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膀胱副神经节瘤:一种在经尿道切除标本中可能被误诊为尿路上皮癌的病变。

Paraganglioma of the urinary bladder: a lesion that may be misdiagnosed as urothelial carcinoma in transurethral resection specimens.

作者信息

Zhou Ming, Epstein Jonathan I, Young Robert H

机构信息

Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland 02114, USA.

出版信息

Am J Surg Pathol. 2004 Jan;28(1):94-100. doi: 10.1097/00000478-200401000-00011.

Abstract

Paraganglioma of the urinary bladder is a rare tumor with characteristic histologic and immunohistochemical features. However, in our experience, it may be misdiagnosed as urothelial cancer because of 1) its frequent involvement of the muscularis propria; 2) morphology that may suggest urothelial cancer in transurethral resection specimens, particularly if there are artifactual changes induced by that procedure; 3) failure of pathologists to include it in their differential diagnosis when evaluating a bladder tumor; and 4) only a minority of the cases are associated with symptoms that might prompt consideration of the diagnosis. Distinction between paraganglioma and urothelial cancer is important because of likely different therapeutic options. In this report, we describe our experience with the histopathology of paragangliomas of the urinary bladder with emphasis on the histologic features that have led to their being misdiagnosed as conventional urothelial cancer and, most importantly, those that will help pathologists recognize this rare tumor of the bladder. Fifteen cases of paraganglioma of the urinary bladder were studied, 11 of them consult cases. They affected patients (8 male, 7 female) with a mean age of 49.5 years; only two had symptoms suggestive of the diagnosis, including hypertension during cystoscopy and episodic headache. Three consult cases were submitted with a diagnosis of "transitional cell carcinoma" and 4 with a diagnosis only of "bladder tumor." Histologically, "zellballen" and diffuse patterns were present in 12 (80%) and 3 (20%) of the cases. A delicate fibrovascular stroma was obvious in 14 (93%) cases. Other patterns included irregular nests and pseudorosette formation. Tumor necrosis, significant cautery artifact, and muscularis propria invasion were present in 1 (7%), 3 (20%) cases, and 10 (67%) cases, respectively. All 15 tumors were composed of large polygonal cells with abundant granular cytoplasm. Focal clear cells were present in 3 (20%). The nuclei were mostly uniform, although occasional pleomorphic nuclei were seen in 6 (40%) cases, and 2 (13%) had frequent pleomorphic nuclei. Mitoses were rare overall, and no abnormal mitotic figures were found. The major histologic features that led to misdiagnosis included a diffuse growth pattern, focal clear cells, necrosis, and muscularis propria invasion, with significant cautery artifact compounding the diagnostic problems. Immunohistochemically, 2 of 2 tumors were positive for neuron-specific enolase, 9 of 10 tumors for chromogranin, and 2 of 3 tumors for synaptophysin; 3 of 3 tumors were negative for cytokeratin and 1 of 1 tumor negative for HMB-45. Paraganglioma of the urinary bladder may be misdiagnosed as urothelial cancer, but a careful search for the characteristic histologic features and, if necessary, supportive immunohistochemical studies, should lead to a correct diagnosis.

摘要

膀胱副神经节瘤是一种罕见肿瘤,具有特征性的组织学和免疫组化特征。然而,根据我们的经验,它可能会被误诊为尿路上皮癌,原因如下:1)它常累及固有肌层;2)在经尿道切除标本中的形态可能提示尿路上皮癌,特别是如果该操作引起人为改变时;3)病理学家在评估膀胱肿瘤时未将其纳入鉴别诊断;4)只有少数病例伴有可能促使考虑该诊断的症状。由于可能有不同的治疗选择,区分副神经节瘤和尿路上皮癌很重要。在本报告中,我们描述了膀胱副神经节瘤的组织病理学经验,重点关注导致其被误诊为传统尿路上皮癌的组织学特征,最重要的是,那些有助于病理学家识别这种罕见膀胱肿瘤的特征。研究了15例膀胱副神经节瘤,其中11例为会诊病例。患者(8例男性,7例女性)平均年龄49.5岁;只有2例有提示该诊断的症状,包括膀胱镜检查时的高血压和发作性头痛。3例会诊病例的诊断为“移行细胞癌”,4例仅诊断为“膀胱肿瘤”。组织学上,12例(80%)呈“细胞巢”和弥漫性模式,3例(20%)呈其他模式。14例(93%)可见纤细的纤维血管间质。其他模式包括不规则巢状和假菊形团形成。肿瘤坏死、明显的烧灼假象和固有肌层浸润分别见于1例(7%)、3例(20%)和10例(67%)。所有15个肿瘤均由大的多边形细胞组成,细胞质丰富且呈颗粒状。3例(20%)可见局灶性透明细胞。细胞核大多均匀一致,尽管6例(40%)可见偶尔的核异型,2例(13%)有频繁的核异型。总体上有丝分裂罕见,未发现异常有丝分裂象。导致误诊的主要组织学特征包括弥漫性生长模式、局灶性透明细胞、坏死和固有肌层浸润,明显的烧灼假象使诊断问题更加复杂。免疫组化方面,2例肿瘤中2例神经元特异性烯醇化酶阳性,10例肿瘤中9例嗜铬粒蛋白阳性,3例肿瘤中2例突触素阳性;3例肿瘤细胞角蛋白阴性,1例肿瘤HMB-45阴性。膀胱副神经节瘤可能被误诊为尿路上皮癌,但仔细寻找特征性组织学特征,并在必要时进行支持性免疫组化研究,应能得出正确诊断。

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