Toonstra J, van Weelden H, Gmelig Meyling F H, van der Putte S C, Schiere S I, Baart de la Faille H
Arch Dermatol Res. 1985;277(3):159-66. doi: 10.1007/BF00404310.
A report is given on two male patients who showed all the main characteristics of Sézary syndrome (SS). When phototested, however, they proved to be extremely photosensitive, which suggested a diagnosis of actinic reticuloid (AR). This was supported by the predominance in blood and skin specimens of lymphoid cells with a suppressor/cytotoxic phenotype, the absence of clonal cell proliferation and a benign clinical course. Differential diagnostic problems of SS and erythrodermic AR are discussed.
报告了两名男性患者,他们表现出蕈样肉芽肿综合征(SS)的所有主要特征。然而,经光试验,他们被证明对光极度敏感,这提示诊断为光化性类网状细胞增多症(AR)。血液和皮肤标本中具有抑制/细胞毒性表型的淋巴细胞占优势、不存在克隆性细胞增殖以及临床病程良性,这些均支持该诊断。文中讨论了SS与红皮病型AR的鉴别诊断问题。