Membranous lipodystrophy (lipomembranous polycystic osteodysplasia). Two case reports.

@article{Hasegawa1983MembranousL,
  title={Membranous lipodystrophy (lipomembranous polycystic osteodysplasia). Two case reports.},
  author={Yoshihisa Hasegawa and Yoshiaki Inagaki},
  journal={Clinical orthopaedics and related research},
  year={1983},
  volume={181},
  pages={229-32}
}
Membranous lipodystrophy, a hereditary disease, is characterized by symmetric multiple cystic bone lesions and progressive neuropsychiatric symptoms. In two patients, a 22-year-old woman and a 30-year-old man, as in others reported in the literature, neither the etiology nor the pathogenesis was apparent. Histologically, the lesions consisted of convoluted membranes interlaced with lipoid structures.