Atypical teratoid rhabdoid tumor historical perspective: Difference between revisions
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{{Atypical teratoid rhabdoid tumor}} | {{Atypical teratoid rhabdoid tumor}} | ||
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==Overview== | ==Overview== | ||
Atypical teratoid rhabdoid tumor was first reported by Bonnin et al., in 1984. It was incorporated as a separate entity into the [[World Health Organization|WHO]] [[classification]] of [[Tumor|tumors]] of the [[nervous system]], in 1993. | |||
==Historical Perspective== | ==Historical Perspective== | ||
*Atypical teratoid rhabdoid tumor was first reported by Bonnin et al., in 1984.<ref name="GinnGajjar2012">{{cite journal|last1=Ginn|first1=Kevin F.|last2=Gajjar|first2=Amar|title=Atypical Teratoid Rhabdoid Tumor: Current Therapy and Future Directions|journal=Frontiers in Oncology|volume=2|year=2012|issn=2234-943X|doi=10.3389/fonc.2012.00114}}</ref> | |||
*It was incorporated as a separate entity into the [[World Health Organization|WHO]] [[classification]] of [[tumors]] of the [[nervous system]], in 1993. | |||
*After the first case of atypical teratoid rhabdoid tumor was reported, it was followed by a series of multiple [[Case report|case reports]] by Biggs et al. (1987); Ho et al. (1990); Chou and Anderson (1991); Agranovich et al. (1992); and Satoh et al. (1993). | |||
*Previously reported cases of atypical teratoid rhabdoid tumor were often associated with [[Malignant rhabdoid tumor|malignant rhabdoid tumors (MRT)]] of the [[kidney]], which had been identified a decade earlier upon central review of [[Wilms' tumor]] treated in a collaborative group. This group noted that certain patients had [[Tumor|tumors]] with different [[Pathology|pathologic]] features and that these features were associated with significantly worse outcomes.<ref name="GinnGajjar2012">{{cite journal|last1=Ginn|first1=Kevin F.|last2=Gajjar|first2=Amar|title=Atypical Teratoid Rhabdoid Tumor: Current Therapy and Future Directions|journal=Frontiers in Oncology|volume=2|year=2012|issn=2234-943X|doi=10.3389/fonc.2012.00114}}</ref> | |||
*Similarly, atypical teratoid rhabdoid tumor was often categorized with [[Primitive neuroectodermal tumors|primitive neuroectodermal tumors (PNETs)]], along with [[medulloblastoma]], due to [[Histology|histologic]] similarities, but they are now separated from other [[Germ cell tumor|embryonal tumors]] by the presence of rhabdoid [[Cell (biology)|cells]] and specific [[immunohistochemistry]]. | |||
*Atypical teratoid rhabdoid tumor was only recognized as an entity in 1996 and added to the [[World Health Organization|World Health Organization (WHO)]] [[brain tumor]] [[classification]] in 2000 (grade IV).<ref name="hi9atrtjhjh">Atypical teratoid rhabdoid tumor. Wikipedia 2015. https://en.wikipedia.org/wiki/Atypical_teratoid_rhabdoid_tumor. Accessed on December 14, 2015</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
[[Category:Types of cancer]] | |||
[[Category:Rare cancers]] | |||
[[Category:Rare diseases]] | |||
[[Category:Pathology]] | |||
[[Category:Pediatrics]] | |||
[[Category:Neurology]] | |||
[[Category:Pediatric cancers]] | |||
[[Category:Disease]] | |||
[[Category:Oncology]] | |||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Latest revision as of 19:10, 14 May 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]
Overview
Atypical teratoid rhabdoid tumor was first reported by Bonnin et al., in 1984. It was incorporated as a separate entity into the WHO classification of tumors of the nervous system, in 1993.
Historical Perspective
- Atypical teratoid rhabdoid tumor was first reported by Bonnin et al., in 1984.[1]
- It was incorporated as a separate entity into the WHO classification of tumors of the nervous system, in 1993.
- After the first case of atypical teratoid rhabdoid tumor was reported, it was followed by a series of multiple case reports by Biggs et al. (1987); Ho et al. (1990); Chou and Anderson (1991); Agranovich et al. (1992); and Satoh et al. (1993).
- Previously reported cases of atypical teratoid rhabdoid tumor were often associated with malignant rhabdoid tumors (MRT) of the kidney, which had been identified a decade earlier upon central review of Wilms' tumor treated in a collaborative group. This group noted that certain patients had tumors with different pathologic features and that these features were associated with significantly worse outcomes.[1]
- Similarly, atypical teratoid rhabdoid tumor was often categorized with primitive neuroectodermal tumors (PNETs), along with medulloblastoma, due to histologic similarities, but they are now separated from other embryonal tumors by the presence of rhabdoid cells and specific immunohistochemistry.
- Atypical teratoid rhabdoid tumor was only recognized as an entity in 1996 and added to the World Health Organization (WHO) brain tumor classification in 2000 (grade IV).[2]
References
- ↑ 1.0 1.1 Ginn, Kevin F.; Gajjar, Amar (2012). "Atypical Teratoid Rhabdoid Tumor: Current Therapy and Future Directions". Frontiers in Oncology. 2. doi:10.3389/fonc.2012.00114. ISSN 2234-943X.
- ↑ Atypical teratoid rhabdoid tumor. Wikipedia 2015. https://en.wikipedia.org/wiki/Atypical_teratoid_rhabdoid_tumor. Accessed on December 14, 2015