In:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics), The National Academy of Pediatric Science and Innovation, Vol. 64, No. 4 ( 2019-09-15), p. 83-87
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.
Type of Medium:
Online Resource
ISSN:
2500-2228
,
1027-4065
DOI:
10.21508/1027-4065-2019-64-4
DOI:
10.21508/1027-4065-2019-64-4-83-87
Language:
Unknown
Publisher:
The National Academy of Pediatric Science and Innovation
Publication Date:
2019
detail.hit.zdb_id:
2953971-7
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