Hamman–Rich syndrome in a young child-Reference-Cited by-同舟云学术

Hamman–Rich syndrome in a young child

Published:2019-09-15 Issue:4 Volume:64 Page:83-87
ISSN:2500-2228
Container-title:Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
language:
Short-container-title:Ross. vestn. perinatol. pediatr.

Author:

Minenkova T. A.¹^ORCID,Mizernitsky Yu. L.²^ORCID,Razinkova N. S.¹^ORCID,Serezhkina A. V.²^ORCID,Kostyuchenko M. V.²

Affiliation:

1. Kursk State Medical University

2. Veltischev Research and Clinical Institute for Pediatrics of the Pirogov Russian National Research Medical University

Abstract

Hamman–Rich syndrome (idiopathic fibrosing alveolitis) is a lung disease of unknown nature, characterized by non-infectious inflammation of the interstitium, alveoli and terminal bronchioles with an outcome in progressive pulmonary fibrosis. Idiopathic fibrosing alveolitis in young children, despite the timely verification of the diagnosis and therapy, is characterized by an unfavorable prognosis and rapidly progressive course. The article describes the clinical case of Hamman–Rich syndrome in a child of 8 months, its main clinical manifestations and diagnostic features.

Publisher

The National Academy of Pediatric Science and Innovation

Subject

Pediatrics, Perinatology, and Child Health

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