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Case report describes intracranial WHO Grade II ependymoma with rare lipomatous metaplasiaDoctors report rare case of brain tumor containing fat tissue in young man

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Key Takeaway
Consider lipomatous metaplasia in the differential for intracranial masses with significant fat signal on MRI.

A case report and systematic literature review details a 28-year-old male with recent-onset dizziness and an incidentally discovered intracranial mass. The patient underwent gross-total resection. Histopathology confirmed a World Health Organization (WHO) Grade II ependymoma with lipomatous metaplasia, a rare pathological variant. Immunohistochemical analysis highlighted features of both ependymal differentiation and fatty metaplasia. Preoperative MRI of the left frontotemporal lesion showed significant fat signal, progressive enhancement, and mass effect on adjacent structures.

Safety and tolerability data were not reported for this single case. The follow-up duration and any adverse events related to the resection were also not reported.

Key limitations stem from the evidence being based on a single case report combined with a review of other reported cases. This severely limits generalizability and any conclusions about long-term outcomes, prognosis, or optimal management for this rare entity. The study does not establish treatment efficacy or compare interventions.

For clinical practice, this report underscores the importance of meticulous radiological and pathological evaluation to guide diagnosis when encountering similar imaging findings. It aims to raise awareness of this rare ependymoma subtype among clinicians and pathologists. Management decisions should be based on standard principles for intracranial tumors, as evidence specific to this variant is anecdotal.

Doctors reported on a single case of a 28-year-old man who had a brain tumor discovered after he experienced dizziness. The tumor was located in the frontotemporal area of his brain. Imaging scans showed the mass contained significant fat signal and was pressing on nearby brain structures. The man underwent surgery to completely remove the tumor.

After surgery, laboratory analysis of the tumor tissue confirmed it was a specific type of brain tumor called a World Health Organization Grade II ependymoma. What made this case unusual was that the tumor also contained areas of fatty tissue, a rare change called lipomatous metaplasia. Special staining tests highlighted features of both the typical tumor cells and the fatty tissue.

This report combines this single case with a review of previously published similar cases in medical literature. The authors note this fatty change within this type of brain tumor is extremely rare. The goal of the report is to help other doctors and pathologists recognize this rare variant if they encounter it.

Readers should understand this is a description of one very rare case. It does not provide information on how common this is, what causes it, or long-term outcomes for patients. The main takeaway is that doctors sometimes encounter unusual variations in tumors, and careful analysis is needed for accurate diagnosis.

What this means for you:
A single case report describes an extremely rare brain tumor variant containing fat tissue. This finding is not common.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Ependymomas are uncommon tumors arising from ependymal cells of the central nervous system, with lipomatous metaplasia representing an extremely rare pathological variant. We report a case of a 28-year-old male who presented with a 5-year history of an incidentally discovered intracranial mass and recent-onset dizziness. Magnetic resonance imaging (MRI) revealed a left frontotemporal lesion characterized by significant fat signal, progressive enhancement, and mass effect on adjacent structures. The patient underwent gross-total resection, and histopathology confirmed a World Health Organization (WHO) Grade II ependymoma with lipomatous metaplasia. Immunohistochemical analysis further supported the diagnosis, highlighting features of both ependymal differentiation and fatty metaplasia. We also provide a comprehensive literature review of previously reported cases, emphasizing the rarity, imaging characteristics, differential diagnosis, and surgical considerations for this unique pathological variant. This case underscores the importance of careful radiological and pathological evaluation to guide diagnosis and management, and aims to raise awareness of this rare subtype among clinicians and pathologists.
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