» Articles » PMID: 23243005

Successful Treatment of Pulmonary Hypertension with Beraprost and Sildenafil After Cord Blood Transplantation for Infantile Leukemia

Overview
Journal Int J Hematol
Specialty Hematology
Date 2012 Dec 18
PMID 23243005
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Pulmonary hypertension (PH) is an infrequently reported complication after hematopoietic stem cell transplantation, and its etiology and therapeutic strategies, especially in infants, remain unclear. We report a case of severe PH that developed in an infant with acute leukemia following administration of busulfan as a preconditioner for cord blood transplantation; the case was successfully treated with sildenafil and beraprost, which to our knowledge is the first reported successful use of this regimen in PH following transplantation for infantile leukemia. From a review of all previous reports, use of busulfan in infants may raise the risk of developing PH, and unlike definitive pulmonary veno-occlusive disease, PH in this subgroup may be reversible by early detection and treatment.

Citing Articles

Synchrotron-Based Phase-Contrast Micro-CT Combined With Histology to Decipher Differences Between Hereditary and Sporadic Pediatric Pulmonary Veno-Occlusive Disease.

Jeremiasen I, Peruzzi N, Lampei E, Meyer S, Akyurek L, Gebre-Medhin E Pulm Circ. 2024; 14(4):e70024.

PMID: 39678731 PMC: 11638014. DOI: 10.1002/pul2.70024.


Pulmonary veno-occlusive disease in childhood-a rare disease not to be missed.

Pfluger M, Humpl T Cardiovasc Diagn Ther. 2021; 11(4):1070-1079.

PMID: 34527533 PMC: 8410504. DOI: 10.21037/cdt-20-320.


Toxicities of busulfan/melphalan versus carboplatin/etoposide/melphalan for high-dose chemotherapy with stem cell rescue for high-risk neuroblastoma.

Desai A, Heneghan M, Li Y, Bunin N, Grupp S, Bagatell R Bone Marrow Transplant. 2016; 51(9):1204-10.

PMID: 27159174 DOI: 10.1038/bmt.2016.84.


Resource Utilization and Toxicities After Carboplatin/Etoposide/Melphalan and Busulfan/Melphalan for Autologous Stem Cell Rescue in High-Risk Neuroblastoma Using a National Administrative Database.

Desai A, Seif A, Li Y, Getz K, Fisher B, Huang V Pediatr Blood Cancer. 2016; 63(5):901-7.

PMID: 26797923 PMC: 5672623. DOI: 10.1002/pbc.25893.


Pediatric pulmonary arterial hypertension.

Wu D, Zhang H, Jing Z Curr Hypertens Rep. 2013; 15(6):606-13.

PMID: 24163011 DOI: 10.1007/s11906-013-0399-3.

References
1.
Limsuwan A, Pakakasama S, Hongeng S . Reversible course of pulmonary arterial hypertension related to bone marrow transplantation. Heart Vessels. 2011; 26(5):557-61. DOI: 10.1007/s00380-010-0100-6. View

2.
Lopes A . Pathophysiological basis for anticoagulant and antithrombotic therapy in pulmonary hypertension. Cardiovasc Hematol Agents Med Chem. 2006; 4(1):53-9. DOI: 10.2174/187152506775268794. View

3.
Resten A, Maitre S, Humbert M, Rabiller A, Sitbon O, Capron F . Pulmonary hypertension: CT of the chest in pulmonary venoocclusive disease. AJR Am J Roentgenol. 2004; 183(1):65-70. DOI: 10.2214/ajr.183.1.1830065. View

4.
Itoh T, Nagaya N, Fujii T, Iwase T, Nakanishi N, Hamada K . A combination of oral sildenafil and beraprost ameliorates pulmonary hypertension in rats. Am J Respir Crit Care Med. 2003; 169(1):34-8. DOI: 10.1164/rccm.200303-346OC. View

5.
Shankar S, Choi J, Dermody T, Head D, Bunin N, Iannone R . Pulmonary hypertension complicating bone marrow transplantation for idiopathic myelofibrosis. J Pediatr Hematol Oncol. 2004; 26(6):393-7. DOI: 10.1097/00043426-200406000-00013. View