| Literature DB >> 16813111 |
Takuma Tsukioka1, Kiyotoshi Inoue, Takashi Iwata, Shinjiro Mizuguchi, Ryuhei Morita, Shigefumi Suehiro.
Abstract
A 29-year-old female was admitted to our hospital complaining of severe dry cough and low-grade fever. A chest roentgenogram and a chest computed tomographic scan revealed a huge tumor and massive pleural effusion in the left pleural cavity. Pathological examination revealed spindle shaped malignant cells. SYT-SSX fusion gene transcripts were detected, so we diagnosed the tumor as a synovial sarcoma in the pleural cavity. After neoadjuvant chemotherapy we resected the tumor completely. A synovial sarcoma in the pleural cavity is extremely rare. To the best of our knowledge, this is the thirteenth case, and the first case to undergo neoadjuvant chemotherapy and complete resection. Because a synovial sarcoma in the pleural cavity has a poor prognosis and is characterized by a high incidence of recurrence, we must carefully follow up this patient.Entities:
Mesh:
Year: 2006 PMID: 16813111 DOI: 10.1007/pl00022249
Source DB: PubMed Journal: Jpn J Thorac Cardiovasc Surg ISSN: 1344-4964