Fibrolipomatous Hamartoma of Digital Branch of the Median Nerve without Macrodystrophy: Two Case Reports with Magnetic Resonance Imaging Findings

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منابع مشابه

Fibrolipomatous Hamartoma of the Median Nerve

A case of fibrolipomatous hamartoma of the median nerve is presented. The operative findings were characteristic. The diagnosis should be confirmed by histological examination of a biopsy from an involved palmar cutaneous branch, and treatment should be limited to decompression of the ligament or fascia over the involved area.

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Fibrolipomatous hamartoma of the median nerve

http://www.sajr.org.za doi:10.4102/sajr.v19i2.886 Fibrolipomatous hamartoma is a rare benign tumour most commonly affecting the median nerve and is characterised by fibro-fatty nerve infiltration. It results in fusiform nerve enlargement with a pathognomonic ‘spaghetti-like’ imaging appearance. Patients present with numbness and paraesthesia and later with motor deficits in the affected nerve d...

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Fibrolipomatous hamartoma of the median nerve on CT

Fibrolipomatous hamartomas are rare lesions with a pathognomonic appearance on MRI. I describe CT findings that parallel the pathognomonic description on MRI. While these lesions are typically evaluated on MRI, they may be discovered incidentally on a CT scan of the upper extremity. In addition, contraindications to MRI may require CT evaluation in some cases. The findings of soft tissue with c...

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Fibrolipomatous hamartoma in the median nerve in the arm - an unusual location but with MR imaging characteristics: a case report

Fibrolipomatous hamartoma of the median nerve are usually located distally in the forearm and may have characteristic features on MR imaging. Here we report a patient with an extensive fibrolipomatous hamartoma at an unusual location proximally in the arm, where a preoperative MR imaging was pathognomonic and diagnosis was verified by an incisional biopsy. We suggest that MRI should be performe...

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ژورنال

عنوان ژورنال: Journal of the Korean Society of Radiology

سال: 2012

ISSN: 1738-2637

DOI: 10.3348/jksr.2012.67.6.483