Maroto P, Tabernero J M, Villavicencio H, Mesía R, Marcuello E, Solé-Balcells F J, Sola C, Mora J, Algaba F, Pérez C, León X, López López J J
Medical Oncology Service, Hospital de Sant Pau, Barcelona, Spain.
Eur Urol. 1997;32(3):305-9.
To analyze the clinical outcome of patients diagnosed with growing teratoma syndrome (GTS) at a single center during a long follow-up.
Eleven patients with GTS are reported. GTS lesions were located in the metastatic sites involved at disease presentation. Involved sites were: retroperitoneum in 9 patients; lung in 3; supraclavicular lymph nodes in 2, and inguinal lymph nodes in 1. Surgical resection of the masses was the treatment of choice.
Twenty-four surgical procedures were performed: 4 thoracotomies; 2 supraclavicular; 1 inguinal, and 17 retroperitoneal node resections. Three patients have not relapsed since surgery of the masses, at 37+, 110+ and 118+ months. Eight patients have relapsed, 6 with mature teratoma and 2 (22%) with cancer. To date, all the patients are alive, 6 of them without disease and 5 with teratoma after resection of the masses.
GTS is an infrequent entity. Involved sites are only at locations previously affected by the disease. The treatment of choice is surgical resection but recurrence is common. Efforts should be done to complete resection of the masses.
分析在单一中心长期随访期间被诊断为成熟性畸胎瘤综合征(GTS)患者的临床结局。
报告了11例GTS患者。GTS病灶位于疾病初发时累及的转移部位。受累部位如下:9例位于腹膜后;3例位于肺部;2例位于锁骨上淋巴结;1例位于腹股沟淋巴结。手术切除肿块是首选治疗方法。
共进行了24次手术:4次开胸手术;2次锁骨上手术;1次腹股沟手术以及17次腹膜后淋巴结切除术。3例患者自肿块手术后未复发,时间分别为37 +、110 +和118 +个月。8例患者复发,6例为成熟性畸胎瘤,2例(22%)为癌症。迄今为止,所有患者均存活,其中6例无疾病,5例在切除肿块后患有畸胎瘤。
GTS是一种罕见疾病。受累部位仅在先前受疾病影响的位置。首选治疗方法是手术切除,但复发很常见。应努力完整切除肿块。