A CASE OF SEIP-LAWRENCE SYNDROME WITH ACANTHOSIS NIGRICANS
نویسندگان
چکیده
منابع مشابه
A case of Seip-Lawrence syndrome with acanthosis nigricans.
Seip-Lawrence syndrome is the total lipodystrophy which unites the con genital and acquired forms of the disease under one eponym.1) In 1946, Lawrence2) originally characterized this syndrome by absence of subcutaneous fat tissue, insulin-resistant diabetes unassociated with ketosis, hepatic cirrhosis, hypermeta bolism under the presence of euthyroidism, and hyperlipemia. Since then we only rec...
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.
متن کاملA 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 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 کاملCutaneous features of Crouzon syndrome with acanthosis nigricans.
IMPORTANCE Crouzon syndrome with acanthosis nigricans is a distinct disorder caused by a mutation in the FGFR3 gene, featuring craniosynostosis, characteristic facial features, and atypical and extensive acanthosis nigricans. Other cutaneous findings have not been thoroughly described. OBSERVATIONS We report 6 cases and summarize the existing literature with regard to the cutaneous manifestat...
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ژورنال
عنوان ژورنال: The Keio Journal of Medicine
سال: 1966
ISSN: 1880-1293,0022-9717
DOI: 10.2302/kjm.15.101