Cristian Surcel, Cristian Mirvald, Cristian Pavelescu, Constantin Gingu, Savu Carmen, Huri Emre, Sinescu Ioanel
Center of Urological Surgery and Renal Transplantation, Fundeni Clinical Institute, Bucharest, Romania.
Department of Intensive Care and Anesthesiology, Fundeni Clinical Institute, Bucharest, Romania.
Ther Adv Urol. 2015 Apr;7(2):85-99. doi: 10.1177/1756287214565637.
Idiopathic retroperitoneal fibrosis (IRF) is a rare disease characterized by a fibrotic reaction that affects retroperitoneal organs, especially the urinary tract. In this review we analyze the current imaging techniques, morphological characteristics, clinical aspects and therapeutic aspects of idiopathic retroperitoneal disease.
A PubMed search was conducted in December 2013 to find original articles, bibliographic reviews and series reports published in the past 15 years on idiopathic retroperitoneal fibrosis, its management and outcomes by combining terms like retroperitoneal fibrosis, periaortitis, treatment and autoimmune. A total of 89 articles were included in this review that referred strictly to IRF. We analyzed the imaging tools used for diagnostic and the decision making protocol used by physicians in the management of IRF.
A computerized tomography (CT) scan represents the most commonly used imaging technique for diagnosis. Magnetic resonance imaging (MRI) is unable to differentiate more accurately between benign and malignant retroperitoneal fibrosis (RF) than a CT scan. Biopsy remains the most reliable diagnostic tool for IRF. However, the histological characteristics of IRF are not yet well-defined and the protocol for biopsy is not standardized in terms of template, number of biopsies and the immunohistochemical panel needed for positive diagnosis. The most common treatment reported is corticosteroid therapy alone or in combination with other immunosuppressants, whereas surgical treatment is reserved for severe cases. Indwelling ureteric stents represent the most common procedure for renal drainage, but their efficacy is questionable. Open ureterolysis remains the gold standard for surgical treatment, but its purpose is only to resolve the ureteric obstruction, not to treat the retroperitoneal fibrosis. Laparoscopic and robotic approaches have been reported to be feasible, but no prospective, comparative trials have been performed due to the rarity of the disease. Surgical technique is not standardized and the outcome of the treatment only evaluates the recovery of the renal function.
The imaging procedures available today are unable to accurately differentiate between idiopathic and malignant RF. A biopsy is mandatory to confirm the diagnosis, but there is no consensus regarding the template, timing and number of biopsies needed to exclude malignancy. Open ureterolysis represents the main surgical treatment for cases with severe IRF, and laparoscopic or robotic approach may be an option in selected cases. The recovery of the renal function is a surrogate for evaluating the success of the treatment. More clinical studies are needed in order standardize the protocol for diagnostic, treatment and follow up after medical or surgical management.
特发性腹膜后纤维化(IRF)是一种罕见疾病,其特征为影响腹膜后器官尤其是泌尿道的纤维化反应。在本综述中,我们分析了特发性腹膜后疾病的当前成像技术、形态学特征、临床方面及治疗方面。
2013年12月在PubMed上进行检索,通过结合“腹膜后纤维化”“主动脉周炎”“治疗”及“自身免疫”等术语,查找过去15年发表的关于特发性腹膜后纤维化及其管理与结局的原始文章、文献综述及系列报告。本综述共纳入89篇严格涉及IRF的文章。我们分析了用于诊断的成像工具以及医生在IRF管理中使用的决策方案。
计算机断层扫描(CT)是诊断中最常用的成像技术。与CT扫描相比,磁共振成像(MRI)无法更准确地区分良性和恶性腹膜后纤维化(RF)。活检仍是IRF最可靠的诊断工具。然而,IRF的组织学特征尚未明确界定,活检方案在取材模板、活检次数及阳性诊断所需的免疫组化指标方面均未标准化。报道的最常见治疗方法是单独使用皮质类固醇疗法或与其他免疫抑制剂联合使用,而手术治疗仅用于严重病例。留置输尿管支架是肾引流最常见的操作,但其疗效存疑。开放性输尿管松解术仍是手术治疗的金标准,但其目的仅为解除输尿管梗阻,而非治疗腹膜后纤维化。已报道腹腔镜和机器人手术方法可行,但由于该疾病罕见,尚未进行前瞻性对比试验。手术技术未标准化,治疗结局仅评估肾功能的恢复情况。
目前可用的成像程序无法准确区分特发性和恶性RF。必须进行活检以确诊,但在排除恶性肿瘤所需的取材模板、时机和活检次数方面尚无共识。开放性输尿管松解术是重度IRF病例的主要手术治疗方法,在特定病例中腹腔镜或机器人手术方法可能是一种选择。肾功能的恢复是评估治疗成功与否的替代指标。需要更多临床研究来规范诊断、治疗及药物或手术治疗后随访的方案。