# Invasive Fungal Granuloma of the Skull Base Mimicking Spindle Cell Neoplasm in a Young Immunocompetent Patient: A Diagnostic Challenge

**Authors:** Huzaifa Ali Khan, Qaiser Yaseen, Hafiz Muhammad Usama Amjad, Sajjad Dasti

PMC · DOI: 10.7759/cureus.92672 · Cureus · 2025-09-18

## TL;DR

A young healthy man's skull base tumor was initially misdiagnosed as a blood vessel tumor but later found to be a rare fungal infection, highlighting the need for careful testing.

## Contribution

This case highlights the diagnostic challenge of invasive fungal granuloma mimicking a spindle cell neoplasm in an immunocompetent patient.

## Key findings

- Initial biopsy and imaging were inconclusive, suggesting a vascular neoplasm.
- Repeat biopsy with fungal stains confirmed invasive fungal sinusitis caused by Aspergillus.
- The patient improved with surgical debridement and antifungal therapy.

## Abstract

Skull base lesions presenting with proptosis and sinonasal involvement in young patients are commonly attributed to vascular neoplasms such as juvenile nasopharyngeal angiofibroma. However, rare infectious etiologies such as invasive fungal granulomas may present with overlapping radiological features, leading to diagnostic challenges. We report a rare case of a 19-year-old immunocompetent male presenting with progressive bilateral proptosis and a large skull base mass involving the clivus, nasal cavity, and orbits. Initial imaging suggested a vascular neoplasm, and biopsy revealed a spindle cell lesion with inconclusive immunohistochemistry. Fungal cultures were negative. The patient was lost to follow-up but returned four months later with worsening symptoms. Repeat biopsy demonstrated necrotizing granulomatous inflammation with septate, acute-angle branching fungal hyphae, consistent with Aspergillus species on GMS (Grocott methenamine silver) and PAS (periodic acid-Schiff) staining. The final diagnosis was invasive fungal sinusitis mimicking a skull base neoplasm. The patient underwent surgical debridement followed by antifungal therapy with voriconazole and showed clinical improvement. This case underscores the importance of considering fungal granulomas in the differential diagnosis of skull base lesions, even in immunocompetent individuals. It highlights the critical role of repeat biopsy, fungal stains, and a multidisciplinary approach in arriving at an accurate diagnosis when imaging and histology are inconclusive.

## Linked entities

- **Chemicals:** voriconazole (PubChem CID 71616)
- **Diseases:** juvenile nasopharyngeal angiofibroma (MONDO:0017340)

## Full-text entities

- **Diseases:** vascular neoplasm (MESH:D019043), Skull base lesions (MESH:D019292), Invasive (MESH:D009361), Spindle Cell Neoplasm (MESH:D002277), juvenile nasopharyngeal angiofibroma (MESH:D018322), proptosis (MESH:D005094), granulomatous inflammation (MESH:D007249), fungal sinusitis (MESH:D000092562), Granuloma (MESH:D006099), Fungal (MESH:D009181)
- **Chemicals:** voriconazole (MESH:D065819)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12535620/full.md

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Source: https://tomesphere.com/paper/PMC12535620