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X‐Linked reticulate pigmentary disorder in a female patient
Author(s) -
Kim Byung Soo,
Seo SangHee,
Jung Hong Dae,
Kwon KyungSool,
Kim MoonBum
Publication year - 2010
Publication title -
international journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 93
eISSN - 1365-4632
pISSN - 0011-9059
DOI - 10.1111/j.1365-4632.2010.04102.x
Subject(s) - reticulate , medicine , dermatology , biology , paleontology
Background  X‐Linked reticulate pigmentary disorder is a very rare cutaneous condition characterized by different clinical manifestations according to sex. Methods  We report a 31‐year‐old woman with X‐linked reticulate pigmentary disorder. Results  On examination, there were multiple, asymptomatic, brownish macules in linear and whorled patterns over the trunk, axillae, groin, and extremities. The woman had not experienced any systemic manifestations involving the gastrointestinal, pulmonary, or ocular systems. Her hair, teeth, and nails were normal on close observation. All laboratory data were within the normal range. A genetic study was not performed. Conclusions  Although a genetic study was not performed, we believe that our patient can be diagnosed with X‐linked reticulate pigmentary disorder according to the clinical and histopathologic findings.

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