| Autor: |
Demirci, Harun, Kahraman, Devrim, Kuzucu, Pelin, Şenol, Özde, Uğur, Kadriye Şerife, Ergün, Mehmet Ali, Keskil, Semih, Akdemir Özışık, Pınar |
| Předmět: |
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| Zdroj: |
British Journal of Neurosurgery; Oct2024, Vol. 38 Issue 5, p1144-1150, 7p |
| Abstrakt: |
Objectives: Double pituitary adenoma is a rare entity that can pose a significant challenge. The incidence of double or multiple pituitary adenomas is ∼1% in autopsy cases and 0.4–1.3% in surgical series. Its definition varies, including 'double adenomas' in the literature in contrast to 'multiple adenomas', which is more specific and suitable. While some authors require separating topographically unique tumours, others have used a looser definition of separate immunohistochemistry. Case presentation: We presented the case of a 26-year-old patient with recurrent carpal tunnel syndrome symptoms, with double pituitary adenomas secreting growth hormone (GH) and thyroid-stimulating hormone (TSH). To date, 89 patients have been reported in the literature with symptomatic carpal tunnel syndrome, but only five had GH-TSH secretion. Conclusions: Double adenoma resection is of great importance for ensuring successful biochemical treatment. To ensure a successful operation, a careful preoperative 3T MRI examination is of great importance. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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