Markovits P, Bergiron C, Chauvel C, Castellino R A
AJR Am J Roentgenol. 1977 May;128(5):835-8. doi: 10.2214/ajr.128.5.835.
Ovarian dysgerminomas are distinguished from other ovarian neoplasms by their rarity, their predilection for metastases via lymphatic pathways, and their radiosensitivity and favorable prognosis. After the initial surgery, which provides the histologic diagnosis and defines the local extent of pelvic involvement, lymphography is the single most useful tool to determine whether retroperitoneal lymph nodes are involved. Results of the study guide the radiotherapeutic approach, including field size and dosage. In an unselected group of 31 previously untreated patients, 10 had positive lymphograms. The response to therapy and the detection of relapse of disease may be evaluated by monitoring the residually opacified lymph nodes with surveillance abdominal radiographs. If necessary, a repeat lymphogram can be performed. The 2 year survival rate of 84% for ovarian dysgerminomas is lower than that for testicular seminomas, probably due to later recognition of the tumor. Failuresare related to local extension or to hematogenous dissemination.
卵巢无性细胞瘤与其他卵巢肿瘤的区别在于其罕见性、通过淋巴途径转移的倾向、放射敏感性和良好的预后。初始手术可提供组织学诊断并确定盆腔受累的局部范围,术后淋巴造影是确定腹膜后淋巴结是否受累的最有用的单一工具。研究结果指导放射治疗方法,包括照射野大小和剂量。在一组未经选择的31例未经治疗的患者中,10例淋巴造影呈阳性。通过监测腹部X线平片上残留的显影淋巴结来评估对治疗的反应和疾病复发情况。如有必要,可重复进行淋巴造影。卵巢无性细胞瘤的2年生存率为84%,低于睾丸精原细胞瘤,可能是由于肿瘤发现较晚。治疗失败与局部扩展或血行播散有关。