Pulmonary alveolar microlithiasis: A literature review and case report of a lung biopsy-confirmed disease in an infant

The article provides up-to-date information on epidemiology, etiology, genetics, pathogenesis, pathomorphology, clinical manifestation, X-ray and computed tomography (CT) semiotics, features in childhood, treatment of a rare genetic interstitial lung disease pulmonary alveolar microlithiasis (PAM). A clinical observation of a child with PAM manifestation, confirmed by lung biopsy in infancy, is presented. The results of X-ray and CT of the patient's chest organs are presented, the unique features of the course of the disease are listed. © 2021, Pediatria Ltd.. All rights reserved.

Авторы
Ovsyannikov D.Yu. 1, 2 , Alekseeva O.V. 1 , Taniya R.V. 1 , Frolov P.A. 1, 2 , Skobeev D.A.2 , Topilin O.G. 2 , Berezhanskiy P.V. 1, 2 , Gorev V.V.2
Номер выпуска
5
Язык
Русский
Страницы
170-175
Статус
Опубликовано
Том
100
Год
2021
Организации
  • 1 Peoples’ Friendship University of Russia, 6 Miklukho-Maclay ul, Moscow, 117198, Russian Federation
  • 2 Morozov Children’s Municipal Clinical Hospital, 6 Miklukho-Maclay ul, Moscow, 117198, Russian Federation
Ключевые слова
Children; Clinical observation; Computed tomography; Lung biopsy; Pulmonary alveolar microlithiasis
Цитировать
Поделиться

Другие записи