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原发性、纯大细胞神经内分泌膀胱癌

Primary, pure, large-cell neuroendocrine carcinoma of the urinary bladder.

作者信息

Hailemariam S, Gaspert A, Komminoth P, Tamboli P, Amin M

机构信息

University of Zurich, Switzerland.

出版信息

Mod Pathol. 1998 Oct;11(10):1016-20.

PMID:9796733
Abstract

We report what to our knowledge is the first case in the English-language literature of a primary, pure, undifferentiated large-cell neuroendocrine carcinoma of the urinary bladder. To date, only one case of a large-cell neuroendocrine carcinoma was reported, and it was associated with an adenocarcinoma most likely of urachal origin. On the other hand, slightly more than 100 cases of undifferentiated small-cell carcinoma of the urinary bladder were reported, approximately one-half of which were associated with poorly differentiated transitional-cell carcinoma of the conventional type. The patient in our case was a 73-year-old man with a history of prostatic cancer treated with radiation therapy. He presented with hematuria, leading to the discovery of a solitary tumor on the dorsal wall of the urinary bladder. A diagnosis of large-cell neuroendocrine carcinoma was made, supported by immunohistochemical reactivity for chromogranin, neuron-specific enolase, and synaptophysin; a variety of other hormonal markers of neuroendocrine tumors were negative. The radical cystoprostatectomy and bilateral pelvic lymphadenectomy specimen showed a transmurally invasive tumor, without regional lymph node metastases. The patient died 2 months after surgery, and the autopsy revealed disseminated metastases histologically identical to the urinary bladder neoplasm. Awareness of the occurrence of large-cell neuroendocrine carcinoma of the urinary bladder seems to be important because of the possible aggressive outcome associated with this tumor and because of differential diagnostic considerations, which include malignant lymphoma and metastasis from another primary, especially in tumors occurring in a pure form.

摘要

据我们所知,我们报告了英文文献中首例原发性、纯的、未分化大细胞神经内分泌癌累及膀胱的病例。迄今为止,仅报告过1例大细胞神经内分泌癌,且它与1例很可能起源于脐尿管的腺癌相关。另一方面,已报告了100多例膀胱未分化小细胞癌,其中约半数与传统类型的低分化移行细胞癌相关。我们病例中的患者是一名73岁男性,有前列腺癌放疗史。他因血尿就诊,结果发现膀胱后壁有一个孤立性肿瘤。通过嗜铬粒蛋白、神经元特异性烯醇化酶和突触素的免疫组化反应确诊为大细胞神经内分泌癌;神经内分泌肿瘤的多种其他激素标志物均为阴性。根治性膀胱前列腺切除术及双侧盆腔淋巴结清扫标本显示肿瘤呈透壁性浸润,无区域淋巴结转移。患者术后2个月死亡,尸检发现有组织学上与膀胱肿瘤相同的播散性转移。认识到膀胱大细胞神经内分泌癌的发生似乎很重要,因为该肿瘤可能具有侵袭性,且存在鉴别诊断问题,包括恶性淋巴瘤以及来自其他原发部位的转移,尤其是对于以纯形式出现的肿瘤。

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