Posterior petrosal approach for retrochiasmatic craniopharyngioma

Craniophyringiomas are histologically benign tumors arising from embryonic epithelial cells of the craniopharyngeal duct. They are locally aggressive and their location in the sellar/supra-sellar region is associated with a high rate of recurrence and morbidity. It is generally recognized that surgi...

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Main Authors: Baha'eddin A. Muhsen, MD, Bilal Ibrahim, MD, Edinson Najera, MD, Hamid Borghei-Razavi, MD, Badih Adada, MD
Format: Article
Language:English
Published: Elsevier 2020-12-01
Series:Interdisciplinary Neurosurgery
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214751920304060
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spelling doaj-3db7005c136649f688eb5c68a74511c02020-11-25T03:37:42ZengElsevierInterdisciplinary Neurosurgery2214-75192020-12-0122100845Posterior petrosal approach for retrochiasmatic craniopharyngiomaBaha'eddin A. Muhsen, MD0Bilal Ibrahim, MD1Edinson Najera, MD2Hamid Borghei-Razavi, MD3Badih Adada, MD4Corresponding author at: Department of Neurosurgery, Braathen Center, Cleveland Clinic Florida, 3121 Cleveland Clinic Blvd, Weston, FL 33331, USA.; Department of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, FL, USADepartment of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, FL, USADepartment of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, FL, USADepartment of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, FL, USADepartment of Neurosurgery, Cleveland Clinic Florida Egil and Pauline Braathen Center, Neurological Institute, Cleveland Clinic, Weston, FL, USACraniophyringiomas are histologically benign tumors arising from embryonic epithelial cells of the craniopharyngeal duct. They are locally aggressive and their location in the sellar/supra-sellar region is associated with a high rate of recurrence and morbidity. It is generally recognized that surgical resection is the first treatment option. Craniopharyngiomas located in the retrochiasmatic area are among the most challenging to treat. They grow superiorly pushing floor of third ventricle, and posteriorly in the prepontine and interpeduncular cisterns. Different skull base approaches have been utilized to tackle tumors in this location. In this video we illustrate the surgical steps and nuances for resection of a large retrochiasmatic craniopharyngioma in a 25 YO RHF who presented with progressive headaches and visual decline. On neurological examination she was found to have bi-temporal hemianopia. An MRI scan of the brain showed a 4.5 × 3.2 × 4.3 cm mixed solid and cystic suprasellar mass with obstructive hydrocephalus located behind the optic chiasm. A brain CTA showed no displacement of the anterior communicating artery confirming the retrochiasmatic location of the tumor. The preoperative endocrine work up showed central hypothyroidism and low cortisol levels. Postoperatively the patient was extubated in the operating room, she had intact extra-ocular movements. She developed Diabetes insipidus and oculomotor nerve palsy on postoperative day 3. Her third nerve palsy recovered when she was seen 3 weeks postoperatively. The histopathology showed an adamantinomatous craniopharyngioma. The posterior petrosal approach should be considered in treating patients with Retrochiasmatic Craniopharyngiomas. The consent was obtained.http://www.sciencedirect.com/science/article/pii/S2214751920304060CraniopharyngiomaRetrochiasmatic CraniopharyngiomaPosterior petrosal approach
collection DOAJ
language English
format Article
sources DOAJ
author Baha'eddin A. Muhsen, MD
Bilal Ibrahim, MD
Edinson Najera, MD
Hamid Borghei-Razavi, MD
Badih Adada, MD
spellingShingle Baha'eddin A. Muhsen, MD
Bilal Ibrahim, MD
Edinson Najera, MD
Hamid Borghei-Razavi, MD
Badih Adada, MD
Posterior petrosal approach for retrochiasmatic craniopharyngioma
Interdisciplinary Neurosurgery
Craniopharyngioma
Retrochiasmatic Craniopharyngioma
Posterior petrosal approach
author_facet Baha'eddin A. Muhsen, MD
Bilal Ibrahim, MD
Edinson Najera, MD
Hamid Borghei-Razavi, MD
Badih Adada, MD
author_sort Baha'eddin A. Muhsen, MD
title Posterior petrosal approach for retrochiasmatic craniopharyngioma
title_short Posterior petrosal approach for retrochiasmatic craniopharyngioma
title_full Posterior petrosal approach for retrochiasmatic craniopharyngioma
title_fullStr Posterior petrosal approach for retrochiasmatic craniopharyngioma
title_full_unstemmed Posterior petrosal approach for retrochiasmatic craniopharyngioma
title_sort posterior petrosal approach for retrochiasmatic craniopharyngioma
publisher Elsevier
series Interdisciplinary Neurosurgery
issn 2214-7519
publishDate 2020-12-01
description Craniophyringiomas are histologically benign tumors arising from embryonic epithelial cells of the craniopharyngeal duct. They are locally aggressive and their location in the sellar/supra-sellar region is associated with a high rate of recurrence and morbidity. It is generally recognized that surgical resection is the first treatment option. Craniopharyngiomas located in the retrochiasmatic area are among the most challenging to treat. They grow superiorly pushing floor of third ventricle, and posteriorly in the prepontine and interpeduncular cisterns. Different skull base approaches have been utilized to tackle tumors in this location. In this video we illustrate the surgical steps and nuances for resection of a large retrochiasmatic craniopharyngioma in a 25 YO RHF who presented with progressive headaches and visual decline. On neurological examination she was found to have bi-temporal hemianopia. An MRI scan of the brain showed a 4.5 × 3.2 × 4.3 cm mixed solid and cystic suprasellar mass with obstructive hydrocephalus located behind the optic chiasm. A brain CTA showed no displacement of the anterior communicating artery confirming the retrochiasmatic location of the tumor. The preoperative endocrine work up showed central hypothyroidism and low cortisol levels. Postoperatively the patient was extubated in the operating room, she had intact extra-ocular movements. She developed Diabetes insipidus and oculomotor nerve palsy on postoperative day 3. Her third nerve palsy recovered when she was seen 3 weeks postoperatively. The histopathology showed an adamantinomatous craniopharyngioma. The posterior petrosal approach should be considered in treating patients with Retrochiasmatic Craniopharyngiomas. The consent was obtained.
topic Craniopharyngioma
Retrochiasmatic Craniopharyngioma
Posterior petrosal approach
url http://www.sciencedirect.com/science/article/pii/S2214751920304060
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