揭示瓦尔德曼病的渗出性肠病:罕见病例报告

Sara Dilal, S. Mechhor, Manal Cherkaoui Malki, H. Elbacha, N. Benzzoubeir, Ikram Errabih
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摘要

简介:瓦尔德曼氏病或原发性肠淋巴管扩张症(PIL)是一种不常见的疾病,以消化道淋巴管扩张为特征,主要见于儿童,成人很少见。该病于 1961 年首次被描述,病因至今不明,表现多种多样,从慢性腹泻到腹水不等。诊断需要进行肠道活检和放射学评估,治疗主要集中在饮食调整上,在特殊情况下也可进行手术。观察:本报告详细介绍了一例独特的瓦尔德曼病,患者为一名 52 岁的男性,曾患 2 型糖尿病。患者的临床表现复杂,包括全身水肿综合征、慢性腹泻和腹水表现,经过全面诊断评估,排除了肾脏、肝脏和心脏疾病的病因。内镜检查发现多处十二指肠淋巴管扩张,支持了渗出性胃肠病的诊断。患者对中链甘油三酯的饮食干预反应积极,症状明显缓解。讨论瓦尔德曼病是一种罕见的病症,发病率不详,通常在儿童早期发病。然而,本文所介绍的病例强调了在成年期发病的不典型性,强调了在早期发病的渗出性肠病病例中考虑这一诊断的重要性。下肢水肿、慢性腹泻和内脏渗出物等临床症状可能各不相同,因此明确诊断具有挑战性。影像学检查、活组织切片检查和 Alpha-1 抗胰蛋白酶清除率等专门检查等诊断方法在确诊病情方面起着至关重要的作用。并发症,包括肿瘤和免疫异常的风险,需要警惕随访。治疗方法主要包括药物和饮食疗法,效果令人鼓舞。可考虑手术切除 .........。
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Exudative Enteropathy Revealing Waldmann’s Disease: A Rare Case Report
Introduction: Waldmann's disease, or primary intestinal lymphangiectasia (PIL), is an uncommon condition characterized by digestive lymphatic dilatations, predominantly observed in the pediatric population and rarely in adults. First described in 1961, its etiology remains unknown, and it presents with diverse manifestations, from chronic diarrhea to ascites. Diagnosis involves intestinal biopsies and radiological assessments, with treatment primarily focused on dietary modifications and, in exceptional cases, surgery. Observation: This report details a unique case of Waldmann's disease diagnosed in a 52-year-old man with a history of type 2 diabetes. Presenting with a complex clinical picture including generalized edematous syndrome, chronic diarrhea, and ascitic manifestations, the patient underwent a comprehensive diagnostic evaluation ruling out renal, hepatic, and cardiac causes. Endoscopic examinations revealed multiple duodenal lymphangiectasias, supporting the diagnosis of exudative gastroenteropathy. The patient responded positively to dietary interventions with medium-chain triglycerides, showing a significant regression of symptoms. Discussion: Waldmann's disease, a rare pathology with unknown prevalence, typically manifests in early childhood. However, the case presented here highlights the atypical onset in adulthood, emphasizing the importance of considering this diagnosis in cases of exudative enteropathy with an early onset. Clinical signs, including lower limb edema, chronic diarrhea, and visceral effusions, may vary, making a definitive diagnosis challenging. Diagnostic modalities such as imaging, biopsies, and specialized tests like Alpha-1 antitrypsin clearance play a crucial role in confirming the condition. Complications, including the risk of neoplasia and immunological abnormalities, require vigilant follow-up. Treatment primarily involves medical and dietary approaches, with encouraging results. Surgical resection may be considered .........
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