...
首页> 外文期刊>American Journal of Case Reports >Association of Appendicitis, Helicobacter Pylori Positive Gastritis and Thrombotic Thrombocytopenic Purpura in an Adolescent
【24h】

Association of Appendicitis, Helicobacter Pylori Positive Gastritis and Thrombotic Thrombocytopenic Purpura in an Adolescent

机译:阑尾炎,幽门螺杆菌阳性胃炎与青少年血栓性血小板减少性紫癜的关联

获取原文
           

摘要

Patient: Male, 16 Final Diagnosis: Thrombotic thrombocytopenic purpura Symptoms: Anemia Medication: — Clinical Procedure: — Specialty: Pediatrics and Neonatology Objective: Unusual clinical course Background: Thrombotic thrombocytopenic purpura (TTP) in children is a rare life-threatening syndrome, characterized by microangiopathic hemolytic anemia, thrombocytopenia with renal dysfunction, neurologic symptoms, and fever. TTP is usually caused by deficient activity of von Willebrand factor cleaving protease (ADAMTS13), due to either gene mutations or acquired via anti-ADAMTS13 autoantibodies. It can be triggered by bone marrow or solid organ transplantation, cardiothoracic-, abdominal-, and orthopedic surgeries, infections including very rarely Helicobacter pylori infection. Case Report: Here we report a case of a 16-year-old male with TTP, who presented with thrombocytopenia before an appendectomy. Seven days after surgery, our patient started to vomit, developed melena, and was admitted to our pediatric intensive care unit (PICU) with clinical presentation of shock. Gastroscopy revealed H. pylori positive hemorrhagic gastritis. The patient was treated by erythrocyte transfusions, fresh frozen plasma, human albumin, glucose-electrolyte solutions, vitamin K, platelet transfusion before implantation of central venous catheter, and antibiotics. After 36 hours, we started plasma exchange (PEX). Blood tests showed deficiency of ADAMTS13. Due to the presence of anti-ADAMTS13 autoantibodies, rituximab was administered. Due to generalized tonic-clonic seizures, he was artificially ventilated. Brain MR angiography showed small ischemic cerebro-vascular insult in the arteria cerebri media region. Despite immunosuppressive therapy and PEX, the patient did not improve completely until the H. pylori infection was eradicated. After which, he recovered completely. Conclusions: We present a rare case of TTP accompanied with appendicitis and gastritis caused by H. pylori , where TTP improvement was dependent on H. pylori infection eradication.
机译:患者:男性,16岁最终诊断:血栓性血小板减少性紫癜症状:贫血药物:-临床程序:-专科:儿科和新生儿科目的:异常的临床过程背景:儿童血栓性血小板减少性紫癜(TTP)是一种罕见的威胁生命的综合征,其特征是微血管性溶血性贫血,血小板减少症伴肾功能不全,神经系统症状和发烧。 TTP通常是由于基因突变或通过抗ADAMTS13自身抗体获得的von Willebrand因子裂解蛋白酶(ADAMTS13)活性不足引起的。它可以由骨髓或实体器官移植,心胸,腹部和整形外科手术(包括极少数幽门螺杆菌感染)引起。病例报告:在此我们报告一例16岁男性TTP,在阑尾切除术前出现血小板减少症。手术后7天,我们的病人开始呕吐,发展为黑斑病,并因电击的临床表现被送入我们的儿科重症监护病房(PICU)。胃镜检查发现幽门螺杆菌阳性出血性胃炎。通过红细胞输注,新鲜冷冻血浆,人白蛋白,葡萄糖电解质溶液,维生素K,植入中心静脉导管前的血小板输注以及抗生素对患者进行了治疗。 36小时后,我们开始进行血浆置换(PEX)。验血显示ADAMTS13缺乏。由于存在抗ADAMTS13自身抗体,因此使用了利妥昔单抗。由于全身性强直-阵挛性癫痫发作,他被人工通气。脑MR血管造影显示脑小动脉中部区域有缺血性小脑血管损伤。尽管进行了免疫抑制治疗和PEX,但直到幽门螺杆菌感染根除后,患者才能完全康复。之后,他完全康复了。结论:我们目前罕见的由幽门螺杆菌引起的TTP伴有阑尾炎和胃炎的病例,其中TTP的改善取决于根除幽门螺杆菌的感染。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号