Anais Brasileiros de Dermatologia (Jun 2016)

Primary cutaneous aspergillosis and idiopathic bone marrow aplasia

  • Karina Colossi Furlan,
  • Mario Cezar Pires,
  • Priscila Kakizaki,
  • Juliana Cabral Nunes Chartuni,
  • Neusa Yuriko Sakai Valente

DOI
https://doi.org/10.1590/abd1806-4841.20164889
Journal volume & issue
Vol. 91, no. 3
pp. 381 – 383

Abstract

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Abstract: We describe the case of a 9-year-old boy with idiopathic bone marrow aplasia and severe neutropenia, who developed skin ulcers under cardiac monitoring electrodes. The diagnosis of primary cutaneous aspergillosis was made after the second biopsy and culture. Imaging investigation did not reveal internal fungal infection. The child was treated, but did not improve and died 3 months after admission. The report highlights and discusses the preventable risk of aspergillus skin infection in immunocompromised patients.

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