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Gangliosides in Neuroblastomas
Neurochemical Pathology, 1988Neuroblastomas from children presenting with tumors at various ages and different primary sites (abdominal, adrenals, pelvic, and thoracic) were studied. Analysis of the ganglioside patterns of 53 tumors indicated that patients who were either disease positive 2 yr following surgery or dead of disease, had significantly (p less than 0.005) less GT1b ...
C L, Schengrund, S J, Shochat
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Archives of Pediatrics & Adolescent Medicine, 1969
SECOND only to accidents, cancer is the most frequent cause of death in children older than 1 year. 1 In the California Tumor Registry neuroblastoma accounts for 5% of the childhood malignancies, and in children's centers 10% to 12% of the malignant neoplasms are neuroblastomas.
A A, DeLorimier, K U, Bragg, G, Linden
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SECOND only to accidents, cancer is the most frequent cause of death in children older than 1 year. 1 In the California Tumor Registry neuroblastoma accounts for 5% of the childhood malignancies, and in children's centers 10% to 12% of the malignant neoplasms are neuroblastomas.
A A, DeLorimier, K U, Bragg, G, Linden
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World Journal of Urology, 1995
Neuroblastoma, a disease primarily of infants and younger children, is a tumor deriving from sympathetic neuroblasts. The variety of tumor location, growth and biologic characteristics represents the clinical manifestations: the range comprises spontaneous regression up to eminently malignant development with resistance to any therapy.
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Neuroblastoma, a disease primarily of infants and younger children, is a tumor deriving from sympathetic neuroblasts. The variety of tumor location, growth and biologic characteristics represents the clinical manifestations: the range comprises spontaneous regression up to eminently malignant development with resistance to any therapy.
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Opsomyoclonus and Neuroblastoma
Clinical Pediatrics, 1985Three cases of neuroblastoma with opsomyoclonus are reported, reconfirming favorable prognostic significance of the association. In one case, computed tomography of the abdomen was the only confirmatry diagnostic study. Two of the cases also were unusual in that the patients had a concomitantly inherited genetic disorder not known to be associated with
R P, Warrier +4 more
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Acta Pathologica Japonica, 1982
Two cases of neuroblastoma in situ incidentally found in young infants at autopsy are reported. One was an 8‐day‐old female infant of large for dates clinically diagnosed as fetal erythroblastosis. Histologically, several foci of tumor were scattered within the medulla of the left adrenal gland.
R, Hasegawa +6 more
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Two cases of neuroblastoma in situ incidentally found in young infants at autopsy are reported. One was an 8‐day‐old female infant of large for dates clinically diagnosed as fetal erythroblastosis. Histologically, several foci of tumor were scattered within the medulla of the left adrenal gland.
R, Hasegawa +6 more
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European Journal of Cancer, 1997
The neuroblastic tumours, derived from primordial neural crest cells which ultimately populate the sympathetic ganglia, adrenal medulla and other sites, (Brodeur GM and Castleberry RP. Neuroblastoma. In Pizzo PA, Poplack DG, eds, Principles and Practice of Pediatric Oncology. Philadelphia, J. B.
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The neuroblastic tumours, derived from primordial neural crest cells which ultimately populate the sympathetic ganglia, adrenal medulla and other sites, (Brodeur GM and Castleberry RP. Neuroblastoma. In Pizzo PA, Poplack DG, eds, Principles and Practice of Pediatric Oncology. Philadelphia, J. B.
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Neuroblastoma or not neuroblastoma
Human Pathology, 2014Risa, Teshiba +2 more
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Seminars in Perinatology, 1999
Neuroblastoma is the most common malignant neoplasm occurring in the neonate and arguably the most variable in its presentation. This review examines differences in the tumor's clinical course in the context of known biologic determinants of behavior.
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Neuroblastoma is the most common malignant neoplasm occurring in the neonate and arguably the most variable in its presentation. This review examines differences in the tumor's clinical course in the context of known biologic determinants of behavior.
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1989
Over a 33-month period, 31 infants and children had surgery for neuroblastoma. Twenty-three of the total had stage IV disease at the time of presentation and all but five had an abdominal primary tumour. In only two children was the tumour considered unresectable. The operative mortality was 3%.
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Over a 33-month period, 31 infants and children had surgery for neuroblastoma. Twenty-three of the total had stage IV disease at the time of presentation and all but five had an abdominal primary tumour. In only two children was the tumour considered unresectable. The operative mortality was 3%.
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