Craniopharyngioma epidemiology and demographics: Difference between revisions
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==Overview== | ==Overview== | ||
The demographic patterns of craniopharyngioma are not well described because the tumor is rare. In addition, most cancer registries collect data only on malignant conditions and, therefore, they are not useful in the study of craniopharyngioma | The [[Demographics|demographic patterns]] of craniopharyngioma are not well described because the [[tumor]] is rare. In addition, most [[Cancer registry|cancer registries]] collect [[data]] only on [[Malignant|malignant conditions]] and, therefore, they are not useful in the study of craniopharyngioma which is considered to be a [[Borderline|borderline histological malignancy]]. [[Incidence]] [[rates]] are similar in males and females and between caucasians and African Americans. [[Tumor|Tumors]] are more common among children of age 5 to 15 years and older adults of greater than 65 years, while the lowest rates occur among those aged 15 to 34 years. [[Survival analysis|Survival]] is highest for patients [[Diagnosis|diagnosed]] at a younger age. | ||
==Epidemiology and demographics== | ==Epidemiology and demographics== | ||
===Prevalence=== | ===Prevalence=== | ||
*Craniopharyngiomas constitute approximately 3% of all intracranial neoplasms. | *Craniopharyngiomas constitute approximately 3% of all [[Intracranial hemorrhage|intracranial]] [[Neoplasm|neoplasms]].<ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | ||
*They are the most common pediatric brain tumor of nonglial origin, yet nearly half of all cases of craniopharyngiomas occur in adults . | *In children, craniopharyngiomas account for 5% of all [[Tumor|tumours]] and 50% of all [[Sella turcica|sellar and parasellar]] [[Tumor|tumours]].<ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | ||
*They appear to be more common, with higher incidence rates reported in Japan and some parts of Africa. | *They are the most common [[Brain tumor|pediatric brain tumor]] of [[Glial|nonglial origin]], yet nearly half of all cases of craniopharyngiomas occur in adults.<ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | ||
*They are approximately equally common in males and females. | *They appear to be more common, with [[Incidence|higher incidence rates]] reported in Japan and some parts of Africa. | ||
*They are approximately equally common in males and females.<ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | |||
===Incidence=== | ===Incidence=== | ||
The [[incidence]] of craniopharyngioma | *The [[Incidence (epidemiology)|overall incidence]] of craniopharyngioma is approximately 0.5 to 2 per 100,000 per year.<ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | ||
*The age distribution is [[Bimodal distribution|bimodal]] with a peak in childhood and a second peak among middle-aged and older adults.<ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | |||
*No definite [[Genetic|genetic relationship]] has been found and few familial cases reported. <ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | |||
===Age=== | ===Age=== | ||
A [[bimodal distribution]] by age was noted with peak incidence rates in children (aged 5-14 years; more common) and among older adults | *A [[bimodal distribution]] by age was noted with [[Incidence (epidemiology)|peak incidence rates]] in children (aged 5-14 years; more common) and among older adults.<ref>Incidence. Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM. Pubmed. http://www.ncbi.nlm.nih.gov/pubmed/9761047</ref> | ||
===Gender=== | ===Gender=== | ||
There appears to be a similar incidence in both males and females.<ref>Epidemiology. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/craniopharyngioma</ref> | *There appears to be a similar incidence in both males and females.<ref>Epidemiology. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/craniopharyngioma</ref> | ||
===Race=== | ===Race=== | ||
No racial predilection is seen in craniopharyngioma cases. | *No [[Race|racial predilection]] is seen in craniopharyngioma cases. | ||
*Few studies show that there is a higher [[Incidence (epidemiology)|incidence]] rates reported in Japan and some parts of Africa. <ref name="pmid9761047">{{cite journal |vauthors=Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM |title=The descriptive epidemiology of craniopharyngioma |journal=J. Neurosurg. |volume=89 |issue=4 |pages=547–51 |date=October 1998 |pmid=9761047 |doi=10.3171/jns.1998.89.4.0547 |url=}}</ref> | |||
==References== | ==References== | ||
Latest revision as of 15:11, 26 February 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Marjan Khan M.B.B.S.[2]
Overview
The demographic patterns of craniopharyngioma are not well described because the tumor is rare. In addition, most cancer registries collect data only on malignant conditions and, therefore, they are not useful in the study of craniopharyngioma which is considered to be a borderline histological malignancy. Incidence rates are similar in males and females and between caucasians and African Americans. Tumors are more common among children of age 5 to 15 years and older adults of greater than 65 years, while the lowest rates occur among those aged 15 to 34 years. Survival is highest for patients diagnosed at a younger age.
Epidemiology and demographics
Prevalence
- Craniopharyngiomas constitute approximately 3% of all intracranial neoplasms.[1]
- In children, craniopharyngiomas account for 5% of all tumours and 50% of all sellar and parasellar tumours.[1]
- They are the most common pediatric brain tumor of nonglial origin, yet nearly half of all cases of craniopharyngiomas occur in adults.[1]
- They appear to be more common, with higher incidence rates reported in Japan and some parts of Africa.
- They are approximately equally common in males and females.[1]
Incidence
- The overall incidence of craniopharyngioma is approximately 0.5 to 2 per 100,000 per year.[1]
- The age distribution is bimodal with a peak in childhood and a second peak among middle-aged and older adults.[1]
- No definite genetic relationship has been found and few familial cases reported. [1]
Age
- A bimodal distribution by age was noted with peak incidence rates in children (aged 5-14 years; more common) and among older adults.[2]
Gender
- There appears to be a similar incidence in both males and females.[3]
Race
- No racial predilection is seen in craniopharyngioma cases.
- Few studies show that there is a higher incidence rates reported in Japan and some parts of Africa. [1]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM (October 1998). "The descriptive epidemiology of craniopharyngioma". J. Neurosurg. 89 (4): 547–51. doi:10.3171/jns.1998.89.4.0547. PMID 9761047.
- ↑ Incidence. Bunin GR, Surawicz TS, Witman PA, Preston-Martin S, Davis F, Bruner JM. Pubmed. http://www.ncbi.nlm.nih.gov/pubmed/9761047
- ↑ Epidemiology. Dr Dylan Kurda and Dr Frank Gaillard et al. Radiopaedia 2015. http://radiopaedia.org/articles/craniopharyngioma