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Solide Kindertumoren : Ein Streifzug durch das Raritätenkabinett

Gürtl-Lackner, B.; Gisselsson-Nord, D. LU and Vujanic, Gordan (2017) In Pathologe 38(4). p.278-285
Abstract

Solid tumors in childhood are extremely rare entities, which are usually treated in specialized centers. Diagnosis and therapy are carried out according to a joint European protocol, whereby the pathological evaluation and therapy are carried out according to international guidelines. For the correct diagnosis and/or therapy of most tumors, analysis of specific genetic changes is mandatory; therefore, tumors have to be adequately sampled for parallel genetic analysis during the pathological work-up. A second opinion reference of the histopathological assessment is part of the international guidelines. Neuroblastomas, congenital mesoblastic nephromas and rhabdoid tumors are examples of solid tumors in childhood that are not restricted to... (More)

Solid tumors in childhood are extremely rare entities, which are usually treated in specialized centers. Diagnosis and therapy are carried out according to a joint European protocol, whereby the pathological evaluation and therapy are carried out according to international guidelines. For the correct diagnosis and/or therapy of most tumors, analysis of specific genetic changes is mandatory; therefore, tumors have to be adequately sampled for parallel genetic analysis during the pathological work-up. A second opinion reference of the histopathological assessment is part of the international guidelines. Neuroblastomas, congenital mesoblastic nephromas and rhabdoid tumors are examples of solid tumors in childhood that are not restricted to one organ and occur exclusively during childhood.

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Please use this url to cite or link to this publication:
author
organization
alternative title
Solid pediatric tumors : A brief survey of the rarity cabinet
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Congenital mesoblastic nephroma, INI1/SMARCB1, MYC-N, Neuroblastoma, Rhabdoid tumors
in
Pathologe
volume
38
issue
4
pages
8 pages
publisher
Springer Verlag
external identifiers
  • scopus:85021106049
  • wos:000405553500009
ISSN
0172-8113
DOI
10.1007/s00292-017-0312-y
language
German
LU publication?
yes
id
20f82154-0c03-4763-859c-6f599320a966
date added to LUP
2017-08-07 15:18:45
date last changed
2018-01-07 12:14:11
@article{20f82154-0c03-4763-859c-6f599320a966,
  abstract     = {<p>Solid tumors in childhood are extremely rare entities, which are usually treated in specialized centers. Diagnosis and therapy are carried out according to a joint European protocol, whereby the pathological evaluation and therapy are carried out according to international guidelines. For the correct diagnosis and/or therapy of most tumors, analysis of specific genetic changes is mandatory; therefore, tumors have to be adequately sampled for parallel genetic analysis during the pathological work-up. A second opinion reference of the histopathological assessment is part of the international guidelines. Neuroblastomas, congenital mesoblastic nephromas and rhabdoid tumors are examples of solid tumors in childhood that are not restricted to one organ and occur exclusively during childhood.</p>},
  author       = {Gürtl-Lackner, B. and Gisselsson-Nord, D. and Vujanic, Gordan},
  issn         = {0172-8113},
  keyword      = {Congenital mesoblastic nephroma,INI1/SMARCB1,MYC-N,Neuroblastoma,Rhabdoid tumors},
  language     = {ger},
  month        = {07},
  number       = {4},
  pages        = {278--285},
  publisher    = {Springer Verlag},
  series       = {Pathologe},
  title        = {Solide Kindertumoren : Ein Streifzug durch das Raritätenkabinett},
  url          = {http://dx.doi.org/10.1007/s00292-017-0312-y},
  volume       = {38},
  year         = {2017},
}