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Your search keyword '"Patrizi, Annalisa"' showing total 36 results
Start Over Author "Patrizi, Annalisa" Journal journal of the american academy of dermatology
36 results on '"Patrizi, Annalisa"'

1. The clinical spectrum of COVID-19–associated cutaneous manifestations: An Italian multicenter study of 200 adult patients

Author

Marzano, Angelo Valerio, Genovese, Giovanni, Moltrasio, Chiara, Gaspari, Valeria, Vezzoli, Pamela, Maione, Vincenzo, Misciali, Cosimo, Sena, Paolo, Patrizi, Annalisa, Offidani, Annamaria, Quaglino, Pietro, Arco, Renato, Caproni, Marzia, Rovesti, Miriam, Bordin, Giorgio, Recalcati, Sebastiano, Potenza, Concetta, Guarneri, Claudio, Fabbrocini, Gabriella, Tomasini, Carlo, Sorci, Mariarita, Lombardo, Maurizio, Gisondi, Paolo, Conti, Andrea, Casazza, Giovanni, Peris, Ketty, Calzavara-Pinton, Piergiacomo, and Berti, Emilio

Published
2021
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14. Late-onset hidradenitis suppurativa: A cluster analysis of the National Italian Registry IRHIS

Author

Cazzaniga, Simone, primary, Pezzolo, Elena, additional, Garcovich, Simone, additional, Naldi, Luigi, additional, Bettoli, Vincenzo, additional, Abeni, Damiano, additional, Marzano, Angelo V., additional, Patrizi, Annalisa, additional, Atzori, Laura, additional, Fabbrocini, Gabriella, additional, Offidani, Annamaria, additional, Lasagni, Claudia, additional, Dini, Valentina, additional, Caproni, Marzia, additional, and Cannavò, Serafinella Patrizia, additional

Published
2021
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27. Focal facial dermal dysplasia: two familial cases

Author

Di Lernia, Vito, Neri, Iria, and Patrizi, Annalisa

Subjects
Face -- Abnormalities, Ectodermal dysplasia -- Case studies, Birth defects -- Evaluation, Ectodermal dysplasia -- Genetic aspects, Familial diseases -- Genetic aspects, Health
Abstract

Focal facial dermal dysplasia is an inherited skin disease characterized by birth-related, scar-like, depressed skin lesions on the temples of the face. Tissue microscopic features include thinning of the inner and outer skin layers and absence of adnexal, or appending skin structures. In addition, focal facial dermal dysplasia may be accompanied by other abnormalities of the face. A case is described of an infant boy who was born with various facial abnormalities. The infant had a short neck, low-set hairline, fine hair on the forehead, a flat broad nose, thick lips with the upper lip bent, and prominent, rubbery chin. He had sparse eyebrows, puckered skin around the eyes, and no lower eyelashes; discolored, depressed scars over the temples, and abnormalities of abdominal rectus muscles. The infant's mother had similar skin lesion on the temples and similar facial features, including a low-set hairline, no lower eyelashes, a bent upper lip, and rubbery chin. Microscopic examination of the skin lesion on the mother's temple reveled thinning of the skin layers, absence of skin appendages, and little elastic tissue in the inner skin layer. The genetic aspects of focal facial dermal dysplasia are discussed. (Consumer Summary produced by Reliance Medical Information, Inc.)

Published
1991

29. Alitretinoin and Darier disease: 'All that glisters is not gold'

Author

Federico Bardazzi, Patrizi Annalisa, Riccardo Balestri, Alessandro Pileri, Balestri R, Patrizi A, and Bardazzi F

Subjects
medicine.medical_specialty, darier desease, business.industry, alitretinoin, MEDLINE, Antineoplastic Agents, Tretinoin, Dermatology, Alitretinoin, Darier Disease, medicine, Humans, Female, business, medicine.drug
Abstract

not available

Published
2015
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30. Porokeratosis palmaris et plantaris disseminata: an unusual clinical presentation

Author

Patrizi, Annalisa, Passarini, Beatrice, Minghetti, Giulio, and Masina, Marco

Subjects
Keratosis -- Case studies, Keratosis -- Identification and classification, Skin diseases -- Case studies, Keratinization -- Abnormalities, Health
Abstract

Porokeratosis is a chronic disorder of keratinization, the formation of the hard protein in the skin called keratin. It is characterized by annular or ring-shaped patches bordered by hyperkeratotic, or horny, tissue. This inherited disease is controlled by non-sex-linked, or autosomal, dominant genes. When a trait is controlled by a dominant gene (X), the trait will be expressed in the offspring when the dominant gene is paired with another dominant gene (XX) or with a recessive gene (Xx). Porokeratosis may be classified into five categories, one of which is porokeratosis palmaris et plantaris disseminata. A case of this form of the disease is described. A 54-year-old man and his son had porokeratoses located on the trunk and extremities, mainly on the palms and soles of the feet. In addition, within the mouth, there were many slightly depressed, opalescent, round-shaped lesions bordered by hyperemic, or congested, areas. The varieties of porokeratosis palmaris et plantaris disseminata and other forms of porokeratosis are discussed. The older patient was treated successfully with etretinate, but a relapse occurred five weeks after the treatment was discontinued. (Consumer Summary produced by Reliance Medical Information, Inc.)

Published
1989

33. Cutaneous squamous cell carcinoma progression during imiquimod treatment

Author

Giulia Maria Ravaioli, Giulia Veronesi, Martina Lambertini, Alba Guglielmo, Emi Dika, Federica Scarfì, Pier Alessandro Fanti, Annalisa Patrizi, Carlotta Baraldi, Dika, Emi, Fanti, Pier Alessandro, Lambertini, Martina, Scarfì, Federica, Maria Ravaioli, Giulia, Veronesi, Giulia, Baraldi, Carlotta, Guglielmo, Alba, and Patrizi, Annalisa

Subjects
Administration, Cutaneou, Cutaneous squamous cell carcinoma, Skin Neoplasms, Imiquimod, Dermatology, Administration, Cutaneous, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Text mining, Aminoquinoline, medicine, Humans, Skin Neoplasm, Aminoquinolines, business.industry, Disease progression, 030220 oncology & carcinogenesis, Cancer research, Carcinoma, Squamous Cell, Disease Progression, business, Human, medicine.drug
Published
2018

34. Comment on 'Desquamative gingivitis: Clinical findings and diseases'

Author

Carlotta Baraldi, Carlotta Gurioli, Annalisa Patrizi, Marco Adriano Chessa, Emi Dika, Chessa, Marco Adriano, Dika, Emi, Gurioli, Carlotta, Baraldi, Carlotta, and Patrizi, Annalisa

Subjects
Desquamative gingivitis, medicine.medical_specialty, Gingivitis, business.industry, medicine, Dermatology, medicine.symptom, medicine.disease, business, Human
Published
2019
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35. An asymptomatic subungual nodule

Author

Cosimo Misciali, Pier Alessandro Fanti, Bianca Maria Piraccini, Annalisa Patrizi, Emi Dika, Holly Christman, Dika, Emi, Patrizi, Annalisa, Fanti, Pier Alessandro, Christman, Holly, Misciali, Cosimo, and Piraccini, Bianca Maria

Subjects
medicine.medical_specialty, Skin Neoplasms, Dermoscopy, Dermatology, Asymptomatic, 030207 dermatology & venereal diseases, 03 medical and health sciences, Nail Diseases, 0302 clinical medicine, 0502 economics and business, Medicine, Humans, nail apparatu, Melanoma, Nail Apparatus, Asymptomatic Diseases, business.industry, clinical characteristic, 05 social sciences, Nodule (medicine), Middle Aged, medicine.disease, symptom, Nail disease, 050211 marketing, feature, Female, amelanotic, medicine.symptom, business
Abstract

an asymptomaric subungual nodule should always be biopsied

Published
2015

36. Congenital pseudoclubbing of a fingernail caused by subungual hemangioma

Author

Giulia Rech, Matilde Iorizzo, Angela Antonucci, Annalisa Patrizi, Antonella Tosti, Bianca Maria Piraccini, Iria Neri, Piraccini, BIANCA MARIA, Antonucci, Angela, Rech, Giulia, Iorizzo, Matilde, Neri, Iria, Patrizi, Annalisa, and Tosti, Antonella

Subjects
Male, Pathology, medicine.medical_specialty, Skin Neoplasms, Physical examination, Pseudoclubbing, Dermatology, Hemangioma, Angioma, Nail Diseases, medicine, Humans, integumentary system, medicine.diagnostic_test, business.industry, Vascular disease, Soft tissue, Infant, medicine.disease, Numerical digit, medicine.anatomical_structure, Nail (anatomy), Female, business
Abstract

Background Nail dystrophies in newborns are rare and are particularly frightening when they appear as masses involving a single digit, suggesting the possibility of a tumor. Objective The aim of this study is to report 3 infants with a congenital pseudoclubbing appearance of a digit and with a reddish discoloration caused by the presence of a subungual hemangioma. Methods Diagnosis was based on clinical examination and ultrasonography. Results Clinical presentation and vitrocompression showed the presence of a vascular mass. Ultrasonography confirmed the diagnosis of a subungual hemangioma. The lesions showed a spontaneous regression on follow-up. Conclusion Localization of hemangioma under the proximal nailfold is extremely rare and produces nail pseudoclubbing caused by capillary vessel proliferation in the soft tissue of the subungual region, which is associated with a reddish discoloration of the nail that typically fades with compression. Hemangiomas of infancy located in the proximal nailfold are rare, and, in our opinion, not at risk to become big masses with tissue damage and compression.

Published
2005

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