Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants-Reference-Cited by-同舟云学术

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Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants

Published:2023-01 Issue: Volume:31 Page:42-45
ISSN:2352-5126
Container-title:JAAD Case Reports
language:en
Short-container-title:JAAD Case Reports

Author:

Trupiano Nicole,Koeppe Erika,Jacobs Michelle F.,Else Tobias,Cha Kelly B.

Publisher

Elsevier BV

Subject

Dermatology

Reference13 articles.

1. Guidelines of care for the management of primary cutaneous melanoma;Swetter;J Am Acad Dermatol,2019

2. Selection criteria for genetic assessment of patients with familial melanoma;Leachman;J Am Acad Dermatol,2009

3. Familial atypical multiple mole melanoma syndrome;Eckerle Mize,2009

4. BRCA1-and BRCA2-associated hereditary breast and ovarian cancer;Petrucelli,1998

5. American Society of Clinical Oncology expert statement: collection and use of a cancer family history for oncology providers;Lu;J Clin Oncol,2014

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