Case Report: Psychogenic purpura in a uremic patient on peritoneal dialysis.

IF 5.9 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI:10.3389/fimmu.2025.1625126
Lin Zhang, Hanqing Zhang, Yuetong Zhao, Tao Zhang, Zhengjie Zhu, Yanheng Qiao, Yongming Tian, Hang Su, Jie Li, Bo Yang
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引用次数: 0

Abstract

Psychogenic purpura (Gardner-Diamond syndrome) is a rare autoimmune vasculopathy characterized by the spontaneous onset of painful edema and infiltrative cutaneous lesions that rapidly develop into ecchymosis after severe psychological stress events. In this article, we report an 87-year-old female uremic patient who was admitted to the hospital with erythema and subcutaneous ecchymoses on the head and face following an Aedes mosquito sting. She was previously diagnosed with "toxic insect stings and skin bacterial infections" and was given anti-infective treatment by an outside hospital, which was ineffective. Subsequent laboratory tests at our hospital revealed only an increase in fibrinogen and leukocytosis. Tracing the history revealed that the patient's purpura episodes were related to a major life event, the death of her husband. After consultation with the dermatology department, the patient's autoerythrocyte sensitization test was positive, and she was finally diagnosed with "psychogenic purpura". Treatment included glucocorticoids and immunomodulators, supplemented by anti-infective and renal replacement therapy, and the patient's ecchymosis gradually subsided and resolved after one month of follow-up. This case highlights the complexity of diagnosing psychogenic purpura and the significance of medical history in the diagnosis. Only accurate and timely diagnosis can effectively avoid unnecessary treatment.

病例报告:一例腹膜透析尿毒症患者的心因性紫癜。
心因性紫癜(加德纳-戴蒙德综合征)是一种罕见的自身免疫性血管病变,其特征是在严重的心理应激事件后,自发发生疼痛性水肿和浸润性皮肤病变,并迅速发展为瘀斑。在这篇文章中,我们报告了一位87岁的女性尿毒症患者,她在被伊蚊叮咬后头部和面部出现红斑和皮下瘀斑。她之前被诊断为“有毒昆虫叮咬和皮肤细菌感染”,并在外部医院接受了抗感染治疗,但无效。随后在本院进行的实验室检查仅显示纤维蛋白原和白细胞增多。追踪病史显示,患者的紫癜发作与她丈夫的死亡有关。经皮肤科会诊,患者自体红细胞致敏试验阳性,最终诊断为“心因性紫癜”。治疗以糖皮质激素和免疫调节剂为主,辅以抗感染和肾脏替代治疗,随访1个月后患者瘀斑逐渐消退。本病例强调了心因性紫癜诊断的复杂性和病史在诊断中的重要性。只有准确及时的诊断才能有效避免不必要的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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