Ozdemir Kutbay N, Sarer Yurekli B, Yasar Z, Akinci B
Celal Bayar University, Faculty of Medicine, Division of Endocrinology and Metabolism, Manisa, Izmir, Turkey.
Ege University - Endocrinology, Izmir, Turkey.
Acta Endocrinol (Buchar). 2019 Jan-Mar;-5(1):129-130. doi: 10.4183/aeb.2019.129.
About 250 patients with acquired partial lipodystrophy (Barraquer-Simons) syndrome have been reported so far. It is characterized by the loss of adipose tissue from the face and upper extremities, and accumulated fat in the rest of the body. The disease usually starts in females during childhood or adolescence, and usually after a febrile illness. Fat loss often comes into view in months or years. We present a 23-year-old female patient with acquired partial lipodystrophy , which is rarely seen.
迄今为止，已报道了约250例获得性部分脂肪营养不良（Barraquer-Simons）综合征患者。其特征为面部和上肢脂肪组织缺失，而身体其他部位脂肪堆积。该病通常始于儿童期或青春期的女性，且通常在发热性疾病之后。脂肪流失常在数月或数年内显现。我们报告了1例23岁患有获得性部分脂肪营养不良的女性患者，此病例较为罕见。
