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成人伴发肠型杜氏利什曼原虫病的致命性过敏性紫癜。

Fatal Henoch-Schönlein purpura in an adult with Dieulafoy lesions.

机构信息

Rheumatology Division, Roger Williams Medical Center, Boston University, Boston, MA, USA.

出版信息

J Clin Rheumatol. 2012 Aug;18(5):253-6. doi: 10.1097/RHU.0b013e318262e3f9.

DOI:10.1097/RHU.0b013e318262e3f9
PMID:22832298
Abstract

Henoch-Schönlein purpura (HSP) is considered a benign disease of children. We report a severe case of HSP in an adult causing renal failure and gastrointestinal (GI) hemorrhage. Despite aggressive treatment with corticosteroids, cyclophosphamide, and plasmapheresis, the patient developed massive GI bleeding from 2 Dieulafoy lesions and died weeks after bowel resection. Although uncommon, when massive GI hemorrhage occurs, actively bleeding Dieulafoy lesions, although uncommon, should be suspected and evaluated early.

摘要

过敏性紫癜(HSP)被认为是儿童的良性疾病。我们报告了一例成人严重 HSP 病例,导致肾功能衰竭和胃肠道(GI)出血。尽管使用皮质类固醇、环磷酰胺和血浆置换进行了积极治疗,但患者仍因 2 处Dieulafoy 病变发生大量胃肠道出血,并在肠切除数周后死亡。尽管不常见,但当发生大量胃肠道出血时,应怀疑并早期评估是否存在活动性出血的 Dieulafoy 病变。

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Case Rep Gastrointest Med. 2019 Jul 3;2019:9402968. doi: 10.1155/2019/9402968. eCollection 2019.