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BMJ Case Rep. 2012 Feb 25;2012. pii: bcr1220115357. doi: 10.1136/bcr.12.2011.5357.

Coccidioidomycosis masquerading as malignancy.

Author information

1
Department of Internal Medicine, Wayne State University School of Medicine, Detroit Medical Center, Detroit, Michigan, USA. narora@med.wayne.edu

Abstract

Skeletal coccidioidomycosis is extremely rare and in the non-endemic areas, diagnosis is often delayed or missed resulting in extensive and unnecessary medical investigation for other diseases. The authors report a case of disseminated skeletal coccidioidomycosis in a previously healthy person living in a non-endemic area, who was initially thought to have a malignancy. Due to the presence of multiple expansile lytic bone lesions on x-rays and CT scan, an extensive investigation for malignancy was done. Diagnosis of coccidioidomycosis was made when H&E and Gomori's methenamine silver staining of a bone biopsy sample revealed multiple fungal spherules, which were confirmed to be Coccidioides immitis by culture and PCR. On questioning, the patient admitted to have spent 2 weeks in Arizona (an endemic area) few months ago. He was discharged home on long-term fluconazole. At 1 month clinical follow-up, a significant improvement in his lesions was noticed.

PMID:
22665569
PMCID:
PMC3291038
DOI:
10.1136/bcr.12.2011.5357
[Indexed for MEDLINE]
Free PMC Article

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