Results 121 to 130 of about 10,442 (240)

Large Adrenal Ganglioneuroma

open access: yesInternal Medicine, 2012
We herein report the case of a 41-year-old male patient with an incidentally identified large adrenal ganglioneuroma (GN). His endocrine examinations were normal except for one episode of elevated urinary dopamine and noradrenaline levels. Abdominal computed tomography (CT) and magnetic resonance imaging (MRI) showed a large solid tumor with ...
Shugo, Sasaki   +16 more
openaire   +3 more sources

Pancreatic ganglioneuroma: a rare entity with a difficult approach: a case report and systematic review

open access: yes, 2019
Ganglioneuroma is a very rare benign tumor, arising from neural crest cells in the sympathetic ganglia and adrenal medulla, that is generally located in the retroperitoneum and in the mediastinum; pancreatic involvement is unusual with less than 10 cases
M. Mazzola   +9 more
semanticscholar   +1 more source

Neuroendocrine Tumors (NETs) : A population-based study of incidence and survival in Girona province, 1994-2004 [PDF]

open access: yes, 2012
Els tumors neuroendocrins (TNEs) són un grup de neoplàsies poc freqüents i heterogènies i amb un ampli espectre d'agressivitat. Hi ha molt poca informació epidemiològica a nivell mundial, l'objectiu d'aquest estudi ha estat el de reportar-ne les dades a ...
Alsina Maqueda, Maria   +3 more
core  

Giant Ganglioneuroma of Thoracic Spine: A Case Report and Review of Literature

open access: yesJournal of Korean Neurosurgical Society, 2017
Ganglioneuroma (GN) is a rare benign tumor of neural crest origin usually found in the abdomen, but may occasionally present at uncommon sites including the cervical, lumbar, or sacral spine. However, GNs of thoracic spine are extremely rare.
Yong Huang   +3 more
semanticscholar   +1 more source

Long-term outcome of ten children with opsoclonus-myoclonus syndrome [PDF]

open access: yes, 2018
Opsoclonus-myoclonus syndrome (OMS) in children is a rare neurological condition with opsoclonus, myoclonus, ataxia and irritability in the first 2 years of life.
Boltshauser, Eugen   +2 more
core  

Laparoscopic technologies in the treatment of retroperitoneal ganglioneuroma

open access: yesКреативная хирургия и онкология
Introduction. In the routine practice of a medical oncologist, ganglioneuroma is a rare pathology, and no clearly defined, modern protocols and guidelines for its diagnosis and treatment are available.Aim.
D. V. Erygin   +5 more
doaj   +1 more source

A case report of primary presacral neuroblastoma in a 9-month infant [PDF]

open access: yes, 2014
زمینه و هدف: نوروبلاستوما شایع ترین تومور جامد در کودکان است. در واقع، نزدیک به یک سوم موارد نوروبلاستوما در کودکان زیر 1 سال تشخیص داده می شود؛ اما تومورهایی با محل اولیه در قدام ساکروم نادرند.
Motamedi, Akram.   +2 more
core  

Nódulos incidentais da glândula suprarrenal: a experiência de um serviço de urologia [PDF]

open access: yes, 2017
info:eu-repo/semantics ...
Antunes, H   +7 more
core  

Retro-Peritoneal Extra-Adrenal Ganglioneuroma Encasing Major Blood Vessels

open access: yesPakistan Journal of Medicine and Dentistry
Ganglioneuroma is a rare, benign, slow-growing asymptomatic tumor of the neural crest cells. It occurs in one per million population with female predominance. It most commonly occurs in the retro=peritoneum. Although CT scan and other imaging modalities
Asad Abbas   +3 more
doaj  

Cervical Ganglioneuroma. A Pediatric Case Presentation and Review of the Literature

open access: yesRevista Finlay, 2021
The ganglioneuroma is a benign primitive neuroectodermal tumor, which derives from the ganglia of the sympathetic system and is composed of mature Schwann cells, ganglion cells, and nerve fibers.
Mányeles Brito Vázquez   +2 more
doaj  

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