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炎性假瘤:血尿和休克的罕见病因。

Inflammatory pseudotumor: a rare cause of hematuria and shock.

作者信息

Lantz Andrea G, Power Nicholas E, Gupta Rekha, Grantmyre John

机构信息

Department of Urology, Dalhousie University Faculty of Medicine, Halifax, Nova Scotia, Canada.

出版信息

Urology. 2007 Aug;70(2):372.e3-6. doi: 10.1016/j.urology.2007.04.006.

DOI:10.1016/j.urology.2007.04.006
PMID:17826517
Abstract

We report the clinical, radiologic, and pathologic findings of a case of inflammatory pseudotumor in an otherwise healthy 44-year-old woman, who presented with dysuria and hematuria causing hemodynamic instability. Computed tomography revealed a 4.3-cm by 3.5-cm densely enhancing mass arising from the anterior bladder wall. Pathologic examination showed spindle-shaped cells with mild nuclear pleomorphism, rare mitotic activity, and a strong reaction to vimentin, with focal positivity to alpha-actin and S100 protein. Monokeratin, CK7, and CK20 were negative. After two transurethral resections, the patient underwent partial cystectomy.

摘要

我们报告了一例炎性假瘤患者的临床、影像学和病理学检查结果。该患者为一名44岁健康女性,因排尿困难和血尿导致血流动力学不稳定。计算机断层扫描显示,一个4.3厘米×3.5厘米的肿块从前膀胱壁长出,强化明显。病理检查显示梭形细胞,核轻度异形,有罕见的有丝分裂活性,波形蛋白反应强烈,α-肌动蛋白和S100蛋白呈局灶性阳性。单克隆角蛋白、CK7和CK20均为阴性。经过两次经尿道切除术后,患者接受了部分膀胱切除术。

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Inflammatory pseudotumor: a rare cause of hematuria and shock.炎性假瘤:血尿和休克的罕见病因。
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