Craniopharyngioma epidemiology and demographics: Difference between revisions
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===Prevalence=== | ===Prevalence=== | ||
*Craniopharyngiomas constitute approximately 3% of all intracranial neoplasms. | *Craniopharyngiomas constitute approximately 3% of all intracranial 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 tumours and 50% of all sellar/para sellar 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 are the most common pediatric brain tumor of 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 appear to be more common, with higher incidence rates reported in Japan and some parts of Africa. | *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. | *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 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 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> | ||
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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, considered to be of 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,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/para sellar 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 (aged 65-74 years in CBTRUS and 50-74 years in Los Angeles county).[2]
Gender
There appears to be a similar incidence in both males and females.[3]
Race
No racial predilection is seen in craniopharyngioma cases.
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 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