Malignant ovarian tumor composed of endometrioid adenocarcinoma, clear cell adenocarcinoma, squamous cell carcinoma, yolk sac tumor and immature teratoma with prominent neuroectodermal and rhabdomyosarcomatous differentiation: A case study

被引:5
|
作者
Ohishi, Yoshihiro
Kaku, Tsunehisa
Kaneki, Eisuke
Wake, Norio
Tsuneyoshi, Masazumi
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Anat Pathol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Sch Med, Dept Hlth Sci, Div Maternal Hlth, Fukuoka 812, Japan
[3] Kyushu Univ Hosp, Dept Obstet & Gynecol, Fukuoka 812, Japan
关键词
endomettioid adenocarcinoma; clear cell adenocarcinoma; yolk sac tumor; immature teratoma; neuroectodermal and rhabdomyosarcomatous differentiation;
D O I
10.1016/j.ygyno.2007.02.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Cases of malignant ovarian tumor composed of mullerian-type epithelial tumor and malignant germ cell tumor are extremely rare. Case. We herein report the case of a 34-year-old woman with an ovarian tumor which was composed of endometrioid adenocarcinoma (EAC), clear cell adenocarcinoma (CCC), squamous cell carcinoma, yolk sac tumor (YST) and immature teratoma with prominent neuroectodermal and rhabdomyosarcomatous differentiation. Even after systemic chemotherapy, this intriguing tumor recurred again and again, which is in contrast to pure germ cell tumor which is known to be sensitive to chemotherapy. Conclusion. No previous cases with an identical composition have been found in the literature. Correct diagnosis of this complex and aggressive tumor is paramount. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:548 / 552
页数:5
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