Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
BMJ Case Rep ; 20162016 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-27358095

RESUMEN

Misdiagnosis of phosphatase and tensin homologue hamartoma syndromes is common. Correct diagnosis has a relevant impact on patients, as the risk of malignancies is high and treatment options are limited. We report the case of a 24-year-old man who presented with symptomatic vascular intramuscular lesions of the left forearm and right calf, macrocephaly, post Hashimoto thyroiditis, a multicystic intracranial paratrigonal lesion, lentiginous hyperpigmented maculae on the foreskin and multiple skin lesions. MRI showed extended fibrofatty changes and malformed vessels in the forearm and calf lesions, also, arteriovenous shunting was present in these lesions. The patient had been treated by embolisation and surgically in the past, with limited results. A multidisciplinary assessment and genetic counselling were undertaken and a surveillance programme was initiated. Treatment options of the symptomatic vascular lesions include excision or possibly cryoablation. Physiotherapy to prevent progression of the contractures should be initiated meanwhile.


Asunto(s)
Síndrome de Hamartoma Múltiple/genética , Fosfohidrolasa PTEN/genética , Malformaciones Vasculares/genética , Anomalías Múltiples/genética , Diagnóstico Diferencial , Antebrazo/irrigación sanguínea , Síndrome de Hamartoma Múltiple/diagnóstico , Humanos , Extremidad Inferior/irrigación sanguínea , Angiografía por Resonancia Magnética , Masculino , Megalencefalia/genética , Músculo Esquelético/irrigación sanguínea , Dolor Musculoesquelético/etiología , Ultrasonografía Doppler en Color , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...