Pleuropulmonary Blastoma in a Young Adult Presenting as a Ruptured Cystic Teratoma in Radiology.
10.3346/jkms.2003.18.4.595
- Author:
Chang Hun LEE
1
;
Keun Il KIM
;
Young Dae KIM
;
Min Ki LEE
;
Jee Yeon KIM
;
Do Youn PARK
;
Mee Young SOL
;
Kang Suek SUH
Author Information
1. Department of Pathology, Internal Medicine Pusan National University College of Medicine, Busan, Korea.cnlee@pusan.ac.kr
- Publication Type:Case Report
- Keywords:
Mediastinal Neoplasms;
Pulmonary Blastoma;
Teratoma;
Adult
- MeSH:
Adult;
Diagnosis, Differential;
Human;
Immunohistochemistry;
Lung Neoplasms/*diagnosis/radiography/surgery;
Male;
Pulmonary Blastoma/*diagnosis/radiography/surgery;
Teratoma/*diagnosis/*radiography/surgery;
Tomography, X-Ray Computed;
Vimentin/biosynthesis
- From:Journal of Korean Medical Science
2003;18(4):595-598
- CountryRepublic of Korea
- Language:English
-
Abstract:
Pleuropulmonary blastoma (PPB) is a rare malignant dysontogenetic neoplasm primarily affecting children and is characterized histologically by a variably mixed blastematous and sarcomatous patterns. We herein report a very exceptional adult case of PPB. A 21-yr-old male patient presented with a left chest pain of two weeks' duration. A computed tomography scan revealed a large, multicystic tumor occupying the left lower hemithorax, leading to the impression of a ruptured mediastinal cystic teratoma. A thoracotomy for resection of the tumor was performed. On histologic examination, the tumor consisted of cystic walls and associated solid lesions which showed undifferentiated blastemal tissues with focal fibrosarcomatous and rhabdoid features. Immunohistochemically the tumor cells only showed diffuse strong positivity for vimentin. The histologic findings corresponded to a type II PPB. The authors suggest that PPB, especially of type I or II, should be included in the radiologic differential diagnosis of mediastinal cystic neoplasms in a young adult.