Results 61 to 70 of about 10,442 (240)

Ganglioneuroma Always A Histopathological Diagnosis [PDF]

open access: yes, 2011
Neuroblastoma, ganglioneuroblastoma and ganglioneuroma arise from sympathetic tissue in the neck, posterior mediastinum, adrenal gland, retroperitoneum and pelvis Ganglioneuromas are commonly seen in childhood.
K, Balaiah   +3 more
core   +1 more source

The Enigma of a Traumatic Neuroma: A Case of Nerve Proliferation Without Documented History of Trauma

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
Intraoperative photograph showing the reflection of full thickness flap over the body of mandible exposing the lesion and specimen following excisional biopsy. ABSTRACT In the differential diagnosis of nerve‐related lesions, even when there is no documented trauma, this case emphasizes the significance of taking traumatic neuroma into account.
Shristi Maharjan   +7 more
wiley   +1 more source

Mediastinal ganglioneuroma: An incidentaloma of childhood

open access: yesIndian Journal of Medical and Paediatric Oncology, 2013
Ganglioneuroma is a rare benign neurogenic tumor which represents the final maturation stage of neuroblast tumors. Here, we are discussing an interesting case of incidentally detected posterior mediastinal ganglioneuroma which should be kept in mind when
Ram Mohan Shukla   +3 more
doaj   +1 more source

Giant adrenal ganglioneuroma in children: a case report

open access: yesDiscover Oncology, 2022
Background Ganglioneuromas (GNs) arise from the Schwann cells, ganglion cells, and neuronal tissues, and are extremely rare, slow-growing, benign tumors.
Mingqiu Hu   +3 more
doaj   +1 more source

Posterior Mediastinal Ganglioneuroma [PDF]

open access: yesRadioGraphics, 2004
History The patient was a 20-year-old female college student with no medical history who enrolled in a study at the University of Connecticut that assessed the role that genetics plays in muscle development following weight training. The study included initial magnetic resonance (MR) imaging of the thorax prior to a regimen of lifting weights and ...
Allen, Forsythe   +2 more
openaire   +2 more sources

A Rare Case of an Adrenal Ganglioneuroma Treated Laparoscopically in a Patient with Left-Sided Inferior Vena Cava.

open access: yesJournal of Endourology Case Reports, 2020
Background: Ganglioneuroma is a rare tumor derived from the neural crest that can occur in any sympathetic tissue. It corresponds to 0.3% to 2% of incidental adrenal tumors and
João Rafael Silva Simões Estrela   +3 more
semanticscholar   +1 more source

Mature Cystic Teratoma of the Right Adrenal Gland in a Pediatric Patient: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Adrenal teratomas are rare neoplasms, most often benign but with potential for malignant transformation, particularly in the pediatric population. A seven‐year‐old girl from kawasoti, Nepal, presented with intermittent right‐sided abdominal pain for 2 months, initially attributed to dietary factors such as junk food intake.
Amit Gautam   +4 more
wiley   +1 more source

Ganglioneuroma tumors associated with chronic diarrhea in infants [PDF]

open access: yes, 1961
Thesis (M.D.)—Boston ...
LeMaire, Roger
core  

Dopamine secreting adrenal tumor-ganglioneuroma rather than pheochromocytoma: case report.

open access: yesGland surgery, 2020
Ganglioneuromas are rare, benign, well-differentiated neural crest tumors arising in the paravertebral sympathetic chain, and are classically non-secretory and clinically asymptomatic.
A. Burns   +4 more
semanticscholar   +1 more source

Pigmented Birthmarks and Spinal Neurofibromas in KRAS Mosaicism—Not to Be Confused With NF1

open access: yesPediatric Dermatology, Volume 43, Issue 1, Page 128-131, January/February 2026.
ABSTRACT We report a child presenting with pigmentary skin lesions and spinal neurofibromas who was diagnosed molecularly with KRAS mosaicism. We review the previous literature of two cases of congenital skin lesions and neurofibromas and spinal nerve root hypertrophy caused by KRAS variants and highlight this presentation as an important differential ...
Karina M. Forde   +3 more
wiley   +1 more source

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