Malakoplakia:儿科患者血尿的罕见病因

JPGN Reports Pub Date : 2024-05-01 DOI:10.1002/jpr3.12075
Ariel Porto, Jonathan Lebowitz, Robert Byrd, Elaine Morgan, Joshua D. Prozialeck
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引用次数: 0

摘要

马立克白斑病是一种罕见的炎症,其特点是巨噬细胞功能受损,无法完全消化和杀死吞噬的细菌,导致部分消化的细菌成分积聚在吞噬溶酶体内。由于潜在疾病或药物影响,马立克氏病通常发生在免疫力低下的人群中,很少在儿童中确诊。泌尿道是最常受累的部位,其次是胃肠道,主要影响降结肠、乙状结肠和直肠。治疗的重点是使用能在巨噬细胞内聚集的抗生素,如喹诺酮类和三甲双胍-磺胺甲噁唑,以及胆碱能药物,如倍他乐克,后者能提高巨噬细胞内环磷酸鸟苷的水平,从而提高杀菌活性。我们报告了一例罕见的正在接受白血病治疗的儿童消化道恶性肿瘤病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malakoplakia: A rare cause of hematochezia in pediatric patients
Malakoplakia is a rare inflammatory condition characterized by impaired macrophages unable to completely digest and kill phagocytized bacteria, resulting in partially digested bacterial components accumulating within the phagolysosome. Malakoplakia typically presents in immunocompromised individuals due to underlying disease or to medication effects and is rarely diagnosed in the pediatric population. The urinary tract is the most commonly involved site, followed by the gastrointestinal (GI) tract, mainly affecting the descending colon, sigmoid colon, and rectum. Treatment focuses on the use of antibiotics that concentrate in macrophages such as quinolones and trimethoprim‐sulfamethoxazole as well as cholinergic agents such as bethanechol, which raise intracellular levels of cyclic guanosine monophosphate in macrophages to improve bactericidal activity. We report a rare case of GI tract malakoplakia in a pediatric patient undergoing treatment for leukemia.
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