Hirai Yoshimitsu, Yoshimasu Tatsuya, Oura Shoji, Okamura Yoshitaka
Department of Thoracic and Cardiovascular Surgery, Wakayama Medical University, 811-1 Kimiidera, Wakayama 641-0012, Japan.
Interact Cardiovasc Thorac Surg. 2011 Jan;12(1):96-7. doi: 10.1510/icvts.2010.242867. Epub 2010 Oct 12.
A 39-year-old man was referred to hospital with a giant mediastinal mass, thrombocytopenia and high levels of serum tumor markers. Flow cytometry of bone marrow and peripheral blood samples led to the diagnosis of a mediastinal germ cell tumor associated with hematologic neoplasia. He was treated with combination chemotherapy for a germ cell tumor and acute myeloid leukemia. After chemotherapy, the tumor was enlarged, although serum tumor marker levels had decreased. After induction therapy, the tumor was surgically resected. This syndrome is rare, and more cases need to be studied to enable effective treatment.
一名39岁男性因巨大纵隔肿块、血小板减少和血清肿瘤标志物水平升高被转诊至医院。对骨髓和外周血样本进行流式细胞术检查后,诊断为与血液系统肿瘤相关的纵隔生殖细胞肿瘤。他接受了针对生殖细胞肿瘤和急性髓系白血病的联合化疗。化疗后,尽管血清肿瘤标志物水平有所下降,但肿瘤仍增大。诱导治疗后,肿瘤被手术切除。这种综合征很罕见,需要研究更多病例以实现有效治疗。