94 results on '"Kazandjieva J"'
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2. Use of SEM/EDX methods for the analysis of ambient particulate matter adhering to the skin surface.
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Mirakovski, D., Damevska, K., Simeonovski, V., Nikolovska, S., Boev, B., Petrov, A., Sijakova Ivanova, T., Zendelska, A., Hadzi‐Nikolova, M., Boev, I., Dimov, G., Darlenski, R., Kazandjieva, J., Damevska, S., and Situm, M.
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PARTICULATE matter ,FLY ash ,AIR pollutants ,SILICON detectors ,AIR pollution - Abstract
Background: The skin is exposed to numerous particulate and gaseous air pollutants. The ones that need particular attention are the particles that adhere to the skin surface, which can later cause direct skin damage. This study aimed to characterize air pollution (AP) particles adhered to the human skin by using scanning electron microscopy (SEM) combined with X‐ray dispersive energy spectrometry (EDX). Methods: Tape stripping was performed from six healthy volunteers exposed to urban AP to collect stratum corneum samples from the cheeks and forehead. The samples were analysed using SEM equipped with EDX system with a silicon drift detector at an accelerating voltage of 20 keV. After the preliminary examination, the particles were located and counted using 1000× magnification. Each particle was analysed, increasing magnification up to 5000× for precise dimension measurement and elemental composition analysis. At least 100 fields or a surface of approximately 1 mm2 were examined. Results: Particles adhered to the skin were identified in all samples, with a particle load ranging from 729 to 4525. The average area and perimeter of all particles identified were 302 ± 260 μm2 and 51 ± 23 μm subsequently, while the equivalent circular diameter was, on average, 14 ± 6 μm. The particles were classified into ten groups based on morphology and elemental composition. Chlorides were the most numerous particle group (21.9%), followed by carbonaceous organic particles (20.3%), silicates (18%), carbonates (16.4%), metal‐rich particles (14%), and a minor number of bioaerosols, quartz‐like, and fly ash particles. Conclusion: The SEM–EDX analysis provides evidence of the contamination of exposed skin to various airborne PM of natural or anthropogenic origin. This method may provide new insights into the link between exposure to AP and AP‐induced skin damage. [ABSTRACT FROM AUTHOR]
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- 2022
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3. Topical timolol maleate for treatment of infantile haemangiomas: preliminary results of a prospective study
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Semkova, K. and Kazandjieva, J.
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- 2013
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4. Scoring the proliferative activity of haemangioma of infancy: state of the art
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Semkova, K. and Kazandjieva, J.
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- 2013
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5. Skin barrier damage correlates with increased skin irritation and sensitization in atopic dermatitis: FC4.08
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Darlenski, R., Kazandjieva, J., Nikolova, A., and Tsankov, N.
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- 2010
6. Foreign-body granuloma of the penis in sexually active individuals (penile paraffinoma)
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Pehlivanov, G, Kavaklieva, S, Kazandjieva, J, Kapnilov, D, and Tsankov, N
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- 2008
7. The Objective Severity Assessment of Atopic Dermatitis (OSAAD) score: validity, reliability and sensitivity in adult patients with atopic dermatitis
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Angelova-Fischer, I., Bauer, A., Hipler, U. C., Petrov, I., Kazandjieva, J., Bruckner, T., Diepgen, T., Tsankov, N., Williams, M., Fischer, T. W., Elsner, P., and Fluhr, J. W.
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- 2005
8. Henna: allergic reactions due to temporary tattoos
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Kazandjieva, J., Balabanova, M., and Tsankov, N.
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- 2003
9. Angiotensin-converting enzyme inhibitors and psoriasis: FC21–1
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Kazandjieva, J., Drenovska, K., Mashal, R., and Tsankov, N.
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- 1998
10. Drug-Induced Psoriasis: Recognition and Management.
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Tsankov, N., Angelova, I., and Kazandjieva, J.
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PSORIASIS treatment ,DRUG side effects - Abstract
As psoriasis is a common skin disorder, knowledge of the factors that may induce, trigger, or exacerbate the disease is of primary importance in clinical practice. Drug intake is a major concern in this respect, as new drugs are constantly being added to the list of factors that may influence the course of the disease. Drug ingestion may result in exacerbation of pre-existing psoriasis, in induction of psoriatic lesions on clinically uninvolved skin in patients with psoriasis, or in precipitation of the disease in persons without family history of psoriasis or in predisposed individuals. In view of their relationship to drug-provoked psoriasis, therapeutic agents may be classified as drugs with strong evidence for a causal relationship to psoriasis, drugs about which there are considerable but insufficient data to support the induction or aggravation of the disease, and drugs that are occasionally reported to be associated with aggravation or induction. This review focuses on the most common causative agents for drug-induced, drug-triggered, or drug-aggravated psoriasis, such as β-blockers, lithium, synthetic antimalarial drugs, nonsteroidal anti-inflammatory agents, and tetracyclines. Latency periods, pathogenetic mechanisms of action, clinical and histologic findings, and management guidelines for each drug are discussed to help clinicians to treat patients with suspected drug-influenced psoriasis. [ABSTRACT FROM AUTHOR]
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- 2000
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11. Unprofessional tattoos in Bulgaria - psychological aspects.
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Kazandjieva, J., Kamarashev, J., Kadurina, M., and Tsankov, N.
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TATTOOING , *BODY art , *BODY marking , *COMMUNISTS , *SOCIALISTS - Abstract
Background People suffered many psychic traumas during the period of the communist rule which altered their perception of the outer world and of themselves. For many their skin became a place where their frustration could be expressed. Up to now the psychological aspects of tattoos in the countries from Eastern Europe have been decidedly understudied. Method We have studied over 100 tattoos, done after the end of World War II in Bulgaria. Aim To examine the motivations for getting tattoos and their symbolic meanings. Conclusions On the ground of motivation three main groups were differentiated. The first group comprises lines and drawings without any meaning or sense, which could be interpreted as a pure form of autoaggression. The second group consisted of symbols of resistance - anticommunist, promonarchic, etc. The closed character of the socialist society brought to life the third group of motives - symbols of the "west" and of the so called "western way of life". Many of the tattoos observed by us were self-made and carried an element of self-inflicted injury. [ABSTRACT FROM AUTHOR]
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- 1995
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12. Tufted hair folliculitis: a case report and literature review.
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Broshtilova, Valentina, Bardarov, Emil, Kazandjieva, J., and Marina, S.
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- 2011
13. Granuloma formation after oil-soluble vitamin D injection for lip augmentation - case report.
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Kamouna, B., Litov, I., Bardarov, E., Broshtilova, V., Miteva, L., and Kazandjieva, J.
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GRANULOMA ,DISEASES in women - Abstract
A letter to the editor is presented on the case of nodular fibrosis and granuloma formation in a woman.
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- 2016
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14. Acute inflammatory tinea manuum caused by Nannizzia gypsea transmitted by an African pygmy hedgehog.
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Gergovska M, Hitova M, Manuelyan K, and Kazandjieva J
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- Animals, Humans, Acute Disease, Female, Adult, Hedgehogs microbiology, Tinea microbiology, Tinea diagnosis
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- 2024
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15. Skin Cryobranding-A Worrisome Trend among Bulgarian Children.
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Milkova K, Kazandjieva J, and Darlenski R
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- Child, Humans, Bulgaria, Cold Temperature, Burns
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- 2024
16. A new case of contact allergic reaction caused by topical timolol and literature review.
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Mahmoud I, Gergovska M, and Kazandjieva J
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- Humans, Patch Tests, Female, Adrenergic beta-Antagonists adverse effects, Adrenergic beta-Antagonists administration & dosage, Middle Aged, Timolol adverse effects, Timolol administration & dosage, Dermatitis, Allergic Contact etiology, Dermatitis, Allergic Contact diagnosis
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- 2024
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17. Lues maligna and HIV mimicking aggressive epidermotropic CD8+ cutaneous T-cell lymphoma.
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Petrova E, Mateeva V, Kafelova A, Saleva-Stateva M, Radeva I, Yancheva N, Dikov T, Kazandjieva J, Miteva L, and Dourmishev L
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- 2023
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18. Allergic contact dermatitis caused by topical propranolol therapy for infantile haemangioma.
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Mahmoud I, Kotirkova D, Gospodinova K, Darlenski R, and Kazandjieva J
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- Humans, Infant, Propranolol adverse effects, Adrenergic beta-Antagonists adverse effects, Dermatitis, Allergic Contact diagnosis, Dermatitis, Allergic Contact etiology, Hemangioma drug therapy
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- 2023
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19. Delayed type hypersensitivity injection site reaction and tolerance induction to liraglutide for the treatment of obesity.
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Yaneva M, Handjieva-Darlenska T, Kazandjieva J, and Darlenski R
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Competing Interests: None disclosed.
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- 2023
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20. Figurate annulare erythemas.
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Kazandjieva J, Bogdanov G, Bogdanov I, and Tsankov N
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T. Colcott Fox (1849-1916) first introduced in 1889 the term "figurate erythemas." According to the clinical pattern, figurate erythemas are annular, circinate, concentric, polycyclic, or arciform. The most important figurate annulare erythemas are erythema annulare centrifugum, erythema marginatum, erythema gyratum repens, erythema migrans, erythema chronicum migrans, and the pediatric annular erythemas. Erythema annulare centrifugum might be due to fungal, bacterial, or viral infections or drugs. It tends to spread centrifugally while developing central clearing. The most common locations are the trunk and the proximal extremities. Individual lesions last from several days to weeks and may resolve spontaneously. Erythema marginatum is one of the criteria for the diagnosis of acute rheumatic fever, but it also might be seen as a symptom of other diseases such as hereditary angioedema with C1-inhibitor deficiency and psittacosis. The typical clinical picture is presented by serpiginous erythematous macules and plaques with central clearing and accentuated borders. Erythema gyratum repens is a figurate erythema associated with internal malignancy. It has been linked especially to lung, esophageal, and breast cancers. Erythema gyratum repens is characterized by multiple erythematous, rounded macules or papules, rapidly progressing and forming concentric bands with an unique wood-grained appearance with desquamation on the edges of the erythema. Erythema chronicum migrans is the most common sign of infection with Borrelia burgdorferi and other Borrelia species. It is characterized by a round or oval erythematous or livid macule with a central depressed or raised area on the spot of a previous tick bite. Erythema migrans grows centrifugally and slowly in a matter of days or weeks. Central clearing is observed in 60% of patients, thus forming a targetoid appearance of the lesion. Many other figurate erythemas can be observed in infancy (pediatric annular erythemas). To this group belong neonatal lupus, erythema gyratum atrophicans transiens neonatale, annular centrifugal erythema, familial annular erythema, annular erythema of infancy, eosinophilic annular erythema, and figurate neutrophilic erythema of infancy. The treatment of the various types of figurate erythemas should be etiologic, and when the underlying condition is addressed, the therapy usually is successful., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Inc.)
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- 2023
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21. COVID-19 vaccine-related eruption of papules and plaques-A case report.
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Kafelova A, Mateeva V, Kazandjieva J, Miteva L, and Dourmishev L
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- Humans, Pruritus, COVID-19 diagnosis, COVID-19 Vaccines adverse effects, Exanthema
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- 2022
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22. Efficacy of a retinoid complex plus anti-inflammatory component cream alone or in combination with prebiotic food supplement in adult acne: A randomized, assessor-blinded, parallel-group, multicenter trial on 184 women.
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Kazandjieva J, Dimitrova J, Sankeva M, Yankov D, Bocheva V, Kircheva K, Gincheva V, Gospodinova K, Andasorova R, Milanova M, Jeleva D, Zlateva P, Vasileva I, Yankova R, Gotseva S, Dakova T, Zografova E, Marina S, Kateva M, Broshtilova V, Todeva V, Tsankov N, Mitova Z, Boyanova N, and Milani M
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- Humans, Adult, Female, Anti-Inflammatory Agents, Emollients therapeutic use, Treatment Outcome, Dietary Supplements adverse effects, Double-Blind Method, Retinoids therapeutic use, Acne Vulgaris drug therapy
- Abstract
Background: Adult female acne (AFA) nowadays is a very common skin condition affecting mainly women aged between 25 and 40. The treatment of AFA could be challenging., Study Aim: We evaluate and compare the efficacy and tolerability of a cream formulation containing two retinoid molecules (hydroxypinacolone/retinyl palmitate) combined with Iris Florentina root extract and a complex of three oligopeptides (C) applied twice a day (morning and evening) alone or in combination (C + O) with a food supplement containing a mixture of prebiotic molecules (FOS&GOS) zinc, lactoferrin, and niacinamide., Subjects and Methods: In a multicenter, randomized, assessor-blinded, 12-week trial, we assessed the efficacy of these two regimens in the evolution of AFA lesions (non-inflammatory: NI-L; inflammatory: IL; and total number of lesions: TL). Additional efficacy endpoints were the evolution of the 6-point (from 0 to 5) GEA and Adult Female Acne Scoring Tool (AFAST) scores., Results: One hundred and eighty-four women (mean age 32 ± 6 years) with AFA agreed to participate after obtaining informed consent. They were randomized (2:1) to the topical product (n = 123) (Group C) or to the combination (n = 61) (Group C + O) treatment. All enrolled patients concluded the trial with no drop-out. At baseline, NI-L, IL, and TL acne lesion count were 15 ± 9, 9 ± 5, and 24 ± 14 in the Group C and 19 ± 8, 9 ± 4, and 29 ± 10 in Group C + O. In comparison with the number of the acne lesions at the baseline, both treatment regimens induced a significant reduction (p = 0.0001, ANOVA test) at Week 12 in NI-L, IL, and TL by -54%, -63%, and - 59% in Group C and by -55%, -73%, and - 61% in the Group C + O, respectively. At Week 12, the absolute IL count reduction vs. baseline was significantly (p = 0.0158) greater in Group C + O (-7.0) in comparison with Group C (-5.5). The GEA absolute score reduction in Group C + O group was significantly greater in comparison with Group C (-1.5 vs. -1.1; p = 0.0097). In the Group C + O, a greater percentage of success treatment (defined as a GEA score of 0/1 at Week 12) was observed in comparison with Group C (39% vs. 27%; p = 0.06). AFAST score at baseline was 2.4 ± 0.5 in group C and 2.8 ± 0.6 in group C + O. AFAST score was reduced by 21% and by 51% after 6 and 12 weeks of treatment in group C and by 22% and 55% in group C + O, respectively. Both treatment regimens were well tolerated. Not relevant adverse events were recorded., Conclusion: A cream containing retinoid molecules and Iris Florentina root extract is effective and well tolerated in the management of AFA. The treatment combination with a prebiotic and anti-inflammatory food supplement offers an additional clinical benefit mainly in reducing inflammatory lesions and improving the severity acne score., (© 2022 Wiley Periodicals LLC.)
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- 2022
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23. Contact pemphigus: does it exist?
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Darlenski R, Kazandjieva J, and Tsankov N
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- Humans, Pemphigus physiopathology, Pemphigus chemically induced
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The entity "contact pemphigus" has been recognized for more than 50 years, however existence of the disease, which is opposed and supported by many, is questionable. Contact pemphigus is defined as pemphigus occurring at the site of local skin contact with different chemicals. Many products have been disclosed as aetiological factors such as pesticides, topical drugs (imiquimod, ketoprofen, phenol, bezoin, polymyxin B sulphate, neomycin and bacitracin), cosmetics, garlic and others. This paper summarizes the current knowledge on contact pemphigus and the chemicals responsible for its aetiology, with an emphasis on mechanisms that may elicit the disease.
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- 2021
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24. Immunopathogenesis and management of polymorphic light eruption.
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Kadurina M, Kazandjieva J, and Bocheva G
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- Humans, Phototherapy, Skin pathology, Sunlight, Sunscreening Agents therapeutic use, Ultraviolet Rays adverse effects, Photosensitivity Disorders drug therapy, Photosensitivity Disorders etiology
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Polymorphic light eruption (PLE) is the most common immunologically mediated photodermatosis, demonstrating many abnormalities caused by critical failure of ultraviolet (UV)-induced immunosuppression. The unique expression of antimicrobial peptides in PLE, which is most likely determined by alteration of microbiome components upon UV exposure, implicates their possible triggering role and pathogenic significance in the eruption. The review aims to clarify current knowledge regarding the immunological disturbances correlated with PLE that serve a base for better understanding of molecular pathogenesis of the disease and the development of new therapeutic strategies. Preventive treatment with broad-spectrum suncreens and sunscreens containing DNA repair enzymes, as well as natural photohardening with graduate exposure to sunlight in early spring could be sufficient in milder cases. Antioxidants and topical calcipotriol are promising approach for adjuvant prevention. Phototherapy, mainly with narrow band UVB rays, is more appropriate method in severe cases of the disease. The established treatment options for PLE include local and systemic glucocorticoids, systemic nonsedative antihistamines for itch relief, and rarely, immunosuppressive drugs in the refractory cases. Like medical photohardening, afamelanotide has the potential of photoprotection by inducing a melanization of the skin. Afamelanotide is believed to be a possible new treatment option for very severe and refractory cases of PLE. Targeting the main pruritogenic cytokine, IL-31, opens a new road for the development of novel therapeutic approaches to combat moderate and severe itching in cases of PLE with intense pruritus., (© 2021 Wiley Periodicals LLC.)
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- 2021
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25. Dermatophyte infection transmitted by an African pygmy hedgehog.
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Gergovska M, Manuelyan K, Hitova M, and Kazandjieva J
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- Animals, Humans, Dermatomycoses diagnosis, Dermatomycoses drug therapy, Hedgehogs
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- 2021
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26. Cutaneous adverse effects of the available COVID-19 vaccines.
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Bogdanov G, Bogdanov I, Kazandjieva J, and Tsankov N
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- Animals, COVID-19 Vaccines, Humans, SARS-CoV-2, COVID-19, Drug-Related Side Effects and Adverse Reactions, Vaccines
- Abstract
Vaccination has played a crucial role in the improvement of global health. Some of the world's deadliest diseases, like smallpox and rinderpest, have been eradicated with the help of vaccines, and many others have been restrained. The appearance of the strain of coronavirus disease 2019 (COVID-19) severe acute respiratory syndrome coronavirus 2 and its impact on global health have made the development of effective and safe vaccines crucial for this new lethal disease. So far, there are three main types of COVID-19 vaccines in use around the world: messenger RNA-based vaccines, adenoviral vector vaccines, and inactivated whole-virus vaccines. Some of them have passed through phase 3 of safety and efficacy trials and are widely used for prophylaxis of COVID-19 infection. A plethora of cutaneous adverse events have been reported, most of them mild or moderate injection-site reactions. Some rare delayed inflammatory reactions such as "COVID arm" have also been reported, posing questions on their pathophysiology and clinical importance. Some rare serious adverse events, such as vaccine-induced prothrombotic immune thrombocytopenia and anaphylaxis, have been described raising great concerns on the safety of some widely spread vaccines. More data need to be collected with further and more detailed analysis. The overall risk of such severe adverse reactions remains extremely low, and the benefits of the existing vaccines in combating the widespread threat of COVID-19 continue to outweigh the risk of their side effects., (Copyright © 2021 Elsevier Ltd. All rights reserved.)
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- 2021
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27. Prevention and occupational hazards for the skin during COVID-19 pandemic.
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Darlenski R, Kazandjieva J, and Tsankov N
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- COVID-19 prevention & control, Disease Progression, Humans, Occupational Diseases etiology, Occupational Diseases prevention & control, Occupational Injuries etiology, Occupational Injuries prevention & control, SARS-CoV-2, Skin Diseases etiology, Skin Diseases prevention & control, COVID-19 epidemiology, Health Personnel, Occupational Diseases classification, Personal Protective Equipment adverse effects, Skin injuries, Skin Diseases classification
- Abstract
The life of medical specialists worldwide has dramatically changed due to the spread of the coronavirus disease 2019 (COVID-19) pandemic. Health care professionals (HCPs) have personally faced the outbreak by being on the first line of the battlefield with the disease and, as such, compose a significant number of people who have contracted COVID-19. We propose a classification and discuss the pathophysiology, clinical findings, and treatments and prevention of the occupational skin hazards COVID-19 poses to HCPs. The multivariate pattern of occupational skin diseases during the COVID-19 pandemic can be classified into four subgroups: mechanical skin injury, moisture-associated skin damage, contact reactions, and exacerbation of preexisting dermatoses. The clinical pattern is versatile, and the most affected skin sites were the ones in contact with the protective equipment. Dermatologists should recognize the plethora of HCPs' occupational skin reactions that are occurring during the COVID-19 pandemic and implement treatment and preventive strategies., Competing Interests: Conflict of interest The authors declare no conflict of interest., (Copyright © 2021 Elsevier Ltd. All rights reserved.)
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- 2021
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28. Aquagenic Syringeal Acrokeratoderma from Extensive Water Immersion during the COVID-19 Pandemic Outbreak.
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Kazandjieva J, Tsankov N, and Darlenski R
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- COVID-19, Child, Coronavirus Infections complications, Coronavirus Infections epidemiology, Female, Humans, Pneumonia, Viral complications, Pneumonia, Viral epidemiology, SARS-CoV-2, Time Factors, Betacoronavirus, Coronavirus Infections prevention & control, Hand Disinfection, Keratoderma, Palmoplantar diagnosis, Keratoderma, Palmoplantar etiology, Pandemics prevention & control, Pneumonia, Viral prevention & control, Water adverse effects
- Published
- 2020
29. Nickel Allergy of the Skin and Beyond.
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Gergovska M, Darlenski R, and Kazandjieva J
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- Diagnosis, Differential, Humans, Immune System Diseases chemically induced, Immune System Diseases diagnosis, Immune System Diseases epidemiology, Immune System Diseases therapy, Nickel adverse effects, Prevalence, Dermatitis, Allergic Contact diagnosis, Dermatitis, Allergic Contact epidemiology, Dermatitis, Allergic Contact etiology, Dermatitis, Allergic Contact therapy, Nickel toxicity
- Abstract
Background: Hypersensitization to nickel is one of the most common contact allergies in the modern world and it is considered to be a major cause of contact dermatitis, especially for hand eczema., Objective: The aim of this paper is to describe many faces of the nickel allergy and to find out different diagnostic, potential strategies for treatment and prevention in hypersensitized patients. A personal clinical experience with practical clinical cases of contact dermatitis to nickel has also been presented., Methods: Electronic databases on this topic was carried out using PubMed-Medline., Results: The literature review identified many articles reporting for nickel contact allergy and pointing the metal as number one allergen in the frequency of positive skin patch test reactions in a large population worldwide. Herein, a summary of the current understanding and evidence on nickel allergy with practical approach and proposed recommendations to the dermatologist, general practitioner, and the allergist were prepared., Conclusion: The prevalence of nickel allergy represents an important socio-economical and health issue. Metal is one of the most common sensitizing agents worldwide. The morbidity due to this metal represents the allergic contact dermatitis and it is constantly growing in many countries. There are also cases of systemic allergic contact dermatitis, where they could be easily misdiagnosed as adverse drug reactions, which lead to delay of the correct diagnosis and inappropriate treatment., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
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- 2020
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30. The rash that becomes purpuric, petechial, hemorrhagic, or ecchymotic.
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Antonov D, Kamarashev J, Kazandjieva J, Neykova T, and Tsankov N
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- Diagnosis, Differential, Exanthema complications, Exanthema diagnosis, Hemorrhage etiology, Hemorrhage pathology, Humans, Exanthema pathology, Skin pathology
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Hemorrhagic rashes are observed in a wide variety of conditions, ranging from harmless to life-threatening. This review offers a stepwise approach, which helps limit the possible differential diagnoses based on the clinical manifestations and the clinical picture. The most common and most important conditions, including infectious, coagulation and embolic disorders, vasculitides, and vasculopathies, are briefly reviewed focusing on morphology. Dermatologists often need to distinguish among infectious, reactive, or autoimmune etiologies of the rash and determine if the condition is dangerous or even life-threatening in order to make the right decision. Dermatologic expertise provides vital input in the diagnosis and care of complex interdisciplinary patients, such as those with sepsis, purpura fulminans, and thrombotic thrombocytopenic purpura., (Copyright © 2019. Published by Elsevier Inc.)
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- 2020
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31. Angioedema as a systemic disease.
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Kazandjieva J and Christoff G
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- Angioedemas, Hereditary, Bradykinin metabolism, Diagnosis, Differential, Histamine metabolism, Humans, Inflammation Mediators metabolism, Leukemia, Lymphocytic, Chronic, B-Cell complications, Lymphoma, Non-Hodgkin complications, Mast Cells pathology, Multiple Myeloma complications, Angioedema diagnosis, Angioedema etiology, Angioedema metabolism, Angioedema pathology
- Abstract
Angioedema is a clinical entity defined as self-limiting edema localized in the deeper layers of the skin and mucosa and lasting for several days. Angioedema can be provoked by bradykinin and/or mast cell mediators, including histamine. Four types of acquired and three types of hereditary angioedema have been identified. The most obvious form of angioedema associated with other systemic disease is acquired angioedema due to C1-inhibitor deficiency. It is characterized by acquired consumption of C1 inhibitor and various underlying disorders, such as multiple myeloma, chronic lymphocytic leukemia, rectal carcinoma, and non-Hodgkin lymphoma. Suspected cases need an accurate differential diagnosis to exclude all other types of acquired and hereditary angioedema., (Copyright © 2019 Elsevier Inc. All rights reserved.)
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- 2019
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32. The skin as a target organ in multisystemic diseases III.
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Tsankov N, Kazandjieva J, and Darlenski R
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- Humans, Skin, Skin Diseases, Skin Physiological Phenomena
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- 2019
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33. Dermatomyositis: Current concepts.
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Bogdanov I, Kazandjieva J, Darlenski R, and Tsankov N
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- Calcineurin Inhibitors therapeutic use, Dermatomyositis epidemiology, Dermatomyositis etiology, Humans, Immunosuppressive Agents therapeutic use, Paraneoplastic Syndromes etiology, Adrenal Cortex Hormones therapeutic use, Dermatomyositis diagnosis, Dermatomyositis drug therapy, Immunologic Factors therapeutic use
- Abstract
Dermatomyositis (DM) is a multifactorial chronic autoimmune disorder with characteristic skin changes and involvement of different organ systems, including the muscles, blood vessels, joints, esophagus, and lungs. In terms of epidemiology, DM affects both children and adults. It is most often observed beyond the age of 40, but there is also a peak of incidence between 5 and 12 years of age. The current paradigm describing the pathophysiology of DM is an autoimmune attack on affected organs that is triggered by environmental factors such as UV exposure, drugs, infection, and lifestyle decisions in genetically susceptible individuals. Importantly, DM is also regarded as a paraneoplastic phenomenon, as cancer may precede, occur concurrently with, or follow the development of the clinical signs of DM. The cutaneous manifestations of DM can be categorized as pathognomonic, characteristic, compatible, less common, rare, recent, and nonspecific. The treatment of DM is a difficult task due to its rarity, its multiple phenotypes, and the fact that the disease may affect multiple organs and is commonly treatment-refractory. The lack of randomized, controlled intervention trials and, until recently, the insufficiency of validated, clinically meaningful outcome instruments in part contribute to the lack of approved treatments., (Copyright © 2018 Elsevier Inc. All rights reserved.)
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- 2018
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34. Drug-induced acne.
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Kazandjieva J and Tsankov N
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- Acne Vulgaris pathology, Adrenal Cortex Hormones adverse effects, Age of Onset, Antineoplastic Agents adverse effects, Antitubercular Agents adverse effects, Humans, Isoniazid adverse effects, Lithium Compounds adverse effects, Testosterone adverse effects, Acne Vulgaris chemically induced
- Abstract
A variety of drugs may provoke acne, with drug-induced acne (DIA) often having some specific clinical and histopathologic features. DIA is characterized by a medical history of drug intake, sudden onset, and an unusual age of onset, with a monomorphous eruption of inflammatory papules or papulopustules. The location of the acne lesions is beyond the seborrheic zone. Corticosteroids, anabolic steroids, testosterone, halogens, isoniazid, lithium, and some new anticancer agents are drugs with undoubted causal relationship to acne. The diagnosis of DIA is made by a detailed history with a record of drug onset, dosage regimen and therapy duration, absence of additional triggering factors, and clinical relationship between the introduction of the drug and the onset of an acne-like eruption. In all cases, the withdrawal of the drug should be followed by lessening of the acne lesions., (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Published
- 2017
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35. Acrally distributed dermatoses: Vascular dermatoses (purpura and vasculitis).
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Kazandjieva J, Antonov D, Kamarashev J, and Tsankov N
- Subjects
- Arm, Churg-Strauss Syndrome complications, Churg-Strauss Syndrome pathology, Embolism complications, Granulomatosis with Polyangiitis complications, Humans, IgA Vasculitis complications, IgA Vasculitis diagnosis, IgA Vasculitis therapy, Pigmentation Disorders complications, Pigmentation Disorders diagnosis, Pigmentation Disorders pathology, Polyarteritis Nodosa complications, Polyarteritis Nodosa pathology, Purpura diagnosis, Purpura pathology, Purpura Fulminans complications, Vasculitis diagnosis, Vasculitis drug therapy, Vasculitis pathology, Foot Dermatoses etiology, Hand Dermatoses etiology, Leg Dermatoses etiology, Purpura complications, Skin Diseases, Vascular complications, Vasculitis complications
- Abstract
Purpuric lesions appear in acral distribution in a variety of conditions and often provide clues to the clinical diagnosis. Purpuric means "hemorrhagic"-that is, the lesions do not blanch from pressure. This review focuses on dermatoses that produce hemorrhagic lesions in acral distribution from the large groups of the vasculitic diseases and their mimics. Cutaneous small vessel vasculitis is confined to the skin, involves mainly postcapillary venules, and has the hallmark manifestation of palpable purpura. Henoch-Schönlein purpura is an immune complex-mediated systemic vasculitis of the small vessels with manifestations from the skin, joints, kidneys, and gastrointestinal system. Only cases where the immune complexes contain immunoglobulin A type are classified as Henoch-Schönlein purpura. Cryoglobulinemic vasculitis is induced by the deposition of cold-precipitated immune complexes in the small vessels. Urticarial vasculitis comprises a spectrum of conditions with the characteristic course of chronic urticaria, with wheals that persist longer than 24 hours, leave hyperpigmentation, and have leukocytoclastic vasculitis on histologic examination. Polyarteritis nodosa is a rare multisystem, segmental necrotizing vasculitis of mainly the medium-sized vessels. Pigmented purpuric dermatoses are chronic benign dermatoses characterized by petechiae, purpura, and increased skin pigmentation. The hallmark of pigmented purpuric dermatoses is their orange-brown, speckled, cayenne pepper-like discoloration., (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Published
- 2017
- Full Text
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36. Reaching a consensus on scoring instruments for infantile hemangioma: are we there yet?
- Author
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Semkova K and Kazandjieva J
- Subjects
- Hemangioma, Humans, Infant, Consensus, Hemangioma, Capillary
- Published
- 2016
- Full Text
- View/download PDF
37. The skin as a target organ in multisystemic diseases II.
- Author
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Tsankov N, Kazandjieva J, and Darlenski R
- Subjects
- Humans, Skin Diseases etiology
- Abstract
Progress in medical science has given a new reading to the claim that the skin could be a mirror of the pathological changes found in the internal organs. The concept that we previously promoted is furthered in this issue; namely that the greatest part of skin diseases are systemic ones. In this issue we focus on another group of diseases with systemic involvement and skin manifestations. We review such inflammatory conditions as lichen planus, autoinflammatory syndromes, and pyoderma gangrenosum focusing on their systemic involvement. We have not missed such classic examples of systemic involvement as scleroderma. In this issue we have included two infectious diseases with multi-organ involvement: Lyme disease and Herpes simplex. In contrast to our previous work, we have also addressed neoplastic diseases - namely mycosis fungoides., (Copyright © 2015. Published by Elsevier Inc.)
- Published
- 2015
- Full Text
- View/download PDF
38. Systemic drug reactions with skin involvement: Stevens-Johnson syndrome, toxic epidermal necrolysis, and DRESS.
- Author
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Darlenski R, Kazandjieva J, and Tsankov N
- Subjects
- Humans, Male, Middle Aged, Drug Eruptions diagnosis, Drug Eruptions etiology, Drug Hypersensitivity Syndrome diagnosis, Drug Hypersensitivity Syndrome etiology, Stevens-Johnson Syndrome diagnosis, Stevens-Johnson Syndrome etiology
- Abstract
Skin is often affected in adverse drug reactions. Although the majority of cutaneous adverse drug reactions are benign and self-limiting, Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug rash with eosinophilia and systemic symptoms (DRESS), affecting multiple organs and systems, are potentially fatal. Many organs can be affected, including the mucosal membranes, gastrointestinal tract, liver, lungs, kidneys, and eyes. We discuss the causes, pathophysiologic aspects, and main clinical features of SJS, TEN, and DRESS as systemic diseases with skin involvement., (Copyright © 2015 Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
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39. Hyperhidrosis, bromhidrosis, and chromhidrosis: Fold (intertriginous) dermatoses.
- Author
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Semkova K, Gergovska M, Kazandjieva J, and Tsankov N
- Subjects
- Biopsy, Needle, Eccrine Glands metabolism, Female, Humans, Hyperhidrosis epidemiology, Hyperhidrosis physiopathology, Immunohistochemistry, Incidence, Intertrigo epidemiology, Intertrigo physiopathology, Male, Prognosis, Risk Assessment, Severity of Illness Index, Skin Care methods, Skin Diseases epidemiology, Skin Diseases pathology, Skin Diseases physiopathology, Sweat Glands metabolism, Sweat Glands physiopathology, Eccrine Glands physiopathology, Hygiene, Hyperhidrosis pathology, Intertrigo pathology
- Abstract
Human sweat glands disorders are common and can have a significant impact on the quality of life and on professional, social, and emotional burdens. It is of paramount importance to diagnose and treat them properly to ensure optimal patient care. Hyperhidrosis is characterized by increased sweat secretion, which can be idiopathic or secondary to other systemic conditions. Numerous therapeutic options have been introduced with variable success. Novel methods with microwave-based and ultrasound devices have been developed and are currently tested in comparison to the conventional approaches. All treatment options for hyperhidrosis require frequent monitoring by a dermatologist for evaluation of the therapeutic progress. Bromhidrosis and chromhidrosis are rare disorders but are still equally disabling as hyperhidrosis. Bromhidrosis occurs secondary to excessive secretion from either apocrine or eccrine glands that become malodorous on bacterial breakdown. The condition is further aggravated by poor hygiene or underlying disorders promoting bacterial overgrowth, including diabetes, intertrigo, erythrasma, and obesity. Chromhidrosis is a rare dermatologic disorder characterized by secretion of colored sweat with a predilection for the axillary area and the face. Treatment is challenging in that the condition usually recurs after discontinuation of therapy and persists until the age-related regression of the sweat glands., (Copyright © 2015 Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
40. Hemangioma Activity and Severity Index (HASI), an instrument for evaluating infantile hemangioma: development and preliminary validation.
- Author
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Semkova K, Kazandjieva J, Kadurina M, and Tsankov N
- Subjects
- Humans, Infant, Pilot Projects, Reproducibility of Results, Hemangioma pathology, Severity of Illness Index
- Abstract
Background: Infantile hemangiomas (IHs) are the most common benign vascular tumors of infancy. Their evaluation is important and requires the use of a unified scoring system., Objectives: We designed a novel scoring index, the Hemangioma Activity and Severity Index (HASI), for the clinical evaluation of IHs. The purpose of this pilot study was to validate the HASI., Methods: The HASI was evaluated for validity by an external panel of experts. The reliability study included 59 children with superficial and mixed hemangiomas. Patients attended an assessment visit and a subsequent visit three days later for a second scoring. They were then followed up monthly for six months and scored at each visit by two investigators separately., Results: Interclass correlation coefficients (ICCs) for inter-rater reliability were 0.82 (95% confidence interval [CI] 0.75-0.88) for IH activity and 0.94 (95% CI 0.91-0.96) for IH severity. Intra-rater reliability was high, with negligible mean differences of 0.3 and 0.4 points between the two ratings. The average time required to complete the scoring was 2.5 minutes., Conclusions: Our preliminary studies on the HASI show promising results in terms of its clinical utility and applicability in practice. It could be used by physicians as an objective instrument for the scoring of IHs., (© 2014 The International Society of Dermatology.)
- Published
- 2015
- Full Text
- View/download PDF
41. Complications of injected vitamin E as a filler for lip augmentation: case series and therapeutic approach.
- Author
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Kamouna B, Darlenski R, Kazandjieva J, Balabanova M, Dourmishev L, Negentsova Z, Etugov D, Mirchevska B, and Tsankov N
- Subjects
- Adolescent, Adrenal Cortex Hormones therapeutic use, Adult, Anti-Bacterial Agents therapeutic use, Biopsy, Dermal Fillers administration & dosage, Drug Therapy, Combination, Female, Granuloma, Foreign-Body diagnosis, Granuloma, Foreign-Body drug therapy, Humans, Injections, Subcutaneous, Lip Diseases diagnosis, Lip Diseases drug therapy, Treatment Outcome, Vitamin E administration & dosage, Young Adult, Cosmetic Techniques adverse effects, Dermal Fillers adverse effects, Granuloma, Foreign-Body chemically induced, Lip Diseases chemically induced, Rejuvenation, Vitamin E adverse effects
- Abstract
The strive for proficient cosmetic facial appearance is growing in the past decades. Fillers for tissue augmentation are gaining wide popularity. Uncertified products based on oleic solutions are applied by untrained staff, thus growing the risk for certain complications such as infections, allergic and irritant contact dermatitis, and lipogranuloma formation. We present a series of three cases lipogranuloma after liquid vitamin E injection for lip augmentation. In all cases, painful edema at the injected area followed the procedure. The patients were presented with erythema, firm indurations of the lips and the perioral skin, and tenderness. Histological examination of skin biopsies showed round-ovoid cavities of varying sizes, resulting in a Swiss cheese-like appearance, consistent with a lipogranuloma. In this paper, we propose a protocol for treatment of this specific complication with systemic corticosteroids and a broad spectrum antibiotics., (© 2015 Wiley Periodicals, Inc.)
- Published
- 2015
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42. Lactic acid sting test does not differentiate between facial and generalized skin functional impairment in sensitive skin in atopic dermatitis and rosacea.
- Author
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Darlenski R, Kazandjieva J, Fluhr JW, Maurer M, and Tsankov N
- Subjects
- Dermatitis, Atopic diagnosis, Humans, Rosacea diagnosis, Dermatitis, Atopic physiopathology, Lactic Acid, Rosacea physiopathology, Skin physiopathology
- Published
- 2014
- Full Text
- View/download PDF
43. Phytodermatitis to Euphorbia trigona.
- Author
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Darlenski R, Kazandjieva J, and Tsankov N
- Subjects
- Acute Disease, Dermatitis, Contact drug therapy, Dermatitis, Contact pathology, Erythema drug therapy, Erythema etiology, Erythema pathology, Facial Dermatoses drug therapy, Facial Dermatoses pathology, Female, Humans, Loratadine administration & dosage, Loratadine analogs & derivatives, Loratadine therapeutic use, Methylprednisolone administration & dosage, Methylprednisolone analogs & derivatives, Methylprednisolone therapeutic use, Middle Aged, Patch Tests, Pruritus etiology, Dermatitis, Contact etiology, Euphorbia adverse effects, Facial Dermatoses etiology
- Abstract
A 56-year-old Caucasian woman presented with acute onset of dermatitis on her face accompanied by intense itching. The patient reported that the condition began after cleaning a decorative plant, Euphorbia trigona, and contact with some drops of the plant's latex sap released upon cutting its leaves. The clinical examination revealed erythema and edema of the infraorbital and perioral regions (Figure 1). The patient was in otherwise good general health, had no personal or family history of systemic or skin disease, and was not receiving any concomitant medications. Therapy with topical methylprednisolone aceponate 0.1% cream once daily was initiated and systemic desloratadine 5 mg tablets once daily was administered for the intense itch. Seven days after the introduction of the treatment a significant improvement was noticed (Figure 2). Patch testing with the leaves of the plant as well as with the latex sap was undertaken in order to prove the causative role (Figures 3 and 4). Strongly positive reactions with bulla formation were observed on day 2 and 3, most likely suggesting acute irritation instead of true delayed hypersensitivity.
- Published
- 2014
44. Chronic urticaria as a systemic disease.
- Author
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Darlenski R, Kazandjieva J, Zuberbier T, and Tsankov N
- Subjects
- Autoimmune Diseases complications, Bacterial Infections complications, Central Nervous System Diseases complications, Chronic Disease, Dermatitis, Atopic complications, Humans, Urticaria psychology, Urticaria complications, Urticaria immunology
- Abstract
Urticaria is one of the most common diseases seen in everyday dermatologic practice, characterized by the development of wheals, angioedema, or both. While acute urticaria is mostly related to allergic or pseudoallergic reaction to food, drugs, or infections, chronic urticaria is a more complex disease with different additional ethiopathologic mechanisms and evoking factors. While urticaria is an undisputed disease of the skin, growing evidence supports, like in other dermatologic diseases, the concept of urticaria as a systemic disease with clinical symptoms and signs predominantly presenting on the skin. In this review, we describe the evidence and association between chronic urticaria and a variety of disorders, such as autoimmune diseases, atopy, infections, metabolic conditions, and neoplastic disorders. Beyond the mechanistic association, the possible common underlying pathomechanisms, such as systemic immunologic processes, are discussed., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2014
- Full Text
- View/download PDF
45. Are skin diseases systemic ones?: I.
- Author
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Tsankov N, Kazandjieva J, and Darlenski R
- Subjects
- Autoimmune Diseases complications, Digestive System Diseases complications, Eye Diseases complications, Hematologic Diseases complications, Humans, Inflammation complications, Lung Diseases complications, Metabolic Diseases complications, Otorhinolaryngologic Diseases complications, Urologic Diseases complications, Vascular Diseases complications, Skin Diseases complications
- Published
- 2014
- Full Text
- View/download PDF
46. Atopic dermatitis as a systemic disease.
- Author
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Darlenski R, Kazandjieva J, Hristakieva E, and Fluhr JW
- Subjects
- Autoimmune Diseases complications, Dermatitis, Atopic immunology, Dermatitis, Atopic psychology, Disease Progression, Eye Diseases complications, Gastrointestinal Diseases complications, Humans, Kidney Diseases complications, Metabolic Syndrome complications, Dermatitis, Atopic complications, Epidermis physiopathology
- Abstract
Atopic dermatitis (AD) is a chronic inflammatory disease that seriously affects the quality of life of these patients. Both immune deviations and epidermal barrier deficiency have been defined as pathophysiologic mechanisms in the disease development. The atopic march, or the natural progression form atopic dermatitis in infancy to asthma and allergic rhinitis, is a classic example for the multiorgan involvement in atopy. It has been hypothesized that epidermal barrier impairment is the primary pathologic condition responsible for the atopic march. In recent decades, a growing body of evidence has accumulated that AD can be accompanied by a variety of systemic diseases, such as autoimmune disorders, ophthalmologic involvement, eosinophilic gastroenteritis, inflammatory bowel disease, nephritic syndrome, and metabolic diseases. This contribution reviews these associations and focuses on the possible common underlying mechanisms of AD and the associated syndromes. We present a concept on AD as a multiorgan systemic disease., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2014
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- View/download PDF
47. Contact dermatitis in a child from methlychloroisothiazolinone and methylisothiazolinone in moist wipes.
- Author
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Kazandjieva J, Gergovska M, and Darlenski R
- Subjects
- Buttocks, Child, Preschool, Female, Humans, Patch Tests, Dermatitis, Contact etiology, Preservatives, Pharmaceutical adverse effects, Thiazoles adverse effects
- Abstract
Contact allergic reactions to methlychloroisothiazolinone/methylisothiazolinone also widely known as Kathon CG have been reported extensively reported. It is one of the most commonly used preservatives in rinse-off products, cosmetics, and others. Herein, a case of a 50-year-old girl is presented with chronic dermatitis in the anogenital area. The patient was patch tested and had positive reaction to Kathon CG. The detailed history taking revealed that the allergen was present in the moist cleaning wipes used instead of dry toilet paper. The presented case serves as a basis for a appraisal of the use of this preservative in wet wipes. In addition, the duration of the patch test protocol in children has also been discussed., (© 2012 Wiley Periodicals, Inc.)
- Published
- 2014
- Full Text
- View/download PDF
48. Rapid complete regression of an early infantile hemangioma with topical timolol gel.
- Author
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Semkova K and Kazandjieva J
- Subjects
- Administration, Cutaneous, Adrenergic beta-Antagonists administration & dosage, Gels, Humans, Infant, Male, Timolol administration & dosage, Treatment Outcome, Adrenergic beta-Antagonists therapeutic use, Head and Neck Neoplasms drug therapy, Hemangioma, Capillary drug therapy, Neoplastic Syndromes, Hereditary drug therapy, Scalp, Skin Neoplasms drug therapy, Timolol therapeutic use
- Published
- 2014
- Full Text
- View/download PDF
49. The red face revisited: connective tissue disorders.
- Author
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Kazandjieva J, Tsankov N, and Pramatarov K
- Subjects
- Erythema etiology, Humans, Mixed Connective Tissue Disease complications, Dermatomyositis complications, Facial Dermatoses etiology, Lupus Erythematosus, Discoid complications, Lupus Erythematosus, Systemic complications, Scleroderma, Systemic complications
- Abstract
Red face is not a rare finding in patients with connective tissue disorders. The malar eruption is the most frequent cutaneous manifestation of systemic lupus erythematosus (LE). This condition is more apparent among fair-skinned individuals, and it usually appears after sun exposure. A very important clinical sign is that nasolabial folds remain free of any erythematous or other changes. With subacute cutaneous LE, sun exposure can provoke a red face that resembles the malar eruption of systemic LE. The typical clinical findings of chronic cutaneous LE are the discoid lesions. There is a clinical form of chronic cutaneous LE called erythema perstans faciei. This form is purely erythematous, and it usually appears on the face. Other rare "red face" forms of chronic cutaneous LE are LE tumidus and LE telangiectaticus. Red face is not typical of systemic sclerosis, but facial telangiectasias are frequent, especially with CREST (calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) syndrome. The differential diagnoses of other red face manifestations are easy due to the additional findings. Telangiectasias are accompanied by calcinosis, sclerodactyly, digital ischemia, and Raynaud disease. Many studies mention telangiectasias as markers of the severity of the systemic sclerosis, the disease duration, any pulmonary arterial hypertension, and any esophageal involvement. Purple- or violet-colored upper eyelids are the hallmark and one of the first clinical signs that is helpful for the diagnosis of dermatomyositis. This violaceous to dusky erythema can extend over the whole face and the upper aspects of the trunk. Erythematous changes on the face that are different from those of the heliotrope sign which occurs with dermatomyositis may be observed in both sun-exposed skin and non-sun-exposed skin. Malar and facial erythema, linear extensor erythema, V-sign or shawl sign, and other photodistributed eruptions can also appear., (© 2013 Elsevier Inc. All rights reserved.)
- Published
- 2014
- Full Text
- View/download PDF
50. Acute irritant threshold correlates with barrier function, skin hydration and contact hypersensitivity in atopic dermatitis and rosacea.
- Author
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Darlenski R, Kazandjieva J, Tsankov N, and Fluhr JW
- Subjects
- Adult, Case-Control Studies, Dermatitis, Atopic chemically induced, Epidermis drug effects, Female, Humans, Male, Middle Aged, Patch Tests, Permeability, Rosacea chemically induced, Skin drug effects, Skin pathology, Sodium Dodecyl Sulfate chemistry, Water Loss, Insensible physiology, Dermatitis, Atopic physiopathology, Dermatitis, Contact physiopathology, Irritants chemistry, Rosacea physiopathology
- Abstract
The aim of the study was to disclose interactions between epidermal barrier, skin irritation and sensitization in healthy and diseased skin. Transepidermal water loss (TEWL) and stratum corneum hydration (SCH) were assessed in adult patients with atopic dermatitis (AD), rosacea and healthy controls. A 4-h patch test with seven concentrations of sodium lauryl sulphate was performed to determine the irritant threshold (IT). Contact sensitization pattern was revealed by patch testing with European baseline series. Subjects with a lower IT had higher TEWL values and lower SCH. Subjects with positive allergic reactions had significantly lower IT. In AD, epidermal barrier deterioration was detected on both volar forearm and nasolabial fold, while in rosacea, impeded skin physiology parameters were observed on the facial skin only, suggesting that barrier impediment is restricted to the face in rosacea, in contrast with AD where the abnormal skin physiology is generalized., (© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
- Published
- 2013
- Full Text
- View/download PDF
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