| Literature DB >> 22665569 |
Natasha Purai Arora1, Vikas Taneja, Carlos ReyesSacin, Ravinder Bhanot, Suganthini Krishnan Natesan.
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.Entities:
Mesh:
Year: 2012 PMID: 22665569 PMCID: PMC3291038 DOI: 10.1136/bcr.12.2011.5357
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X