Autoreactive Antibodies Associated with Castleman Disease Triad.

IF 1.5 Q4 IMMUNOLOGY Case Reports in Immunology Pub Date : 2024-03-06 eCollection Date: 2024-01-01 DOI:10.1155/2024/9382107
Jacqueline A Turner, Ali Hakimi, Hannah Lee, Jeffrey T Schowinsky, Jeffrey M Sippel, Bradford J Siegele, Raul M Torres, William A Robinson
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Abstract

The Castleman triad has been described in a select few patients presenting with a retroperitoneal mass, mucocutaneous pemphigus vulgaris, and bronchiolitis obliterans. Here, we describe the Castleman triad in a 19-year-old male with unicentric hyaline vascular type Castleman disease (HV-CD). This patient presented with an array of positive antibodies, including anti-cyclic citrullinated peptide, anti-double-stranded DNA, and Sjogren's IgG. Interestingly, the patient's rheumatologic symptoms resolved after tumor resection, while his antibody profile remained relatively unchanged. HV-CD, with a triad presentation, was thought to be from a paraneoplastic syndrome secondary to an underlying lymphoproliferative disorder. The findings presented here identify multiple autoantibodies potentially contributing to this patient's presentation with HV-CD.

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与卡斯特曼病三联征相关的自身抗体
卡斯特曼三联征在少数患者中有所描述,这些患者表现为腹膜后肿块、寻常型粘膜天疱疮和阻塞性支气管炎。在这里,我们描述了一名患有单中心透明血管型卡斯特曼病(HV-CD)的 19 岁男性患者的卡斯特曼三联征。该患者出现了一系列阳性抗体,包括抗环瓜氨酸肽、抗双链DNA和Sjogren's IgG。有趣的是,肿瘤切除后,患者的风湿病症状缓解了,而抗体谱却相对保持不变。具有三联征表现的 HV-CD 被认为是继发于潜在淋巴增生性疾病的副肿瘤综合征。本文的研究结果发现,多种自身抗体可能是导致该患者出现HV-CD的原因。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
14
审稿时长
15 weeks
期刊介绍: Case Reports in Immunology is a peer-reviewed, Open Access journal that publishes case reports and case series related to allergies, immunodeficiencies, autoimmune diseases, immune disorders, cancer immunology and transplantation immunology.
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