| Literature DB >> 25406225 |
Jagadeesan Dhanasekaran1, Ajit Kumar Reddy1, Radha Sarawagi1, Prakash Manikka Lakshmanan1.
Abstract
Macrodystrophia lipomatosa (MDL), a rare non-hereditary congenital disorder of localised gigantism, is characterised by progressive proliferation of all mesenchymal elements, with a disproportionate increase in fibroadipose tissue. We report a case of a 19-year-old man who presented with a history of painless enlargement of the left upper limb since childhood, which was gradually increasing in size and predominantly involving the radial aspect of the upper limb with relative sparing of the ulnar aspect. The patient was imaged with X-ray and MRI. Imaging and clinical features were classical of MDL. The patient underwent stage 1 reduction plasty of the left forearm; preoperative and histopathological findings confirmed the preoperative diagnosis. 2014 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2014 PMID: 25406225 PMCID: PMC4244489 DOI: 10.1136/bcr-2014-204899
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X