Valencia Deray Kristen G, Kellermayer Richard, Gomez Alexis C, Patel Kalyani R, Imani Peace, Kitagawa Seiji, Bocchini Claire E, Orjuela Alvaro
Division of Infectious Diseases, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
Division of Pediatric Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
SAGE Open Med Case Rep. 2024 Mar 18;12:2050313X241239866. doi: 10.1177/2050313X241239866. eCollection 2024.
Malakoplakia is a rare, chronic granulomatous disease that mainly affects the genitourinary system of immunocompromised adults. It is caused by a bactericidal deficit in macrophages and, therefore, the treatment includes antimicrobials that reach high concentrations in macrophages. To our knowledge, we present the first case of malakoplakia in a pediatric solid organ transplant recipient. Our patient is a 15-year-old male renal transplant recipient who presented with recurrent diarrhea. Blood, urine, and gastrointestinal pathogen panel testing were positive for enteroaggregative A colonoscopy revealed diffuse malakoplakia. He had a complete resolution of symptoms with trimethoprim-sulfamethoxazole therapy. Unfortunately, his malakoplakia recurred after 9 months prompting the transition of therapy to oral gentamicin with subsequent remission. Malakoplakia should be considered in the differential of solid organ transplant recipients with recurrent gastrointestinal infections.
软斑病是一种罕见的慢性肉芽肿性疾病,主要影响免疫功能低下成年人的泌尿生殖系统。它是由巨噬细胞杀菌功能缺陷引起的,因此,治疗包括使用能在巨噬细胞中达到高浓度的抗菌药物。据我们所知,我们报告了首例小儿实体器官移植受者患软斑病的病例。我们的患者是一名15岁男性肾移植受者,出现反复腹泻。血液、尿液和胃肠道病原体检测显示肠聚集性大肠杆菌呈阳性。结肠镜检查发现弥漫性软斑病。他接受甲氧苄啶 - 磺胺甲恶唑治疗后症状完全缓解。不幸的是,9个月后他的软斑病复发,促使治疗改为口服庆大霉素,随后病情缓解。对于反复发生胃肠道感染的实体器官移植受者,鉴别诊断时应考虑软斑病。