Ma'koseh Mohammad, Al-Ibraheem Akram, Almasri Nidal, Hamed Eman, Alrabi Kamal
Medical Oncology, King Hussein Cancer Center, Amman, JOR.
Nuclear Medicine, King Hussein Cancer Center, Amman, JOR.
Cureus. 2023 Sep 8;15(9):e44930. doi: 10.7759/cureus.44930. eCollection 2023 Sep.
Castleman disease (CD) is a rare lymphoproliferative disorder that is associated with an increased risk for lymphoma. The association between CD and classical Hodgkin lymphoma (HL) is rare. The patient described here is a 44-year-old, HIV-seronegative male who presented with significant weight loss, fever, night sweats, and right axillary swelling. Imaging showed bulky infraclavicular, subpectoral, and axillary lymph nodes. A biopsy revealed classical HL on the background of a human herpesvirus-8 (HHV-8)-negative plasma cell variant of CD. The patient had a complete remission after six cycles of doxorubicin, bleomycin, vincristine, and dacarbazine (ABVD) that were followed by consolidative radiotherapy and continued to be disease-free for more than two years.
卡斯特尔曼病(CD)是一种罕见的淋巴增生性疾病,与淋巴瘤风险增加相关。CD与经典型霍奇金淋巴瘤(HL)之间的关联罕见。本文所述患者为一名44岁的HIV血清阴性男性,表现为显著体重减轻、发热、盗汗及右腋窝肿胀。影像学检查显示锁骨下、胸肌下及腋窝有肿大淋巴结。活检显示在HHV-8阴性的CD浆细胞变异型背景下为经典型HL。该患者接受六个周期的阿霉素、博来霉素、长春新碱及达卡巴嗪(ABVD)化疗后完全缓解,随后接受巩固放疗,且持续无病生存超过两年。