Prasad Pallavi, Gupta Neelima, Verma Ritu, Prasad Narayan, Kaul Anupama, Agrawal Vinita, Jain Manoj
Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Nephrology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Indian J Nephrol. 2024 May-Jun;34(3):257-260. doi: 10.4103/ijn.ijn_129_23. Epub 2024 Jan 8.
Microfilarial parasites can obstruct the lymphatic tree giving rise to varying lymphatic and extra-lymphatic symptoms. Renal manifestations can range from asymptomatic proteinuria, chyluria, and nephrotic syndrome, to acute glomerulonephritis. The diagnosis of filariasis is usually made by the demonstration of the parasite in the peripheral blood smear, with or without eosinophilia. The renal involvement by this parasite has been sparsely reported in the literature. We hereby report five cases of filariasis detected on histopathological examination of renal biopsies, performed for other indications, along with a brief report of the additional histological findings. Three native and two graft biopsies were included. All our patients were male, with a mean age of 47 years (range 37 to 66 years). The serum creatinine ranged from 1.2 to 12.9 mg/dL. The mean 24-hour urinary protein was 3.6 gm/day. Peripheral blood eosinophilia was not recorded in any case, however, ESR was raised in all cases. Urine examination revealed varying proteinuria, with hematuria in two cases. Histological examination revealed microfilaria in all five biopsies, along with focal segmental glomerulosclerosis in two cases, combined cellular and humoral rejection, minimal change disease and acute tubular necrosis in one case each respectively. All patients were treated with diethylcarbamazine 6mg/kg/day or 12 days, in addition to the renal medications. Diagnosing the parasite is crucial as the patient is likely to benefit due to the timely treatment of the disease. Reporting this case series highlights an interesting finding in nephropathology.
微丝蚴寄生虫可阻塞淋巴系统,引发各种淋巴及淋巴外症状。肾脏表现可从无症状蛋白尿、乳糜尿和肾病综合征,到急性肾小球肾炎不等。丝虫病的诊断通常通过在外周血涂片中发现寄生虫来确定,无论有无嗜酸性粒细胞增多。该寄生虫引起的肾脏受累在文献中报道较少。我们在此报告5例在因其他指征进行的肾活检组织病理学检查中发现的丝虫病病例,并简要报告其他组织学发现。其中包括3例自体肾活检和2例移植肾活检。所有患者均为男性,平均年龄47岁(范围37至66岁)。血清肌酐范围为1.2至12.9mg/dL。24小时尿蛋白平均为3.6g/天。所有病例均未记录外周血嗜酸性粒细胞增多,但所有病例血沉均升高。尿液检查显示不同程度的蛋白尿,2例有血尿。组织学检查显示,所有5例活检均发现微丝蚴,2例有局灶节段性肾小球硬化,1例分别有细胞和体液混合性排斥反应、微小病变病和急性肾小管坏死。除肾脏药物治疗外,所有患者均接受乙胺嗪6mg/kg/天,共12天的治疗。诊断出该寄生虫至关重要,因为及时治疗该病患者可能会受益。报告这一系列病例突出了肾病病理学中的一个有趣发现。