Results 121 to 130 of about 131,868 (167)
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NEUROBLASTOMA—EMPHASIS ON THE MEDIASTINAL NEUROBLASTOMA
American Journal of Roentgenology, 19681. Seventeen cases of neuroblastoma are reported with special emphasis on those manifested as thoracic masses.2. Three unusual cases are described in detail—one, with bone metastasis and survival.3. It has been shown that the prognosis is better in neuroblastomas of the mediastinum than of other locations.4.
L C, Griff, R E, Griff
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The American Journal of Dermatopathology, 1993
Cutaneous neuroblastoma (CN) is a rare tumor in adults. Histologically CN can be confused with other small, round cell tumors, especially with Merkel cell tumor. This is the second case that we have encountered in a 6-year period. A 46-year-old man with severe adult respiratory distress syndrome had a 2.5 x 2.0 x 2.0-cm, rapidly growing, fleshy nodule ...
A, Van Nguyen, Z B, Argenyi
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Cutaneous neuroblastoma (CN) is a rare tumor in adults. Histologically CN can be confused with other small, round cell tumors, especially with Merkel cell tumor. This is the second case that we have encountered in a 6-year period. A 46-year-old man with severe adult respiratory distress syndrome had a 2.5 x 2.0 x 2.0-cm, rapidly growing, fleshy nodule ...
A, Van Nguyen, Z B, Argenyi
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Journal of Urology, 1989
Neuroblastoma usually presents as an upper abdominal mass arising from the adrenal gland. Recent experience with neuroblastoma of the spermatic cord, bladder and pelvis demonstrates the propensity of this tumor to arise in unusual areas. The need for unusual and unexpected masses in children to be evaluated thoroughly for neuroblastoma and for therapy ...
C J, Knoedler +3 more
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Neuroblastoma usually presents as an upper abdominal mass arising from the adrenal gland. Recent experience with neuroblastoma of the spermatic cord, bladder and pelvis demonstrates the propensity of this tumor to arise in unusual areas. The need for unusual and unexpected masses in children to be evaluated thoroughly for neuroblastoma and for therapy ...
C J, Knoedler +3 more
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2020
Olfactory neuroblastoma is a rare tumor. Nasal endoscopy typically identifies a soft mass arising from the olfactory cleft. Computer tomography and magnetic resonance imaging are mandatory for staging (in association with 18F-fluorodeoxyglucose positron emission tomography) in high-grade and/or high-stage tumors.
Mathieu, Veyrat +6 more
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Olfactory neuroblastoma is a rare tumor. Nasal endoscopy typically identifies a soft mass arising from the olfactory cleft. Computer tomography and magnetic resonance imaging are mandatory for staging (in association with 18F-fluorodeoxyglucose positron emission tomography) in high-grade and/or high-stage tumors.
Mathieu, Veyrat +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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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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Australian and New Zealand Journal of Surgery, 1965
Summary1. A rase of congenital neuroblastonia is reported.2. Forty‐five other cases reported since 19·10 are reviewed.3. Twenty‐six cases (56 per cent.) survived fifteen months or longer without evidence of metastases.4. Of 14 cases arising apart from the adrenals, 13 survived.5.
D C, MACKENZIE, J M, HAM, R S, HYSLOP
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Summary1. A rase of congenital neuroblastonia is reported.2. Forty‐five other cases reported since 19·10 are reviewed.3. Twenty‐six cases (56 per cent.) survived fifteen months or longer without evidence of metastases.4. Of 14 cases arising apart from the adrenals, 13 survived.5.
D C, MACKENZIE, J M, HAM, R S, HYSLOP
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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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Acta Oto-Laryngologica, 1975
A case of olfactory neuroblastoma, type 1 (olfactory neurocytoma), in a 44-year-old man is described. The tumour grew extensively in the right nasal cavity with involvement of the maxillary sinus and ethmoidal region, but was radically removed at operation. The prognosis and treatment are discussed in the light of earlier literature.
C G, Lindström, D W, Lindström
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A case of olfactory neuroblastoma, type 1 (olfactory neurocytoma), in a 44-year-old man is described. The tumour grew extensively in the right nasal cavity with involvement of the maxillary sinus and ethmoidal region, but was radically removed at operation. The prognosis and treatment are discussed in the light of earlier literature.
C G, Lindström, D W, Lindström
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Pediatrics, 1965
Four cases of neonatal neuroblastoma are reported. The literature has been reviewed in an attempt to distinguish characteristics peculiar to neuroblastoma in the newborn. The various therapeutic modalities are discussed.
J M, Becker, K M, Schneider, I H, Krasna
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Four cases of neonatal neuroblastoma are reported. The literature has been reviewed in an attempt to distinguish characteristics peculiar to neuroblastoma in the newborn. The various therapeutic modalities are discussed.
J M, Becker, K M, Schneider, I H, Krasna
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