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Pediatric Neurology 2014-Jun

Pituitary apoplexy in a teenager--case report.

Només els usuaris registrats poden traduir articles
Inicieu sessió / registreu-vos
L'enllaç es desa al porta-retalls
Chen-Cheng Chao
Chun-Ju Lin

Paraules clau

Resum

BACKGROUND

Pituitary apoplexy is a rare clinical emergency which results from hemorrhage or infarction in the pituitary gland.

METHODS

We present a 14-year-old girl with pituitary apoplexy and review the literature.

RESULTS

Our patient experienced blurred vision, nausea, and headache. Her best-corrected visual acuity was 20/200 and 20/20. Confrontation test visual field testing revealed bitemporal hemianopsia. Brain imaging demonstrated a suprasellar mass. The microscopic endonasal transsphenoidal approach only found 5-10 mL brownish fluid-like material. Pathology confirmed no malignancy. Pituitary apoplexy was diagnosed. Her nausea and headache gradually improved. Six months after operation, her best-corrected visual acuity had improved to 20/30 and 20/20.

CONCLUSIONS

Although pituitary apoplexy is rare in pediatric patients, prompt evaluation including detailed ophthalmic examination, biochemical evaluation, endocrine workup, and image study are very important.

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