Craniopharyngioma historical perspective: Difference between revisions
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*in 1932 the name “craniopharyngioma” was introduced by Cushing.<ref name="pmid17425791">{{cite journal |vauthors=Garnett MR, Puget S, Grill J, Sainte-Rose C |title=Craniopharyngioma |journal=Orphanet J Rare Dis |volume=2 |issue= |pages=18 |date=April 2007 |pmid=17425791 |pmc=1855047 |doi=10.1186/1750-1172-2-18 |url=}}</ref> | *in 1932 the name “craniopharyngioma” was introduced by Cushing.<ref name="pmid17425791">{{cite journal |vauthors=Garnett MR, Puget S, Grill J, Sainte-Rose C |title=Craniopharyngioma |journal=Orphanet J Rare Dis |volume=2 |issue= |pages=18 |date=April 2007 |pmid=17425791 |pmc=1855047 |doi=10.1186/1750-1172-2-18 |url=}}</ref> | ||
*In the International Classification of Diseases for Oncology 3rd revision the code number 9350 refers to "unspecified craniopharyngioma", whilst 9351 and 9352 correspond to the two histological subtypes, adamantinous and papillary craniopharyngiomas, respectively.<ref name="pmid17425791">{{cite journal |vauthors=Garnett MR, Puget S, Grill J, Sainte-Rose C |title=Craniopharyngioma |journal=Orphanet J Rare Dis |volume=2 |issue= |pages=18 |date=April 2007 |pmid=17425791 |pmc=1855047 |doi=10.1186/1750-1172-2-18 |url=}}</ref> | *In the International Classification of Diseases for Oncology 3rd revision the code number 9350 refers to "unspecified craniopharyngioma", whilst 9351 and 9352 correspond to the two histological subtypes, adamantinous and papillary craniopharyngiomas, respectively.<ref name="pmid17425791">{{cite journal |vauthors=Garnett MR, Puget S, Grill J, Sainte-Rose C |title=Craniopharyngioma |journal=Orphanet J Rare Dis |volume=2 |issue= |pages=18 |date=April 2007 |pmid=17425791 |pmc=1855047 |doi=10.1186/1750-1172-2-18 |url=}}</ref> | ||
===History and evolution of transsphenoidal surgery=== | |||
*Initial attempts at transcranial approaches to the pituitary gland in the late 1800s and early 1900s resulted in a mortality rate that was generally considered prohibitive | |||
==References== | ==References== | ||
Revision as of 16:47, 3 January 2019
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Overview
Historical perspective
- In 1840, von Mohr described the rapid development of obesity in a case of a pituitary tumor.
- Zenker in 1857 was the first to identify masses of cells resembling squamous epithelium along the pars tuberalis and pars distalis of the pituitary.[1]
- In 1932, squamous epithelial cells were detected in the pituitary glands of childhood populations.[1]
- in 1932 the name “craniopharyngioma” was introduced by Cushing.[1]
- In the International Classification of Diseases for Oncology 3rd revision the code number 9350 refers to "unspecified craniopharyngioma", whilst 9351 and 9352 correspond to the two histological subtypes, adamantinous and papillary craniopharyngiomas, respectively.[1]
History and evolution of transsphenoidal surgery
- Initial attempts at transcranial approaches to the pituitary gland in the late 1800s and early 1900s resulted in a mortality rate that was generally considered prohibitive