Lipomembranous polycystic osteodysplasia
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Virchows Archiv
- Vol. 372 (3) , 245-251
- https://doi.org/10.1007/bf00433283
Abstract
A case of lipomembranous polycystic Osteodysplasia is presented. The clinical features were characterized by multiple cystic changes of the bones and progressive psychomotor retardation. Although the diagnosis of polyostotic fibrous dysplasia of bone was made first because of expanded tumorlike lesions in bones, pathology of bone and bone marrow confirmed the diagnosis of lipomembranous polycystic Osteodysplasia. Light microscopy showed a great number of peculiar undulating membranous structures in the adipose tissue. With the electron microscope the membrane seemed to be composed of an accumulation of endoplasmic reticulum-like tubular profiles. They appear first, in close connection with fat droplets, within the mesenchymal cell.Keywords
This publication has 1 reference indexed in Scilit:
- Farber's disease: Report of a case with observations on its histogenesis and notes on the nature of the stored materialThe Journal of Pediatrics, 1962