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具有微乳头和筛状模式的卵巢浆液性交界性肿瘤:40例研究及与44例无这些模式的病例对比。

Ovarian serous borderline tumors with micropapillary and cribriform patterns: a study of 40 cases and comparison with 44 cases without these patterns.

作者信息

Eichhorn J H, Bell D A, Young R H, Scully R E

机构信息

Massachusetts General Hospital, and the Department of Pathology, Harvard Medical School, Boston 02114, USA.

出版信息

Am J Surg Pathol. 1999 Apr;23(4):397-409. doi: 10.1097/00000478-199904000-00004.

Abstract

A group of investigators have proposed that the presence of micropapillary or cribriform patterns within ovarian serous tumors diagnosed as borderline according to World Health Organization (WHO) criteria identifies a subset of these neoplasms that are apt to be associated with invasive peritoneal implants and therefore should be designated as "micropapillary carcinoma." The authors of the current article identified 40 serous borderline tumors that showed one or both of these patterns, using the earlier investigators' published criteria for so-called micropapillary carcinoma, and compared them with 44 tumors that lacked these patterns (controls). Twenty-six patients with micropapillary tumors were aged 21 to 76 years (mean 38); 11 with cribriform tumors were aged 34 to 79 years (mean 60); and 3 with tumors having both patterns were aged 21 to 58 years (mean 38); the control patients were aged 22 to 83 years (mean 54). An advanced stage, bilaterality, and ovarian surface growth were features of the "micropapillary" tumors more often than of the control tumors. Except for a postoperative death related to sepsis, all 11 patients with Stage I tumors with either or both patterns who were followed until their death, or for at least 5 years (mean 7.9 years), survived without evidence of disease; a twelfth patient had a recent removal of recurrent pelvic tumor at 2.8 years and was alive at 3.3 years. Six of the eight patients with Stage II or III tumors with either or both patterns who were followed for at least 5 years (mean 7.5 years) survived disease-free. No deaths from tumor or progressive recurrences occurred in 27 control cases with 5-14 (mean 7.9) years of follow-up data. The two tumor-related deaths in the entire series, one from a micropapillary tumor and one from a cribriform tumor, occurred in patients who had Stage III tumors with invasive peritoneal implants. No patient with "micropapillary" tumors and noninvasive implants had progressive disease. Two women with "micropapillary" tumors and two control subjects had stable recurrent tumor or a newly developed tumor in a contralateral ovary that had been spared during the initial operation. Our findings confirm those of previous investigators that noninvasive serous tumors with a micropapillary or cribriform pattern or both patterns may be accompanied by invasive peritoneal implants more often than tumors without such patterns and that in such cases the disease is likely to be progressive and fatal. Since so-called micropapillary carcinomas lack obvious stromal invasion within the ovary, and their prognosis when they spread to the peritoneum is much closer to that associated with typical Stage II and III serous borderline tumors than to that associated with similarly staged serous carcinomas, the authors believe that this newly described category of tumors should remain as a subset within the borderline category, with a notation that their prognosis is poor if they are associated with invasive peritoneal implants.

摘要

一组研究人员提出,根据世界卫生组织(WHO)标准诊断为交界性的卵巢浆液性肿瘤中,微乳头或筛状结构的存在表明这些肿瘤的一个亚组易于伴有侵袭性腹膜种植,因此应被指定为“微乳头癌”。本文作者根据早期研究人员发表的所谓微乳头癌标准,识别出40例显示这两种结构之一或两者皆有的浆液性交界性肿瘤,并将其与44例缺乏这些结构的肿瘤(对照组)进行比较。26例微乳头型肿瘤患者年龄为21至76岁(平均38岁);11例筛状型肿瘤患者年龄为34至79岁(平均60岁);3例具有两种结构的肿瘤患者年龄为21至58岁(平均38岁);对照组患者年龄为22至83岁(平均54岁)。与对照组肿瘤相比,“微乳头型”肿瘤更常具有晚期、双侧性和卵巢表面生长的特征。除了1例与败血症相关的术后死亡外,11例患有I期肿瘤且具有其中一种或两种结构的患者,在随访至死亡或至少5年(平均7.9年)期间均存活,无疾病证据;第12例患者在2.8年时近期切除复发性盆腔肿瘤,在3.3年时仍存活。8例具有其中一种或两种结构的II期或III期肿瘤患者中,6例接受了至少5年(平均7.5年)的随访,无疾病存活。27例对照组病例有5至14年(平均7.9年)的随访数据,无肿瘤死亡或疾病进展复发。整个系列中两例与肿瘤相关的死亡,1例来自微乳头型肿瘤,1例来自筛状型肿瘤,均发生在患有III期肿瘤且伴有侵袭性腹膜种植的患者中。没有“微乳头型”肿瘤且无侵袭性种植的患者出现疾病进展。两名患有“微乳头型”肿瘤的女性和两名对照受试者在对侧卵巢出现稳定的复发性肿瘤或新发生的肿瘤,对侧卵巢在初次手术时未受累。我们的研究结果证实了先前研究人员的发现,即具有微乳头或筛状结构或两者皆有的非侵袭性浆液性肿瘤比没有这些结构的肿瘤更常伴有侵袭性腹膜种植,并且在这种情况下疾病可能进展并致命。由于所谓的微乳头癌在卵巢内缺乏明显的间质浸润,并且它们扩散至腹膜时的预后与典型的II期和III期浆液性交界性肿瘤更接近,而不是与同样分期的浆液性癌更接近,作者认为这种新描述的肿瘤类别应保留在交界性类别中,并注明如果它们与侵袭性腹膜种植相关,其预后较差。

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