Results 41 to 50 of about 281 (139)
Acrokeratosis verruciformis of Hopf [PDF]
Our Dermatology Online, 2019 A 30-year-old female presented with multiple nodules, grouped, hyperkeratotic, brownish and malodorous on his feet (Fig. 1), which had been present for more than 3 years.Histopathological examination showed classical feature of "church spires" appearance without dyskeratosis (Fig.
openaire +1 more source
Type 2 segmental darier's disease in a twelve-year old Nigerian male - A case report [PDF]
, 2010 No ...
Mohammed, AZ, Oloko, AE, Yusuf, SM
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Guttate leukoderma and acrokeratosis verruciformis of Hopf: a rare combination in Darier disease [PDF]
, 2020 A distinct Darier phenotype presenting with confetti-like hypopigmented macules was first described in 1965. Designated as "guttate leukoderma," this skin finding is a rarely-reported presentation of Darier disease.
Grossman, Shoshana K +4 more
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Atypical Steatocystoma Multiplex with Calcification
International Scholarly Research Notices, Volume 2011, Issue 1, 2011., 2011 A 60‐year‐old male reported to us with an atypical case of giant steatocystoma multiplex in the scrotum with calcification. There was no family history of similar lesions. Yellowish, creamy material was expressed from a nodule during punch biopsy. The diagnosis was based on clinical as well as histological findings.
Muhammad Hasibur Rahman +6 more
wiley +1 more source
Diagnosis dan Tatalaksana Steatosistoma [PDF]
, 2018 Steatosistoma adalah suatu kista intradermal yang umumnya asimtomatik dimana kista tersebut berisi sebum dengan karakteristik khas terdapat kelenjar sebasea pada dinding kista yang dilapisi epitel berlapis gepeng.
Kampar, Puridelko, Lestari, Sri
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Acrokeratosis verruciformis of Hopf: A rare case report
Indian Journal of Pathology and Oncology, 2023 Acrokeratosis verruciformis of Hopf (AKV) is a rare cutaneous autosomal dominant genodermatosis described by Hopf in 1931. It usually presents at birth or may appear as late as 5 decade of life. It is characterized by multiple hyperkeratotic, verrucous papules/plaques to multiple planar wart like lesions on dorsal aspects of hand and feet.
Shushruta Mohanty +3 more
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New Described Dermatological Disorders [PDF]
, 2014 Many advances in dermatology have been made in recent years. In the present review article, newly described disorders from the last six years are presented in detail. We divided these reports into different sections, including syndromes, autoinflammatory
Bengu Cevirgen Cemil +3 more
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Epidermodysplasia Verruciformis: A Case Report [PDF]
, 2020 Epidermodysplasia verruciformis (EDV) is a rare, inherited disorder that is characterized by an increased susceptibility to infection with specific human papilloma viruses (HPV) and a greater propensity for developing malignant skin tumors. A 26 years
Anisha Joshi, Bibush Amatya
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A Case of Acrokeratosis Verruciformis Treated with Acitretin [PDF]
, 2009 Acrokeratosis Verruciformis is a rare autosomal dominant genodermatosis. Typically, the lesions are small, verrucous, flat papules on the dorsal aspects of the hands and feet, elbows and knees.
Ayten Ferahbaş +3 more
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