Takahashi S, Asamoto M, Nakazawa T, Kosaki T, Katsumi K, Shirai T
First Department of Pathology, Nagoya City University Medical School.
Jpn J Clin Oncol. 1994 Dec;24(6):327-30.
A 22-year-old Japanese man with a mediastinal germ cell tumor with mixed teratoma and hepatoid alpha-fetoprotein positive, and glandular yolk sac components, also demonstrated widely disseminated malignant histiocytosis involving the lungs, liver, pancreas, spleen, bone marrow and lymph nodes. Sensitivity to chemotherapy was acute and the patient died of disseminated intravascular coagulation syndrome within four months of his initial presentation.
一名22岁的日本男性，患有纵隔生殖细胞肿瘤，伴有混合性畸胎瘤、肝样甲胎蛋白阳性及腺性卵黄囊成分，同时还表现为广泛播散的恶性组织细胞增多症，累及肺、肝、胰腺、脾、骨髓和淋巴结。对化疗的敏感性很高，患者在首次就诊后的四个月内死于弥散性血管内凝血综合征。
