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Immunoproliferative small intestinal disease presented with ascites and edema.

机译:免疫增生性小肠疾病伴有腹水和水肿。

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摘要

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
机译:免疫增生性小肠疾病(IPSID)是一种罕见疾病,可发展为恶性肿瘤和侵袭性疾病。在此,男性患者五年前出现了次白蛋白性腹水和慢性腹泻病史。小肠活检和免疫组织化学研究提示IPSID的诊断。然后该患者已成功使用抗生素治疗。考虑到IPSID在初期阶段对抗生素具有良好的治疗反应,临床医生应注意其各种表现形式,以便尽早开始治疗

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