Patel Jay P, Patel Deep P, Amin Trishul H, Dave Rushikesh K, Hardaswani Daksh, Saiyed Faizanali, Goswami Rushita J
Research, Chirayu Medical College and Hospital, Bhopal, IND.
Research, AMA School of Medicine, Makati, PHL.
Cureus. 2024 Sep 11;16(9):e69149. doi: 10.7759/cureus.69149. eCollection 2024 Sep.
Castleman disease (CD) includes rare and intricate lymphoproliferative disorders characterized by the abnormal growth of lymph nodes and immune system disturbances. It primarily presents in two forms: unicentric Castleman disease (UCD), which affects a single lymph node area, and multicentric Castleman disease (MCD), which involves multiple lymph nodes and systemic manifestations. The disease's underlying mechanisms are often linked to immune system irregularities, especially involving interleukin-6 (IL-6). The condition was first documented by Dr. Benjamin Castleman in 1954, laying the groundwork for understanding this complex disorder. MCD can be further divided into idiopathic MCD (iMCD), which includes thrombocytopenia, ascites, fibrosis, renal impairment, and organ enlargement (TAFRO) syndrome, and human herpesvirus-8 (HHV-8)-associated MCD, which can occur in individuals with or without HIV. The prevalence of CD shows a higher occurrence of UCD, with the disease typically presenting in individuals in their fifth to seventh decades of life and being more common in areas with high HIV prevalence. The clinical presentation of CD can include symptoms such as swollen lymph nodes, fever, anemia, and systemic inflammation. Diagnostic challenges arise due to the disease's rarity, and its symptoms overlap with other conditions. Treatment approaches differ based on the subtype. UCD generally responds favorably to the surgical removal of the affected lymph nodes, while MCD often requires antiviral treatments, interleukin-6 (IL-6) inhibitors, and new biologic therapies. Recent advances in treatment, including innovative biologic agents and combination therapies, offer promising prospects for improving patient outcomes. Accurate diagnosis and customized treatment strategies are essential for the effective management of this complex disease.
卡斯特尔曼病(CD)是一种罕见且复杂的淋巴增殖性疾病,其特征为淋巴结异常生长及免疫系统紊乱。它主要有两种表现形式:单中心型卡斯特尔曼病(UCD),仅累及单个淋巴结区域;多中心型卡斯特尔曼病(MCD),涉及多个淋巴结并伴有全身症状。该疾病的潜在机制通常与免疫系统异常有关,尤其是白细胞介素-6(IL-6)。1954年本杰明·卡斯特尔曼医生首次记录了这种疾病,为了解这一复杂病症奠定了基础。MCD可进一步分为特发性MCD(iMCD),包括血小板减少、腹水、纤维化、肾功能损害及器官肿大(TAFRO)综合征,以及与人类疱疹病毒8型(HHV-8)相关的MCD,后者可发生于有或无HIV感染的个体。CD的患病率显示UCD更为常见,该病通常在50至70岁的人群中出现,在HIV高流行地区更为普遍。CD的临床表现可包括淋巴结肿大、发热、贫血及全身炎症等症状。由于该病罕见且症状与其他病症重叠,诊断存在挑战。治疗方法因亚型而异。UCD通常通过手术切除受累淋巴结可取得良好疗效,而MCD往往需要抗病毒治疗、白细胞介素-6(IL-6)抑制剂及新型生物疗法。包括创新生物制剂和联合疗法在内的治疗新进展为改善患者预后带来了希望。准确诊断和定制治疗策略对于有效管理这种复杂疾病至关重要。