Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review

Libman-Sacks endocarditis (LSE) is a cardiac condition characterized by the growth of verrucous vegetation. Although relatively rare in children, LSE is nevertheless a known cardiac manifestation of autoimmune diseases, including systemic lupus erythematosus (SLE). The mitral valve is the most commo...

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Main Authors: Jingyi Lu, Shengfang Bao, Xuemei Xu, Yingying Jin, Chenxi Liu, Yuqi Zhang, Qian Wang, Yanliang Jin
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-01-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2024.1323943/full
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author Jingyi Lu
Shengfang Bao
Xuemei Xu
Yingying Jin
Chenxi Liu
Yuqi Zhang
Qian Wang
Yanliang Jin
author_facet Jingyi Lu
Shengfang Bao
Xuemei Xu
Yingying Jin
Chenxi Liu
Yuqi Zhang
Qian Wang
Yanliang Jin
author_sort Jingyi Lu
collection DOAJ
description Libman-Sacks endocarditis (LSE) is a cardiac condition characterized by the growth of verrucous vegetation. Although relatively rare in children, LSE is nevertheless a known cardiac manifestation of autoimmune diseases, including systemic lupus erythematosus (SLE). The mitral valve is the most commonly affected region, followed by the aortic valve, while the tricuspid and pulmonary valves are rarely affected. The management of established Libman-Sacks vegetation poses significant challenges, often necessitating surgical interventions, although surgery is not the primary treatment modality. Herein, we present the case of a 14-year-old Chinese female patient whose initial lupus manifestation included LSE, among other symptoms and signs that provided insights into the final diagnosis of SLE. After early comprehensive pharmacological treatment, tricuspid regurgitation and vegetation disappeared within 28 days without necessitating cardiac surgery, indicating that the resolution of LSE vegetation in this patient was achieved through a combination of immunosuppressive and anticoagulant therapy. These findings suggest the potential of this treatment approach as a viable model for the management of LSE in young patients.
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spelling doaj.art-b2217a4f01494735a654a084c18c97912024-01-31T04:36:06ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602024-01-011210.3389/fped.2024.13239431323943Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature reviewJingyi Lu0Shengfang Bao1Xuemei Xu2Yingying Jin3Chenxi Liu4Yuqi Zhang5Qian Wang6Yanliang Jin7Department of Rheumatology and Immunology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Rheumatology and Immunology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Rheumatology and Immunology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Rheumatology and Immunology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Rheumatology and Immunology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Pediatric Cardiology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDiagnostic Imaging Center, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDepartment of Rheumatology and Immunology, Shanghai Children’s Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaLibman-Sacks endocarditis (LSE) is a cardiac condition characterized by the growth of verrucous vegetation. Although relatively rare in children, LSE is nevertheless a known cardiac manifestation of autoimmune diseases, including systemic lupus erythematosus (SLE). The mitral valve is the most commonly affected region, followed by the aortic valve, while the tricuspid and pulmonary valves are rarely affected. The management of established Libman-Sacks vegetation poses significant challenges, often necessitating surgical interventions, although surgery is not the primary treatment modality. Herein, we present the case of a 14-year-old Chinese female patient whose initial lupus manifestation included LSE, among other symptoms and signs that provided insights into the final diagnosis of SLE. After early comprehensive pharmacological treatment, tricuspid regurgitation and vegetation disappeared within 28 days without necessitating cardiac surgery, indicating that the resolution of LSE vegetation in this patient was achieved through a combination of immunosuppressive and anticoagulant therapy. These findings suggest the potential of this treatment approach as a viable model for the management of LSE in young patients.https://www.frontiersin.org/articles/10.3389/fped.2024.1323943/fullLibman-Sacks endocarditissystemic lupus erythematosusimmunosuppressive therapychildrencase report
spellingShingle Jingyi Lu
Shengfang Bao
Xuemei Xu
Yingying Jin
Chenxi Liu
Yuqi Zhang
Qian Wang
Yanliang Jin
Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review
Frontiers in Pediatrics
Libman-Sacks endocarditis
systemic lupus erythematosus
immunosuppressive therapy
children
case report
title Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review
title_full Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review
title_fullStr Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review
title_full_unstemmed Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review
title_short Libman-Sacks endocarditis in a child with systemic lupus erythematosus: a case report and literature review
title_sort libman sacks endocarditis in a child with systemic lupus erythematosus a case report and literature review
topic Libman-Sacks endocarditis
systemic lupus erythematosus
immunosuppressive therapy
children
case report
url https://www.frontiersin.org/articles/10.3389/fped.2024.1323943/full
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