ArticleBalkan medical journal2019
Recent Progress in the Pathology and Genetics of Pilocytic and Pilomyxoid Astrocytomas
Article in Balkan medical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Neuro-Ophthalmic Manifestations of Suprasellar Pilomyxoid Astrocytoma.Neuro-ophthalmology (Aeolus Press) · 2026Article
- Circumscribed Pilocytic Astrocytoma Including Pilomyxoid and Intermediate Pilomyxoid Variants - A Single Institutional, Retrospective Study.Indian journal of surgical oncology · 2025Article
- Article
- A molecular study of pediatric pilomyxoid and pilocytic astrocytomas: Genome-wide copy number screening, retrospective analysis of clinicopathological features and long-term clinical outcome.Frontiers in oncology · 2023Article
- Oncologic causes of oculopalatal tremors: neurophysiology and treatment.Acta neurologica Belgica · 2021Review
- Pineal region pilocytic astrocytoma showing uncommon growth: a case report.Radiology case reports · 2021Article
- Imaging of brain tumors in children: the basics-a narrative review.Translational pediatrics · 2021Review
- Failure to Thrive Revealing a Pilomyxoid Astrocytoma: An Uncommon Case Report with Literature Review.Case reports in pediatrics · 2021Article
- Article
- Survival rates of children and young adolescents with CNS tumors improved in the Netherlands since 1990: A population-based study.Neuro-oncology advancesArticle
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pilocytic and pilomyxoid astrocytomas are some of the most common gliomas in children and young adults. These gliomas are indolent neoplasms with long overall survival probability. The genetic characteristics of these neoplasms are well known, and our deepened understanding of their associated molecular alterations has led to the development of novel treatment strategies and approaches. Currently, we can account for some of the unusual behavior, such as oncogene-induced senescence, associated spontaneous regression, anaplastic transformation, and cerebrospinal dissemination, of these gliomas. Nevertheless, enigmatic issues continue to surround these chronic tumors. Here, we review the classical and uncommon clinical pathological and genetic features of these indolent gliomas.
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