Klippel-Trenaunay syndrome presenting with acanthocytosis and splenic and retroperitoneal lymphangioma: a case report

INTRODUCTION: Klippel-Trenaunay syndrome is a rare congenital mesodermal abnormality characterized by bone and soft tissue hypertrophy, extensive hemangioma and venous abnormalities. We report the case of a patient with two additional rare clinical manifestations in the background of Klippel-Trenaun...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Med Case Rep
Päätekijät: Withana, Milinda, Rodrigo, Chaturaka, Shivanthan, Mitrakrishnan Chrishan, Warnakulasooriya, Sachini, Wimalachandra, Manu, Gooneratne, Lallindra, Rajapakse, Senaka
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2014
Aiheet:
Case Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4289367/
https://ncbi.nlm.nih.gov/pubmed/25427442
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-8-390
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