Abstract:
:A familial cancer aggregation comprising sarcomas, brain tumors, leukemias, and carcinomas of breast, larynx, lung, adrenal, cortex, and other sites has been studied from a pathologic--genetic standpoint. Based upon sibships segregating for cancer, the genetic segregation parameter is estimated to be 45.6 +/- 11% which is compatible with that expected for a rare deleterious autosomal gene showing complete dominance. Pathologic review of 16 tumors by bright field microscopy revealed variable occurrences of intranuclear cytoplasmic invaginations, intranucleolar bodies, and acidophilic intracytoplasmic inclusions in eight lesions. Two tumors showed both intranuclear cytoplasmic invaginations and intranucleolar inclusions. Morphological findings coupled with the observed pattern and distribution of cancer in the subject kindred suggest that the cancer-prone genotype interacts with one or more exogenous factors in causing this familial tumor association.
journal_name
Cancerjournal_title
Cancerauthors
Lynch HT,Mulcahy GM,Harris RE,Guirgis HA,Lynch JFdoi
10.1002/1097-0142(197805)41:5<2055::aid-cncr282041subject
Has Abstractpub_date
1978-05-01 00:00:00pages
2055-64issue
5eissn
0008-543Xissn
1097-0142journal_volume
41pub_type
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