Van Winter J T, Ogburn P L, Engen D E, Webb M J
Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN 55905.
Mayo Clin Proc. 1991 Feb;66(2):179-82. doi: 10.1016/s0025-6196(12)60490-x.
Spontaneous rupture of the renal parenchyma or renal pelvis during pregnancy has been previously reported in 16 cases. In the case we describe in this report, the patient initially had right flank pain and nausea for 48 hours, which progressed to severe abdominal symptoms that necessitated exploratory laparotomy. Cystoscopic placement of a ureteral stent relieved the obstruction and allowed spontaneous healing of the renal pelvis. Dilatation of the urinary collecting system commonly occurs during pregnancy. Spontaneous rupture of the renal parenchyma or renal pelvis, however, is unusual and often associated with diseased kidneys. Our case is the 8th one of spontaneous rupture of the renal collecting system with no identifiable underlying pathologic condition and the 17th case of spontaneous renal rupture overall.
此前已有16例关于孕期肾实质或肾盂自发性破裂的报道。在本报告所描述的病例中,患者最初右侧胁腹疼痛并恶心48小时,之后进展为严重的腹部症状,因而需要进行剖腹探查术。通过膀胱镜放置输尿管支架缓解了梗阻,并使肾盂实现了自愈。孕期泌尿系统集合系统扩张较为常见。然而,肾实质或肾盂的自发性破裂并不常见,且常与患肾有关。我们的病例是第8例肾集合系统自发性破裂且无明确潜在病理状况的病例,也是总体上第17例自发性肾破裂病例。