Galakhoff C, Hospitel S, Dana A, Michel J R
J Radiol. 1986 Jun-Jul;67(6-7):463-8.
A series of 40 cases of cystic pyeloureteritis (CPU) is reported, this affection being considered as rare since only about 150 cases have been described in the literature. The lesion is probably more prevalent than was once believed but many cases probably remain unrecognized because of the paucity of radiologic signs. Based on findings in these 40 patients, results of radiologic imaging are described, the technical precautions needed for its detection emphasized and differential diagnoses discussed, none of which presents insurmountable obstacles since these are more theoretical than real. Pathogenesis is thought to be an acquired particular form of urinary mucosa metaplasia associated with urinary tract lesions responsible for stasis or chronic inflammation. Treatment should be conservative because of the usual benign nature of the lesion, although exceptional but possible occlusion by the lesions necessitates a certain surveillance.
本文报告了40例囊性肾盂输尿管炎(CPU)病例。由于文献中仅描述了约150例,这种疾病被认为较为罕见。该病变可能比以往认为的更为普遍,但由于放射学征象较少,许多病例可能未被识别。基于这40例患者的检查结果,描述了放射学成像的结果,强调了检测所需的技术注意事项,并讨论了鉴别诊断。由于这些问题更多是理论上而非实际存在的,因此均未构成不可逾越的障碍。发病机制被认为是一种后天获得的特殊形式的尿路上皮化生,与导致尿液潴留或慢性炎症的泌尿系统病变有关。由于该病变通常具有良性性质,治疗应采取保守治疗,尽管病变导致梗阻的情况罕见但有可能发生,因此需要进行一定的监测。