Abstract | OBJECTIVE: METHODS: We present a case report and review the available literature on this topic. RESULTS: CONCLUSION: Overall, pituitary carcinomas are extremely rare. To date, about 100 cases have been reported in the world's literature, and of these, only 19 cases originated from GH-secreting cells. Our examination of the symptoms, signs, diagnosis, and treatment of our patient, in comparison with the previously reported cases, should enhance awareness of this unusual disease process.
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Authors | Michele A Manahan, Alan P B Dackiw, Douglas W Ball, Martha A Zeiger |
Journal | Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
(Endocr Pract)
2007 Jan-Feb
Vol. 13
Issue 1
Pg. 72-6
ISSN: 1934-2403 [Electronic] United States |
PMID | 17360306
(Publication Type: Case Reports, Journal Article, Review)
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Topics |
- Acromegaly
(etiology)
- Adenoma
(complications, pathology, surgery)
- Aged
- Female
- Growth Hormone-Secreting Pituitary Adenoma
(complications, pathology, surgery)
- Humans
- Lymphatic Metastasis
- Parathyroid Neoplasms
(complications, secondary, surgery)
- Thymus Neoplasms
(complications, secondary, surgery)
- Thyroid Neoplasms
(complications, secondary, surgery)
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