Vickers S M, Niederhuber J E
Department of Surgery, Johns Hopkins University School of Medicine, Baltimore Md., USA.
South Med J. 1997 Aug;90(8):839-44. doi: 10.1097/00007611-199708000-00015.
In this case of neurologic paraneoplastic syndrome in a patient with Hodgkin's disease, both the Hodgkin's disease and the associated neurologic syndrome were cured by surgical intervention and postoperative adjuvant chemotherapy. The patient's tumor was removed en bloc. Postoperative chemotherapy consisted of doxorubicin (Adriamycin), etoposide, and vinblastine. At 5-year follow-up in August 1996, the patient was active and tumor-free, without evidence of recurrent Hodgkin's disease or paraneoplastic syndrome. The possibility that this patient's syndrome was the result of a cross-reacting monoclonal idiotype produced by his tumor is suggested by the rapid recovery associated with tumor debulking. The role of surgery in the treatment of patients with Hodgkin's disease is limited, well defined, and even more infrequent in recurrent disease. Systemic chemotherapy is the treatment of choice for these patients, but surgery may play an important role in the initial cytoreduction of the recurrent tumor, especially in cases of localized bulky disease.
在这位患有霍奇金病的患者发生神经副肿瘤综合征的病例中,霍奇金病及相关神经综合征均通过手术干预和术后辅助化疗得以治愈。患者的肿瘤被整块切除。术后化疗方案包括多柔比星(阿霉素)、依托泊苷和长春碱。在1996年8月的5年随访中,患者情况良好且无肿瘤,没有霍奇金病复发或副肿瘤综合征的迹象。肿瘤体积减小后患者迅速康复,这提示该患者的综合征可能是由其肿瘤产生的交叉反应性单克隆独特型所致。手术在霍奇金病患者治疗中的作用有限,界定明确,在复发性疾病中更为少见。全身化疗是这些患者的首选治疗方法,但手术可能在复发性肿瘤的初始细胞减灭中发挥重要作用,尤其是在局限性大块疾病的病例中。