# Case Report: Intracranial hemophilic pseudotumor mimicking an aggressive neoplasm: a rare skull-invasive presentation

**Authors:** Moksada Regmi, Junyi Liu, Shikun Liu, Ying Xiong, Zihan Zhao, Xu Zhang, Chenlong Yang

PMC · DOI: 10.3389/fsurg.2025.1709321 · Frontiers in Surgery · 2026-01-12

## TL;DR

A rare case of a hemophilic pseudotumor in a man with hemophilia A was mistaken for a brain tumor but successfully treated with surgery and factor VIII replacement.

## Contribution

Presents a unique case of a skull-invasive hemophilic pseudotumor mimicking an aggressive brain tumor in a hemophilia patient.

## Key findings

- A 36-year-old man with hemophilia A had a pseudotumor that mimicked a meningioma on MRI.
- Surgical resection under factor VIII replacement led to significant neurological improvement and no recurrence at 12 months.

## Abstract

Hemophilic pseudotumor is a rare complication of hemophilia in which a chronic, expanding hemorrhagic mass erodes adjacent bone; intracranial presentations are exceedingly uncommon and can mimic neoplasms. We describe a 36-year-old man with severe hemophilia A who developed a five-year, progressively enlarging left frontoparietal swelling with worsening right-sided hemiparesis. MRI demonstrated a heterogeneously enhancing extra-axial lesion destroying the left cranial vault with “mushroom-like” extracranial extension, marked mass effect, and midline shift, initially interpreted as a possible meningioma. Given progressive deficits, the patient underwent resection under intensive factor VIII replacement. Intraoperatively, a 10 × 10 × 5 cm encapsulated lesion containing organizing clot and fibrous tissue was excised en bloc; the skull defect was reconstructed in a staged procedure. Histopathology confirmed hemophilic pseudotumor. Postoperatively, hemiparesis improved markedly; a small epidural hematoma was managed conservatively. At 12 months, MRI showed no recurrence and the patient remained neurologically intact on prophylactic factor VIII. This case highlights the need to include hemophilic pseudotumor in the differential diagnosis of skull lesions in patients with hemophilia and underscores the value of early recognition and multidisciplinary management—particularly meticulous perioperative hemostatic support—to enable safe resection and excellent outcomes.

## Linked entities

- **Diseases:** hemophilia A (MONDO:0010602)

## Full-text entities

- **Diseases:** hematoma (MESH:D006406), hemiparesis (MESH:D010291), frontoparietal swelling (MESH:C536673), hemorrhagic (MESH:D006470), Hemophilic pseudotumor (MESH:D006104), neoplasm (MESH:D009369), hemophilia (MESH:D006467), skull defect (MESH:D012888), meningioma (MESH:D008579)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12832656/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832656/full.md

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Source: https://tomesphere.com/paper/PMC12832656