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Dergiler / Erciyes Medical Journal / 2018 / Cilt: 40 - Sayı: 1

A Rare Cause of Headache: Rathke Cleft Cyst

Zeynep Özözen AYAS
Kıyasettin ASİL
Sayfa
39–41
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

We report a case of a 36-year-old man with big-sized RCC diagnosed after presenting with a 3-month history of headache in the light of the existing literature.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Headache is the most common symptom encountered in clinical practice.
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Temel Bulgular & Veri:Although the causes of primary headaches are common, intracranial space-occupying lesions also cause headaches, albeit more rarely.
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Sonuç & Katkı:We report a case of a 36-year-old man with big-sized RCC diagnosed after presenting with a 3-month history of headache in the light of the existing literature.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Headache is the most common symptom encountered in clinical practice. Although the causes of primary headaches are common, intracranial space-occupying lesions also cause headaches, albeit more rarely. Rathke cleft cyst (RCC) is a rare, usually asymptomatic cystic lesion of the sellar/suprasellar region. Despite being benign in nature, these should be immediately treated in case they display compressive signs. We report a case of a 36-year-old man with big-sized RCC diagnosed after presenting with a 3-month history of headache in the light of the existing literature.

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Bu Makaleye Atıf Yap

AYAS, Z. Ö., ASİL, K. (2018). A Rare Cause of Headache: Rathke Cleft Cyst. Erciyes Medical Journal, Cilt: 40 - Sayı: 1, 39–41. https://ajindex.com/articles/196099

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Kaynakça (2)

  1. Teramoto A, Hirakawa K, Sanno N, Osamura Y. Incidental Pituitary lesions in 1000 unselected autuopsy specimens. Radiology 1994; 193(1): 161-4. [CrossRef] Ross DA, Norman D, Wilson CB. Radiological characteristics and results of surgical management of Rathke’s cysts in 43 patients. Neurosurgery 1992; 30(2): 173-9. [CrossRef] Sivaraju L, Anantha Sai, Kiran N, Rao AS, Ghosal N, Hegde AS. Giant multi-compartmental suprasellar Rathke’s cleft cyst with restriction on diffusion weighted images. Neuroradiol J 2017; 30(3): 1971400916682512. [CrossRef] Zada G. Rathke cleft cysts: a review of clinical and surgical management. Neurosurg Focus 2011; 31(1): E1. [CrossRef] Saeki N, Sunami K, Sugaya Y, Yamaura A. MRI findings and clinical manifestations in Rathke cleft cyst. Acta Neurochir (Wien) 199; 141(10): 1055-61.
  2. Naiken VS, Tellen M, Merance DR. Pituitary cyst of Rathkes cleft origin with hypopituitarism. J Neurosurg 1961; 18(5): 70-706. [CrossRef] Sumida M, Arita K, igita K, Tominaga, Lida K, Kurisiu K. Concomitant pituitary adenoma and Rathke cleft cyst. Neuroradiology 2001; 43(9): 755-9. [CrossRef] Kim CW, Hwang K, Joo JD, Kim YH, Han JH, Kim CY. Spontaneus involution of Rathke’s cleft cysts without visual symptoms. Brain Tumor Res Treat 2016; 4(2): 58-62. [CrossRef] Çakabay M, Iplikçioğlu AC, Gökduman CA, Dinç C, San A. Rathke cleft cysts; Clinical hormonal features, pathology, surgical treatment. Turk Neurosurg 2006; 16: 35-41. (bulamadım) Wilson CB. Surgical management of pituitary tumors. J Clin Endocrinol Metab 1997; 82(8): 2381-5. [CrossRef]