Acanthosis Nigricans and Eruptive Xanthoma

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منابع مشابه

Eruptive xanthoma.

History A two-month-old girl with unremarkable birth history presented with sudden onset of erythematous papules on the limbs and face for one week. There was no systemic upset, and she remained asymptomatic. Her sister had a history of hypertriglyceridaemia under treatment. The patient's other family members enjoyed good physical health and there was no family history of premature coronary hea...

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[Acanthosis nigricans].

Acanthosis nigricans is thickened, velvety, hyperpigmented skin associated with a variety of endocrine disorders, malignancies and medications.

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Generalized benign acanthosis nigricans.

with normal growth and developmental milestones, presented with asymptomatic generalized hyperpigmentation. It started spontaneously at the age of 2 years, around the neck and axilla, and spread insidiously to involve the other parts of body. The skin gradually became thickened and rugose. There was no history of drug intake, polyuria, polydypsia, loss of appetite, excess weight gain or loss. C...

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Linear Acanthosis Nigricans

Acathosis nigricans (AN) typically presents as symmetric, brownish-black, velvety, hypertrophic, verrucous, and at times papillomatous plaques most commonly involving the flexural sites [1]. It is a cutaneous marker, most frequently of insulin resistance and less frequently of malignancy [2]. AN has been classified into 8 types: benign, obesity-related, syndromic, malignant, unilateral, acral, ...

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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...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1976

ISSN: 0035-9157

DOI: 10.1177/003591577606900430