A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome

Ehlers-Danlos Syndrome (EDS) refers to a group of connective tissue disorders characterized by significant clinical and genetic variability, affecting multiple systems in the body. Classified as a rare disease, EDS includes 14 subtypes, all marked by joint hypermobility, skin extensibility, and tiss...

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Main Authors: QingHua Liu, Ganhua Zeng, Yu Xiong, Chenyang Xu
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Medicine
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Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2025.1514349/full
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author QingHua Liu
Ganhua Zeng
Yu Xiong
Chenyang Xu
author_facet QingHua Liu
Ganhua Zeng
Yu Xiong
Chenyang Xu
author_sort QingHua Liu
collection DOAJ
description Ehlers-Danlos Syndrome (EDS) refers to a group of connective tissue disorders characterized by significant clinical and genetic variability, affecting multiple systems in the body. Classified as a rare disease, EDS includes 14 subtypes, all marked by joint hypermobility, skin extensibility, and tissue fragility. These subtypes present with a wide range of clinical manifestations and severities, including frequent joint dislocations, scoliosis, arterial dissections, and organ ruptures. Hypermobile EDS (hEDS) is the most common subtype, with newly established clinical diagnostic guidelines. In this case, a patient presented with minor hemoptysis over 8 h, and a chest CT scan revealed a massive hematoma in the left lower lung. Due to the complexity and varied presentations of EDS, misdiagnosis is common. This report shares our experience with diagnosis and treatment in this case, highlighting the importance of increasing awareness for improved survival outcomes.
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spelling doaj-art-c5fac0414a2847e5a5d2c0894f1167522025-01-28T06:41:21ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2025-01-011210.3389/fmed.2025.15143491514349A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndromeQingHua LiuGanhua ZengYu XiongChenyang XuEhlers-Danlos Syndrome (EDS) refers to a group of connective tissue disorders characterized by significant clinical and genetic variability, affecting multiple systems in the body. Classified as a rare disease, EDS includes 14 subtypes, all marked by joint hypermobility, skin extensibility, and tissue fragility. These subtypes present with a wide range of clinical manifestations and severities, including frequent joint dislocations, scoliosis, arterial dissections, and organ ruptures. Hypermobile EDS (hEDS) is the most common subtype, with newly established clinical diagnostic guidelines. In this case, a patient presented with minor hemoptysis over 8 h, and a chest CT scan revealed a massive hematoma in the left lower lung. Due to the complexity and varied presentations of EDS, misdiagnosis is common. This report shares our experience with diagnosis and treatment in this case, highlighting the importance of increasing awareness for improved survival outcomes.https://www.frontiersin.org/articles/10.3389/fmed.2025.1514349/fullpulmonary hematomacase reporthypermobile Ehlers-Danlos syndrome (hEDS)hemoptysisthoracic surgery
spellingShingle QingHua Liu
Ganhua Zeng
Yu Xiong
Chenyang Xu
A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome
Frontiers in Medicine
pulmonary hematoma
case report
hypermobile Ehlers-Danlos syndrome (hEDS)
hemoptysis
thoracic surgery
title A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome
title_full A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome
title_fullStr A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome
title_full_unstemmed A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome
title_short A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome
title_sort case of massive hematoma reflections on hypermobile ehlers danlos syndrome
topic pulmonary hematoma
case report
hypermobile Ehlers-Danlos syndrome (hEDS)
hemoptysis
thoracic surgery
url https://www.frontiersin.org/articles/10.3389/fmed.2025.1514349/full
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