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Cerebral phaeohyphomycosis: The 'Dark Side' of fungal infections
Archit Latawa1, Ipsita Panda2, Harsimran Kaur3
1Department of Neurosurgery, PGIMER, Chandigarh, India.
Purpose:
Cerebral phaeohyphomycosis is a rare and fatal fungal infection of the central nervous system (CNS) caused by dematiaceous fungi. The aim of this study was to analyse the clinico- radiological presentation, pathology and outcome of cerebral phaeohyphomycosis and discuss the relevant literature.
Patients And Methods:
Data of 7 patients diagnosed with cerebral phaeohyphomycosis and managed at our institute between 2014 and 2020 was collected and reviewed retrospectively. The diagnosis was established after surgery on KOH mount, Sabouraud dextrose agar, frozen section or histopathology. The clinical, radiological and pathological characteristics along with outcomes were analysed.
Results:
Three patients with underlying comorbidities [chronic renal failure-2 and haematological malignancy -1] presented with brain abscess. The remaining 4 had no comorbidities. Two of them mimicked cystic glioma and one patient presented as intraventricular tumour. Another patient on anti- tubercular treatment for suspected pulmonary tuberculosis presented with encephalitis. Histopathology in all patients showed diffuse micro abscesses with coarse and reactive gliosis in the adjacent brain parenchyma and chronic lymphomononuclear inflammation without angioinvasion or vasculitis. Four showed granuloma formation. Antifungals were started after diagnosis. Six out of seven patients died and one was lost to follow up.
Conclusion:
Cerebral phaeohyphomycosis presents as abscesses in immunocompromised patients and mimics tumours in immunocompetent patients. KOH mount and frozen section examination is simple yet effective tool for establishing early diagnosis. Overall, the prognosis is dismal. Administering antifungals early in the course of management along with aggressive surgical excision may improve outcomes.
Insights
Cerebral phaeohyphomycosis, a rare central nervous system fungal infection, often presents as brain abscesses in immunocompromised individuals and mimics tumors in others. Early diagnosis and treatment are crucial, though outcomes remain poor.
Area of Science:
- Neurology
- Infectious Diseases
- Mycology
Background:
- Cerebral phaeohyphomycosis is a rare, fatal central nervous system (CNS) infection caused by dematiaceous fungi.
- Understanding its clinico-radiological presentation, pathology, and outcomes is critical for patient management.
Purpose of the Study:
- To analyze the clinical, radiological, and pathological features of cerebral phaeohyphomycosis.
- To evaluate the outcomes of patients diagnosed with this infection.
- To discuss relevant literature and potential management strategies.
Main Methods:
- Retrospective review of 7 patients diagnosed with cerebral phaeohyphomycosis between 2014 and 2020.
- Diagnosis confirmed via KOH mount, fungal cultures, frozen section, or histopathology.
- Analysis of clinical, radiological, pathological data, and patient outcomes.
Main Results:
- Three patients had comorbidities (chronic renal failure, hematological malignancy) presenting as brain abscesses.
- Four immunocompetent patients presented with varied imaging findings, including cystic glioma mimicry and intraventricular tumors.
- Histopathology revealed microabscesses, gliosis, and inflammation; 6 out of 7 patients died, and one was lost to follow-up.
Conclusions:
- Cerebral phaeohyphomycosis presents differently in immunocompromised versus immunocompetent patients.
- KOH mount and frozen sections are effective for early diagnosis.
- Prognosis is generally poor; early antifungal treatment and aggressive surgical excision may improve outcomes.
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