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Surgery and Sample Processing for Correlative Imaging of the Murine Pulmonary Valve
Published on: August 5, 2021
Histologic evidence of intrapulmonary anastomoses by three-dimensional reconstruction in severe bronchopulmonary
Csaba Galambos1, Sunder Sims-Lucas, Steven H Abman
11 Department of Pathology.
Insights
New findings reveal abnormal blood vessels in the lungs of infants with severe bronchopulmonary dysplasia (BPD). These precapillary arteriovenous anastomoses may cause hypoxemia and contribute to BPD severity.
Area of Science:
- Neonatal Medicine
- Pulmonary Pathology
- Pediatric Cardiology
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease in premature infants, often leading to refractory hypoxemia.
- While fetal lungs have vascular communications, their role in BPD-related hypoxemia is unclear.
Purpose of the Study:
- To investigate the presence of intrapulmonary anastomotic vessels in infants with severe BPD.
- To determine if these vessels contribute to hypoxemia in BPD.
Main Methods:
- Histological examination of lung tissues from infants deceased with severe BPD.
- Immunohistochemistry and high-precision 3D reconstruction techniques were employed.
Main Results:
- Histologic evidence of vessels connecting pulmonary arteries and veins in the distal lungs of BPD infants was found.
- These vessels resemble those seen in alveolar capillary dysplasia.
Conclusions:
- Precapillary arteriovenous anastomotic vessels are present in severe BPD lungs.
- Persistence of these vessels post-birth may cause intrapulmonary shunting and hypoxemia, contributing to BPD morbidity and mortality.
Rationale:
Bronchopulmonary dysplasia (BPD) is the chronic lung disease of infancy that occurs in premature infants after oxygen and ventilator therapy for acute respiratory disease at birth. Despite improvement in current therapies, the clinical course of infants with BPD is often characterized by marked hypoxemia that can become refractory to therapy. Preacinar anatomic and functional communications between systemic and pulmonary vascular systems has been established in fetal lungs, but whether increased intrapulmonary anastomotic vessels or their failure to regress after birth contributes to hypoxemia in preterm infants with BPD is unknown.
Objectives:
We sought to find histologic evidence of intrapulmonary anastomotic vessels in lungs of patients who died of severe BPD.
Methods:
We collected lung tissues from fatal BPD cases and performed histology, immunohistochemistry, and high-precision three-dimensional reconstruction techniques.
Measurements And Main Results:
We report histologic evidence of intrapulmonary vessels that bridge pulmonary arteries and veins in the distal lungs of infants dying with severe BPD. These prominent vessels appear similar to "misaligned pulmonary veins" described in the lethal form of congenital lung disorder, alveolar capillary dysplasia.
Conclusions:
We found striking histological evidence of precapillary arteriovenous anastomotic vessels in the lungs of infants with severe bronchopulmonary dysplasia. We propose that persistence or expansion of these vessels after premature birth provides the anatomic basis for intrapulmonary shunt and hypoxemia in neonates with severe bronchopulmonary dysplasia and may play a significant role in the morbidity and mortality of BPD.
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