Spontaneous Haemothorax as Initial Presentation of Pleural Ewing Sarcoma: A Case Report.

Q4 Medicine
Case Reports in Pulmonology Pub Date : 2026-05-20 eCollection Date: 2026-01-01 DOI:10.1155/crpu/2865406
Alishba Khan, Andrew Mcdougall, Jon Tomas, Saddam Ibrahim, David Snead, Joshua Dale, Beatriz Lara
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引用次数: 0

Abstract

This case report discusses a middle-aged patient with metastatic pleuro-pulmonary Ewing sarcoma, with the rare initial presentation of spontaneous haemothorax. The patient had a prior history of Ewing sarcoma of the pelvis in young age, which had been treated with chemoradiotherapy with remission. There was a 2-week history of right sided chest pain and shortness of breath, and a chest x-ray showed complete opacification of the right hemithorax, with subsequent CT arising suspicion of a heterogeneous soft tissue pleural lesion with fluid in the pleural cavity. While awaiting further treatment including biopsy, the patient deteriorated rapidly and was eventually started on end-of-life care. Postmortem examination showed large right pleural haemorrhage with lung collapse, and histological examination of pleural lesions confirmed a diagnosis of recurrent Ewing's sarcoma. Extraskeletal presentations of Ewing's sarcoma, particularly with spontaneous haemothorax as the initial presentation have been rarely reported in the literature in adult patients. Diagnosing pleural Ewing's sarcoma requires a multimodal approach, utilising investigations such as contrast-enhanced CT imaging, pleural fluid analysis, thoracoscopy, and PET-CT to evaluate for disease spread. Treating pleural Ewing's sarcoma can be challenging; early diagnosis and management of complications such as haemothorax is essential with thoracocentesis or thoracotomy. Ongoing treatment can include multimodal therapies including chemotherapy and radiotherapy with or without surgery, depending on disease extent.

自发性血胸作为胸膜尤文氏肉瘤的初始表现:1例报告。
本病例报告讨论了一名中年患者转移性胸膜肺尤文氏肉瘤,罕见的初始表现为自发性血胸。患者年轻时曾有骨盆尤文氏肉瘤病史,经放化疗治疗后缓解。患者有2周的右侧胸痛和呼吸短促病史,胸部x线片显示右侧半胸完全混浊,随后的CT显示怀疑胸膜软组织病变异质性,胸膜腔积液。在等待包括活检在内的进一步治疗期间,患者病情迅速恶化,最终开始接受临终关怀。尸检显示右侧大量胸膜出血并肺萎陷,胸膜病变的组织学检查证实了复发性尤文氏肉瘤的诊断。尤文氏肉瘤的骨骼外表现,特别是以自发性血胸为首发表现,在成人患者中很少有文献报道。诊断胸膜尤文氏肉瘤需要多模式方法,利用造影增强CT成像、胸膜液分析、胸腔镜检查和PET-CT等检查来评估疾病的扩散。治疗胸膜尤文氏肉瘤具有挑战性;早期诊断和处理并发症,如血胸是至关重要的胸穿刺或开胸术。持续治疗可包括多模式治疗,包括化疗和放疗,伴或不伴手术,视疾病程度而定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Pulmonology
Case Reports in Pulmonology Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.80
自引率
0.00%
发文量
23
审稿时长
13 weeks
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