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一名患有膜性肾病的女孩,与脑室-腹腔分流感染相关。

A girl with membranous nephropathy associated with ventriculoperitoneal shunt infection.

机构信息

Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, Japan.

Department of Pediatrics, Tokyo Ohtsuka Metropolitan Hospital, 2-8-1, Minamiohtsuka, Toshima-ku, Tokyo, Japan.

出版信息

CEN Case Rep. 2023 Feb;12(1):130-134. doi: 10.1007/s13730-022-00732-z. Epub 2022 Sep 10.

Abstract

Glomerulopathy associated with shunt infection is commonly membranoproliferative glomerulonephritis, whereas the causative organisms of secondary membranous nephropathy are usually viruses. We report a case of membranous nephropathy associated with shunt infection. The patient was born at 29-week gestation with a birth weight of 1178 g. Ventriculoperitoneal shunt surgery had been performed for congenital hydrocephalus. Thereafter, she had experienced seven shunt infections. At the age 13 years, proteinuria was detected in a school urinary screening. Urinalysis at our hospital demonstrated 3 + protein and 3 + blood. Laboratory testing demonstrated a serum creatinine 0.5 m/dl, albumin 2.5 g/dl, C-reactive protein (CRP) 13.7 mg/dl, and C3 182 mg/dl. Prior to repeat urinalysis, the patient developed vomiting and was admitted with suspected shunt infection. On admission, her body temperature was 36.0 ºC. Physical examination was unremarkable other than small stature and a palpable mass in the left upper quadrant. Urinalysis demonstrated 2 + protein and 1 + blood with no cells or casts. The urinary protein excretion was 3 g/day. Abnormal laboratory tests included erythrocyte sedimentation rate 102 mm/hr, CRP 11.67 mg/dl, IgG 2442 mg/dl, C3 177 mg/dl, and C4 44 mg/dl. Antibiotic therapy was initiated for a presumptive diagnosis of shunt infection and the shunt catheter was removed. Cultures obtained after antibiotic administration were negative. Proteinuria persisted after control of the shunt infection. Histology of a renal biopsy demonstrated membranous nephropathy with diffuse granular IgG staining and subepithelial deposits. Three possible pathomechanisms for her membranous nephropathy were considered.

摘要

与分流感染相关的肾小球病通常为膜增生性肾小球肾炎,而继发性膜性肾病的病原体通常为病毒。我们报告一例与分流感染相关的膜性肾病。患者 29 孕周出生,出生体重 1178g。因先天性脑积水行脑室-腹腔分流术。此后,她经历了 7 次分流感染。13 岁时,在学校尿液筛查中发现蛋白尿。我院尿液分析显示 3+蛋白和 3+血。实验室检查显示血清肌酐 0.5mg/dl,白蛋白 2.5g/dl,C 反应蛋白(CRP)13.7mg/dl,C3 182mg/dl。在重复进行尿液分析之前,患者出现呕吐并因疑似分流感染而入院。入院时,患者体温为 36.0°C。除身材矮小和左上象限可触及肿块外,体格检查无明显异常。尿液分析显示 2+蛋白和 1+血,无细胞或管型。尿蛋白排泄量为 3g/天。异常实验室检查包括红细胞沉降率 102mm/hr,CRP 11.67mg/dl,IgG 2442mg/dl,C3 177mg/dl 和 C4 44mg/dl。鉴于疑似分流感染,给予抗生素治疗并移除分流导管。抗生素治疗后获得的培养物为阴性。分流感染得到控制后,蛋白尿仍持续存在。肾活检组织学显示膜性肾病,弥漫性颗粒 IgG 染色和上皮下沉积物。考虑到她的膜性肾病有 3 种可能的发病机制。

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