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Case ReportInternational Surgery Journal

Publication:
Rare site and size of a neurofibroma: a case report

Int Surg J. 2015;2(1):88-90.DOI10.5455/2349-2902.isj20150218

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Abstract

Neurofibromas are tumor of neural connective tissue, mainly composed of Schwann cells and fibroblasts. They can occur anywhere in the body, presenting as a feature of neurofibromatosis or as a solitary mass except in the brain and spinal cord. A large neurofibroma in the inguino-scrotal region is a rare condition with few reports available in the literature. We report a case of a 32 year old male with a large mass extending from the inguinal region into the thigh, mimicking an indirect inguinal hernia. Since he had multiple nodules on his body suggestive of neurofibromatosis, a diagnosis of benign neurofibroma was made, the mass excised and the diagnosis confirmed by histo-pathological examination. Elongated, spindle shaped neoplastic cells with poorly defined cytoplasm was observed. No evidence of atypical mitotic figures noted.

Keywords

Affiliations

  1. Consultant surgeon, Apollo KH Hospitals, Ranipet, Tamil Nadu
  2. Department of Anatomy, ESIC Medical College, Chennai, Tamil Nadu

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