| Literature DB >> 29260248 |
N S Häring1, R Strohal2, S Dertinger3, F Offner3.
Abstract
The epithelioid sarcoma classic, "distal" type was first published in 1970. It is a very rare, malignant, aggressive subcutaneous soft tissue sarcoma that shows characteristic positivity for both epithelial and mesenchymal immunohistochemical markers. It grows very slowly and mostly presents in young men. Clinically the tumor is characterized as a coarse cutaneous or subcutaneous nodular induration that often ulcerates in the course of the disease. An association with trauma is often described and can lengthen time to diagnosis. Most frequently it is found on the flexural side of fingers, the back of the hands, soles of the feet, and extensor sides of arms and legs. Specific for this type of sarcoma is the progression along nerves, tendons, and fasciae. Treatment of choice should be wide excision of the tumor, sentinel node biopsy, and possibly even localized postoperative radiation therapy. Unfortunately the epithelioid sarcoma is very likely to recur and is then associated with metastases in the lung and lymph nodes.Entities:
Keywords: Excision; Radiation therapy; Recurrence; Sentinel lymph node biopsy; Soft tissue neoplasms
Mesh:
Year: 2018 PMID: 29260248 DOI: 10.1007/s00105-017-4087-0
Source DB: PubMed Journal: Hautarzt ISSN: 0017-8470 Impact factor: 0.751