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伴有罕见巨大胃溃疡的腹痛:1例IgA血管炎合并巨细胞病毒感染病例报告

Abdominal pain with curious massive gastric ulcer: A case report of IgA vasculitis complicated with cytomegalovirus infection.

作者信息

Zhang Yueyi, Yang Aiming, Wang Qiang

机构信息

Department of Gastroenterology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Department of Gastroenterology, The People's Hospital of Xizang Autonomous Region, Lhasa, Xizang Autonomous Region, China.

出版信息

Medicine (Baltimore). 2025 Jul 4;104(27):e43050. doi: 10.1097/MD.0000000000043050.

Abstract

RATIONALE

Immunoglobulin A (IgA) vasculitis is a relatively rare autoimmune disorder in adults, typically affecting the skin, joints, kidneys, and gastrointestinal tract. It is often an overlooked cause of abdominal pain, and the diagnostic challenge is compounded when it coexists with infections. IgA vasculitis complicated by cytomegalovirus infection is a rare clinical scenario that presents significant challenges for diagnosis and treatment. This case is reported to raise awareness of the condition.

PATIENT CONCERNS

A 56-year-old female presented with abdominal pain, hematochezia, purpura, and reduced urine output. After corticosteroid treatment, her condition initially improved. However, 1 week later, the abdominal pain worsened, and gastroscopy revealed multiple large ulcers.

DIAGNOSES

The diagnosis of IgA vasculitis with concomitant cytomegalovirus (CMV) infection was confirmed based on clinical and endoscopic findings, CMV-DNA titer changes, and the patient's response to antiviral therapy.

INTERVENTIONS

Antiviral treatment for CMV was initiated, while corticosteroid therapy was gradually tapered.

OUTCOMES

The patient's abdominal pain significantly relieved, CMV-DNA levels decreased to normal, and follow-up gastroscopy showed a marked reduction in ulcer size.

LESSONS

During corticosteroid treatment for IgA vasculitis, if abdominal pain intensifies and multiple gastric ulcers are found on endoscopy, a high index of suspicion for an underlying infection, particularly CMV infection, is crucial. Raising awareness of this clinical scenario can improve diagnostic accuracy and enable prompt treatment adjustments.

摘要

原理

免疫球蛋白A(IgA)血管炎在成人中是一种相对罕见的自身免疫性疾病,通常累及皮肤、关节、肾脏和胃肠道。它常常是腹痛被忽视的原因,当与感染并存时,诊断挑战更加复杂。IgA血管炎合并巨细胞病毒感染是一种罕见的临床情况,对诊断和治疗提出了重大挑战。报告该病例以提高对这种疾病的认识。

患者关注

一名56岁女性出现腹痛、便血、紫癜和尿量减少。经皮质类固醇治疗后,她的病情最初有所改善。然而,1周后,腹痛加重,胃镜检查发现多个大溃疡。

诊断

根据临床和内镜检查结果、巨细胞病毒DNA滴度变化以及患者对抗病毒治疗的反应,确诊为IgA血管炎合并巨细胞病毒(CMV)感染。

干预措施

开始针对CMV的抗病毒治疗,同时逐渐减少皮质类固醇治疗。

结果

患者腹痛明显缓解,CMV-DNA水平降至正常,随访胃镜显示溃疡大小明显缩小。

经验教训

在对IgA血管炎进行皮质类固醇治疗期间,如果腹痛加剧且内镜检查发现多个胃溃疡,高度怀疑存在潜在感染,尤其是CMV感染至关重要。提高对这种临床情况的认识可以提高诊断准确性并及时调整治疗。

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