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...

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Detalles Bibliográficos
Autores principales: Withana, Milinda, Rodrigo, Chaturaka, Shivanthan, Mitrakrishnan Chrishan, Warnakulasooriya, Sachini, Wimalachandra, Manu, Gooneratne, Lallindra, Rajapakse, Senaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289367/
https://www.ncbi.nlm.nih.gov/pubmed/25427442
http://dx.doi.org/10.1186/1752-1947-8-390

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289367/
https://www.ncbi.nlm.nih.gov/pubmed/25427442
http://dx.doi.org/10.1186/1752-1947-8-390

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