Meningothelial Hamartoma Masquerading as a Lipoma: A Case Report and Review of Literature

Meningothelial hamartoma is a rare, benign scalp lesion that is often misdiagnosed as common soft tissue tumors such as lipomas. It is characterized by ectopic meningothelial elements and is classified as a type of cutaneous meningioma. Due to its rarity and histological overlap with other lesions, diagnosis requires histopathological examination and immunohistochemistry (IHC). A 36-year-old female presented with a painless, slow-growing lump on the left forehead persisting for 10 years. Magnetic resonance imaging (MRI) findings suggested a lipoma, and fine needle aspiration cytology (FNAC) indicated a fibro lipomatous lesion of neoplastic nature. It was surgically excised, and histopathology revealed mature adipose tissue with meningothelial cells. IHC showed epithelial membrane antigen (EMA) and vimentin positivity, confirming meningothelial hamartoma. The patient recovered well postoperatively, with no recurrence after one year. Meningothelial hamartoma is often misdiagnosed due to its resemblance to more common scalp tumors. Surgical excision is the mainstay of treatment, and IHC markers such as EMA and vimentin are essential for diagnosis. Given its potential hormonal influences and association with nevus sebaceous, further research is warranted. Clinicians should consider meningothelial hamartoma in atypical scalp lesions to ensure accurate diagnosis and appropriate management.

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Publication Details

Journal
Cureus
Published
2025-02-26
DOI
https://doi.org/10.7759/cureus.79732
Primary Topic
Teratomas and Epidermoid Cysts
Type
article
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article

Meningothelial Hamartoma Masquerading as a Lipoma: A Case Report and Review of Literature

Rekha Gupta, Saransh Gupta
Cureus
Teratomas and Epidermoid Cysts
article

Meningothelial Hamartoma Masquerading as a Lipoma: A Case Report and Review of Literature

Rekha Gupta, Saransh Gupta
article en

Abstract

Meningothelial hamartoma is a rare, benign scalp lesion that is often misdiagnosed as common soft tissue tumors such as lipomas. It is characterized by ectopic meningothelial elements and is classified as a type of cutaneous meningioma. Due to its rarity and histological overlap with other lesions, diagnosis requires histopathological examination and immunohistochemistry (IHC). A 36-year-old female presented with a painless, slow-growing lump on the left forehead persisting for 10 years. Magnetic resonance imaging (MRI) findings suggested a lipoma, and fine needle aspiration cytology (FNAC) indicated a fibro lipomatous lesion of neoplastic nature. It was surgically excised, and histopathology revealed mature adipose tissue with meningothelial cells. IHC showed epithelial membrane antigen (EMA) and vimentin positivity, confirming meningothelial hamartoma. The patient recovered well postoperatively, with no recurrence after one year. Meningothelial hamartoma is often misdiagnosed due to its resemblance to more common scalp tumors. Surgical excision is the mainstay of treatment, and IHC markers such as EMA and vimentin are essential for diagnosis. Given its potential hormonal influences and association with nevus sebaceous, further research is warranted. Clinicians should consider meningothelial hamartoma in atypical scalp lesions to ensure accurate diagnosis and appropriate management.

CureusVol. 17(2)
Central University of Punjab (IN), Dr. B. R. Ambedkar National Institute of Technology Jalandhar (IN)
Openalex Percentile: Top 94%
Teratomas and Epidermoid Cysts
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