Familial multiple lipomatosis associated with multiple cherry hemangiomas and moles: a rare case report

Author:

Guntupalli Gopalaswamy1,Ramadugu Rithika1,Suvvari Tarun K2,Ravipati Shivani3ORCID,Thomas Vimal4ORCID

Affiliation:

1. Department of Surgery, Kamineni Academy of Medical Sciences and Research Centre , LB Nagar, Hyderabad, Telangana 508254 , India

2. Rangaraya Medical College , Kakinada, Andhra Pradesh 533001 , India

3. Department of Surgery, Dr. Pinnamaneni Siddhartha Institute of Medical Sciences & Research Foundation , Gannavaram, Andhra Pradesh 521286 , India

4. Tbilisi State Medical University , Tbilisi 0186 , Georgia

Abstract

Abstract Lipomas are common benign mesenchymal tumours, whereas lipomatoses are uncommon. Familial multiple lipomatosis (FML) is a rare syndrome characterized by multiple usually painless lipomas which may be associated with other conditions. FML is considered to be genetic, with various patterns of inheritance suggested. In this case report, we described a case of multiple familial lipomatosis that was misdiagnosed as dercum’s disease.

Publisher

Oxford University Press (OUP)

Reference21 articles.

1. Familial multiple lipomatosis;Shanks;Can Med Assoc J,1957

2. Familial multiple lipomatosis with clear autosomal dominant inheritance and onset in early adolescence;Lee;BMJ Case Rep,2011

3. Familial multiple lipomatosis: a case report;Veger;Acta Chir Belg,2010

4. Familial multiple lipomatosis;Keskin;Israel Med Assoc J,2002

5. Multiple familial lipomatosis with polyneuropathy, an inherited dominant condition;Stoll;Ann Genet,1996

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