Spark R P, Gleason D M, DeBenedetti C D, Gigax J H
Department of Pathology, Tucson Medical Center, Arizona 85733.
J Urol. 1991 Jun;145(6):1256-60. doi: 10.1016/s0022-5347(17)38594-4.
The characteristics of eosinophilic ureteritis and idiopathic segmental ureteritis are sufficiently overlapping and so uncommonly reported as to raise a nosological issue. In an attempt to address that question, we compared 2 new cases and 8 previous reports of eosinophilic ureteritis with a series of 21 idiopathic segmental ureteritis patients. One of our patients also had renal pelvic involvement, while 1 is the youngest (3 years old) patient reported and the first instance of bilateral eosinophilic ureteritis. Our review found that eosinophilic ureteritis largely occurs in atopic or hypereosinophilic syndromes, often with a traumatic history. Eosinophilic and idiopathic segmental ureteritis causes ureteral obstruction due to mural involvement. However, eosinophilic ureteritis never forms an intraluminal mass and is not associated with mucosal ulceration. In addition, we found no case reported with features that bridge the 2 conditions. We conclude that the clinical and pathological features of eosinophilic and idiopathic segmental ureteritis are sufficiently distinct to separate the 2 conditions.
嗜酸性粒细胞性输尿管炎和特发性节段性输尿管炎的特征有足够的重叠,且报道罕见,从而引发了一个疾病分类学问题。为了回答这个问题,我们将2例新的嗜酸性粒细胞性输尿管炎病例和8例既往报道与21例特发性节段性输尿管炎患者进行了比较。我们的1例患者还伴有肾盂受累,1例是报道的最年轻(3岁)患者且为双侧嗜酸性粒细胞性输尿管炎的首例。我们的综述发现,嗜酸性粒细胞性输尿管炎主要发生于特应性或嗜酸性粒细胞增多综合征,常伴有外伤史。嗜酸性粒细胞性和特发性节段性输尿管炎因壁层受累导致输尿管梗阻。然而,嗜酸性粒细胞性输尿管炎从不形成腔内肿块,也不伴有黏膜溃疡。此外,我们未发现有兼具这两种情况特征的病例报道。我们得出结论,嗜酸性粒细胞性和特发性节段性输尿管炎的临床和病理特征足够不同,足以区分这两种疾病。