FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2007202911> ?p ?o ?g. }

• W2007202911 endingPage "822" @default.
• W2007202911 startingPage "816" @default.
• W2007202911 abstract "We reviewed all cases of malignant melanoma in children younger than 17 years of age who were evaluated at Sainte Justine Hospital, a tertiary care pediatric center, between 1980 and 2002. The medical records and histologic features of all cases were reviewed. Thirteen cases were identified, 4 boys and 9 girls. Fifty-three percent of patients were prepubescent. None of the patients had a predisposing condition (eg, giant congenital nevi, dysplastic nevus syndrome, or xeroderma pigmentosum). One patient had had chemoradiotherapy previously for an undifferentiated pleuropulmonary malignant tumor (blastoma) and another patient had Down syndrome. The most frequent reason for initial consultation was a recent increase in size of the lesion. Three patients had pyogenic granuloma–like lesions. Eighty-five percent of the observed melanomas were nodular in type. Tumor thickness ranged from 0 to 6 mm with a median and mean thickness of 2.8 and 3.2 mm, respectively. The overall 5-year survival rate was 58.8%. Lack of awareness and delay in diagnosis may lead to a higher incidence of thick and intermediate melanoma in children. Because it appears that the majority of melanomas in childhood and adolescence occur de novo, clinicians should consider this condition in the differential diagnosis of any suspect lesion in children and adolescents even without an identified predisposing factor. We reviewed all cases of malignant melanoma in children younger than 17 years of age who were evaluated at Sainte Justine Hospital, a tertiary care pediatric center, between 1980 and 2002. The medical records and histologic features of all cases were reviewed. Thirteen cases were identified, 4 boys and 9 girls. Fifty-three percent of patients were prepubescent. None of the patients had a predisposing condition (eg, giant congenital nevi, dysplastic nevus syndrome, or xeroderma pigmentosum). One patient had had chemoradiotherapy previously for an undifferentiated pleuropulmonary malignant tumor (blastoma) and another patient had Down syndrome. The most frequent reason for initial consultation was a recent increase in size of the lesion. Three patients had pyogenic granuloma–like lesions. Eighty-five percent of the observed melanomas were nodular in type. Tumor thickness ranged from 0 to 6 mm with a median and mean thickness of 2.8 and 3.2 mm, respectively. The overall 5-year survival rate was 58.8%. Lack of awareness and delay in diagnosis may lead to a higher incidence of thick and intermediate melanoma in children. Because it appears that the majority of melanomas in childhood and adolescence occur de novo, clinicians should consider this condition in the differential diagnosis of any suspect lesion in children and adolescents even without an identified predisposing factor." @default.
• W2007202911 created "2016-06-24" @default.
• W2007202911 creator A5005987239 @default.
• W2007202911 creator A5006719943 @default.
• W2007202911 creator A5050067306 @default.
• W2007202911 creator A5056708332 @default.
• W2007202911 creator A5059531889 @default.
• W2007202911 creator A5068003083 @default.
• W2007202911 creator A5088246713 @default.
• W2007202911 creator A5090706039 @default.
• W2007202911 date "2005-11-01" @default.
• W2007202911 modified "2023-09-30" @default.
• W2007202911 title "Malignant melanoma in childhood and adolescence: Report of 13 cases" @default.
• W2007202911 cites W1543634324 @default.
• W2007202911 cites W1825121097 @default.
• W2007202911 cites W1842392377 @default.
• W2007202911 cites W1965201362 @default.
• W2007202911 cites W1968515762 @default.
• W2007202911 cites W1969152840 @default.
• W2007202911 cites W1974687777 @default.
• W2007202911 cites W1977544164 @default.
• W2007202911 cites W1980083709 @default.
• W2007202911 cites W1980752323 @default.
• W2007202911 cites W1992582263 @default.
• W2007202911 cites W1997684002 @default.
• W2007202911 cites W1998938134 @default.
• W2007202911 cites W1999423655 @default.
• W2007202911 cites W2000326099 @default.
• W2007202911 cites W2002406176 @default.
• W2007202911 cites W2005701028 @default.
• W2007202911 cites W2007210451 @default.
• W2007202911 cites W2010306279 @default.
• W2007202911 cites W2011257826 @default.
• W2007202911 cites W2012204911 @default.
• W2007202911 cites W2013238087 @default.
• W2007202911 cites W2021934199 @default.
• W2007202911 cites W2024639069 @default.
• W2007202911 cites W2025005487 @default.
• W2007202911 cites W2031494390 @default.
• W2007202911 cites W2033504127 @default.
• W2007202911 cites W2040801753 @default.
• W2007202911 cites W2043971416 @default.
• W2007202911 cites W2044657311 @default.
• W2007202911 cites W2046512602 @default.
• W2007202911 cites W2052447509 @default.
• W2007202911 cites W2055720263 @default.
• W2007202911 cites W2058134455 @default.
• W2007202911 cites W2063854919 @default.
• W2007202911 cites W2064436242 @default.
• W2007202911 cites W2074441576 @default.
• W2007202911 cites W2076856767 @default.
• W2007202911 cites W2082371364 @default.
• W2007202911 cites W2086233817 @default.
• W2007202911 cites W2089398095 @default.
• W2007202911 cites W2089577571 @default.
• W2007202911 cites W2090691993 @default.
• W2007202911 cites W2090704428 @default.
• W2007202911 cites W2092062062 @default.
• W2007202911 cites W2093072027 @default.
• W2007202911 cites W2093519640 @default.
• W2007202911 cites W2098807286 @default.
• W2007202911 cites W2129491469 @default.
• W2007202911 cites W2133157220 @default.
• W2007202911 cites W2162297071 @default.
• W2007202911 cites W2166928613 @default.
• W2007202911 cites W2168836794 @default.
• W2007202911 cites W227934341 @default.
• W2007202911 cites W2330305032 @default.
• W2007202911 cites W23844752 @default.
• W2007202911 cites W2413806308 @default.
• W2007202911 cites W4231279699 @default.
• W2007202911 cites W4233743410 @default.
• W2007202911 cites W4237908080 @default.
• W2007202911 cites W4251391836 @default.
• W2007202911 cites W4299163522 @default.
• W2007202911 doi "https://doi.org/10.1016/j.jaad.2005.07.013" @default.
• W2007202911 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16243130" @default.
• W2007202911 hasPublicationYear "2005" @default.
• W2007202911 type Work @default.
• W2007202911 sameAs 2007202911 @default.
• W2007202911 citedByCount "67" @default.
• W2007202911 countsByYear W20072029112012 @default.
• W2007202911 countsByYear W20072029112013 @default.
• W2007202911 countsByYear W20072029112014 @default.
• W2007202911 countsByYear W20072029112015 @default.
• W2007202911 countsByYear W20072029112016 @default.
• W2007202911 countsByYear W20072029112017 @default.
• W2007202911 countsByYear W20072029112018 @default.
• W2007202911 countsByYear W20072029112019 @default.
• W2007202911 countsByYear W20072029112020 @default.
• W2007202911 countsByYear W20072029112021 @default.
• W2007202911 countsByYear W20072029112022 @default.
• W2007202911 countsByYear W20072029112023 @default.
• W2007202911 crossrefType "journal-article" @default.
• W2007202911 hasAuthorship W2007202911A5005987239 @default.
• W2007202911 hasAuthorship W2007202911A5006719943 @default.
• W2007202911 hasAuthorship W2007202911A5050067306 @default.
• W2007202911 hasAuthorship W2007202911A5056708332 @default.

• next