Two cases of fibrolipomatous hamartomas of the median nerve: A rare entity with pathognomonic MRI features

Fibrolipomatous hamartomas of the median nerve are rare, benign tumors characterized by the overgrowth of fibro-fatty tissue within the nerve sheath, often leading to nerve compression. This report presents 2 cases: a 33-year-old man with a gradually enlarging wrist mass and a 48-year-old woman, initially diagnosed with De Quervain's tenosynovitis for radial pain, who was found to have an incidental fibrolipomatous hamartoma on MRI. In both cases, MRI played a pivotal role in diagnosis, revealing characteristic features that enabled a definitive, noninvasive diagnosis. Early recognition of these MRI findings is essential for guiding management and preventing unnecessary surgical interventions.

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Publication Details

Journal
Radiology Case Reports
Published
2024-11-08
DOI
https://doi.org/10.1016/j.radcr.2024.10.015
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
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article

Two cases of fibrolipomatous hamartomas of the median nerve: A rare entity with pathognomonic MRI features

Evangelos Petsatodis, Anastasia Theocharidou, Antonios Michailidis, Ola Furmaga-Rokou et al.
Radiology Case Reports
Neurofibromatosis and Schwannoma Cases
article

Two cases of fibrolipomatous hamartomas of the median nerve: A rare entity with pathognomonic MRI features

Evangelos Petsatodis, Anastasia Theocharidou, Antonios Michailidis, Ola Furmaga-Rokou, Ioannis Tsifountoudis
article en

Abstract

Fibrolipomatous hamartomas of the median nerve are rare, benign tumors characterized by the overgrowth of fibro-fatty tissue within the nerve sheath, often leading to nerve compression. This report presents 2 cases: a 33-year-old man with a gradually enlarging wrist mass and a 48-year-old woman, initially diagnosed with De Quervain's tenosynovitis for radial pain, who was found to have an incidental fibrolipomatous hamartoma on MRI. In both cases, MRI played a pivotal role in diagnosis, revealing characteristic features that enabled a definitive, noninvasive diagnosis. Early recognition of these MRI findings is essential for guiding management and preventing unnecessary surgical interventions.

Radiology Case ReportsVol. 20(1)
424 General Military Hospital (GR), G. Papanikolaou General Hospital (GR), Asklepios (DE)
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Openalex Percentile: Top 69%
Neurofibromatosis and Schwannoma Cases
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