Fisch R O, Tsai M Y, Gentry W C
J Am Acad Dermatol. 1981 Mar;4(3):284-90. doi: 10.1016/s0190-9622(81)70029-x.
A comprehensive study was undertaken of two patients who had typical phenylketonuria (PKU) and chronic dermatitis. Hematologic, immunologic, and histologic (light and electron microscopy) studies and quantitative intracellular amino acid measurements were made from the skin and cultured fibroblasts of these patients. Findings were: (1) the complement receptor-bearing lymphocytes (EAC rosettes) were decreased; (2) both light and electron microscopic findings revealed nonspecific dermatitis; (3) fibroblastic studies suggested little or no phenylalanine hydroxylase activity in cells of patients with PKU and controls; (4) the intracellular concentration of phenylalanine was significantly higher in the skin of PKU patients than in the controls; and (5) patch tests using 50% phenylalanine in petrolatum were negative in four untreated adult PKU patients and four controls.
对两名患有典型苯丙酮尿症(PKU)和慢性皮炎的患者进行了一项全面研究。对这些患者的皮肤和培养的成纤维细胞进行了血液学、免疫学和组织学(光镜和电镜)研究以及细胞内氨基酸定量测定。结果如下:(1)携带补体受体的淋巴细胞(EAC玫瑰花结)减少;(2)光镜和电镜检查结果均显示为非特异性皮炎;(3)成纤维细胞研究表明,PKU患者和对照组细胞中的苯丙氨酸羟化酶活性很低或没有;(4)PKU患者皮肤中苯丙氨酸的细胞内浓度显著高于对照组;(5)在四名未经治疗的成年PKU患者和四名对照组中,使用凡士林加50%苯丙氨酸进行的斑贴试验均为阴性。