Teratoma epidemiology and demographics: Difference between revisions

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===Incidence===
===Incidence===
*The incidence of mature teratoma is approximately 1.2-14.2 cases per 100,000 individuals worldwide.<ref name="pmid3166898">{{cite journal| author=Westhoff C, Pike M, Vessey M| title=Benign ovarian teratomas: a population-based case-control study. | journal=Br J Cancer | year= 1988 | volume= 58 | issue= 1 | pages= 93-8 | pmid=3166898 | doi=10.1038/bjc.1988.171 | pmc=2246492 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3166898  }} </ref>
*The incidence of mature teratoma is approximately 1.2-14.2 cases per 100,000 individuals worldwide.<ref name="pmid3166898">{{cite journal| author=Westhoff C, Pike M, Vessey M| title=Benign ovarian teratomas: a population-based case-control study. | journal=Br J Cancer | year= 1988 | volume= 58 | issue= 1 | pages= 93-8 | pmid=3166898 | doi=10.1038/bjc.1988.171 | pmc=2246492 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3166898  }} </ref>
*In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.


===Prevalence===
===Prevalence===
*The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
*The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
*In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
*The prevalence of [disease/malignancy] is estimated to be [number] cases annually.
*The prevalence of [disease/malignancy] is estimated to be [number] cases annually.


Line 20: Line 18:


===Age===
===Age===
*Patients of all age groups may develop [disease name].
*Immature is mostly seen in younger patients and postpubertal males.<ref name="pmid30256256">{{cite journal| author=Kao CS, Bangs CD, Aldrete G, Cherry AM, Ulbright TM| title=A Clinicopathologic and Molecular Analysis of 34 Mediastinal Germ Cell Tumors Suggesting Different Modes of Teratoma Development. | journal=Am J Surg Pathol | year= 2018 | volume= 42 | issue= 12 | pages= 1662-1673 | pmid=30256256 | doi=10.1097/PAS.0000000000001164 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30256256  }} </ref><ref name="OutwaterSiegelman2001">{{cite journal|last1=Outwater|first1=Eric K.|last2=Siegelman|first2=Evan S.|last3=Hunt|first3=Jennifer L.|title=Ovarian Teratomas: Tumor Types and Imaging Characteristics|journal=RadioGraphics|volume=21|issue=2|year=2001|pages=475–490|issn=0271-5333|doi=10.1148/radiographics.21.2.g01mr09475}}</ref>
*The incidence of [disease name] increases with age; the median age at diagnosis is [#] years.
*Mature teratoma commonly affects aldolescent, but it occurs in all age groups.<ref name="pmid30256256">{{cite journal| author=Kao CS, Bangs CD, Aldrete G, Cherry AM, Ulbright TM| title=A Clinicopathologic and Molecular Analysis of 34 Mediastinal Germ Cell Tumors Suggesting Different Modes of Teratoma Development. | journal=Am J Surg Pathol | year= 2018 | volume= 42 | issue= 12 | pages= 1662-1673 | pmid=30256256 | doi=10.1097/PAS.0000000000001164 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30256256  }} </ref>
*[Disease name] commonly affects individuals younger than/older than [number of years] years of age.  
*[Chronic disease name] is usually first diagnosed among [age group].
*[Acute disease name] commonly affects [age group].


===Race===
===Race===

Latest revision as of 17:48, 18 November 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Gertrude Djouka, M.D.[2]

Overview

Epidemiology and Demographics

Incidence

  • The incidence of mature teratoma is approximately 1.2-14.2 cases per 100,000 individuals worldwide.[1]

Prevalence

  • The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
  • The prevalence of [disease/malignancy] is estimated to be [number] cases annually.

Case-fatality rate/Mortality rate

  • In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate/mortality rate of [number range]%.
  • The case-fatality rate/mortality rate of [disease name] is approximately [number range].

Age

  • Immature is mostly seen in younger patients and postpubertal males.[2][3]
  • Mature teratoma commonly affects aldolescent, but it occurs in all age groups.[2]

Race

  • There is no racial predilection to [disease name].
  • [Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].

Gender

  • [Disease name] affects men and women equally.
  • [Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1.

Region

  • The majority of [disease name] cases are reported in [geographical region].
  • [Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2].

Developed Countries

Developing Countries

References

  1. Westhoff C, Pike M, Vessey M (1988). "Benign ovarian teratomas: a population-based case-control study". Br J Cancer. 58 (1): 93–8. doi:10.1038/bjc.1988.171. PMC 2246492. PMID 3166898.
  2. 2.0 2.1 Kao CS, Bangs CD, Aldrete G, Cherry AM, Ulbright TM (2018). "A Clinicopathologic and Molecular Analysis of 34 Mediastinal Germ Cell Tumors Suggesting Different Modes of Teratoma Development". Am J Surg Pathol. 42 (12): 1662–1673. doi:10.1097/PAS.0000000000001164. PMID 30256256.
  3. Outwater, Eric K.; Siegelman, Evan S.; Hunt, Jennifer L. (2001). "Ovarian Teratomas: Tumor Types and Imaging Characteristics". RadioGraphics. 21 (2): 475–490. doi:10.1148/radiographics.21.2.g01mr09475. ISSN 0271-5333.

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