NON-GERM-CELL OR TERATOMATOUS MALIGNANT-TUMORS SHOWING ADDITIONAL RHABDOMYOBLASTIC DIFFERENTIATION, WITH EMPHASIS ON THE MALIGNANT TRITON TUMOR

Citation
Jm. Woodruff et G. Perino, NON-GERM-CELL OR TERATOMATOUS MALIGNANT-TUMORS SHOWING ADDITIONAL RHABDOMYOBLASTIC DIFFERENTIATION, WITH EMPHASIS ON THE MALIGNANT TRITON TUMOR, Seminars in diagnostic pathology, 11(1), 1994, pp. 69-81
Citations number
NO
Categorie Soggetti
Medical Laboratory Technology",Pathology
ISSN journal
07402570
Volume
11
Issue
1
Year of publication
1994
Pages
69 - 81
Database
ISI
SICI code
0740-2570(1994)11:1<69:NOTMSA>2.0.ZU;2-S
Abstract
Non-germ-cell or teratomatous malignant tumors showing additional rhab domyoblastic differentiation can be divided into three groups. Group I consists of tumors with only sarcomatous differentiation. Included in this group are malignant mesenchymoma, dedifferentiated chondrosarcom a, and the dedifferentiated retroperitoneal liposarcoma. Epithelial or Sertoli-Leydig cell elements represent the second component of tumors in group II. The best known tumor in this group is the malignant mull erian mixed tumor, but other well described tumors with rhabdomyosarco matous differentiation are the carcinosarcoma, mullerian adenosarcoma, Sertoli-Leydig cell tumor, mammary cystosarcoma, and blastomas. Most of the tumors in groups I and II are derived from mesenchymal tissue. A neuroectodermal origin is shared by all tumors in group III. This in cludes the medulloblastoma, retinoblastoma and, most frequently, the m alignant Triton tumor. The tumors in all three groups are clinically m alignant to a varying degree. Copyright (C) 1994 by W.B. Saunders Comp any