Indian Journal of Dermatology (Jan 2015)

Acral acanthosis nigricans in a case of scleroderma

  • Mahendra M Kura,
  • Swapnil A Sanghavi

DOI
https://doi.org/10.4103/0019-5154.160540
Journal volume & issue
Vol. 60, no. 4
pp. 423 – 423

Abstract

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Acanthosis nigricans (AN) is a dermatosis characterized by velvety, papillomatous, brownish-black, hyperkeratotic plaques, typically on the intertriginous surfaces and neck. The majority (80%) of AN occurs idiopathically or in benign conditions such as endocrinopathies like diabetes mellitus, polycystic ovary syndrome; metabolic syndrome and/or heritable disease. Malignancy-associated AN is rare. AN may rarely be associated with autoimmune diseases including systemic lupus erythematosus, due to antibodies to the insulin receptor, so-called type B insulin resistance. Here we report a case of AN in a case of diffuse progressive systemic sclerosis without evidence of insulin resistance.

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