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Case for diagnosis. Steatocystoma multiplex.

Anais brasileiros de dermatologia - 1 Jan 2000

Lima Alexandre Moretti de, Rocha Sheila Pereira da, Batista Carolina Mayana de Ávila, Reis Carmelia Matos Santiago, Leal Isabel Irene Rama, Azevedo Lucas Emanuel de Lima

Abstract excerpt

Steatocystoma multiplex is a rare genetic disorder, autosomal dominant, that is characterized by multiple asymptomatic dermal cysts which vary in size. It is described here the case of a 23 year-old male patient with a typical clinical and evolutional progression of this disease.

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Identifiers

PMID: 21437547
DOI: 10.1590/s0365-05962011000100031

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21437547-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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