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[原发性和继发性腹膜后纤维化的治疗结果]

[Treatment outcomes in primary and secondary retroperitoneal fibrosis].

作者信息

Heidenreich A, Derakhshani P, Neubauer S, Krug B

机构信息

Klinik und Poliklinik für Urologie, Universität zu Köln.

出版信息

Urologe A. 2000 Mar;39(2):141-8. doi: 10.1007/s001200050022.

Abstract

Retroperitoneal fibrosis (RPF) is an uncommon inflammatory disease of the retroperitoneum leading to extensive fibrosis with consecutive obstruction of adjacent organs, namely the ureters. Since no consensus on the standard therapy exists, aim of the current study was to evaluate the outcome of 39 patients with RPF. Between 1986 and 1997 39 cases of RPF were diagnosed: 21 cases had primary RPF and 18 patients had secondary RPF after aortofemoral graft (n = 13), radiation (n = 2), or prior retroperitoneal surgery (n = 2). 21 patients demonstrated unilateral and 16 cases had bilateral hydronephrosis, in 2 patients no dilatation was observed. In 28 cases (n = 12 primary RPF, n = 16 secondary RPF) initial management consisted of DJ-stent placement, whereas in 11 cases (n = 9 primary RPF, n = 2 secondary RPF) percutaneous nephrostomy had to be placed. All patients received oral immunosuppressive agents (prednisolone 1 mg/kg, azathioprine 1 mg/kg/day) for 3 months before reevaluation was performed. In case of complete remission, immunosuppressive medication was continued for another 3 months, in case of stable disease or progression surgery was performed. In 26 cases (n = 15 primary RPF, n = 11 secondary RPF) ureterolysis with intraperitoneal displacement and omental wrapping was performed. 3 patients demonstrated complete remission after oral prednisolone/azathioprine; in 2 cases RPF presented as pelvic mass and was resected followed by immunosuppressive therapy, in another 2 cases bilateral ileal replacement of the ureters had to be performed and 4 cases remained on DJ-stents and nephrostomy, resp. Postoperatively, all patients with primary RPF were continued on immunsuppressive medication for another 3 months. After a follow-up of 6 to 120 months only 3 patients developed a retroperitoneal recurrence and were treated by unilateral nephrectomy or DJ stent placement (n = 2). Our data suggest that the combination of both immunosuppressive medication and surgical management results in an excellent longterm outcome in idiopathic retroperitoneal fibrosis with a recurrence rate of only 8%. Combination therapy should be considered as therapeutic option early in the course of the disease. Primary reconstructive surgery appears to be the most promising approach in secondary retroperitoneal fibrosis with a recurrence rate of only 5%; short external compression of the ureter might be managed by endoluminal balloon dilatation.

摘要

腹膜后纤维化(RPF)是一种罕见的腹膜后炎症性疾病,可导致广泛纤维化,并相继阻塞相邻器官,即输尿管。由于目前尚无关于标准治疗方案的共识,本研究旨在评估39例RPF患者的治疗结果。1986年至1997年间,共诊断出39例RPF:21例为原发性RPF,18例为继发性RPF,继发于主动脉股动脉移植术后(n = 13)、放疗后(n = 2)或既往腹膜后手术(n = 2)。21例患者表现为单侧肾盂积水,16例为双侧肾盂积水,2例未见肾盂扩张。28例患者(n = 12例原发性RPF,n = 16例继发性RPF)初始治疗包括放置DJ支架,而11例患者(n = 9例原发性RPF,n = 2例继发性RPF)必须行经皮肾造瘘术。所有患者在重新评估前接受口服免疫抑制剂(泼尼松龙1mg/kg,硫唑嘌呤1mg/kg/天)治疗3个月。如完全缓解,免疫抑制药物继续使用3个月;如病情稳定或进展,则进行手术治疗。26例患者(n = 15例原发性RPF,n = 11例继发性RPF)行输尿管松解术并将输尿管移位至腹腔内,同时行网膜包裹术。3例患者口服泼尼松龙/硫唑嘌呤后完全缓解;2例患者RPF表现为盆腔肿块,行手术切除并接受免疫抑制治疗;另外2例患者不得不进行双侧输尿管回肠代换术;4例患者分别留置DJ支架和肾造瘘管。术后,所有原发性RPF患者继续接受免疫抑制药物治疗3个月。随访6至120个月后,仅3例患者出现腹膜后复发,分别接受单侧肾切除术或DJ支架置入术(n = 2)治疗。我们的数据表明,免疫抑制药物与手术治疗相结合可使特发性腹膜后纤维化患者获得良好的长期治疗效果,复发率仅为8%。在疾病早期就应考虑联合治疗作为一种治疗选择。原发性重建手术似乎是继发性腹膜后纤维化最有前景的治疗方法,复发率仅为5%;输尿管的短期外部压迫可通过腔内球囊扩张术进行处理。

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