Department of Surgery, Changxing People's Hospital, No. 66, Taihu Road, Changxing, Huzhou, 313100, Zhejiang, China.
BMC Surg. 2021 Mar 25;21(1):162. doi: 10.1186/s12893-021-01162-x.
Retroperitoneal fibrosis (RPF) is a rare disease with a poor prognosis characterized by systemic inflammation and fibroinflammatory tissue. Idiopathic RPF (IRPF) accounts for approximately two-thirds of RPF cases.
A 56-year-old female patient with abdominal distension was admitted to Changxing Hospital. Laboratory tests revealed mild anemia and elevated CA125, while IgG4 and autoantibodies were within the normal ranges. Computed tomography (CT) revealed a gallbladder-occupying lesion, pancreatic cyst and retroperitoneal mass, which may have contributed to bilateral ureteral compression and hydronephrosis. The initial diagnosis was gallbladder carcinoma with lymph node metastasis. Then, abdominal adhesiolysis, cholecystectomy and partial hepatectomy were performed. Histologically, there were fibrosis and inflammation in the retroperitoneal tissue without any malignant cells in the retroperitoneal or gallbladder tissue. Finally, we confirmed the diagnosis of idiopathic retroperitoneal fibrosis, chronic cholecystitis and pancreatic cyst. The patient recovered well following the CT scan, in which dilatation of the bile duct was reduced, and effusion of the bilateral upper ureter was no longer significant.
This atypical case illustrates that RPF can be combined with other biliary tract diseases. The coexistence of other diseases conceals the symptoms of RPF, which increases the difficulty of image identification. A high degree of suspicion is necessary for routine clinical work. As more cases are reported, further advances in the diagnosis and treatment of RPF can be expected.
腹膜后纤维化(RPF)是一种预后不良的罕见疾病,其特征为全身炎症和纤维炎症组织。特发性腹膜后纤维化(IRPF)约占 RPF 病例的三分之二。
一名 56 岁女性患者因腹胀就诊于长兴医院。实验室检查显示轻度贫血和 CA125 升高,而 IgG4 和自身抗体在正常范围内。计算机断层扫描(CT)显示胆囊占位病变、胰腺囊肿和腹膜后肿块,可能导致双侧输尿管受压和肾盂积水。最初的诊断是胆囊癌伴淋巴结转移。随后进行了腹部粘连松解、胆囊切除术和部分肝切除术。组织学上,腹膜后组织存在纤维化和炎症,但腹膜后或胆囊组织中没有恶性细胞。最终,我们确诊为特发性腹膜后纤维化、慢性胆囊炎和胰腺囊肿。CT 扫描后患者恢复良好,胆管扩张减轻,双侧输尿管上段积液不再明显。
本例为非典型病例,表明 RPF 可与其他胆道疾病同时存在。其他疾病的共存掩盖了 RPF 的症状,增加了图像识别的难度。在常规临床工作中需要高度警惕。随着更多病例的报道,预计 RPF 的诊断和治疗将取得进一步进展。