Abstract |
Neonatal lung biopsy guides important medical decisions when the diagnosis is not clear from prior clinical assessment, imaging, or genetic testing. Common scenarios that lead to biopsy include severe acute respiratory distress in a term neonate, pulmonary hypertension disproportionate to that expected for gestational age or known cardiac anomalies, and assessment of suspected genetic disorder based on clinical features or genetic variant of unknown significance. The differential diagnosis includes genetic developmental disorders, genetic surfactant disorders, vascular disorders, acquired infection, and meconium aspiration. This article describes pathologic patterns in the neonatal lung and correlation with molecular abnormalities, where appropriate.
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Authors | Jill Lipsett, Megan K Dishop |
Journal | Surgical pathology clinics
(Surg Pathol Clin)
Vol. 13
Issue 4
Pg. 657-682
(Dec 2020)
ISSN: 1875-9157 [Electronic] United States |
PMID | 33183726
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2020 Elsevier Inc. All rights reserved. |
Topics |
- Biopsy
- Diagnosis, Differential
- Down Syndrome
(complications)
- Heart Defects, Congenital
(complications)
- Humans
- Infant, Newborn
- Infant, Premature
- Infant, Premature, Diseases
(etiology, pathology)
- Lung
(abnormalities, pathology)
- Lung Diseases
(congenital, etiology, pathology)
- Prognosis
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