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BMJ Case Reports 2012; doi:10.1136/bcr.12.2011.5357
  • Rare disease

Coccidioidomycosis masquerading as malignancy

  1. Suganthini Krishnan Natesan2
  1. 1Department of Internal Medicine, Wayne State University School of Medicine, Detroit Medical Center, Detroit, Michigan, USA
  2. 2Department of Internal Medicine, Division of Infectious Diseases, Wayne State University School of Medicine, Detroit Medical Center, Detroit, Michigan, USA
  1. Correspondence to Dr Natasha Purai Arora, narora{at}med.wayne.edu

Summary

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.

Footnotes

  • Competing interests None.

  • Patient consent Obtained.

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