Panhypopituitarism secondary to hypophyseal metastasis

Citation
C. Pinet et al., Panhypopituitarism secondary to hypophyseal metastasis, PRESSE MED, 29(1), 2000, pp. 17-18
Citations number
9
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
PRESSE MEDICALE
ISSN journal
07554982 → ACNP
Volume
29
Issue
1
Year of publication
2000
Pages
17 - 18
Database
ISI
SICI code
0755-4982(20000115)29:1<17:PSTHM>2.0.ZU;2-D
Abstract
BACKGROUND: Hypophyseal metastatic localizations are uncommon and rarely th e first expression of a primary cancer. We report an exceptional case revea led by panhypopituitarism and diabetes insipidis. CASE REPORT: Brain MRI visualized an intra- and suprasellar tumoral formati on found to be a cribiform adenocarcinoma. The primary tumor could not be i dentified. Despite radiotherapy, surgery and chemotherapy combining carbopl atin and etoposide, the tumor progressed with the development of cervical a nd mediastinal nodes. The patient died one year after onset of the clinical signs. DISCUSSION: Diagnosis of hypophyseal metastasis is mainly based on indirect evidence: rapid course, invasion of neighboring structures. Optimal manage ment of these rare tumors remains to be determined.