Epithelioid sarcoma of femoral nerve – A case report

  • Dejan Ivanov Clinical Center of Vojvodina, Clinic for Abdominal, Endocrine Surgery and Transplantation, Novi Sad, Serbia
  • Mirjana Živojinov Clinical Center of Vojvodina, Department for Pathology, Novi Sad, Serbia ; Oncology Institute of Vojvodina, Sremska Kamenica, Serbia
  • Milan Ranisavljević Clinical Center of Vojvodina, Department for Pathology, Novi Sad, Serbia; Faculty of Medicine, Novi Sad, Serbia
Keywords: sarcoma;, soft tissue neoplasms;, femoral nerve;, diagnostic techniques and procedures;, surgical procedures, operative;, radiotherapy.

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), anti-cytokeratin 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.

References

REFERENCE:

Asano N, Yoshida A, Ogura K, Kobayashi E, Susa M, Morioka H, et al. Prognostic Value of Relevant Clinicopathologic Variables in Epithelioid Sarcoma: A Multi-Institutional Retrospective Study of 44 Patients. Ann Surg Oncol 2015; 22(8): 2624–32.

Hee Han C, Li X, Khannaa N. Epithelioid sarcoma of the vulva and its clinical implication: A case report and review of the literature. Gynecol Oncol Rep 2016; 15: 31–3.

Gayatri SP, Amrut VA, Sanjay DD, Shirish SP, Pankaj K. Prox-imal type of epithelioid sarcoma of back with metastasis to humerus at presentation: Indicating aggressive behavior. In-dian J Cancer 2015; 52(1): 97–8.

Lee C, Choe WJ, Kim N. Epithelioid Sarcoma in the Cervical Spine: A Case Report. Korean J Spine 2015; 12(3): 165–8.

Akpinar F, Dervis E, Demirkesen C, Akpinar AC, Ergun SS. Epithelioid sarcoma of the extremities. Indian J Dermatol Ve-nereol Leprol 2014; 80(2): 168–70.

Enzinger FM. Epitheloid sarcoma. A sarcoma simulating a gra-nuloma or a carcinoma. Cancer 1970; 26(5): 1029‒41.

Eyden B, Wang G, Yao L. Epithelioid sarcoma: A case report with ultrastructural confirmation of myofibroblastic differen-tiation based on fibronexus junctions. Ultrastruct Pathol 2009; 33(2): 61–6.

Halling AC, Wollan PC, Pritchard DJ, Vlasak R, Nascimento AG. Epithelioid sarcoma: a clinicopathologic review of 55 cases. Mayo Clin Proc 1996; 71(7): 636–42.

Chbani L, Guillou L, Terrier P, Decouvelaere AV, Grégoire F, Terrier-Lacombe MJ, et al. Epithelioid sarcoma: a clinicopatho-logic and immunohistochemical analysis of 106 cases from the French sarcoma group. Am J Clin Pathol 2009; 131(2): 222–7.

Callister MD, Ballo MT, Pisters PW, Patel SR, Feig BW, Pollock RE, et al. Epithelioid sarcoma: results of conservative surgery and radiotherapy. Int J Radiat Oncol Biol Phys 2001; 51(2): 384–91.

Ross HM, Lewis JJ, Woodruff JM, Brennan MF. Epithelioid sar-coma: clinical behavior and prognostic factors of survival. Ann Surg Oncol 1997; 4(6): 491–5.

Thway K, Jones RL, Noujaim J, Fisher C. Epithelioid sarcoma: diagnostic features and genetics. Adv Anat Pathol 2016; 23(1): 41–9.

Published
2020/12/01
Section
Case report