Nevoid acanthosis nigricans: a rare case with late onset
نویسندگان
چکیده
منابع مشابه
A case of nevoid acanthosis nigricans.
Sir, Naevoid acanthosis nigricans (AN) is an extremely rare form of AN that can manifest with a characteristic naevoid appearance at any age before puberty (1 – 3). It is not associated with any known syndrome, endocrinopathy, drugs or internal malignancy (1 – 3) and, thus far, there have been only 2 case reports in the literature of naevoid AN with a unilateral distribution (1, 2). We report a...
متن کاملUnilateral nevoid acanthosis nigricans with a submammary location.
Unilateral nevoid acanthosis nigricans (AN) is an exceedingly rare form of AN, which is a benign disorder of keratinization. The lesions of unilateral nevoid AN are distributed unilaterally while the histopathologic findings are similar to the common form of AN, and this is characterized by hyperkeratosis, papillomatosis and moderate acanthosis. A 19-year-old female presented with asymptomatic ...
متن کاملUnilateral nevoid acanthosis nigricans treated with CO2 laser
To cite: Campos MA, Varela P, Baptista A, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2016-216073 DESCRIPTION Acanthosis nigricans (AN) can be classified into eight variants, including the benign, obesity associated, syndromic, malignant, acral, unilateral, medication induced and mixed type. Unilateral nevoid AN (UNAN) is an extremely rare form of AN a...
متن کاملMalignant acanthosis nigricans associated with prostate cancer: a case report
BACKGROUND Acanthosis nigricans is characterized by hyperpigmentation and hyperkeratosis of the skin or mucous membranes. Its malignant form is associated with internal neoplasms, especially gastric adenocarcinoma (55-61%). Coexistence with prostate cancer is uncommon. In the paraneoplastic type of this dermatosis, the skin and mucous lesions are characteristically of more sudden onset and more...
متن کاملCrouzon syndrome in association with acanthosis nigricans
Crouzon syndrome is a rare inherited autosomal dominant syndrome characterized by craniosynostosis, midface hypoplasia. Acanthosis nigricans may be associated with Crouzon syndrome, but it differs from the classic crouzon syndrome. This is a report of a 30-year-old-woman who presented acanthosis nigricans coexist with crouzon syndrome.
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ژورنال
عنوان ژورنال: Our Dermatology Online
سال: 2015
ISSN: 2081-9390
DOI: 10.7241/ourd.20153.90