Sina B, Burnett J W
Arch Dermatol. 1983 Mar;119(3):189-97. doi: 10.1001/archderm.119.3.189.
Five new cases of lymphomatoid papulosis are reported. This entity can apparently be divided into at least two subtypes. In one group of patients, papulopustular lesions resembling those of pityriasis lichenoides develop that resolve spontaneously within a few weeks. The lesions contain an epidermotropic dermal infiltration composed predominantly of abnormal lymphocytes. The other group of patients displays larger, more persistent lesions that contain a nonepidermotropic dermal infiltration composed predominantly of histiocytes. Lymphoma eventually develops in about 10% of the patients with lymphomatoid papulosis.
报告了5例新的淋巴瘤样丘疹病病例。该疾病显然可分为至少两个亚型。在一组患者中，出现类似苔藓样糠疹的丘疹脓疱性损害，数周内可自行消退。损害中有以异常淋巴细胞为主的亲表皮性真皮浸润。另一组患者有较大且更持久的损害，其中有以组织细胞为主的非亲表皮性真皮浸润。约10%的淋巴瘤样丘疹病患者最终会发展为淋巴瘤。
