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Bilateral lung transplantation in a 9-year-old girl with bronchopulmonary dysplasia with pulmonary hypertension.
Ota, Chiharu; Saito, Ryoko; Tominaga, Junya; Iwasawa, Shinya; Hirama, Takashi; Matsuda, Yasushi; Ono, Katsunori; Onoki, Takehiko; Kimura, Masato; Kawabata, Yoshinori; Okada, Yoshinori.
Affiliation
  • Ota C; Department of Pediatrics, Tohoku University Hospital, Sendai, Japan.
  • Saito R; Department of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Tominaga J; Department of Diagnostic Radiology, Tohoku University Hospital, Sendai, Japan.
  • Iwasawa S; Department of Pediatrics, Tohoku University Hospital, Sendai, Japan.
  • Hirama T; Department of Thoracic Surgery, Institute of Development, Aging and Cancer, Tohoku University Hospital, Sendai, Japan.
  • Matsuda Y; Department of Thoracic Surgery, Institute of Development, Aging and Cancer, Tohoku University Hospital, Sendai, Japan.
  • Ono K; Department of Diagnostic Radiology, Tohoku University Hospital, Sendai, Japan.
  • Onoki T; Department of Pediatrics, Tohoku University Hospital, Sendai, Japan.
  • Kimura M; Department of Pediatric Cardiology, Miyagi Children's Hospital, Sendai, Japan.
  • Kawabata Y; Division of Diagnostic Pathology, Saitama Cardiovascular and Respiratory Center, Saitama, Japan.
  • Okada Y; Department of Thoracic Surgery, Institute of Development, Aging and Cancer, Tohoku University Hospital, Sendai, Japan.
Pediatr Pulmonol ; 56(10): 3417-3421, 2021 10.
Article in En | MEDLINE | ID: mdl-34350735
ABSTRACT

BACKGROUND:

Bronchopulmonary dysplasia (BPD) is a chronic respiratory disease that occurs in premature infants and the prognosis is variable depending on the comorbidities including fibrosis, emphysema, or pulmonary hypertension (PH). We present a case of a 9-year-old girl who developed PH associated with severe BPD (BPD-PH) and underwent bilateral lung transplantation (BLTx). Case description A 9-year-old girl was admitted to our department to undergo BLTx. She was born at 23 weeks and 4 days gestation with a weight of 507 g. She received ventilation for the first 2 months and required further respiratory care due to repetitive, severe respiratory infections. She was diagnosed with BPD-PH at 6 months of age and oral administration of pulmonary vasodilators were initiated. She was registered as a lung transplant candidate at 4 years of age after the life-threatening exacerbation. Chest computed tomography (CT) revealed severe lung conditions with ground-glass opacities and emphysematous low-density areas in the upper and lower lobes. BLTx from a brain-dead male donor was performed. The pathological findings of her resected lung revealed saccular, hypoplastic lung with alveolar repair/regeneration, and medial hypertrophy and muscularization of peripheral arteries. The postoperative course was mostly uneventful. She was free from oxygen administration and showed no signs of PH after 6 months of the surgery.

CONCLUSION:

This is the first case report of BLTx in a pediatric, irreversible BPD-PH patient with detailed pathohistological findings and clinical examination. Lung transplantation is one of the treatment options for severe BPD-PH.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchopulmonary Dysplasia / Lung Transplantation / Hypertension, Pulmonary Type of study: Prognostic_studies Limits: Child / Female / Humans / Infant / Male / Newborn Language: En Journal: Pediatr Pulmonol Journal subject: PEDIATRIA Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchopulmonary Dysplasia / Lung Transplantation / Hypertension, Pulmonary Type of study: Prognostic_studies Limits: Child / Female / Humans / Infant / Male / Newborn Language: En Journal: Pediatr Pulmonol Journal subject: PEDIATRIA Year: 2021 Document type: Article Affiliation country:
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