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意外发现——肾活检中的微丝蚴

Caught by Surprise - Microfilaria in Renal Biopsies.

作者信息

Prasad Pallavi, Gupta Neelima, Verma Ritu, Prasad Narayan, Kaul Anupama, Agrawal Vinita, Jain Manoj

机构信息

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.

出版信息

Indian J Nephrol. 2024 May-Jun;34(3):257-260. doi: 10.4103/ijn.ijn_129_23. Epub 2024 Jan 8.

DOI:10.4103/ijn.ijn_129_23
PMID:39114403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11302504/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01b2/11302504/3a090edf3926/IJN-34-3-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01b2/11302504/3a090edf3926/IJN-34-3-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01b2/11302504/3a090edf3926/IJN-34-3-257-g001.jpg

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本文引用的文献

1
Filariasis presenting with bicytopenia, progressive splenomegaly and acute renal failure: An unusual case report.血丝虫病表现为两系血细胞减少、进行性脾肿大和急性肾衰竭:一例不常见病例报告。
Trop Doct. 2021 Oct;51(4):588-590. doi: 10.1177/00494755211002027. Epub 2021 May 12.
2
Microfilaria in kidney biopsy: A report of two cases.肾活检中的微丝蚴:两例报告。
J Infect Public Health. 2018 Sep-Oct;11(5):732-734. doi: 10.1016/j.jiph.2018.05.004. Epub 2018 Jun 9.
3
A rare case of reversible acquired AA-type renal amyloidosis in a chronic filariasis patient receiving antifilarial therapy.
一例慢性丝虫病患者接受抗丝虫治疗后出现可逆性获得性 AA 型肾淀粉样变性的罕见病例。
Clin Exp Nephrol. 2011 Aug;15(4):591-5. doi: 10.1007/s10157-011-0448-7. Epub 2011 Apr 26.
4
Extralymphatic disease due to bancroftian filariasis.班氏丝虫病所致的淋巴外疾病
Braz J Med Biol Res. 1999 Dec;32(12):1467-72. doi: 10.1590/s0100-879x1999001200003.
5
Secondary collapsing glomerulopathy associated with Loa loa filariasis.与罗阿丝虫病相关的继发性塌陷性肾小球病。
Am J Kidney Dis. 1997 Dec;30(6):836-9. doi: 10.1016/s0272-6386(97)90090-1.