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12例卵巢子宫恶性中胚叶混合瘤临床病理分析

郝金燕 邓晋芳 刘莉萍 刘文悦 王晨 潘慧 李杰

解放军医学院学报2015,Vol.36Issue(9):896-899,4.
解放军医学院学报2015,Vol.36Issue(9):896-899,4.DOI:10.3969/j.issn.2095-5227.2015.09.011

12例卵巢子宫恶性中胚叶混合瘤临床病理分析

Ovary and uterus malignant mullerian mixed tumor: A clinicopathological study of 12 cases

郝金燕 1邓晋芳 2刘莉萍 1刘文悦 2王晨 2潘慧 2李杰2

作者信息

  • 1. 解放军总医院 病理科,北京 100853
  • 2. 北京市顺义区医院 病理科,北京 101300
  • 折叠

摘要

Abstract

Objective To study the clinicopathological features of ovary and uterus malignant mullerian mixed tumor (MMMT), and investigate its diagnosis and prognosis.Methods Twelve cases with ovary and uterus malignant mullerian mixed tumor in department of pathology, Chinese PLA General Hospital from 2008 to 2013 were enrolled in this study, their macroscopy, microscopy and immunohistochemistry were investigated, and clinical data and literatures were reviewed.Results The average age of MMMT cases was 59.6 years (range from 43 to 74 years). Of the 12 cases, 3 cases were uterus MMMT, 8 cases were unilateral ovary and 1 case was both ovaries and cervix MMMT. The patients usually presented with abnormal vaginal bleeding, abdominal pain and pelvic mass with no specificity in clinic. The morphological changes included epithelial and mesenchymal components. Of the 12 cases, 6 cases were serous papillary carcinoma, 1 case was squamous cell carcinoma, 5 cases were endometrioid carcinoma and 2 cases had chondrosarcoma, 4 cases had leiomyosarcoma, 2 cases had rhabdomyosarcoma, 3 cases had endometrial stromal sarcoma, and 1 case had endometrial stromal sarcoma mixed chondrosarcoma. Immunohistochemically, CK was positive in all epithelial components, Vimentin was positive in all mesenchymal components, H-caldesmon was positive in leiomyosarcoma, Desmin was positive in rhabdomyosarcoma, CD10 was positive in endometrial stromal sarcoma, and S-100 was positive in chondrosarcoma. The main treatment was surgery plus chemotherapy. Ten cases were followed up (2 cases lost follow-up), 1 case died within one month after surgery, 7 cases relapsed during six tofifty-eight months and 2 cases had no tumor progression and metastasis during one and two years after surgery.Conclusion MMMT is a rare subtype of malignant epithelial mesenchymal mixed tumors. Because its clinical features are unspecific,final diagnosis need pathological and immunohistochemical staining and its prognosis is extremely poor.

关键词

恶性中胚叶混合瘤/免疫组织化学/鉴别诊断/卵巢/子宫

Key words

malignant mullerian mixed tumor/immunohistochemistry/differential diagnosis/ovary/uterus

分类

医药卫生

引用本文复制引用

郝金燕,邓晋芳,刘莉萍,刘文悦,王晨,潘慧,李杰..12例卵巢子宫恶性中胚叶混合瘤临床病理分析[J].解放军医学院学报,2015,36(9):896-899,4.

解放军医学院学报

OACSTPCD

2095-5227

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