Case Report: A rare case of familial lung cancer requiring pneumonectomy in three male siblings

Lung cancer is a disease with a unique genetic pattern and is occasionally related to hereditary syndromes such as Lynch, Louis–Bar, and Li–Fraumeni. In some patients, germinal mutations may be discovered in combination with somatic alterations. For instance, Li–Fraumeni syndrome often reveals a mixture of TP53 and EGFR mutations. The development of new target therapies necessitates an extensive search for new pathogenic mutations. In this article, we present a rare case report of lung cancer, requiring a pneumonectomy, in three sibling brothers. Copyright © 2022 Kaprin, Pikin, Ryabov, Aleksandrov, Toneev, Lubchenko and Zelenova.

Авторы
Kaprin A. , Pikin O. , Ryabov A. , Aleksandrov O. , Toneev E. , Lubchenko L. , Zelenova E.
Журнал
Язык
Английский
Статус
Опубликовано
Номер
947210
Том
12
Год
2022
Организации
  • 1 P.Herzen Moscow Oncology Research Institute (MORI), Moscow, Russian Federation
  • 2 Peoples’ Friendship University of Russia, Moscow, Russian Federation
  • 3 Ulyanovsk Oncology Center, Ulyanovsk, Russian Federation
Ключевые слова
familial cancer; genome sequencing; immunotherapy; lung cancer; pneumonectomy
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