Xiao Xin-Yue, Niu Yun, Liu Ping-Ping, Zheng Yu-Ming, Zhang Ming-Gang, Wang Guo-Chun, Wang Xiao-Di, Liu Fang
Department of Rheumatology, China-Japan Friendship Hospital, Beijing, 100029, China.
Department of Pathology, China-Japan Friendship Hospital, Beijing, 100029, China.
J Med Case Rep. 2024 Dec 21;18(1):616. doi: 10.1186/s13256-024-04892-7.
Polyarteritis nodosa is a relatively uncommon type of systemic necrotizing vasculitis that primarily affects medium-sized arteries. While gastrointestinal involvement is known in polyarteritis nodosa, heavy gastrointestinal bleeding due to gastric ulceration is relatively uncommon. We present the case of an 81-year-old male of Chinese ethnicity who experienced severe gastrointestinal bleeding as a result of polyarteritis nodosa and an innovative treatment approach for a better patient outcomes.
Upon admission to the medical intensive care unit, the patient underwent a comprehensive diagnostic assessment, including examinations for cardiovascular and dermatological abnormalities, laboratory tests, autoantibody and tumor marker assessments, and imaging studies (such as endoscopies, whole-body computed tomography, and positron emission tomography-computed tomography scans), and a skin biopsy. The patient had tachycardia, hypotension, and extensive skin abnormalities on the lower extremities along with anemia, low platelets, and abnormal renal function. Upper gastrointestinal endoscopy revealed gastric and duodenal ulcers. Additional examinations, including electronic colonoscopy, capsule endoscopy, and whole-body computed tomography, were negative. A positron emission tomography-computed tomography scan showed increased uptake in the arterial walls and skin, which supported the diagnosis of polyarteritis nodosa, later confirmed by a biopsy of the skin on the lower extremities. Methylprednisolone, octreotide, and omeprazole were administered, leading to improvement in gastrointestinal symptoms, ulcer healing, and skin recovery. The patient continued with prednisone for 1 month.
This case serves to inform gastroenterologists about the need to consider polyarteritis nodosa in severe upper gastrointestinal bleeding and underscores the importance of prompt, medication-based treatment for successful patient outcome.
结节性多动脉炎是一种相对罕见的系统性坏死性血管炎,主要累及中等大小动脉。虽然结节性多动脉炎已知可累及胃肠道,但因胃溃疡导致的严重胃肠道出血相对少见。我们报告一例81岁华裔男性因结节性多动脉炎出现严重胃肠道出血的病例以及一种为改善患者预后的创新治疗方法。
患者入住医学重症监护病房后,接受了全面的诊断评估,包括心血管和皮肤异常检查、实验室检查、自身抗体和肿瘤标志物评估、影像学检查(如内镜检查、全身计算机断层扫描和正电子发射断层扫描 - 计算机断层扫描)以及皮肤活检。患者有心动过速、低血压、下肢广泛皮肤异常,伴有贫血、血小板减少和肾功能异常。上消化道内镜检查发现胃和十二指肠溃疡。包括电子结肠镜检查、胶囊内镜检查和全身计算机断层扫描在内的其他检查均为阴性。正电子发射断层扫描 - 计算机断层扫描显示动脉壁和皮肤摄取增加,支持结节性多动脉炎的诊断,随后下肢皮肤活检得以证实。给予甲泼尼龙、奥曲肽和奥美拉唑治疗后,胃肠道症状改善、溃疡愈合且皮肤恢复。患者继续服用泼尼松1个月。
该病例提醒胃肠病学家在严重上消化道出血时需考虑结节性多动脉炎,并强调及时进行药物治疗对患者成功预后的重要性。