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贾第虫病罕见表现:免疫功能正常宿主的蛋白丢失性肠病的病例报告及文献综述

A Case Report and Literature Review of an Uncommon Manifestation of Giardiasis: Protein-Losing Enteropathy in an Immunocompetent Host.

作者信息

Patro Shubhransu, Sharma Vibha, Goyal Dipleshdeep, Panigrahi Gyanamitra, Pattnaik Sidharth S

机构信息

Internal Medicine, Kalinga Institute of Medical Sciences, Bhubaneswar, IND.

出版信息

Cureus. 2025 Apr 19;17(4):e82601. doi: 10.7759/cureus.82601. eCollection 2025 Apr.

Abstract

Hypoproteinemia can result from multiple etiologies, including malnutrition, hepatic and renal dysfunction, and less commonly, protein-losing enteropathy (PLE). PLE leads to protein loss into the gastrointestinal tract, resulting in decreased oncotic pressure and third-space fluid accumulation. While enteric infections have been implicated in PLE, is a rare causative agent, particularly in immunocompetent adults. We discuss the case of a 41-year-old immunocompetent male who presented with progressive generalized edema, weight gain, and skin hypopigmentation over the past six months. Laboratory investigations revealed significant hypoalbuminemia (1.6 g/dL). An extensive evaluation ruled out hepatic, renal, and gastrointestinal pathologies, but the stool analysis confirmed cysts, with a positive antigen test. The patient was treated with a single dose of tinidazole (2 g) and intravenous albumin. Follow-up after two months showed resolution of edema, weight loss, and improved serum albumin levels (2.7 g/dL) and negative stool cultures. While giardiasis typically causes diarrheal illness, this case highlights its rare but significant role in PLE, even in immunocompetent adults. Clinicians should consider stool testing for in unexplained hypoalbuminemia, as prompt treatment can reverse protein loss and prevent complications. The pathophysiology involves mucosal damage and increased intestinal permeability, leading to excessive protein loss. The few cases of giardiasis-associated PLE highlight the need for heightened clinical suspicion as early recognition and prompt treatment with tinidazole can lead to favorable outcomes, preventing complications associated with prolonged infection.

摘要

低蛋白血症可由多种病因引起,包括营养不良、肝肾功能不全,以及较罕见的蛋白丢失性肠病(PLE)。PLE导致蛋白质丢失到胃肠道,导致胶体渗透压降低和第三间隙液体积聚。虽然肠道感染与PLE有关,但 是一种罕见的病原体,尤其是在免疫功能正常的成年人中。我们讨论了一例41岁免疫功能正常男性的病例,该患者在过去六个月中出现进行性全身水肿、体重增加和皮肤色素减退。实验室检查显示严重低白蛋白血症(1.6 g/dL)。广泛评估排除了肝脏、肾脏和胃肠道疾病,但粪便分析证实有 囊肿,抗原检测呈阳性。患者接受了单剂量替硝唑(2 g)和静脉白蛋白治疗。两个月后的随访显示水肿消退、体重减轻、血清白蛋白水平改善(2.7 g/dL)且粪便培养阴性。虽然贾第虫病通常引起腹泻疾病,但该病例突出了其在PLE中罕见但重要的作用,即使在免疫功能正常的成年人中也是如此。临床医生在不明原因的低白蛋白血症中应考虑进行粪便检测以检测 ,因为及时治疗可逆转蛋白质丢失并预防并发症。其病理生理学涉及黏膜损伤和肠道通透性增加,导致蛋白质过度丢失。少数贾第虫病相关的PLE病例突出了提高临床怀疑的必要性,因为早期识别并及时用替硝唑治疗可带来良好结果,预防与长期感染相关的并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c565/12092956/9ccef0fa5c57/cureus-0017-00000082601-i01.jpg

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