作者: Ryan Ladd , Matthew Davis , Jonathan A. Dyer
DOI: 10.1016/J.CLINDERMATOL.2020.03.007
关键词: Multiple endocrine neoplasia 、 Identification (biology) 、 Genetic therapy 、 Birt–Hogg–Dubé syndrome 、 Intensive care medicine 、 Genetic testing 、 Etiology 、 Medicine 、 Cancer 、 Hereditary Cancer Syndromes
摘要: The hereditary nature of some forms cancer was recognized long ago. Over time, recognition associated findings led to the delineation numerous syndromes. Many these syndromes also have cutaneous manifestations, which can lead their early identification. Recognition allows vigilant surveillance and preemptive treatment, dramatically impact risks morbidity mortality for affected patients. rise rapid accurate genetic testing now identification asymptomatic at risk family members so that monitoring be initiated as possible. dermatologist plays a critical role in and, many cases, treatment. This review summarizes known with findings, etiology, identification, evaluation, management. Importantly, this is an ever evolving topic new will continue recognized. must always alert ensure they are detected.