Caputo R
First Department of Dermatology and Pediatric Dermatology, University of Milano, Italy.
Acta Derm Venereol. 1989;69(5):442-3.
A unique case of Lipodystrophia centrifugalis sacralis infantilis in a caucasian is reported. This case fulfils all the clinical requirements of the centrifugalis lipodystrophy described in Oriental children by Imamura et al. (1) and usually localized on the abdomen. The 15-year follow-up of this case clearly demonstrates the tendency toward spontaneous remission of the disease after puberty.
报告了一例白种人婴儿患离心性骶部脂肪营养不良的独特病例。该病例符合今村等人（1）描述的东方儿童离心性脂肪营养不良的所有临床特征，且通常局限于腹部。对该病例15年的随访清楚地表明，该病在青春期后有自发缓解的趋势。
