2009
DOI: 10.1136/jnnp.2008.149088
|View full text |Cite|
|
Sign up to set email alerts
|

Craniopharyngiomas in the posterior fossa: a rare subgroup, diagnosis, management and outcomes

Abstract: Posterior fossa craniopharyngiomas are rare and may be considered an independent subgroup of classifications. Tumours arising from the sellar region and extending to the posterior fossa present with their own unusual set of characteristics. These tumours can be radically and safely removed with a combined supra- and intratentorial approach.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
9
0
1

Year Published

2009
2009
2020
2020

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 12 publications
(10 citation statements)
references
References 26 publications
0
9
0
1
Order By: Relevance
“…16 Patients < 18 years of age were excluded because pathologies that affect this population and can be treated with anterior petrosectomy are uncommon. 27,28 The trigeminal nerve is a superb landmark in middle fossa and petrous apex surgery. The trigeminal nerve after peeling the middle fossa can be displaced anteriorly, increasing the surgical corridor through the petrous apex.…”
Section: Discussionmentioning
confidence: 99%
“…16 Patients < 18 years of age were excluded because pathologies that affect this population and can be treated with anterior petrosectomy are uncommon. 27,28 The trigeminal nerve is a superb landmark in middle fossa and petrous apex surgery. The trigeminal nerve after peeling the middle fossa can be displaced anteriorly, increasing the surgical corridor through the petrous apex.…”
Section: Discussionmentioning
confidence: 99%
“…Studies were published between 1955 and 2019; 40 of the 84 studies were published in the past 10 years. Twenty-two studies were conducted in the United States of America (USA) [ 28 , 32 , 34 , 35 , 37 , 49 , 51 66 ]; 7 studies in Germany [ 26 , 29 , 67 71 ]; 6 studies in the United Kingdom (UK) [ 9 , 38 , 39 , 42 , 48 , 72 ] and France [ 14 , 24 , 33 , 46 , 73 , 74 ]; 5 studies in China [ 30 , 75 78 ]; 4 studies in India [ 27 , 79 81 ], Israel [ 82 – 85 ] and Japan [ 19 , 86 88 ]; 3 studies in Canada [ 10 , 25 , 89 ], Italy [ 90 92 ] and The Netherlands [ 93 95 ]; 2 studies in Australia [ 6 , 96 ], Korea [ 97 , 98 ], Saudi Arabia [ 99 , 100 ], Turkey [ 32 , 101 ]; 1 study in Bulgaria […”
Section: Resultsmentioning
confidence: 99%
“…Taylor (2012) was the only study that did not provide numbers of children in whom an orthoptic abnormality was found, they only mentioned nystagmus and strabismus as the orthoptic abnormalities seen among their study participants [74]. Fourty-three of 296 children experienced diplopia (14.5%) [7,31,54,55,60,66,75,83,84,89,94,107], 21 of 127 children (16.5%) were diagnosed with strabismus (also called squint by some studies) [6,7,39,66,83,84,96] and in 22 of 331 children (6.6%) nystagmus (monocular, seesaw, horizontal pendular or rotatory) was seen during orthoptic examination [25,38,39,69,83,84,[89][90][91][92][93][94][95][96][97][98][99][100][101][102].…”
Section: Orthoptic Examinationmentioning
confidence: 99%
“…They most commonly occur in the suprasellar area with intrasellar propagation. Symptoms include: endocrine disorders, visual disturbances, hydrocephalus symptoms and very rarely when growing in the posterior fossa-headache, diplopia, ataxia and hearing loss [82]. The diagnosis is made by MRI that displays a tumor with a solid and cystic component and with intratumoral calcifications.…”
Section: Craniopharyngiomamentioning
confidence: 99%