Department of Pathology, Inje University Ilsan Paik Hospital, Goyang, Korea.
Pathol Int. 2010 Dec;60(12):779-83. doi: 10.1111/j.1440-1827.2010.02598.x. Epub 2010 Sep 13.
A 53-year-old man presented with right flank pain for 6 days. Computerized tomography revealed a 3 cm long segment of ureteral narrowing with wall thickening and hydronephrosis, suspicious for ureteral cancer. Under the clinical diagnosis of ureteral carcinoma a right nephroureterectomy was performed. The wall of the distal ureter, 2.5 cm from the bladder cuff, had a luminal-narrowing, firm mass-forming lesion with abrupt transition from the adjacent ureter. Histologically, the resected ureteral mass showed transmural fibrosing, chronic inflammation with numerous plasma cells, epithelioid granulomas, and obliterative phlebitis. Histological findings were consistent with idiopathic segmental ureteritis (ISU) with differential diagnoses of IgG4-related sclerosing disease, including lymphoplasmacytic inflammatory pseudotumor (IPT) and idiopathic retroperitoneal fibrosis. IgG4 immunostaining in this case was barely positive, excluding the possibility of IgG4-related IPT. Although the majority of luminal obliterated segmental lesions of the ureter are neoplastic in nature, non-neoplastic inflammatory processes as seen in this case may occur in the ureter, causing diagnostic confusion with true neoplasms. Herein we report a rare case of ISU that was clinically misdiagnosed as malignancy preoperatively. ISU of the current case may be an IgG4-unrelated subtype of IPT.
一位 53 岁男性因右侧腰痛 6 天就诊。计算机断层扫描显示输尿管有 3cm 长的节段性狭窄,伴有管壁增厚和肾盂积水,提示输尿管癌。临床诊断为输尿管癌,行右肾输尿管切除术。距离膀胱袖口 2.5cm 的远端输尿管壁有腔内狭窄的实性肿块形成病变,与相邻输尿管呈突然过渡。组织学上,切除的输尿管肿块表现为全层纤维化、慢性炎症伴大量浆细胞、上皮样肉芽肿和闭塞性静脉炎。组织学发现符合特发性节段性输尿管炎(ISU),需与 IgG4 相关硬化性疾病进行鉴别诊断,包括淋巴浆细胞性炎性假瘤(IPT)和特发性腹膜后纤维化。本例 IgG4 免疫染色弱阳性,排除 IgG4 相关 IPT 的可能。虽然大多数腔内闭塞性输尿管节段性病变为肿瘤性,但如本例所见,非肿瘤性炎症过程也可能发生在输尿管中,导致与真正的肿瘤混淆。本文报道了一例罕见的术前临床误诊为恶性肿瘤的 ISU 病例。本例 ISU 可能是 IgG4 无关型 IPT。