临床肿瘤学杂志

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女性腹膜恶性间皮瘤的临床病理及预后研究

王 静1,朱 江2

  

  1. 1 610500 成都 成都医学院第一附属医院消化内科 2 1400038 第三军医大学西南医院病理研究所
  • 收稿日期:2012-09-19 修回日期:2012-12-03 出版日期:2013-03-31 发布日期:2013-03-31

Clinicopathological characteristics and prognosis of female peritoneal malignant mesothelioma

WANG Jing,ZHU Jiang.   

  1. Department of Gastroenterology,the First of Affiliated Hospital,Chengdu Medical College,Chengdu 610500,China
  • Received:2012-09-19 Revised:2012-12-03 Online:2013-03-31 Published:2013-03-31

摘要: 目的 探讨女性腹膜恶性间皮瘤(FPMM)的临床病理特点和预后。方法 收集13例FPMM患者的临床病理及随访资料,包括肿瘤组织的病理和免疫组织化学(IHC)染色检测。选取广泛转移性卵巢低分化浆液性癌(MPDOSC)和广泛转移性低分化结直肠腺癌(MPDCC)各5例患者作为对照。结果 13例FPMM中8例发生于盆腔,5例发生于腹腔。13例均行手术切除和术后化疗。病理分型:上皮型12例,双相型1例,未见肉瘤型。组织学表现:立方或低柱状瘤细胞被覆于小管或纤细的不规则乳头上,或多边形细胞镶嵌成片、团、巢状排列。瘤细胞大小一致,胞浆丰富嗜酸;细胞核位于中央,染色质细腻,异型性不明显;部分标本有少数异型性明显的巨核细胞或瘤巨细胞。MPDOSC和MPDCC的组织构型与FPMM相似,但癌细胞异型性更明显。FPMM表现为P-CK、Vimentin、Calretinin阳性,CEA阴性;MPDOSC 表现为CK7、CA125、p53阳性;MPDCC表现为CK20、CA199、CEA阳性;3种肿瘤的Ki-67阳性率均较高。12例FPMM患者随访6~28个月,2例存活,10例死亡,其平均生存期为(12.2±5.3)个月;5例MPDOSC和MPDCC患者分别的平均生存期(10.2±3.7)个月和(6.9±2.1)个月。结论 FPMM更易发生于盆腔。上皮型FPMM有其特征性病理表现,但仍需多种免疫表型综合判断。部分FPMM预后较好,可较长时间存活,应予以积极治疗。

Abstract: Objective To explore the features of the clinicopathology and prognosis for female peritoneal malignant mesothelioma(FPMM). Methods The clinical data and followed up results of 13 cases FPMM were collected and the tumor tissues were studied in histopathology and immunohistochemistry(IHC). The 5 cases of metastatic poorly differentiated serous carcinomas of ovarian(MPDOSC) and 5 cases of female metastatic poorly differentiated colorectal carcinomas(MPDCC) were studied as contrast. Results Eight cases tumors occurred in pelvic cavity,5 cases occurred in peritonium. All the 13 cases were operated and carried out chemotherapy. There were 12 epithelioid patterns and 1 biopolar pattern in FPMM. The cubic or low columnar tumor cells were covered on tubules or slender and irregular papillae,or polygonal cells were arrayed in solid sheets. The size of the tumor cells with abundant and eosinophilic cytoplasm were similar, nuclear/cytoplasmic area ratio were equal. The nuclei located in center and showed well distributed fine chromatin with a light atypical and a few mitosis. Among the epithelioid tumor cells, there were dispersive giant cells or multinucleations. There was one biphasic differentiation and no sarcomatoid patten. The histological patterns of MPDOSC and MPDCC may be similar to FPMM, but the anaplasia of carcinoma cells was more outstanding. The IHC showed that P-CK, Vimentin,Calretinin were positive and CEA were negative in FPMM. CK7,CA125,p53 were positive in MPDOSC and CK20,CA19-9,CEA were positive in MPDCC. The positive index of Ki-67 was very high in 3 kinds of tumors. Twelve cases were followed up for 6-28 months. Ten cases died and 2 cases survived. The average survival was 14.8±7.8 months. However,the average survival was 10.2±3.7 months in MPDOSC and 6.9±2.1 months in MPDCC respectively. Conclusion The chief sites of FPMM were pelvic cavity. The epithlioid FPMM had their characteristics in histopathology. The IHC phenotype including positive and negative are needed to differential diagnosis. Some FPMM patients can survive longer,so they should be treated positively.

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