A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis
Tekijät: Klockars Tuomas, Renkonen Suvi, Leivo Ilmo, Hagström Jaana, Mäkitie Antti A
Kustantaja: SPRINGER
Julkaisuvuosi: 2010
Journal: Familial Cancer
Tietokannassa oleva lehden nimi: FAMILIAL CANCER
Lehden akronyymi: FAM CANCER
Vuosikerta: 9
Numero: 3
Aloitussivu: 401
Lopetussivu: 403
Sivujen määrä: 3
ISSN: 1389-9600
DOI: https://doi.org/10.1007/s10689-010-9331-z
Tiivistelmä
Juvenile nasopharyngeal angiofibromas (JNAs) are rare tumors with prominent vascularity and locally destructive growth. The pathogenesis of JNA is largely unknown. A causal association between JNA and familial adenomatous polyposis has been suggested. Twenty-one patients diagnosed with juvenile angiofibroma filled out a detailed patient questionnaire. No patients reported any relatives with nasopharyngeal angiofibroma or familial adenomatous polyposis. No significant regional clustering suggestive for founder effect could be identified. We believe that if there were a strong genetic predisposition or association with familial adenomatous polyposis, it should have been seen in this patient sample.
Juvenile nasopharyngeal angiofibromas (JNAs) are rare tumors with prominent vascularity and locally destructive growth. The pathogenesis of JNA is largely unknown. A causal association between JNA and familial adenomatous polyposis has been suggested. Twenty-one patients diagnosed with juvenile angiofibroma filled out a detailed patient questionnaire. No patients reported any relatives with nasopharyngeal angiofibroma or familial adenomatous polyposis. No significant regional clustering suggestive for founder effect could be identified. We believe that if there were a strong genetic predisposition or association with familial adenomatous polyposis, it should have been seen in this patient sample.
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