Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Pediatrics
Volume 2013, Article ID 875683, 3 pages
Case Report

Pulmonary Thromboembolism in a Child with Sickle Cell Hemoglobin D Disease in the Setting of Acute Chest Syndrome

1Pediatrics, The Brooklyn Hospital Center, Brooklyn, NY 11201, USA
2Pediatric Hematology-Oncology, The Brooklyn Hospital Center, Brooklyn, NY 11201, USA
3Hackensack University Medical Center, Hackensack, NJ 07601, USA

Received 3 August 2013; Accepted 24 August 2013

Academic Editors: P. Czauderna and M. Moschovi

Copyright © 2013 Hazel Villanueva et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Introduction. Sickle cell hemoglobin D disease (HbSD) is a rare variant of sickle cell disease (SCD). Incidence of pulmonary thromboembolism (PE) and deep venous thrombosis (DVT) in children with HbSD is unknown. PE and DVT are known complications of SCD in adults but have not been reported in the literature in children with HbSD. Case Report. We are reporting a case of a 12-year-old boy with HbSD with acute chest syndrome (ACS) complicated by complete thrombosis of the branch of the right pulmonary artery and multiple small pulmonary artery emboli seen on computed tomography (CT) pulmonary angiogram and thrombosis of the right brachial vein seen on Doppler ultrasound. Our patient responded to treatment with anticoagulant therapy. Conclusion. There are no cases reported in children with HbSD disease presenting as ACS with pulmonary thromboembolism. We suggest that PE should be suspected in patients presenting with ACS who do not show improvement with standard management. CT pulmonary angiogram should be utilized for early diagnosis and appropriate management as there is no current protocol for management of PE/DVT in pediatric patients with SCD.