Chyloperitoneum in a toddler on peritoneal dialysis.

IF 2.6 3区 医学 Q1 PEDIATRICS
Pediatric Nephrology Pub Date : 2025-05-01 Epub Date: 2024-12-02 DOI:10.1007/s00467-024-06597-x
Veronica Lavelle Bell, Alyssa A Schlotman, Daniel J Benedetti, Tracy E Hunley
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引用次数: 0

Abstract

Chyloperitoneum is an uncommon diagnosis in peritoneal dialysis (PD) patients. While admitted for emesis and feeding intolerance, a 16-month-old male on PD developed milky-colored dialysate with increased triglycerides, indicating chyloperitoneum. In adult PD patients, chyloperitoneum can indicate potentially life-threatening pathologies including malignancies and liver or heart disease. By contrast, pediatric patients on PD with chyloperitoneum had recently undergone PD catheter or gastrostomy tube placement with presumed disruption of abdominal lymphatics. Slowing lymph flow through dietary manipulation and rarely, temporary withholding of PD, resolved chyloperitoneum. We report a toddler on PD with chyloperitoneum in whom abdominal investigation showed multifocal hepatoblastoma. Chemotherapy and a medium chain triglycerides (MCTs)-based diet led to prompt resolution of chyloperitoneum. Intrabdominal malignancy in this patient illustrates the importance of a prompt, thorough evaluation of chyloperitoneum to allow definitive therapy if required.

接受腹膜透析的幼儿乳糜腹膜。
乳糜腹膜是腹膜透析(PD)患者罕见的诊断。在因呕吐和喂养不耐受入院时,一名患有PD的16个月大的男性出现乳白色的透析液,甘油三酯增加,表明乳糜腹膜。在成年PD患者中,乳糜腹膜可以提示潜在的危及生命的病理,包括恶性肿瘤、肝脏或心脏疾病。相比之下,患有乳糜腹膜的儿科PD患者最近接受了PD导管或胃造口管放置,推测腹部淋巴管破坏。通过饮食控制来减缓淋巴流动,偶尔暂时抑制PD,解决乳糜腹膜。我们报告一个患有乳糜腹膜的PD患儿,腹部检查显示多灶性肝母细胞瘤。化疗和以中链甘油三酯(mct)为基础的饮食导致乳糜腹膜迅速消退。腹腔内恶性肿瘤的病人说明了及时,彻底评估乳糜腹膜的重要性,以允许明确的治疗,如果需要的话。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Nephrology
Pediatric Nephrology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
20.00%
发文量
465
审稿时长
1 months
期刊介绍: International Pediatric Nephrology Association Pediatric Nephrology publishes original clinical research related to acute and chronic diseases that affect renal function, blood pressure, and fluid and electrolyte disorders in children. Studies may involve medical, surgical, nutritional, physiologic, biochemical, genetic, pathologic or immunologic aspects of disease, imaging techniques or consequences of acute or chronic kidney disease. There are 12 issues per year that contain Editorial Commentaries, Reviews, Educational Reviews, Original Articles, Brief Reports, Rapid Communications, Clinical Quizzes, and Letters to the Editors.
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