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Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report

Rathke cleft cysts are benign lesions of the sellar and suprasellar region. Extrasellar intrasphenoidal Rathke cleft cysts are rare with only one case reported in pediatric age group. The presenting complaints described include headache and diplopia. We report a case of intrasphenoidal Rathke cleft...

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Autores principales: Gowtham, Mahadevan S., Sunilkumar, Devaraj, Ramesh, Andi S., Srinivas, Bheemanathi H., Verma, Dinesh, Nagarajan, Krishnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757520/
https://www.ncbi.nlm.nih.gov/pubmed/36531764
http://dx.doi.org/10.4103/jpn.JPN_262_20
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author Gowtham, Mahadevan S.
Sunilkumar, Devaraj
Ramesh, Andi S.
Srinivas, Bheemanathi H.
Verma, Dinesh
Nagarajan, Krishnan
author_facet Gowtham, Mahadevan S.
Sunilkumar, Devaraj
Ramesh, Andi S.
Srinivas, Bheemanathi H.
Verma, Dinesh
Nagarajan, Krishnan
author_sort Gowtham, Mahadevan S.
collection PubMed
description Rathke cleft cysts are benign lesions of the sellar and suprasellar region. Extrasellar intrasphenoidal Rathke cleft cysts are rare with only one case reported in pediatric age group. The presenting complaints described include headache and diplopia. We report a case of intrasphenoidal Rathke cleft cyst in a 15-year-old girl who presented with headache and visual disturbances. Neuroimaging showed an expansile cystic lesion involving the sphenoid sinus with mass effect over the pituitary and optic chiasma. Endoscopic decompression of the cystic lesion was done and histopathology of the cyst wall revealed it to be Rathke cleft cyst. Follow-up MRI showed total resection of the cystic lesion with residual partial left optic nerve atrophy.
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spelling pubmed-97575202022-12-17 Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report Gowtham, Mahadevan S. Sunilkumar, Devaraj Ramesh, Andi S. Srinivas, Bheemanathi H. Verma, Dinesh Nagarajan, Krishnan J Pediatr Neurosci Case Reports Rathke cleft cysts are benign lesions of the sellar and suprasellar region. Extrasellar intrasphenoidal Rathke cleft cysts are rare with only one case reported in pediatric age group. The presenting complaints described include headache and diplopia. We report a case of intrasphenoidal Rathke cleft cyst in a 15-year-old girl who presented with headache and visual disturbances. Neuroimaging showed an expansile cystic lesion involving the sphenoid sinus with mass effect over the pituitary and optic chiasma. Endoscopic decompression of the cystic lesion was done and histopathology of the cyst wall revealed it to be Rathke cleft cyst. Follow-up MRI showed total resection of the cystic lesion with residual partial left optic nerve atrophy. Wolters Kluwer - Medknow 2021 2022-01-07 /pmc/articles/PMC9757520/ /pubmed/36531764 http://dx.doi.org/10.4103/jpn.JPN_262_20 Text en Copyright: © 2022 Journal of Pediatric Neurosciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Reports
Gowtham, Mahadevan S.
Sunilkumar, Devaraj
Ramesh, Andi S.
Srinivas, Bheemanathi H.
Verma, Dinesh
Nagarajan, Krishnan
Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report
title Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report
title_full Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report
title_fullStr Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report
title_full_unstemmed Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report
title_short Intrasphenoidal Rathke Cleft Cyst: A Rare Case Report
title_sort intrasphenoidal rathke cleft cyst: a rare case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757520/
https://www.ncbi.nlm.nih.gov/pubmed/36531764
http://dx.doi.org/10.4103/jpn.JPN_262_20
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