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Pediatr Dermatol ; 41(2): 292-295, 2024.
Article in English | MEDLINE | ID: mdl-37800459

ABSTRACT

High-flow vascular malformations have been associated with multiple syndromes including capillary malformation-arteriovenous malformation (CM-AVM) syndrome, hereditary hemorrhagic telangiectasia syndrome, and less commonly, phosphatase and tensin homolog hamartoma tumor syndrome (PHTS). We present a series of three patients with clinically challenging complex AVMs who were found to have underlying PHTS. In all patients, diagnosis was delayed, and the presence of the AVM prompted sampling and genetic testing for PHTS in the absence of other clinical features of the condition. This series highlights the importance of screening for PHTS in the setting of high-flow vascular malformations.


Subject(s)
Arteriovenous Malformations , Capillaries/abnormalities , Hamartoma Syndrome, Multiple , Port-Wine Stain , Telangiectasia, Hereditary Hemorrhagic , Vascular Malformations , Humans , Hamartoma Syndrome, Multiple/complications , Hamartoma Syndrome, Multiple/diagnosis , Hamartoma Syndrome, Multiple/genetics , Arteriovenous Malformations/complications , Arteriovenous Malformations/diagnosis , Arteriovenous Malformations/genetics , Doxorubicin , PTEN Phosphohydrolase/genetics
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