Results 71 to 80 of about 621,587 (217)

Conservative multimodal management of a primitive neuroectodermal tumor of the thyroid

open access: yesRare Tumors, 2013
Primitive neuroectodermal tumors (PNET) represent 1% of sarcomas. Head and neck peripheral PNETs have an intermediate prognosis between abdominopelvic disease and extremities.
Juliette Haudebourg   +9 more
doaj   +1 more source

Peripheral primitive neuroectodermal tumor of the urinary bladder in an Arab woman with history of squamous cell carcinoma: a case report

open access: yesJournal of Medical Case Reports, 2009
Introduction Peripheral primitive neuroectodermal tumors of the urinary bladder are rare and tend to occur in an older age group than do their counterparts in bones and soft tissue.
Al Meshaan Mohd Khaled   +4 more
doaj   +1 more source

A Peripheral Primitive Neuro-ectodermal Tumor (pPNET) of Larynx

open access: yesBengal Journal of Otolaryngology and Head Neck Surgery, 2020
Introduction Primitive neuroectodermal tumors (PNETs) are malignant tumors comprised of small round cells of neuro-ectodermal origin that affect soft tissue and bone.
Raman Wadhera   +4 more
doaj   +1 more source

A 9‐year‐old boy with a posterior fossa tumor

open access: yes
Brain Pathology, EarlyView.
Francesca Arienzo   +14 more
wiley   +1 more source

Reassessing Bone Marrow Aspirate and Trephine Biopsies in Staging for Paediatric and Young Adult Patients With Ewing Sarcoma and Rhabdomyosarcoma

open access: yesPediatric Blood &Cancer, Volume 73, Issue 10, October 2026.
ABSTRACT Ewing sarcoma (ES) and rhabdomyosarcoma (RMS) are aggressive malignancies in children and adolescents where metastases impact prognosis. 18F‐fluoro‐2‐deoxy‐d‐glucose positron emission tomography/computed tomography (FDG‐PET/CT) and bone marrow aspirate and trephine biopsies (BMAT) are used to identify disease involvement.
Imogen Andrews   +3 more
wiley   +1 more source

High-resolution array-based comparative genomic hybridization of medulloblastomas and supratentorial primitive neuroectodermal tumors

open access: yes, 2006
Medulloblastomas and supratentorial primitive neuroectodermal tumors are aggressive childhood tumors. We report our findings using array comparative genomic hybridization (CGH) on a whole-genome BAC/PAC/cosmid array with a median clone separation of 0.97
McCabe, Martin Gerard; id_orcid   +13 more
core   +1 more source

Assessment of Factors and Trends Affecting Different Pathological Types of Cervical Cancer in China From 2013 to 2022

open access: yesCancer Medicine, Volume 15, Issue 10, October 2026.
ABSTRACT Objective Cervical cancer poses a significant burden globally, particularly in developing countries, with China accounting for 20% of the global incidence. This study aimed to examine temporal changes in the pathological distribution of cervical cancer, particularly squamous cell carcinoma (SCC) and adenocarcinoma (ADC), in China from 2013 to ...
Yufei Li   +18 more
wiley   +1 more source

Primitive neuroectodermal tumors of the spine: a comprehensive review with illustrative clinical cases

open access: yes, 2011
Primary spinal primitive neuroectodermal tumors (PNETs) are uncommon malignancies that are increasingly reported in the literature. Spinal PNETs, like their cranial counterparts, are aggressive tumors and patients with these tumors typically have short ...
Paul C. McCormick   +6 more
core   +1 more source

Primitive Neuroectodermal Tumor of the Gallbladder

open access: yesArchives of Pathology & Laboratory Medicine, 2004
Abstract Ewing sarcoma/primitive neuroectodermal tumor (ES/ PNET) most commonly occurs in the soft tissues of the extremities and the paravertebral areas. To our knowledge, no case of PNET has been reported in the gallbladder to date. We report a case of PNET of the gallbladder occurring in a 53-year-old woman.
Dong Eun, Song   +3 more
openaire   +2 more sources

A Rare Instance of Adult Medulloblastoma Presenting Imaging Heterogeneity Correlating With Molecular Subtypes and Anatomical Locations

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT We report an adult medulloblastoma presenting as two imaging‐distinct lesions: a uniformly enhancing torcular mass (WNT‐activated) and a non‐enhancing cerebellar tumor (SHH‐activated). A cohort analysis confirmed torcular location favors uniform enhancement, mimicking meningioma.
Zechen Wang   +8 more
wiley   +1 more source

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