Epithelioid sarcoma of femoral nerve: A case report

Author:

Ivanov Dejan1,Zivojinov Mirjana2,Ranisavljevic Milan3

Affiliation:

1. Clinical Center of Vojvodina, Clinic for Abdominal, Endocrine Surgery and Transplantation, Novi Sad + Clinical Center of Vojvodina, Department for Pathology, Novi Sad

2. Clinical Center of Vojvodina, Department for Pathology, Novi Sad + Oncology Institute of Vojvodina, Sremska Kamenica

3. Clinical Center of Vojvodina, Department for Pathology, Novi Sad + Faculty of Medicine, Novi Sad

Abstract

Introduction. Epithelioid sarcoma is a slow-growing malignant soft tissue tumor and occurs approximately in 1% of all soft tissue malignant tumors. This case report describes epithelioid sarcoma in femoral nerve and as we know it is the first described case of epithelioid sarcoma at this anatomical localisation. Case report. A 44-years-old female patient presented with strong pain in her left leg. On magnetic resonance imaging (MRI), tumor was presented as a node 8 cm in the diameter at left femoral nerve between ileopsoas and iliacus muscle, without infiltration of muscle fascia and tendons. Four enlarged lymph nodes described in left iliac fosa, were suspected on secondary tumor deposits. We preformed radical surgical excision of the tumor and femoral nerve transection with local lymp hnode disection. Histopathological analysis revealed epithelioid sarcoma, and tumor stained highly positive for anti-pan cytokeratin antibody (AE1/AE3), vimentin, cancer antigen 125 (CA125), anticytokeratin antibody (MNF116), hematopoietic progenitor cell antigen (CD34) and epithelial membrane antigen (EMA) markers. After the operation patient recived radiotherapy without chemotherapy. Six months postoperatively, there was no evidence of local relapses or distant metastases. Conclusion. Initial wide surgical resection and adjuvant radiotherapy is beneficial in treatment of epitheloid sarcoma.

Publisher

National Library of Serbia

Subject

Pharmacology (medical),General Medicine

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