Results 41 to 50 of about 1,061 (169)

Diagnostic Challenges in Choroid Plexus Tumours

open access: yesNeuropathology and Applied Neurobiology, Volume 52, Issue 4, August 2026.
In this review, we summarise the diagnostic spectrum of choroid plexus tumours, highlight key age‐dependent differential diagnoses across infants, children/adolescents and adults, and outline how histopathology, immunohistochemistry and molecular profiling support accurate tumour classification.
Christian Thomas, Martin Hasselblatt
wiley   +1 more source

Retrolental vascular membrane in a case of ciliary body medulloepithelioma: Clinicopathologic correlation

open access: yesThe Pan-American Journal of Ophthalmology, 2019
A unilateral nonteratoid malignant ciliary body medulloepithelioma presented in a 13-year-old girl as a leukocoria with an extense vascularized retrolental membrane in her right eye.
Luca Bongiovanni De Miranda Gonçalves   +3 more
doaj   +1 more source

The HIT Network for Children and Adolescents With CNS Tumors Facilitates Improvements of Diagnostic Assessments, Multimodal Treatments, Individual Counseling, and Research in Germany, Austria, and Switzerland

open access: yesPediatric Blood &Cancer, Volume 73, Issue 5, May 2026.
ABSTRACT Background The HIT network was established in 2000 to create a population‐based structure aiming to improve survival rates and reduce late effects for children with central nervous system (CNS) tumors by conducting comprehensive clinical trials.
Stefan Rutkowski   +59 more
wiley   +1 more source

Hybrid CNN–GCN framework for brain tumor MRI classification: A graph‐based approach to smart healthcare diagnostics

open access: yesJournal of Applied Clinical Medical Physics, Volume 27, Issue 4, April 2026.
Abstract Background Accurate classification of brain tumors is a major challenge in neuro‐oncology, as the heterogeneity of tumor morphology and the overlap of radiological features limit the effectiveness of conventional diagnostic approaches. Early and reliable tumor characterization is essential for treatment planning, prognosis, and improved ...
Mus'ab S. Alkasasbeh   +7 more
wiley   +1 more source

Melanoma of the Choroid and Ciliary Body in Children: Remission of Metastatic Melanoma of the Choroid After Treatment With Chemotherapy and Immune Checkpoint Inhibition

open access: yesPediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Background Uveal melanoma is the most common malignant primary intraocular tumor in adults, associated with high mortality. Pediatric uveal melanoma generally has a more favorable course. However, when metastasis occurs, therapeutic options are limited.
Pia Tüller   +18 more
wiley   +1 more source

Eye wall resections for intraocular tumors: Our experience

open access: yesIndian Journal of Ophthalmology, 2014
We conducted a retrospective review of 11 eyes undergoing eye wall resection between October 1998 and October 2009. The median age of 11 patients was 29 years. Decreased vision (eight) was the most common presenting symptom.
Tandava Krishnan   +4 more
doaj   +1 more source

Medulloepithelioma of the ciliary body

open access: yesIndian Journal of Ophthalmology, 1985
Panda A, Dayal Y, Mohan M
doaj   +2 more sources

Fabrication of a facial prosthesis for a 13-year-old child by using a point-and-shoot three-dimensional scanner and CAD/CAM technology

open access: yesTaiwan Journal of Ophthalmology, 2022
Patients cannot wear ocular prostheses after undergoing orbital exenteration. They require a facial prosthesis to obtain a more favorable appearance, which greatly affects their social life and psychological health.
Ming-Hui Sun   +4 more
doaj   +1 more source

Recent Advances in Diagnostics and Therapeutics for Paediatric Thyroid Cancer

open access: yesJournal of Paediatrics and Child Health, Volume 61, Issue 5, Page 666-675, May 2025.
ABSTRACT Purpose of Review Paediatric thyroid cancer management traditionally relied on extrapolation from adult data and, despite good survival outcomes, often involved extensive surgical approaches and radioactive iodine (RAI) therapy with potentially life‐long complications.
Joel A. Vanderniet   +9 more
wiley   +1 more source

Identification of DICER1 Syndrome on the Basis of Familial, Early‐Onset Differentiated Thyroid Cancer

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT DICER1 syndrome encompasses a wide range of phenotypes, and not all individuals with DICER1 syndrome develop aggressive soft tissue tumors. DICER1 syndrome and other genetic conditions predisposing to the development of thyroid tumors should be considered when a young patient presents with thyroid nodules and a positive family history.
Jessica Y. Wong   +5 more
wiley   +1 more source

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