Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-29T17:55:18.835Z Has data issue: false hasContentIssue false

Chronic thromboembolic pulmonary hypertension secondary to Behçet’s disease: an extremely rare pediatric case

Published online by Cambridge University Press:  23 July 2021

Mohammad Mahdavi
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Sanaz Asadian
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Nahid Rezaeian
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Sahar Asl Fallah
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Hossein Shahzadi
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
Yaser Toloueitabar*
Affiliation:
Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
*
Author for correspondence: Yaser Toloueitabar, Cardiac Surgeon, Fellowship of Congenital Cardiac Surgery, Rajaie Cardiovascular Medical and Research Center, Tehran, Iran; Assistant Professor of Iran University of Medical Sciences, Tehran, Iran; Niayesh Intersection, Next to the Mellat Park, Vali-e-Asr Ave, Tehran, Iran. Tel: +98 91 2275 1094; Fax: +98 21 22042026. E-mail: [email protected]

Abstract

Chronic thromboembolic pulmonary hypertension is an uncommon condition in the children. It almost always accompanies a hypercoagulable state. We described a rare case of Behçet’s disease presenting with chronic thromboembolic pulmonary hypertension and initially misdiagnosed as coronavirus disease 2019 pneumonia.

Type
Brief Report
Copyright
© The Author(s), 2021. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Madani, MM, Wittine, LM, Auger, WR, et al. Chronic thromboembolic pulmonary hypertension in pediatric patients. J Thorac Cardiovasc Surg 2011; 141: 624630.CrossRefGoogle ScholarPubMed
Johnson, JN, Driscoll, DJ, McGregor, CG. Pulmonary thromboendarterectomy in adolescents and young adults. Pediatr Pulmonol 2010; 45: 614618.CrossRefGoogle ScholarPubMed
Verbelen, T, Cools, B, Fejzic, Z, et al. Pulmonary endarterectomy in a 12-year-old boy with multiple comorbidities. Pulm Circ 2019; 9: 2045894019886249.CrossRefGoogle Scholar
Fallah, SA, Ghodsi, S, Soleimani, H, et al. Incidence and predictors of chronic thromboembolic pulmonary hypertension following first episode of acute pulmonary embolism. Adv Respir Med 2020; 88: 539547.CrossRefGoogle Scholar
Kumbasar, U, Aypar, E, Karagoz, T, Demircin, M, Dogan, R. Pulmonary thromboendarterectomy in pediatric patients: report of three cases. Turk J Pediatr 2018; 60: 604607.CrossRefGoogle ScholarPubMed
Ma, F, Zhou, K, Hua, Y, et al. Chronic thromboembolic pulmonary hypertension as the first manifestation of nephrotic syndrome in a 12-year-old child. Medicine 2018; 97: e12349.CrossRefGoogle Scholar
La Regina, M, Orlandini, F, Prisco, D, Dentali, F. Homocysteine in vascular Behcet disease: a meta-analysis. Arterioscler Thromb Vasc Biol 2010; 30: 20672074.CrossRefGoogle ScholarPubMed
Wang, AS, Rosenzweig, EB, Takeda, K. A rare childhood case of Behcet’s disease and chronic thromboembolic pulmonary hypertension. J Cardiac Surg 2020; 35: 16691672.CrossRefGoogle ScholarPubMed