9 results on '"Chelitis"'
Search Results
2. Correction of senile drooling using the nasolabial sling.
- Author
-
Pacifico, Marc D. and Ritz, Morris
- Subjects
LABIAL frenulum ,AGING ,SURGICAL flaps ,OPERATIVE surgery ,THERAPEUTIC use of hyaluronic acid ,BOTULINUM toxin ,THERAPEUTICS ,DROOLING - Abstract
Summary: Background: Facial aging, resulting in lower facial ptosis often leads to downward angulation of the oral commissure, which may lead to troublesome angular chelitis. In this paper we present a treatment pathway for management of such patients. Methods: Treatment initially involves a combination of hyaluronic acid injection into the marionette lines and botulinum toxin A to the depressor anguli oris. If this treatment is unsuccessful patients then undergo the creation of a nasolabial sling, using bilateral superiorly-based nasolabial flaps tunnelled through the lower lip with transection of the depressor anguli oris on each side. In addition, two passes of the CO
2 laser are used to resurface the areas of chelitis and to tighten the tissues. Five patients have undergone treatment for their angular chelitis using one or a combination of these methods. Results: All cases were successfully treated and no recurrences occurred. Furthermore, all patients were satisfied with their outcome. Conclusions: Little is available in the literature on the management of this disorder. In this paper we detail our surgical technique, discuss the issues encountered and review the current recommended treatment for this difficult problem. [Copyright &y& Elsevier]- Published
- 2010
- Full Text
- View/download PDF
3. Ectodermal dysplasia-skin fragility syndrome: A rare case report
- Author
-
Subhash Kashyap, Vinay Shanker, and Neelam Sharma
- Subjects
Chelitis ,ectodermal dysplasia/skin fragility syndrome ,granulosis rubra nasi ,McGrath syndrome ,palmoplantar keratoderma ,Dermatology ,RL1-803 - Abstract
Ectodermal dysplasia/skin fragility syndrome (ED-SFS) is a newly described autosomal recessive disorder characterized by skin fragility and blistering, palmoplantar keratoderma, abnormal hair growth, nail dystrophy, and occasionally defective sweating. It results from mutations in the PKP1 gene encoding plakophilin 1 (PKP1), which is an important component of stratifying epithelial desmosomes and a nuclear component of many cell types. Only 12 cases of this rare genodermatosis have been reported so far. We present an unusual case of ED-SFS in a 12-year boy who was normal at birth but subsequently developed skin fragility, hair and nail deformities, abnormal dentition, palmoplantar keratoderma, and abnormal sweating but no systemic abnormality.
- Published
- 2015
- Full Text
- View/download PDF
4. Ectodermal Dysplasia-Skin Fragility Syndrome: A Rare Case Report.
- Author
-
Kashyap, Subhash, Shanker, Vinay, and Sharma, Neelam
- Subjects
- *
ECTODERMAL dysplasia , *DIFFERENTIAL diagnosis , *HISTOLOGY , *SYMPTOMS , *DIAGNOSIS - Abstract
Ectodermal dysplasia/skin fragility syndrome (ED-SFS) is a newly described autosomal recessive disorder characterized by skin fragility and blistering, palmoplantar keratoderma, abnormal hair growth, nail dystrophy, and occasionally defective sweating. It results from mutations in the PKP1 gene encoding plakophilin 1 (PKP1), which is an important component of stratifying epithelial desmosomes and a nuclear component of many cell types. Only 12 cases of this rare genodermatosis have been reported so far. We present an unusual case of ED-SFS in a 12-year boy who was normal at birth but subsequently developed skin fragility, hair and nail deformities, abnormal dentition, palmoplantar keratoderma, and abnormal sweating but no systemic abnormality. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
5. Plasma Cell Cheilitis: A Clinicopathological and Immunohistochemical Study of 13 Cases
- Author
-
Won Joo Kwon, Kwang Ho Kim, Chul Woo Kim, Sang Seok Kim, Jae Won Ha, Ji Eun Hahm, and Jin Yong Lee
- Subjects
Pathology ,medicine.medical_specialty ,Plasma cells ,medicine.diagnostic_test ,business.industry ,H&E stain ,030206 dentistry ,Dermatology ,Plasma cell ,Immunoglobulin light chain ,Chelitis ,Lambda chain ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,medicine.anatomical_structure ,Dermis ,Biopsy ,medicine ,Etiology ,Immunohistochemistry ,Histopathology ,Original Article ,Kappa chain ,business - Abstract
Background Plasma cell cheilitis is an unusual benign plasma cell proliferative disease of an unknown etiology that typically presents on the lip. Objective The aim of this study was to investigate the clinicopathological characteristics of 13 cases of plasma cell cheilitis. Methods The present study investigated the clinical manifestations, treatment modalities, and outcome of 13 patients diagnosed with plasma cell cheilitis from 2011 to 2016 at Kangdong Sacred Heart Hospital and Hallym University Sacred Heart Hospital. Biopsy specimens of the all cases were evaluated using conventional hematoxylin and eosin staining with kappa and lambda immunoglobulin light chain immunohistochemistry. Results The age of the patients ranged from 39 to 86 years (mean, 64.7 years), with male predominance. Histopathologically, 61.5% and 38.5% of patients showed band-like and pan dermal plasmacytic infiltrates, respectively. Eosinophilic infiltration was noted in 69.2% of patients. All cases showed both kappa and lambda immunoglobulin light chain reactivities, and kappa predominance was confirmed in 9 patients (69.2%). A majority of the patients was treated with local therapy, such as intralesional steroid injection with topical tacrolimus. Among the 13 patients, plasma cell cheilitis completely resolved, partially resolved, and recurred in 3 (23.1%), 5 (38.5%), and 5 patients (38.5%), respectively. Conclusion Plasma cell cheilitis presented as erosive edematous circumscribed patches or plaques affecting mainly the lower lip of elderly male patients. The majority of histopathology cases showed characteristic plasma cell aggregation on the upper dermis that was immunopositive for immunoglobulin light chain, with kappa predominance.
- Published
- 2016
6. Análise de queilite actínica por espectroscopia micro FT-IR
- Author
-
Carvalho, Luis Felipe das Chagas e Silva de [UNESP], Universidade Estadual Paulista (Unesp), and Almeida, Janete Dias [UNESP]
- Subjects
Queilite ,Fourier, Espectroscopia de infravermelho por transformada de ,Infrared spectroscopy fourier transform ,Análise espectral ,Chelitis ,Spectrum analysis - Abstract
Made available in DSpace on 2014-06-11T19:33:24Z (GMT). No. of bitstreams: 0 Previous issue date: 2011-06-20Bitstream added on 2014-06-13T20:24:54Z : No. of bitstreams: 1 carvalho_lfcs_dr_sjc.pdf: 1285800 bytes, checksum: e974f0ebe5242c6acaeec015aadb3843 (MD5) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) A queilite actínica (QA) é uma lesão considerada potencialmente cancerizável, localizada principalmente em lábio inferior e causada pela exposição crônica à radiação UV. A Espectroscopia FT-IR fornece informações moleculares através de fenômenos ópticos observado pela vibração de suas moléculas. Tem sido empregada em estudos biológicos para a caracterização de alterações neoplásicas. No entanto, são escassos os estudos que envolvam processos potencialmente cancerizáveis. Objetivou-se avaliar QAs através da espectroscopia micro FT-IR com relação aos seus aspectos moleculares para região de fingerprint (900-1800 cm-1) e altos números de onda (2800-3600 cm-1), e ainda verificar a análise dos componentes principais (PCA) e regressão logística binária (RLB) como modelo de diagnóstico. Foram avaliadas 14 amostras de QA e 14 amostras de mucosas normal (MN), obtendo-se 5 espectros por amostra, totalizando 140 espectros avaliados (70 de cada grupo). Os resultados demonstrados pela análise dos componentes principais revelaram pelo gráfico de scree plot que os dez primeiros PCs deveriam ser utilizados na análise. As maiores variações observadas pelo gráfico de loading plot relacionaram-se aos modos vibracionais do colágeno, ácidos nucléicos, lipídios e água confinada. O modelo de regressão logística binária mostrou 80,6% de pares concordantes para região de fingerprint e 81,7% de pares concordantes para a região de altos números de onda. Concluiu-se que a espectroscopia micro FT-IR provê características moleculares importantes das 19 amostras de QA, evidenciadas tanto na região de fingerprint como na de altos números de onda. Actinic cheilitis (AC) is a potentially precancerous lesion, located primarily in lower lip caused by chronic exposure to UV radiation. The FT-IR spectroscopy provides molecular information through optical properties observed by the vibration of its molecules. This technique has been used in biological studies for characterization of neoplastic tissues. However, there are few studies involving potentially cancerous processes. This study aimed to evaluate molecular changes on AC through micro FT-IR spectroscopy in fingerprint (900-1800 cm-1) and high wave numbers (2800-3600 cm- 1) region, and also to verify the principal components analysis (PCA) and binary logistic regression (BLR) as a model of diagnosis. We evaluated 14 samples of AC and 14 samples of normal mucosa (NM), resulting in 5 spectra per sample, totalling 140 spectra analyzed (70 from each group). The results demonstrated by PCA revealed by scree plot graph showed that the first ten principal components (PCs) should be used in the analysis. The largest variations observed by loading graph plot related to the vibrational modes of collagen, nucleic acids, lipids and confined water. The BLR model showed 80.6% of concordant pairs for the fingerprint region and 81.7% of concordant pairs of high wave numbers region. It was concluded that the micro FT-IR spectroscopy provides important molecular features of AC samples, evidenced both in the fingerprint and in the highwave numbers region.
- Published
- 2011
7. Ectodermal dysplasia-skin fragility syndrome: A rare case report
- Author
-
Neelam Sharma, Vinay Shanker, and Subhash Kashyap
- Subjects
congenital, hereditary, and neonatal diseases and abnormalities ,Ectodermal dysplasia ,Pathology ,medicine.medical_specialty ,McGrath syndrome ,Dermatology ,Plakophilin ,granulosis rubra nasi ,lcsh:Dermatology ,medicine ,skin and connective tissue diseases ,Skin fragility syndrome ,E-IJD Case Report ,integumentary system ,business.industry ,Genodermatosis ,lcsh:RL1-803 ,palmoplantar keratoderma ,ectodermal dysplasia/skin fragility syndrome ,medicine.disease ,Chelitis ,Granulosis rubra nasi ,Palmoplantar keratoderma ,medicine.anatomical_structure ,Nail (anatomy) ,Abnormality ,business - Abstract
Ectodermal dysplasia/skin fragility syndrome (ED-SFS) is a newly described autosomal recessive disorder characterized by skin fragility and blistering, palmoplantar keratoderma, abnormal hair growth, nail dystrophy, and occasionally defective sweating. It results from mutations in the PKP1 gene encoding plakophilin 1 (PKP1), which is an important component of stratifying epithelial desmosomes and a nuclear component of many cell types. Only 12 cases of this rare genodermatosis have been reported so far. We present an unusual case of ED-SFS in a 12-year boy who was normal at birth but subsequently developed skin fragility, hair and nail deformities, abnormal dentition, palmoplantar keratoderma, and abnormal sweating but no systemic abnormality.
- Published
- 2015
- Full Text
- View/download PDF
8. Chelitis from contact allergy to citral in lip salve.
- Author
-
Hindle, E., Ashworth, J., and Beck, M. H.
- Subjects
- *
CONTACT dermatitis , *SKIN inflammation , *LIPS , *ALLERGIES , *SKIN diseases - Abstract
The article discusses a clinical case of chelitis caused by allergy to citral contained in Vaseline® lip balm with aloe vera. Under the case, a 30-year-old woman with a five-year history of chelitis is patch tested. She is then advised to change to plain Vaseline® and avoid use of perfume and nail polish. The patient's citral avoidance resulted in symptomatic improvement of her allergy.
- Published
- 2007
- Full Text
- View/download PDF
9. Plasma Cell Cheilitis: A Clinicopathological and Immunohistochemical Study of 13 Cases.
- Author
-
Lee JY, Kim KH, Hahm JE, Ha JW, Kwon WJ, Kim CW, and Kim SS
- Abstract
Background: Plasma cell cheilitis is an unusual benign plasma cell proliferative disease of an unknown etiology that typically presents on the lip., Objective: The aim of this study was to investigate the clinicopathological characteristics of 13 cases of plasma cell cheilitis., Methods: The present study investigated the clinical manifestations, treatment modalities, and outcome of 13 patients diagnosed with plasma cell cheilitis from 2011 to 2016 at Kangdong Sacred Heart Hospital and Hallym University Sacred Heart Hospital. Biopsy specimens of the all cases were evaluated using conventional hematoxylin and eosin staining with kappa and lambda immunoglobulin light chain immunohistochemistry., Results: The age of the patients ranged from 39 to 86 years (mean, 64.7 years), with male predominance. Histopathologically, 61.5% and 38.5% of patients showed band-like and pan dermal plasmacytic infiltrates, respectively. Eosinophilic infiltration was noted in 69.2% of patients. All cases showed both kappa and lambda immunoglobulin light chain reactivities, and kappa predominance was confirmed in 9 patients (69.2%). A majority of the patients was treated with local therapy, such as intralesional steroid injection with topical tacrolimus. Among the 13 patients, plasma cell cheilitis completely resolved, partially resolved, and recurred in 3 (23.1%), 5 (38.5%), and 5 patients (38.5%), respectively., Conclusion: Plasma cell cheilitis presented as erosive edematous circumscribed patches or plaques affecting mainly the lower lip of elderly male patients. The majority of histopathology cases showed characteristic plasma cell aggregation on the upper dermis that was immunopositive for immunoglobulin light chain, with kappa predominance., Competing Interests: CONFLICTS OF INTEREST: The authors have nothing to disclose.
- Published
- 2017
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.