Parker D, Holford C P, Begent R H, Newlands E S, Rustin G J, Makey A R, Bagshawe K D
Thorax. 1983 Dec;38(12):897-902. doi: 10.1136/thx.38.12.897.
Primary malignant mediastinal teratoma is a rare tumour previously regarded as inevitably fatal. In a series of eight male patients with a mean age of 24 years five remain alive and well. All patients showed raised serum concentrations of human chorionic gonadotrophin or alpha fetoprotein. The patients were treated with intermittent combination chemotherapy that included cisplatin. Six patients responded to chemotherapy with a fall in human chorionic gonadotrophin or alpha fetoprotein to near normal levels and they then had radical excision of the remaining tumour. Living malignant tumour was found in four of the specimens and these patients received postoperative chemotherapy. One patient died after eight months and the remaining five patients are alive and well 13-136 months after the start of treatment. The two patients who did not undergo surgery died at one month and 15 months. Intermittent combination chemotherapy and carefully timed radical excision of these tumours would appear to have produced better results than have been reported in other series.
原发性恶性纵隔畸胎瘤是一种罕见肿瘤,以前被认为必然致命。在一组8例平均年龄24岁的男性患者中,5例仍存活且状况良好。所有患者血清人绒毛膜促性腺激素或甲胎蛋白浓度均升高。患者接受了包括顺铂在内的间歇性联合化疗。6例患者对化疗有反应,人绒毛膜促性腺激素或甲胎蛋白降至接近正常水平,随后对剩余肿瘤进行了根治性切除。在4个标本中发现有存活的恶性肿瘤,这些患者接受了术后化疗。1例患者在8个月后死亡,其余5例患者在治疗开始后13至136个月仍存活且状况良好。另外2例未接受手术的患者分别在1个月和15个月时死亡。这些肿瘤采用间歇性联合化疗并在适当时间进行根治性切除,似乎比其他系列报道的结果更好。