一名接受腹膜透析的多囊性(ADPKD)患者不可抑制的呕吐。

IF 0.7 Q4 UROLOGY & NEPHROLOGY
Case Reports in Nephrology and Dialysis Pub Date : 2021-11-12 eCollection Date: 2021-09-01 DOI:10.1159/000520020
Victor Burguera Vion, R Haridian Sosa Barrios, Maria Delgado Yagüe, Milagros Fernández Lucas, Maite E Rivera Gorrín
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引用次数: 0

摘要

虽然由于多种原因(如输液量过多导致早饱、便秘或腹膜炎)导致的胃肠道症状在 PD 患者中并不少见,但有时鉴别诊断对肾病学家来说更具挑战性。我们介绍了一例因常染色体显性多囊肾病而患有终末期肾病的女性患者的病例。在排除了便秘和感染的可能性后,她接受了腹部 CT 检查,结果显示肝内下腔静脉(ICV)受到外源性压迫,并有从 ICV 到双侧髂股深静脉的大量静脉血栓形成。此外,CT 还显示,由于肝囊肿增大,胃、幽门和十二指肠移位并受到外源性压迫。对压迫胃部的囊肿进行了经皮引流和硬化处理,并开始进行抗凝治疗,患者的临床症状得到了完全改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Incoercible Vomiting in a Polycystic (ADPKD) Patient on Peritoneal Dialysis.

Incoercible Vomiting in a Polycystic (ADPKD) Patient on Peritoneal Dialysis.

Incoercible Vomiting in a Polycystic (ADPKD) Patient on Peritoneal Dialysis.

Incoercible Vomiting in a Polycystic (ADPKD) Patient on Peritoneal Dialysis.

Although gastrointestinal symptoms are not uncommon in PD patients due to several causes, such as infusion volume with early satiety, constipation, or peritonitis, sometimes the differential diagnosis is more challenging for nephrologists. We present the case of a woman with end-stage renal disease due to autosomal dominant polycystic kidney disease on PD who presented with swollen legs and incoercible vomiting. After ruling out constipation and infection, an abdominal CT was done, revealing extrinsic compression of the intrahepatic inferior cava vein (ICV) and massive venous thrombosis from ICV to bilateral iliofemoral deep veins. In addition, CT also showed displacement and extrinsic compression of the stomach, pylorus, and duodenum due to an enlarged liver cyst. Percutaneous drainage and sclerosis of the cyst compressing the stomach was performed, anticoagulation was started, and the patient clinically improved with complete resolution of symptoms.

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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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