Results 21 to 30 of about 126,670 (258)

Giant pediatric de novo parapharyngeal space pleomorphic adenoma: excision by semi trans-parotid cervical approach

open access: yesThe Egyptian Journal of Otolaryngology, 2023
Background Parapharyngeal Space tumors are rare tumors of the head and neck. They most commonly arise from the deep lobe of the parotid gland. Most of these tumors are in seen in adults and de novo origin from the minor salivary glands is extremely rare.
Abhishek Bhardwaj   +5 more
doaj   +1 more source

Desmoplastic Small Round Cell Tumor with “Pure” Spindle Cell Morphology and Novel EWS-WT1 Fusion Transcript: Expanding the Morphological and Molecular Spectrum of This Rare Entity

open access: yesDiagnostics, 2021
Background: Desmoplastic small round cell tumor (DSRCT) is a rare pediatric soft tissue neoplasm composed of small round tumor cells with prominent stromal desmoplasia, polyphenotypic differentiation and EWSR1-WT1 gene fusion.
Gaetano Magro   +7 more
doaj   +1 more source

Large orbital glial heterotopia- A rare entity

open access: yesIndian Journal of Pathology and Microbiology, 2022
A 15-month-old child was brought to the ophthalmology outpatient department with his parents complaining of a large mass located on the nasal side of his right eye since birth. On examination, an irregular mass was seen to be located on the nasal side of
Sujeeth Modaboyina   +4 more
doaj   +1 more source

Neuroblastoma of the Urinary Bladder in an Infant

open access: yesEuropean Journal of Pediatric Surgery Reports, 2019
As it originates from neural crest cells, Neuroblastoma (NBL) can arise anywhere along the sympathetic chain. However, its occurrence in the urinary bladder (UB) is extremely rare.
Ahmed Mohamed   +2 more
doaj   +1 more source

Fusion InPipe, an integrative pipeline for gene fusion detection from RNA-seq data in acute pediatric leukemia

open access: yesFrontiers in Molecular Biosciences, 2023
RNA sequencing (RNA-seq) is a reliable tool for detecting gene fusions in acute leukemia. Multiple bioinformatics pipelines have been developed to analyze RNA-seq data, but an agreed gold standard has not been established. This study aimed to compare the
Clara Vicente-Garcés   +19 more
doaj   +1 more source

Rhabdomyosarcoma of the breast: Report of two cases with the review of literature

open access: yesJournal of Indian Association of Pediatric Surgeons, 2016
Rhabdomyosarcoma (RMS) is a common soft-tissue neoplasm in the pediatric age group. Common locations are head and neck, genitourinary areas, trunk, and extremities. Two pathologic variants of this malignancy are embryonal and alveolar. The involvement of
Nizamudheen M Pareekutty   +3 more
doaj   +1 more source

Rare granular cell tumor affecting a 13-year-old boy

open access: yesIndian Journal of Dental Research, 2018
Granular cell tumor (GCT) is a rare soft-tissue neoplasm, first described in 1926. GCT often manifests as a single, painless nodule that shows a slow enlargement in the cutaneous, subcutaneous, or submucosal tissues.
S M Balaji, Preetha Balaji
doaj   +1 more source

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen   +23 more
wiley   +1 more source

Efficacy and safety of arthroscopy in femoroacetabular impingement syndrome: a systematic review and meta-analysis of randomized clinical trials

open access: yesScientific Reports
This study aimed to compare the efficacy and safety of arthroscopy with physiotherapy or joint lavage in patients with femoroacetabular impingement (FAI).
José María Lamo-Espinosa   +3 more
doaj   +1 more source

Genetic Predisposition to Solid Pediatric Cancers

open access: yesFrontiers in Oncology, 2020
Progresses over the past years have extensively improved our capacity to use genome-scale analyses—including high-density genotyping and exome and genome sequencing—to identify the genetic basis of pediatric tumors.
Mario Capasso   +10 more
doaj   +1 more source

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