Literature DB >> 20306922

Familial multiple lipomatosis: a case report.

H T C Veger1, N J C Ravensbergen, A Ottenhof, S A da Costa.   

Abstract

Lipoma is the most common type of soft tissue tumour. Multiple lipomas localised in different areas of the body are rare and can occur in specific hereditary syndromes. Familial multiple lipomatosis is a rare benign hereditary syndrome with a proposed autosomal-dominant inheritance. We present the case of a 67-year-old man with this disease. Clinical features, genetic evidence, and treatment options are reviewed.

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Year:  2010        PMID: 20306922     DOI: 10.1080/00015458.2010.11680577

Source DB:  PubMed          Journal:  Acta Chir Belg        ISSN: 0001-5458            Impact factor:   1.090


  3 in total

1.  Prominent neurological involvement in Dercum disease.

Authors:  Mariagiovanna Cantone; Giuseppe Lanza; Manuela Pennisi; Rita Bella; Carmelo Schepis; Maddalena Siragusa; Rita Barone; Raffaele Ferri
Journal:  J Neurol       Date:  2017-02-13       Impact factor: 4.849

Review 2.  Review of Dercum's disease and proposal of diagnostic criteria, diagnostic methods, classification and management.

Authors:  Emma Hansson; Henry Svensson; Håkan Brorson
Journal:  Orphanet J Rare Dis       Date:  2012-04-30       Impact factor: 4.123

3.  Subcutaneous adipose tissue fatty acid desaturation in adults with and without rare adipose disorders.

Authors:  Jennifer K Yee; Susan A Phillips; Kambiz Allamehzadeh; Karen L Herbst
Journal:  Lipids Health Dis       Date:  2012-02-03       Impact factor: 3.876

  3 in total

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