Rhabdomyosarcomas in Childhood

Bailey, William C.; Holaday, William J.; Kontras, Stella B.; Clatworthy, W. William

doi:10.1001/archsurg.1961.01300120157018

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% Lack Of Autopsy Data In Children With1

Discussion1

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1964

1969

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Cited by 25 publications

(2 citation statements)

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“…This was similar to the incidence found by Bailey et al 4 T h e predominance of acute lymphocytic leukemia is usual for a pediatric service." T h e ratios between male and female acute leukemics appears to be more homogeneous in children as compared to adults where there is a higher incidence in males.18…”

Section: % Lack Of Autopsy Data In Children Withsupporting

confidence: 89%

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Incidence of second primary tumors in children with cancer and leukemia.A seven-year survey of 150 consecutive autopsied cases

Regelson

Bross

Hananian

et al. 1965

Cancer

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Section: % Lack Of Autopsy Data In Children Withsupporting

confidence: 89%

“…17 Bailey et al 4 and Cuneo and Rand18 indicate that glioblastoma multiforme is present in only 3-3.6% of intracranial neoplasms in children, although it is more common in the brain stem. Its overall frequency in children, according to French28 is 10% although it is the most common brain tumor of adult life.…”

Section: Discussionmentioning

confidence: 99%

Incidence of second primary tumors in children with cancer and leukemia.A seven-year survey of 150 consecutive autopsied cases

Regelson

Bross

Hananian

et al. 1965

Cancer

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Embryonal rhabdomyosarcoma.A clinicopathological study

Lawrence

Jegge

Foote

1964

Cancer

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Embryonal rhabdomyosarcoma. Report of twenty-four cases and study of the effectiveness of radiation therapy upon the primary tumor

Nelson

1968

Cancer

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Twenty‐four cases of embryonal rhabdomyosarcoma seen over a period of 16 years were reviewed and the effectiveness of radiation therapy on the primary tumor was studied. The results in 13 patients treated by radiation therapy alone and in combination with surgery and chemotherapy indicate that this tumor is moderately radiosensitive and can be locally controlled for significant periods of time with radiation therapy. Many patients whose primary lesion has been controlled will die of metastatic disease. In spite of this fact the three patients in this series who survived more than 5 years justify an optimistic approach to the treatment of this disease.

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Rhabdomyosarcomas in Childhood

Cited by 25 publications

References 6 publications

Incidence of second primary tumors in children with cancer and leukemia.A seven-year survey of 150 consecutive autopsied cases

Incidence of second primary tumors in children with cancer and leukemia.A seven-year survey of 150 consecutive autopsied cases

Embryonal rhabdomyosarcoma.A clinicopathological study

Embryonal rhabdomyosarcoma. Report of twenty-four cases and study of the effectiveness of radiation therapy upon the primary tumor

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