Carcinosarcoma of the Urinary Bladder—An Aggressive Tumor With Diverse Histogenesis

2000 ◽  
Vol 124 (8) ◽  
pp. 1172-1178 ◽  
Author(s):  
Dmitry Y. Baschinsky ◽  
Janny H. Chen ◽  
Manjunath S. Vadmal ◽  
Joel G. Lucas ◽  
Robert R. Bahnson ◽  
...  

Abstract Objective.—Carcinosarcomas of urinary bladder are rare malignant neoplasms. Seventy-eight cases have been previously described. The histologic composition of these tumors is variable, but diagnosis requires the presence of both epithelial and mesenchymal malignant components. We report 4 additional cases, with an emphasis on unusual histologic features. Methods.—Histologic and immunohistochemical examinations were performed on bladder tumors from 4 patients. Clinicopathologic features of previously reported and current cases were reviewed and summarized. Results.—Four patients (3 men, 1 woman) age 54 to 77 years were found to have polypoid masses in the urinary bladder. In all cases, histologic examination showed biphasic neoplasms with distinct mesenchymal and epithelial components. The morphologic and immunohistochemical characteristics of the tumors varied. One of the cases was remarkable for the presence of liposarcoma, malignant peripheral nerve sheath tumor, and micropapillary urothelial carcinoma. Two of the patients died 2 years after diagnosis, which is consistent with the previously reported aggressive nature of urinary bladder carcinosarcomas. Conclusions.—Carcinosarcomas of the urinary bladder are rare, aggressive malignant neoplasms. To our knowledge, a liposarcomatous component has been reported in only 1 case previously, and components of micropapillary urothelial carcinoma and malignant peripheral nerve sheath tumor have not been reported previously in carcinosarcomas of the urinary bladder. Because of the aggressive biologic behavior of these tumors, they should be identified promptly and treated appropriately.

1999 ◽  
Vol 3 (5) ◽  
pp. 304-308 ◽  
Author(s):  
Isam A. Eltoum ◽  
R. Jemison Moore ◽  
William Cook ◽  
D. Ralph Crowe ◽  
William H. Rodgers ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Osmond C. Wu ◽  
Berje H. Shammassian ◽  
Arunit J. S. Chugh ◽  
Aparna Harbhajanka ◽  
Manish K. Kasliwal

Primary intradural malignant peripheral nerve sheath tumor (MPNST) is an extremely rare diagnosis and is associated with an extremely poor prognosis. A 77-year-old man diagnosed with an intradural MPNST, more than 40 years after radiation for a testicular seminoma, is reported. Intradural MPNSTs of the spine outside the setting of neurofibromatosis is extremely rare and can masquerade as common benign nerve sheath tumors, on imaging. An older age at presentation with short duration of symptoms and prior regional radiation treatment encompassing the spine in the treatment field regardless of remoteness should alert the oncologists and neurosurgeons to the possible existence of this rare and aggressive tumor, as the management, and overall prognosis of this tumor is distinctly different compared to the usual intradural spinal tumors.


2002 ◽  
Vol 69 (2) ◽  
pp. 156-159 ◽  
Author(s):  
Panagiotis Kalafatis ◽  
Nikolaos Kavantzas ◽  
Petros M. Pavlopoulos ◽  
Emmanuel Agapitos ◽  
Mary Politou ◽  
...  

2016 ◽  
Vol 78 (5) ◽  
pp. 516-521
Author(s):  
Fumihisa SAWADA ◽  
Eiichi MAKINO ◽  
Takenobu YAMAMOTO ◽  
Ryo TANAKA ◽  
Yutaka FUJIWARA ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document