Document Detail


Different lymphscintigraphic patterns in patients with lymphedema distichiasis.
MedLine Citation:
PMID:  20848994     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Mutation of the transcription factor FOXC2 gene has been identified as the cause of lymphedema-distichiasis syndrome (LD). Subjects with LD usually present with lower extremity lymphedema and distichiasis--an additional row of eyelashes. Typically, lymphscintigrams of patients with LD show good transport of the radiotracer from the feet to the inguinal lymph nodes accompanied by reflux of tracer to the skin of the lower extremities ("dermal backflow"). We have examined two patients with LD syndrome and were able to demonstrate two different distinct lymphscintigraphic patterns: lymphatic hyperplasia with reflux and obstructive.
Authors:
E Sutkowska; A Bator; K Trompeta; A Szuba
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Lymphology     Volume:  43     ISSN:  0024-7766     ISO Abbreviation:  Lymphology     Publication Date:  2010 Jun 
Date Detail:
Created Date:  2010-09-20     Completed Date:  2010-10-07     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0155112     Medline TA:  Lymphology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  73-7     Citation Subset:  IM    
Affiliation:
Department and Clinic of Orthopaedic and Traumatologic Surgery, Wroclaw Medical University, Wroclaw, Poland.
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MeSH Terms
Descriptor/Qualifier:
Adult
Child, Preschool
Eyelashes / abnormalities*
Female
Humans
Lymphatic Abnormalities
Lymphatic System / radionuclide imaging*
Lymphedema / radionuclide imaging*,  therapy
Male
Middle Aged
Pedigree
Radiopharmaceuticals / diagnostic use*
Syndrome
Chemical
Reg. No./Substance:
0/Radiopharmaceuticals

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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