Furey N L, Furey W W, Yonan T N, Esterly N B
Acta Derm Venereol. 1975;55(5):381-6.
A 65-year-old black female with Sezary syndrome had generalized intractable pruritus, erythroderma, alopecia, onychogryphosis, lumphadenopathy and hepatomegaly. Abnormal lymphocytes with large, convoluted and grooved nuclei (Sezary cells) were identified in the skin and peripheral blood. A striking feature of her disease was severe, deforming arthropathy of the hands and knees, a clinical finding which has been described previously in only one patient with Sezary syndrome. At necropsy no associated lymphoma was found.
一名65岁患有Sezary综合征的黑人女性,有全身性顽固性瘙痒、红皮病、脱发、甲癣、淋巴结病和肝肿大。在皮肤和外周血中发现了具有大的、卷曲的和有沟的细胞核的异常淋巴细胞(Sezary细胞)。她疾病的一个显著特征是双手和双膝严重的变形性关节病,这一临床发现此前仅在一名Sezary综合征患者中被描述过。尸检时未发现相关淋巴瘤。