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Incidental ganglioneuroblastoma
Urology, 1986A case is described in which an incidental ganglioneuroblastoma was discovered at the time of surgical correction of upper pole hydronephrosis secondary to an obstructing ectopic ureterocele in a duplicated system. We believe this is the first case of incidental ganglioneuroblastoma reported in the urologic literature.
D A, Diamond, R D, Jeffs
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Pediatric cerebral ganglioneuroblastoma
Journal of Clinical Neuroscience, 2014We describe a 4-year-old girl with acute onset headaches and transient blindness who underwent surgical intervention, chemotherapy, and radiotherapy for an intracranial mass. This mass was pathologically confirmed as a primary intracranial ganglioneuroblastoma, a rare finding in the pediatric population. The literature on pediatric primary intracranial
Sean P, Steenberge, Richard A, Prayson
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The Journal of Laryngology & Otology, 1987
A case of primary cervical ganglioneuroblastoma is reported. It is a very rare tumour, only one example of this differentiated form of neuroblastoma having been previously recorded as a primary tumour in the neck. The incidence, clinical features, pathology and prognosis of primary cervical neuroblastoma have been discussed.
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A case of primary cervical ganglioneuroblastoma is reported. It is a very rare tumour, only one example of this differentiated form of neuroblastoma having been previously recorded as a primary tumour in the neck. The incidence, clinical features, pathology and prognosis of primary cervical neuroblastoma have been discussed.
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Primary cervical ganglioneuroblastoma
International Journal of Pediatric Otorhinolaryngology, 2015Ganglioneuroblastomas represent a histological subgroup of the rare neuroblastic tumours with intermediate malignant potential arising from neural crest progenitor cells of sympathetic nerves. Diagnosis can often be difficult based on imaging alone. We describe 4 cases of children presenting with a solitary neck mass with histology ultimately revealing
Joseph G, Manjaly +5 more
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