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免疫增殖性小肠疾病表现为腹水和水肿。

Immunoproliferative small intestinal disease presented with ascites and edema.

作者信息

Shoaran Maryam, Khodadad Ahmad, Mahjoubt Fatemeh, Kiani Mohammad-Ali, Rezaei Nima

机构信息

Department of Pediatrics, Division of Gastroenterology, Children's Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Pediatrics, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Acta Clin Croat. 2013 Sep;52(3):387-90.

Abstract

Immunoproliferative small intestinal disease (IPSID) is a rare disorder, which can progress to malignancy and invasion. Herein, a male patient is presented with hypoalbuminemic ascites and a history of chronic diarrhea five years before. Small intestinal biopsy and immunohistochemical study suggested the diagnosis of IPSID; the patient was then successfully treated with antibiotics. Considering the favorable therapeutic response of IPSID to antibiotics during primary stages, clinicians should be aware of its various presentations in order to initiate treatment at an early

摘要

免疫增殖性小肠疾病(IPSID)是一种罕见的疾病,可进展为恶性肿瘤并发生侵袭。本文介绍了一名男性患者,其有低白蛋白血症性腹水,并有5年前慢性腹泻病史。小肠活检和免疫组化研究提示IPSID诊断;该患者随后用抗生素成功治疗。鉴于IPSID在疾病初期对抗生素有良好的治疗反应,临床医生应了解其各种表现以便早期开始治疗。

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