| Literature DB >> 18266221 |
Elvis Terci Valera1, Bianca Maria Mori, Edgard Eduard Engel, Igor Santos Costa, Daniel Ferraciolli Brandão, Marcello Henrique Nogueira-Barbosa, Rosane Gomes de Paula Queiroz, Vanessa da Silva Silveira, Carlos Alberto Scrideli, Luiz Gonzaga Tone.
Abstract
Paracoccidioides brasiliensis infection causes a systemic mycosis originally described in Latin America but with current reports of worldwide distribution. The clinical presentation of paracoccidiodomycosis as an isolated long-bone lesion in children is quite unusual. This article describes a 10-year-old male with a lytic femoral bone lesion caused by P. brasiliensis infection that was first suspected of being of neoplasic etiology. The text also emphasizes the importance of including endemic fungal infections in the differential diagnosis of bone lesions. (c) 2007 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2008 PMID: 18266221 DOI: 10.1002/pbc.21499
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167