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Multisystemic paracoccidioidomycosis with rare retinal and central nervous system involvement: a case report
Sarah Dos Santos Miguel1, Erika Yuki Mogami Bomfim2, Tiago Pasian Fagundes Santos1
1Departament of Medicine, Irmandade da Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil.
None:
We report a rare case of disseminated paracoccidioidomycosis in an immunocompetent 41-year-old woman presenting with granulomatous skin lesions, neurological involvement, and subretinal fibrosis leading to exudative retinal detachment and permanent vision loss. Diagnosis was confirmed by direct microscopy, histopathology, and serology. The patient was treated with liposomal amphotericin B followed by trimethoprim-sulfamethoxazole, showing significant clinical improvement. This case highlights an atypical presentation of paracoccidioidomycosis with ocular and central nervous system involvement, emphasizing the need to consider the disease in differential diagnoses even in unusual forms, especially in endemic regions.
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