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Case Rep Dermatol Med
January 2020
Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Eruptive syringoma is a rare variant of syringoma presenting with skin-colored or slightly pigmented papules mostly before or during puberty. In this report, we presented a rare case of eruptive syringoma in a 30-year-old woman. She exhibited multiple skin lesions in dorsal areas of her both hands, developed from the age of 15.
View Article and Find Full Text PDFCureus
November 2018
Dermatology, Clinical Pathology Associates, Austin, USA.
Syringomas are benign, eccrine sweat gland tumors frequently found on the eyelids and neck in post-pubescent women and may present in healthy individuals or be associated with various medical comorbidities. We present a case of an otherwise healthy 19-year-old female with an abrupt onset of disseminated syringomas on the bilateral forearms and dorsal hands. Eruptive acral syringomas have not been previously reported in adolescents, and this diagnosis should be considered in patients presenting with a papular eruption on the hands and forearms.
View Article and Find Full Text PDFActas Dermosifiliogr (Engl Ed)
November 2018
Servicio de Dermatología, Hospital Universitario Central de Asturias, Oviedo, Asturias, España.
Indian J Dermatol Venereol Leprol
May 2017
Department of Dermatology, Hospital of León, León, Spain.
Australas J Dermatol
August 2012
Dipartimento di Anestesiologia, Terapia Intensiva e Scienze Dermatologiche, Università degli Studi di Milano, U.O. Dermatologia, Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.
Steatocystoma multiplex (SM) is a hamartomatous malformation of the pilosebaceous duct consisting of dermal cysts filled with a sebum-like material. SM lesions are typically located in areas with sebaceous follicles, although atypical presentations involving sites lacking sebaceous follicles have exceptionally been described. We reviewed retrospectively a series of 32 histologically diagnosed SM observed in our department in the period 2006-2010, evaluating the kinds of lesions and their locations, and family history of SM and associated disorders, to focus on the clinical features of the acral subcutaneous variety of SM and to estimate its prevalence.
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