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Xanthoma striatum palmare and biliary tract atresia: An unusual association
Author(s) -
Joner Mattias Fernanda,
Escobar Gabriela Fortes,
Peruzzo Juliano
Publication year - 2020
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/pde.14225
Subject(s) - xanthoma , medicine , biliary atresia , striatum , dermis , pathology , biliary tract , anatomy , transplantation , liver transplantation , dopamine
Cutaneous xanthomas develop as a result of lipid deposition in the dermis and may be a manifestation of various systemic diseases. The morphology and anatomic location of xanthomas are often a clue to the underlying cause. Xanthoma striatum palmare (XSP) is classically associated with dysbetalipoproteinemia and rarely observed in hepatic disorders. We present a case of a 2‐year‐old child diagnosed with XSP and biliary tract atresia.
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