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SHR Neuro Krebs Kardio Lipid

Gürtl-Lackner, B; Gisselsson-Nord, D; Vujanic, G.
[Solid pediatric tumors : A brief survey of the rarity cabinet].
Pathologe. 2017; 38(4):278-285 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG

 

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
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