Jannot Xavier, Auclair Martine, Martinot Martin, Maazouzi Amin, Boutboul David, Vigouroux Corinne, Dieudonné Yannick
Department of Clinical Immunology and Internal Medicine, National Reference Center for Systemic Autoimmune Diseases (CNR RESO), Tertiary Center for Primary Immunodeficiency, Strasbourg University Hospital, Strasbourg, France.
Faculty of Medicine, Université de Strasbourg, Strasbourg, France.
Eur J Case Rep Intern Med. 2025 Apr 29;12(5):005355. doi: 10.12890/2025_005355. eCollection 2025.
This case study presents the case of a 54-year-old human immunodeficiency virus (HIV)-positive male who developed type B insulin resistance syndrome (TBIRS) in conjunction with a relapse of human herpesvirus 8 (HHV8)-positive multicentric Castleman disease (MCD). This case is only the sixth reported instance of TBIRS associated with HHV8-associated MCD. The diagnosis was confirmed by the presence of anti-insulin receptor autoantibodies, and the patient was treated effectively with rituximab, with no relapse in follow-up. The cases described are discussed, along with the differences between them and our own case. Additionally, the potential for an autoimmune complication of MCD, even when HIV is well controlled, is addressed, as well as the available therapeutic approaches.
Unexplained hypoglycemia can reveal autoimmunity against insulin receptors associated with lymphoproliferative disorders, including multicentric Castleman disease.Autoimmune hypoglycemia can occur independently of inflammatory signs or uncontrolled human immunodeficiency virus infection in patients with multicentric Castleman disease.
本病例研究介绍了一名54岁的男性人类免疫缺陷病毒(HIV)阳性患者,该患者在人类疱疹病毒8(HHV8)阳性多中心Castleman病(MCD)复发时并发了B型胰岛素抵抗综合征(TBIRS)。该病例是第六例报告的与HHV8相关的MCD相关的TBIRS病例。通过抗胰岛素受体自身抗体的存在确诊,患者接受利妥昔单抗有效治疗,随访中无复发。讨论了所描述的病例,以及它们与我们自己病例之间的差异。此外,还探讨了即使HIV得到良好控制,MCD发生自身免疫并发症的可能性,以及可用的治疗方法。
无法解释的低血糖可能揭示与包括多中心Castleman病在内的淋巴增殖性疾病相关的针对胰岛素受体的自身免疫。自身免疫性低血糖可独立于多中心Castleman病患者的炎症体征或未控制的人类免疫缺陷病毒感染而发生。