Vuković I, Stojimirović E, Milutinović S
Bilt Hematol Transfuz. 1978;6(3):57-62.
The paper presents a girl with cutaneous lymphoma. The onset of the illness was two years ago, and followed by cutaneous lesions, typical Mycosis fungoides and Sêzary's syndrome. After a year, the neoplastic cells penetrated into the peripheral blood, and the development of Sézary's variant of Mycosis fungoidses, was shown. The clinical development of the disease, and the application of hystopathological and laboratory investigations, proved that it was the Sézary's syndrome. When the adequete cytostatic therapy, and radiotherapy, was applied, according to the protocol for curing the malignant non Hodgkin lymphoma, the clinical and haematological remission of disease was performed.
该论文介绍了一名患有皮肤淋巴瘤的女孩。疾病于两年前开始,随后出现皮肤病变,典型的蕈样肉芽肿和塞扎里综合征。一年后,肿瘤细胞侵入外周血,显示出蕈样肉芽肿的塞扎里变异型的发展。疾病的临床进展以及组织病理学和实验室检查的应用证明这是塞扎里综合征。按照治疗恶性非霍奇金淋巴瘤的方案应用适当的细胞抑制疗法和放射治疗后,疾病实现了临床和血液学缓解。