Abstract

BackgroundHistoplasmosis is known to cause CNS infection with or without disseminated disease and immunosuppression is a risk factor. It can mimic brain tumor and present a diagnostic challenge.MethodsCase report and literature review using PUBMED.ResultsA 64-year-old white female with myasthenia gravis on mycophenolate mofetil, history of Meniere’s Disease, presented with worsening ataxia and left-sided facial weakness for 4 days. MRI revealed multiple enhancing lesions within the brainstem and supratentorial parenchyma (Figure 1), consistent with metastases but either too small or inaccessible for biopsy. Work up for primary cancer with CT thorax, abdomen-pelvis, transvaginal US, mammogram, bone scan, and CSF cytology were negative. The CSF BioFire PCR and culture were negative. Prednisone taper was started for brain vasogenic edema. Patient presented again two months later with worsening lethargy, vertigo, and recurrent falls. At that time the brain lesions showed continued enlargement on repeat imaging, and stereotactic biopsy was performed. Histopathology showed non-necrotizing granulomas, no evidence of malignancy, but after 12 days a mold was isolated on culture prompting Infectious Diseases consultation. Initial morphologic features were non-diagnostic and empiric voriconazole was initiated. Fungal culture evolved Histoplasma capsulatum and voriconazole was switched to liposomal amphotericin B at 5 mg/kg intravenously every 24 hours. Histoplasma serology was positive at low titer, urine histoplasma antigen was negative. An 8 weeks course of Amphotericin, followed by lifelong suppression with fluconazole, was planned.Figure 1 ConclusionThe diagnosis of our patient’s brain lesions was challenging as biopsy was not an option initially. An anchoring bias likely existed as the investigations had focused on malignancy, while a more robust evaluation for opportunistic endemic fungi, such as Histoplasma, took place at a later stage. Brain lesions in the immunosuppressed patient can masquerade as malignancy. To ensure timely diagnosis, a multimodal investigational approach should be applied early to include imaging and laboratory evaluation for endemic opportunistic pathogens, as well as biopsy when possible.Disclosures All Authors: No reported disclosures

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call