Von Hippel–Lindau disease
Malaysian Family Physician
;
: 29-31, 2017.
Artigo
em Inglês
| WPRIM
| ID: wpr-625500
ABSTRACT
Von Hippel–Lindau (VHL) disease is a rare autosomal dominantly inherited multisystem disorder characterised by the development of a variety of benign and malignant tumours. We report a case of VHL disease that was inherited by a daughter from her father, who both presented at a young age with progressive headache and were found to have a posterior fossa haemangioblastoma (HB) on magnetic resonance imaging (MRI). Multiple benign pancreatic and renal cysts were also noted in both patients.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Idioma:
Inglês
Revista:
Malaysian Family Physician
Ano de publicação:
2017
Tipo de documento:
Artigo
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