scholarly journals Glioblastoma in the optic chiasm: A case report

2022 ◽  
Vol 17 (3) ◽  
pp. 729-734
Author(s):  
Lina F. Merchancano-Esquivel ◽  
Carlos Felipe Marín-Díaz ◽  
Valentina Mejía-Quiñones ◽  
Ana María Granados-Sánchez
Keyword(s):  
2012 ◽  
Vol 17 (1) ◽  
pp. 24 ◽  
Author(s):  
Xianbin Ning ◽  
Kan Xu ◽  
Qi Luo ◽  
Limei Qu ◽  
Jinlu Yu

2008 ◽  
Vol 44 (2) ◽  
pp. 88 ◽  
Author(s):  
Dong Wuk Son ◽  
Sang Weon Lee ◽  
Chang Hwa Choi

F1000Research ◽  
2014 ◽  
Vol 3 ◽  
pp. 171 ◽  
Author(s):  
Chris G. Yedinak ◽  
Shirley McCartney ◽  
Troy H. Dillard ◽  
Kevin S. Wei ◽  
Maria Fleseriu

We present a case of a 21 year old male patient diagnosed with a 2.2 cm prolactin-secreting adenoma in contact with the optic chiasm. The patient was treated with up to 6mg/week of cabergoline (total cumulative dose 814 mg) and developed mild valvulopathy. Valvulopathy was subsequently reversed after discontinuation of cabergoline therapy.


2021 ◽  
pp. 1-4
Author(s):  
Yanire Sánchez Medina ◽  
Yanire Sánchez Medina ◽  
Eric Robles Hidalgo ◽  
Jaime Domínguez Baez ◽  
Luis Gómez Perals

Introduction: Germ Cell Tumors (GCT) represent less than 4% of primary brain tumors. They comprise Germaniums, Non-Germinomatous Germ Cell Tumors and Teratomas. Teratomas represent less than 20% of intracranial GCT. They are tumors of multipotential cells derived from all 3 germ cell layers, frequently arising in midline structures, most commonly in the pineal and suprasellar regions, with a clear excess of male cases and frequently found in children and young adults. We report a case of a mature teratoma in the third ventricle in a 37-year-old male. Case Report: We report a case of a 37-year-old male with a history of headache lasting up to 9 days and refractory to pharmacological treatment. The CT scan revealed a 20mm round hypodense lesion in the anterior third ventricle, with a punctate hyperdensity in the inferior pole causing biventricular hydrocephalus with no periventricular lucency and the MRI showed a well-defined encapsulated mass lesion attached to the roof of the third ventricle, isointense in T1WI with circumferential enhancement and hyperintense in T2WI. Gross total resection was performed. Histopathologic evaluation revealed a mature teratoma. There was no evidence of recurrence on follow up MRI at 2 years. Conclusion: Intracranial teratomas typically originate in midline structures from optic chiasm to pineal region. Presentation after the first two decades of life is exceptional. Complete surgical resection is the only curative treatment for pure mature teratomas. We report the case of a mature teratoma in a 37-year-old male with unusual radiological findings.


2020 ◽  
Vol 19 (4) ◽  
pp. E446-E447
Author(s):  
Ignazio G Vetrano ◽  
Morgan Broggi ◽  
Francesco Acerbi
Keyword(s):  

Author(s):  
Suzan Saylisoy ◽  
Goknur Yorulmaz

Background: The ectopic posterior pituitary (EPP) is a rare condition characterized by the ectopic location of the posterior pituitary lobe associated with varying degrees of stalk anomalies. The arachnoid cysts (AC) are benign lesions of the arachnoid, which account for 1% of all intracranial space-occupying lesions. Sellar/suprasellar ACs account for approximately 1% of all ACs. This is the first case of coexistence EPP with sellar/suprasellar AC. Case Report: A 67-year-old woman presented with 6 months history of fatigue. Her medical history was positive for irregular menstruation. Her endocrine examinations indicated low free thyroxine level with low TSH level, low oestradiol with low gonadotrophin level, slightly elevated prolactin level. Her Insulin-like growth factor-1 was below the normal levels. Dynamic contrast hypophysis MRI revealed a sellar cystic lesion with a dimension of 18 × 14 × 14 mm, extending from the suprasellar cistern, traversing the diaphragma sellae and reaching the level of the floor of the 3rd ventricle, consistent with sellar/suprasellar AC. There was no wall enhancement. The optic chiasm was compressed. The precontrast T1-weighted magnetic resonance images did not demonstrate the characteristic bright spot of posterior pituitary within the sella, which was higher in position, in the region of the median eminence. The pituitary stalk was not present. Conclusion: Although speculative, we have a hypothesis to explain how the EPP and sellar/- suprasellar AC coexist in this patient. Due to the absence of stalk, CSF may enter the sella tursica from the central aperture of the diaphragma sellae through which normally the stalk passes.


2018 ◽  
Vol 42 (6) ◽  
pp. 385-390
Author(s):  
Cynthia K. McClard ◽  
Claudia M. Prospero Ponce ◽  
Aroucha Vickers ◽  
Andrew G. Lee

2001 ◽  
Vol 44 (2) ◽  
pp. 114-116 ◽  
Author(s):  
J. Paladino ◽  
K. Rotim ◽  
N. Pirker ◽  
V. Glunčić ◽  
G. Jurić ◽  
...  

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