Numan Laith, Loku Galappaththy Suguni, Husainat Nedaa M, Abu Ghanimeh Mouhanna
Internal Medicine, University of Missouri-Kansas City School of Medicine, Kansas City, USA.
Kidney Institute, University of Kansas Hospital & Medical Center, Kansas City, USA.
Cureus. 2019 Jun 20;11(6):e4951. doi: 10.7759/cureus.4951.
Angioedema is an allergic reaction that usually involves the face and pharynx. Intestinal angioedema is a rare subtype that is typically linked to the use of angiotensin-converting enzymes inhibitors (ACEIs). Intestinal angioedema is challenging to diagnose, as it can mimic gastroenteritis or other inflammatory bowel conditions. Herein, we present a 34-year-old female who presented with recurrent episodes of abdominal pain. She underwent extensive workup for her abdominal pain and rash, and all was unrevealing except for high Immunoglobulin E (Ig E). Multiple imaging came back negative for any pathology. The allergy and immunology team evaluated the patient, and they believed her symptoms are likely caused by isolated intestinal angioedema with a histamine-related rash. She was started on high doses of antihistamines; her symptoms partially improved. Subsequently, she was started on a trial of omalizumab, which resulted in complete resolution of her symptoms. In conclusion, intestinal angioedema is a rare disease that should be suspected in cases of recurrent abdominal pain with negative workup, especially if the patient is taking ACEIs. Few cases were reported in the literature for patients on ACEI. In our case, the diagnosis was a challenge, as the patient was never on ACEI.
血管性水肿是一种通常累及面部和咽部的过敏反应。肠道血管性水肿是一种罕见的亚型,通常与使用血管紧张素转换酶抑制剂(ACEI)有关。肠道血管性水肿的诊断具有挑战性,因为它可能会模仿肠胃炎或其他炎症性肠病。在此,我们报告一名34岁女性,她反复出现腹痛。她因腹痛和皮疹接受了全面检查,除了高免疫球蛋白E(Ig E)外,所有检查结果均无异常。多项影像学检查均未发现任何病理改变。过敏和免疫科团队对该患者进行了评估,他们认为她的症状可能是由孤立性肠道血管性水肿伴组胺相关性皮疹引起的。她开始服用高剂量的抗组胺药;症状部分改善。随后,她开始试用奥马珠单抗,症状完全缓解。总之,肠道血管性水肿是一种罕见疾病,对于检查结果为阴性的反复腹痛病例应怀疑该病,尤其是患者正在服用ACEI时。文献中报道的服用ACEI的患者病例很少。在我们的病例中,诊断具有挑战性,因为患者从未服用过ACEI。