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微乳头型膀胱癌:20例临床病理研究

Micropapillary bladder carcinoma: a clinicopathological study of 20 cases.

作者信息

Johansson S L, Borghede G, Holmäng S

机构信息

Department of Pathology and Microbiology, Nebraska Medical Center, Omaha, USA.

出版信息

J Urol. 1999 Jun;161(6):1798-802. doi: 10.1016/s0022-5347(05)68807-6.

Abstract

PURPOSE

Micropapillary bladder carcinoma is rare, with only 18 cases reported to date. We report 20 additional cases with long-term followup.

MATERIALS AND METHODS

A total of 680 patients with an initial diagnosis of bladder carcinoma in western Sweden in 1987 and 1989 were prospectively registered. The clinical records of all 816 patients with bladder cancer treated at Sahlgrenska University Hospital with external beam irradiation between 1962 and 1989 were reviewed. The histopathological material was reviewed and immuno-histochemical analyses were performed on 20 cases identified with micropapillary bladder carcinoma.

RESULTS

The incidence of micropapillary bladder carcinoma was 0.7%. Mean patient age at diagnosis was 69 years (range 45 to 82) and the male-to-female ratio was 2.3:1. All but 5 patients had stage T3a disease or higher. There was no difference in stage or prognosis between the 5 prospectively identified patients and those treated with external beam irradiation. Only 2 patients had micropapillary bladder carcinoma as the only pattern, while 1 had 10% and the remainder had 20 to 95% micropapillary bladder carcinoma. Transitional cell carcinoma was noted in 17 patients and 5 had areas of gland forming adenocarcinoma. Carcinoma in situ was noted in 13 patients and 15 had lymphatic invasion. Only 5 patients survived 5 years, 1 of whom died of bladder cancer after 7 years. Radiation and chemotherapy did not seem to be effective.

CONCLUSIONS

The light microscopic appearance, which is strikingly similar to ovarian papillary serous carcinoma, and immunohistochemical staining pattern lend some support to the theory that micropapillary bladder carcinoma is a variant of adenocarcinoma. Since even the focal presence of micropapillary bladder carcinoma is associated with a poor prognosis, recognition of this entity is important. Due to its rarity, the optimal treatment of micropapillary bladder carcinoma needs to be determined in a multicenter study.

摘要

目的

微乳头型膀胱癌较为罕见,迄今为止仅报道过18例。我们报告另外20例并进行长期随访。

材料与方法

前瞻性登记了1987年和1989年在瑞典西部初诊为膀胱癌的680例患者。回顾了1962年至1989年间在萨尔格伦斯卡大学医院接受外照射治疗的所有816例膀胱癌患者的临床记录。对经病理组织学确诊为微乳头型膀胱癌的20例病例进行病理组织学复查和免疫组化分析。

结果

微乳头型膀胱癌的发病率为0.7%。诊断时患者的平均年龄为69岁(范围45至82岁),男女比例为2.3:1。除5例患者外,所有患者均为T3a期或更高分期。5例前瞻性确诊的患者与接受外照射治疗的患者在分期或预后方面无差异。仅2例患者以微乳头型膀胱癌为唯一病理类型,1例为10%,其余患者微乳头型膀胱癌占比为20%至95%。17例患者可见移行细胞癌,5例有腺管状腺癌区域。13例患者有原位癌,15例有淋巴转移。仅5例患者存活5年,其中1例在7年后死于膀胱癌。放疗和化疗似乎无效。

结论

微乳头型膀胱癌的光镜表现与卵巢乳头状浆液性癌极为相似,免疫组化染色模式为微乳头型膀胱癌是腺癌的一种变异这一理论提供了一些支持。由于即使微乳头型膀胱癌呈局灶性存在也与预后不良相关,因此识别这一实体很重要。鉴于其罕见性,微乳头型膀胱癌的最佳治疗方案需要在多中心研究中确定。

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