Macrodystrophia lipomatosa of the left hallux

Author(s):  
C. Cotter ◽  
D. Elias ◽  
S. Pruneddu
1992 ◽  
Vol 33 (6) ◽  
pp. 554-555 ◽  
Author(s):  
R. Jain ◽  
S. Sawhney ◽  
M. Berry

1997 ◽  
Vol 21 (2) ◽  
pp. 135-137 ◽  
Author(s):  
Rafaela Soler ◽  
Esther Rodríguez ◽  
Amelia Bargiela ◽  
Carmen Martĩnez

2017 ◽  
Vol 34 (5) ◽  
pp. e292-e293
Author(s):  
Tyler Willenbrink ◽  
Lindsay Thelin ◽  
Gregory Connor ◽  
Lucia Diaz

2014 ◽  
Vol 18 (2) ◽  
Author(s):  
Andrew J. Van den Heever

Macrodystrophia lipomatosa (MDL) is a rare congenital, but non-hereditary, form of localised gigantism of the fingers or toes. The hallmark of the condition is hypertrophy of all mesenchymal elements in the involved region, with a predominance of fibro-adipose tissue. A clinically subtle case of MDL is presented.


1992 ◽  
Vol 158 (6) ◽  
pp. 1295-1297 ◽  
Author(s):  
M Blacksin ◽  
F J Barnes ◽  
M M Lyons

Hand Surgery ◽  
2013 ◽  
Vol 18 (02) ◽  
pp. 267-272 ◽  
Author(s):  
Steven B. Albright ◽  
Erik M. Wolfswinkel ◽  
Kevin J. Caceres ◽  
William M. Weathers ◽  
Larry H. Hollier

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.


1992 ◽  
Vol 33 (6) ◽  
pp. 554-555
Author(s):  
R. Jain ◽  
S. Sawhney ◽  
M. Berry

2016 ◽  
Vol 61 (3) ◽  
pp. 347
Author(s):  
A Ramesh ◽  
SUma Maheswari ◽  
V Sampath ◽  
K Manoharan

2020 ◽  
Vol 33 (4) ◽  
pp. 250
Author(s):  
Mohd Ilyas ◽  
Zubair Ahmad ◽  
Naseer Choh

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