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Granulomatous pyelitis associated with urinary obstruction: a comprehensive clinicopathologic study

机译:肉芽肿性肾炎合并尿路梗阻:全面的临床病理研究

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Urinary obstruction is rarely associated with a distinct granulomatous inflammation, which involves the pyelocalyceal system and closely simulates infectious conditions including tuberculosis. Its clinicopathologic features, however, have not been adequately studied since there are only seven isolated reported cases. In a comprehensive study of 112 kidney specimens with urinary obstruction, we identified five cases of granulomatous pyelitis. The features of these cases were detailed and compared with the previously reported cases. Among the five identified subjects, three patients had history of urolithiasis and two had ureteral stenosis and all had stent placement 7 weeks to 12 years before nephrectomy for relief of the unilateral urinary obstruction. The age distribution was between 38 and 81 years. Two had end-stage renal disease or chronic renal failure. The pyelocaliceal system showed frank hydronephrosis (1 case) or partial dilatation (4 cases) and contained cheesy and gritty material in its lumen. Each case showed severe granulomatous inflammation, which was limited to the pelvic wall and closely associated with calcified debris, necrotic inflammatory cells, and material consistent with Tamm–Horsfall protein. The kidney showed chronic tubulointerstitial nephritis but without granulomas. Cultures of urine, blood, and the renal pelvic content, and special stains of tissue sections did not show fungi or mycobacteria in any case. Many of these features were also observed in previously reported cases. Granulomatous pyelitis is a rare but distinct cliniocopathologic entity characterized by severe noninfectious granulomatous inflammation limited to the renal pelvis, which is uniformely asociated with urinary obstruction and pyelocalyceal dilatation and may develop in response to accumulated calcified material in the renal pelvis. Awareness of this entity and its characteristic clinicopathologic features also helps eliminate an infectious etiology with obvious treatment and prognostic implications.
机译:尿路阻塞很少伴有明显的肉芽肿性炎症,它涉及胸膜局部腺体系统并紧密模拟包括肺结核在内的传染病。然而,由于仅报告了7例孤立病例,其临床病理特征尚未得到充分研究。在对112例尿路阻塞的肾脏标本进行的全面研究中,我们确定了5例肉芽肿性肾炎。这些案件的特点已被详细介绍并与先前报告的案件进行了比较。在确定的五名受试者中,三名患者有尿路结石病史,两名患者患有输尿管狭窄,所有患者均在肾切除术前7周至12年放置了支架,以缓解单侧尿路阻塞。年龄分布在38至81岁之间。两人患有终末期肾病或慢性肾功能衰竭。胸膜局部器官系统显示出明显的肾积水(1例)或部分扩张(4例),其管腔内含有干酪味和坚硬的物质。每个病例均表现出严重的肉芽肿性炎症,仅限于骨盆壁,并与钙化碎片,坏死性炎性细胞以及与Tamm–Horsfall蛋白一致的物质密切相关。肾脏显示慢性肾小管间质性肾炎,但无肉芽肿。在任何情况下,尿液,血液和肾盂内容物的培养物以及特殊的组织切片染色均未显示真菌或分枝杆菌。在以前报道的病例中也观察到许多这些特征。肉芽肿性肾炎是一种罕见的但独特的淋巴病理学实体,其特征是严重的非感染性肉芽肿性炎症仅限于肾盂,与肾脏梗阻和肾小球黏膜扩张均匀相关,并且可能由于肾盂中钙化物质的累积而发展。意识到该实体及其特征性的临床病理特征也有助于消除具有明显治疗和预后影响的传染病因。

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