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首页> 外文期刊>Journal of the Canadian Association of Gastroenterology >A112 ANGIOEDEMA,A RARE YET AN IMPORTANT CAUSE OF ABDOMINAL PAIN. A CASE STUDY AND LITERATURE REVIEW
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A112 ANGIOEDEMA,A RARE YET AN IMPORTANT CAUSE OF ABDOMINAL PAIN. A CASE STUDY AND LITERATURE REVIEW

机译:A112血管后期,一个罕见的腹痛的重要原因。案例研究与文献综述

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Background Abdominal pain is a common gastroenterological symptom with an extensive deferential diagnoses. Angioedema is an important cause to remember after the more common causes have been excluded.It is caused by a deficiency in the inhibitor of the first component of classical complement pathway and is divided into hereditary or acquired.Acquired angioedema is associated with autoimmune or lymphoproliferative neoplasms.The clinical features of both include recurrent,self-limiting and circumscribed edema affecting the subcutaneous tissue of the upper respiratory airways and gastrointestinal tract. Aims We describe an interesting case of acquired angioedema presenting with recurrent abdominal pain. We also systematically review the current literature on this rare entity. Methods A search of electronic databases was performed inclusive to September 2019, for all studies and reviews of patients with acquired angioedema manifested as recurrent attacks of abdominal pain. Results: Case Report: 65 year old lady ho has an at least 2 year long history of abdominal pain and bloating associated on some occasions with nausea and vomiting.She presented to our emergency department in August,2018 with a day history of severe generalized abdominal pain and was found to have circumferential thickening,edema with mucosal hyperenhancement involving the distal segment of the small bowel.Splenomegaly was noted on that study.A double balloon enteroscopy was planned,but ultimately cancelled as her ileitis had resolved.The patient was discharged home as her pain resolved with conservative management which included intravenous fluid, pain medications and antiemetics.She then represented to the hospital on September 16, 2019 severe abdominal pain and throat tightness associated with shortness of breath. Again,noted was an extremely short segment of ileum with mucosal edema and hyperenhancement which resolved on a repeat CT scan done during that admission on September 18th, 2019.In light of the patient’s symptoms,CT scan findings,progressive anemia, thrombocytopenia and splenomegaly. It was thought that her abdominal pain is related to secondary to angioedema driven by a lymphoproliferative process as evident by the splenomegaly and worsening cytopenia. A bone marrow was done which revealed clonal B, so the diagnosis of lymphoma was made. The patient’s C1 esterase was 0.2 with reduced functional activity.CH50 less 10 perecent. A diagnosis of acquired angioedema was made and the patient was started on BERINERT 3000 IU SQ every three days with 1500 IU for break through with significant improvement in the frequency and severity of abdominal pain episodes. Conclusions Acquired angioedema is to be considered as a cause of recurrent abdominal pain in a patient with a lymphoproliferative malignancy after common causes and etiologies have been ruled out.
机译:背景技术腹痛是一种常见的胃肠学症状,具有广泛的恭敬诊断。在排除较常见的原因之后,血管后美是一个重要的原因。它是由于古典补体途径的第一组分抑制剂的缺陷引起的,并且被分为遗传或获得的.Acquired血管内膜与自身免疫或淋巴抑制性肿瘤有关。两者的临床特征包括反复,自限制和外缘水肿,影响上呼吸道气道和胃肠道的皮下组织。目的是我们描述了患有复发性腹痛患者的有趣案例。我们还系统性地审查了这种罕见实体的当前文献。方法对电子数据库进行搜索,以2019年9月在2019年9月进行,适用于患有血管后期患者的所有研究和评论表现为腹痛的反复发作。结果:案例报告:65岁的女士何历史悠久的腹痛历史至少有2年的腹痛和腹部有关,在某些情况下与恶心和呕吐相关联。她于2018年8月介绍了我们的急诊部门,历史严重的广泛腹部历史疼痛并被发现具有圆周增厚,具有粘膜型粘膜的水肿,涉及小肠的远端段。在该研究中注意到了平面肠球菌。计划了双气球肠镜检查,但最终随着她的对炎已经解决而取消。患者被排出回家由于她的痛苦与保守管理解决,其中包括静脉内液体,止痛药和反助剂。她于2019年9月16日代表着医院,严重的腹痛和喉咙紧绷与呼吸急促相关。再次,注意到是一种极短的回肠片段,粘膜水肿和血清致残,并在2019年9月18日在该录取期间进行的重复CT扫描解决。在患者的症状,CT扫描结果,进步性贫血,血小板减少症和脾肿大。据认为,她的腹痛与由淋巴细胞凋亡的过程驱动的继发性,脾肿大和恶化细胞瘤的淋巴抑制作用。揭示克隆B的骨髓已经完成,因此制备了淋巴瘤的诊断。患者的C1酯酶为0.2,功能活性降低。CH50少10次。诊断出现血管后期的诊断,患者每三天开始每三天在Berinert 3000 IU SQ上进行一次突破,腹痛发作的频率和严重程度显着改善。结论所获得的血管内膜被认为是常见原因和病因术后患者患者在患者中患者的经常性腹痛的原因。

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