Selting Kevin, Hansen Neil J, Harrison W L
University of Nebraska College of Medicine, Department of Radiology, 981045 Nebraska Medical Center, Omaha, NE 68198-1045.
Radiol Case Rep. 2019 Aug 22;14(10):1311-1313. doi: 10.1016/j.radcr.2019.08.007. eCollection 2019 Oct.
We present a 28-year-old female with a rare familial partial lipodystrophy. Originally presenting at the age of 14, she began experiencing hypertrophy of the fat in the mons pubis and labia majora regions. By the age of 24 she had disfiguring hypertrophy of these areas with severe fatty overgrowth, similar in nature to that experienced by her father and paternal grandmother. During her workup and planning for suction lipectomy, she underwent computed tomography angiography with the imaging manifestation of severe massive subcutaneous fat hypertrophy; the imaging appearance was only able to be explained after a thorough review of the patient's history and medical literature.
我们报告一名28岁患有罕见家族性部分脂肪营养不良的女性。她最初在14岁时出现症状，开始经历耻骨联合和大阴唇区域脂肪肥大。到24岁时，这些部位出现毁容性肥大，伴有严重的脂肪过度生长，与她的父亲和祖母所经历的情况类似。在她接受抽脂术的检查和规划过程中，她接受了计算机断层血管造影，成像显示为严重的大量皮下脂肪肥大；只有在全面回顾患者病史和医学文献后，才能解释这种成像表现。
