Vol 11, No 6 (2015)
Case report
Published online: 2016-03-08

open access

Page views 681
Article views/downloads 1268
Get Citation

Connect on Social Media

Connect on Social Media

Synovial sarcoma of the neck

Mariusz Stefański, Paweł Rogoziński, Krzysztof Bruliński
Oncol Clin Pract 2015;11(6):317-321.

Abstract

Soft-tissue sarcomas originate from the mesodermal tissue. They mainly locate within extremities (50% of cases), trunk (30%), head and neck (10%), and in the retroperitoneal space (10%). Sarcomas represent about 1% of all malignant tumours in adults. So far, causes of the soft-tissue sarcomas have not been well recognised. These neoplasms occur more frequently in persons with genetic diseases. Frequent prevalence of sarcomas is observed in subjects with Von Recklinghausen disease (neurofibromatosis), Gardner syndrome, Werner syndrome, tuberous sclerosis, and Li-Fraumeni syndrome (mutation p53). This paper presents the case of a 29-year-old patient with a large tumour of the neck and Von Recklinghausen disease, referred to the Department of Thoracic Surgery with the diagnosis of MPNST (malignant peripheral nerve sheath tumours).

References

  1. Potter BO, Sturgis EM. Sarcomas of the head and neck. Surg Oncol Clin N Am. 2003; 12(2): 379–417.
  2. Sturgis EM, Potter BO. Sarcomas of the head and neck region. Curr Opin Oncol. 2003; 15(3): 239–252.
  3. Rutkowski P, Nowecki ZI. Mięsaki tkanek miękkich u dorosłych — monografia. Medical Tribune, Warszawa 2009.
  4. Lyos AT, Goepfert H, Luna MA, et al. Soft tissue sarcoma of the head and neck in children and adolescents. Cancer. 1996; 77(1): 193–200.
  5. Hruban RH, Shiu MH, Senie RT, et al. Malignant peripheral nerve sheath tumors of the buttock and lower extremity. A study of 43 cases. Cancer. 1990; 66(6): 1253–1265.
  6. Wick MR, Swanson PE, Scheithauer BW, et al. Malignant peripheral nerve sheath tumor. An immunohistochemical study of 62 cases. Am J Clin Pathol. 1987; 87(4): 425–433.
  7. Kransdorf MJ. Malignant soft-tissue tumors in a large referral population: distribution of diagnoses by age, sex, and location. AJR Am J Roentgenol. 1995; 164(1): 129–134.
  8. Spillane AJ, A'Hern R, Judson IR, et al. Synovial sarcoma: a clinicopathologic, staging, and prognostic assessment. J Clin Oncol. 2000; 18(22): 3794–3803.
  9. Burns DK, Kumar V. Układ mięśniowo-szkieletowy. In: Kumar V, Cotran RS, Robbins SL. ed. Patologia Robbinsa. Elsevier Urban & Partner, Wrocław 2003: 863–898.
  10. Dardick I, Ramjohn S, Thomas MJ, et al. Synovial sarcoma. Inter-relationship of the biphasic and monophasic subtypes. Pathol Res Pract. 1991; 187(7): 871–885.
  11. van de Rijn M, Barr FG, Xiong QB, et al. Poorly differentiated synovial sarcoma: an analysis of clinical, pathologic, and molecular genetic features. Am J Surg Pathol. 1999; 23(1): 106–112.
  12. Ruka W, et al. Mięsaki tkanek miękkich u dorosłych — zasady postępowania diagnostyczno-terapeutycznego. Onkol Prakt Klin. 2009; 5: 198–210.
  13. Limon J, Mrozek K, Mandahl N, et al. Cytogenetics of synovial sarcoma: presentation of ten new cases and review of the literature. Genes Chromosomes Cancer. 1991; 3(5): 338–345.
  14. Shah J, Patel S, Singh B. Chirurgia i onkologia głowy i szyi. Vol II. Elsevier Urban & Partner, Wrocław 2012: 144–188.