BILATERAL MACRODYSTROPHIA LIPOMATOSA WITH SYNDACTYLY: A CASE REPORT AND LITERATURE REVIEW

Author:

Albright Steven B.1,Wolfswinkel Erik M.1,Caceres Kevin J.1,Weathers William M.1,Hollier Larry H.1

Affiliation:

1. Division of Plastic Surgery, Michael E. Debakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA

Abstract

Macrodystrophia lipomatosa is a rare, non-hereditary form of congenital local gigantism characterised by enlargement and hypertrophy of all mesenchymal tissue components with a disproportionate increase in adipose tissue. This form of macrodactyly has been reported in association with other anomalies including polydactyly, brachydactyly, syndactyly, and symphalangism. We describe a previously unreported case of bilateral upper extremity macrodystrophia lipomatosa with syndactyly in a 23-month-old boy. In this report, we emphasise the importance of establishing a diagnosis with imaging and review the described surgical approaches to treating this difficult condition.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Medicine

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