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A case of spontaneous intracerebral hemorrhage in neurofibromatosis type 1 associated with pheochromocytoma / 대한내과학회지
Korean Journal of Medicine ; : 103-107, 2008.
Article de Ko | WPRIM | ID: wpr-164618
Bibliothèque responsable: WPRO
ABSTRACT
Spontaneous intracerebral hemorrhage is very rare in patients with neurofibromatosis type 1. A 30-year-old woman was referred to our hospital for evaluation of headaches, nausea, and vomiting. She was diagnosed with neurofibromatosis type 1 and a spontaneous intracerebral hemorrhage. She was treated with conservative management, including antihypertensive medications for 32 months. However, because of sustained hypertension, we performed screening tests for a pheochromocytoma. The 24 hr urine VMA and urine metanephrines were elevated. Abdominal CT showed a right adrenal mass, 7.5 x 5.8 cm in size.. After a successful resection of the tumor, the hypertension resolved without medication for > 1 year. This case illustrates that delayed diagnosis and treatment of pheochromocytoma can cause serious complications from hypertension, such as cerebrovascular hemorrhage. Thus, in patients with neurofibromatosis and hypertension, screening for pheochromocytoma is important for the early detection of an adrenal tumor.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Phéochromocytome / Vomissement / Hémorragie cérébrale / Dépistage de masse / Neurofibromatose de type 1 / Neurofibromatoses / Retard de diagnostic / Céphalée / Hémorragie / Hypertension artérielle Type d'étude: Diagnostic_studies / Screening_studies Limites du sujet: Adult / Female / Humans langue: Ko Texte intégral: Korean Journal of Medicine Année: 2008 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Phéochromocytome / Vomissement / Hémorragie cérébrale / Dépistage de masse / Neurofibromatose de type 1 / Neurofibromatoses / Retard de diagnostic / Céphalée / Hémorragie / Hypertension artérielle Type d'étude: Diagnostic_studies / Screening_studies Limites du sujet: Adult / Female / Humans langue: Ko Texte intégral: Korean Journal of Medicine Année: 2008 Type: Article