Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Gürtl-Lackner, B; Gisselsson-Nord, D; Vujanic, G.
[Solid pediatric tumors : A brief survey of the rarity cabinet].
Pathologe. 2017; 38(4):278-285
Doi: 10.1007/s00292-017-0312-y
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- Führende Autor*innen der Med Uni Graz
- Gürtl-Lackner Barbara
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- 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 one organ and occur exclusively during childhood.
- Find related publications in this database (using NLM MeSH Indexing)
- Child -
- Child, Preschool -
- Female -
- Guideline Adherence -
- Humans -
- Infant -
- Infant, Newborn -
- Kidney Neoplasms - diagnosis
- Kidney Neoplasms - genetics
- Kidney Neoplasms - pathology
- Kidney Neoplasms - therapy
- Neoplasms - diagnosis
- Neoplasms - genetics
- Neoplasms - pathology
- Neoplasms - therapy
- Nephroma, Mesoblastic - diagnosis
- Nephroma, Mesoblastic - genetics
- Nephroma, Mesoblastic - pathology
- Nephroma, Mesoblastic - therapy
- Neuroblastoma - diagnosis
- Neuroblastoma - genetics
- Neuroblastoma - pathology
- Neuroblastoma - therapy
- Pregnancy -
- Proto-Oncogene Proteins c-myc - genetics
- Rare Diseases -
- Referral and Consultation -
- Rhabdoid Tumor - diagnosis
- Rhabdoid Tumor - genetics
- Rhabdoid Tumor - pathology
- Rhabdoid Tumor - therapy
- SMARCB1 Protein - genetics
- Find related publications in this database (Keywords)
- Neuroblastoma
- Congenital mesoblastic nephroma
- Rhabdoid tumors
- MYC-N
- INI1/SMARCB1