Literature DB >> 828300

Macrodactylia fibrolipomatosis.

I Yaghmai, F McKowne, A Alizadeh.   

Abstract

The clinical, pathologic, and roentgenographic features of macrodactylia fibrolipomatosis described are based on 40 cases from the literature and five cases seen by the authors. This condition previously has been described as macrodactyly, megalodactyly, macrodystrophia lipomatosa, dactylomegaly, and local gigantism. We believe macrodactylia fibrolipomatosis is the best term because it describes the characteristics which separate this condition from other forms of macrodactyly. Macrodactylia fibrolipomatosis is a form of macrodactyly noticed soon after birth. Usually affected are multiple adjacent digits on the lateral aspect of the hand or the medial aspect of the foot, although a single digit may be involved. Roentgenograms show bony enlargement, often with medial deviation in the hand and lateral deviation in the foot. The soft tissues ventral to the affected bones are diffusely enlarged and are predominantly of fat density, commonly mixed with bands of denser connective tissue. The cause of this rare condition is obscure but it may be related to fibrofatty tumors, often found at surgery, impinging on nerves supplying the enlarged digits.

Entities:  

Mesh:

Year:  1976        PMID: 828300     DOI: 10.1097/00007611-197612000-00015

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  2 in total

1.  Scintigraphic differentiation of congenital soft-tissue extremity enlargement with Tc-99m DTPA.

Authors:  G A Mandell; C I Scott; H T Harcke; C Sharkey; L Harris
Journal:  Skeletal Radiol       Date:  1989       Impact factor: 2.199

Review 2.  A Review of Macrodystrophia Lipomatosa: Revisitation.

Authors:  Theddeus Oh Prasetyono; Enjeline Hanafi; Windi Astriana
Journal:  Arch Plast Surg       Date:  2015-07-14
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.