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根治性肾切除术治疗腹膜后纤维化:病例报告

Radical nephrectomy for retroperitoneal fibrosis: Case report.

作者信息

Paiva Matheus Miranda, Moccellin Eloi Guilherme Provinciali, Vengjer Alessandro, Stiirmer Guilherme Henrique Silveira, Dos Santos Fernando Oliveira, do Nascimento Paulo Peixoto

机构信息

Santa Casa de Misericordia de Santos, Divisão de Urologia, Departamento de Cirurgia, Santos, São Paulo, Brazil.

Santa Casa de Misericordia de Santos, Divisão de Urologia, Departamento de Cirurgia, Santos, São Paulo, Brazil; Faculdade de Medicina, Universidade Metropolitana de Santos (UNIMES), Departamento de Urologia, Santos, São Paulo, Brazil.

出版信息

Int J Surg Case Rep. 2024 Dec;125:110560. doi: 10.1016/j.ijscr.2024.110560. Epub 2024 Nov 6.

Abstract

INTRODUCTION AND IMPORTANCE

Retroperitoneal fibrosis is a proliferative disease of fibroblasts with a still unclear appearance and low incidence. The clinical manifestations are nonspecific and appear late, pain is the most common symptom present. Elevated serum IgG4 levels are observed in up to 60 % of the patients and the main goal of treating this condition is to preserve kidney function.

CASE PRESENTATION

We present a case of an asymptomatic 34-year-old man. A poorly defined mass in the pre-aortic, pre-caval and right rim regions with possible malignancy was observed. After 3 biopsies, it was treated as low-grade follicular lymphoma with chemotherapy. With new growth after 1 year, right radical nephrectomy was performed to resect the lesion. Pathology showed that it was advanced retroperitoneal fibrosis with negative IgG4.

CLINICAL DISCUSSION

RPF usually presents as an irregular mass of periaortic tissue that frequently has malignancy as a risk factor and may be associated with high levels of IgG4. Most of the time, the disease is asymptomatic. When the patient presents symptoms, pain is the most common, although late. Its diagnosis is made by imaging and histopathological exams. Treatment varies according to the progression of the disease, but aims to try to preserve renal function.

CONCLUSION

RPF is a disease characterized by the accumulation of fibroblasts in the abdominal region with an etiology that has not yet been fully discovered, which can present in several ways, generally identified by imaging exams and can be treated individually depending on the invasiveness of the disease.

摘要

引言与重要性

腹膜后纤维化是一种成纤维细胞增生性疾病,其表现仍不明确且发病率较低。临床表现不具有特异性且出现较晚,疼痛是最常见的症状。高达60%的患者血清IgG4水平升高,治疗该病的主要目标是保护肾功能。

病例介绍

我们报告一例34岁无症状男性病例。在主动脉前、腔静脉前及右侧边缘区域观察到一个边界不清的肿块,怀疑为恶性。经过3次活检后,按低度滤泡性淋巴瘤进行化疗。1年后肿块复发,遂行右侧根治性肾切除术以切除病变。病理显示为晚期腹膜后纤维化,IgG4阴性。

临床讨论

腹膜后纤维化通常表现为主动脉周围组织的不规则肿块,常以恶性肿瘤为危险因素,且可能与高水平的IgG4有关。大多数情况下,该病无症状。当患者出现症状时,疼痛最为常见,但出现较晚。其诊断通过影像学和组织病理学检查。治疗根据疾病进展而异,但目标是尽量保护肾功能。

结论

腹膜后纤维化是一种以腹部成纤维细胞积聚为特征的疾病,其病因尚未完全明确,可表现为多种形式,一般通过影像学检查确定,可根据疾病的侵袭性进行个体化治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f06f/11577170/aeb3ead52915/gr1.jpg

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