揭开罕见出血性恶性胸腔积液的面纱:内科胸腔镜在诊断原发性胸膜血管肉瘤中的作用。

IF 0.8 Q4 RESPIRATORY SYSTEM Respirology Case Reports Pub Date : 2024-11-25 eCollection Date: 2024-11-01 DOI:10.1002/rcr2.70068
Ad Rian Chong, Khai Lip Ng, Nai-Chien Huan, Nur Husna Mohd Aminudin, Maryam Ahmad Sharifuddin, Raja Nor Adilla Raja Rahaizat, Kasuma Mohamed Nordin
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引用次数: 0

摘要

原发性胸膜血管肉瘤(PPA)是一种罕见且难以诊断的肿瘤,由于临床和影像学特征重叠,常被误诊为间皮瘤和肺癌等其他恶性肿瘤。我们报告了一名 52 岁女性的病例,她出现进行性呼吸急促和胸膜炎性胸痛。影像学检查和胸腔穿刺术发现其左胸腔有大量出血性积液。医学胸腔镜检查(MT)显示顶胸膜增厚并呈分叶状,伴有多个结节性病变。组织病理学检查确诊为血管肉瘤,其特点是肿瘤细胞呈多形性,Ki67增殖指数高,免疫组化标记阳性,包括CD31、D2-40、Vimentin和因子VIII。不幸的是,患者在医院感染了病毒,在对血管肉瘤进行明确治疗之前就去世了。该病例凸显了 PPA 诊断的复杂性,并强调了 MT 在鉴别这种罕见恶性肿瘤方面的作用。
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Unveiling a rare haemorrhagic malignant pleural effusion: The role of medical thoracoscopy in diagnosing primary pleural angiosarcoma.

Primary pleural angiosarcoma (PPA) is a rare and challenging tumour to diagnose, often mistaken for other malignancies such as mesothelioma and lung cancer due to overlapping clinical and imaging features. We report a 52-year-old woman who presented with progressive shortness of breath and pleuritic chest pain. Imaging studies and thoracentesis revealed a large haemorrhagic left pleural effusion. Medical thoracoscopy (MT) showed a thickened and lobulated parietal pleura with multiple nodular lesions. Histopathological examination confirmed a diagnosis of angiosarcoma, characterized by pleomorphic tumour cells, a high Ki67 proliferation index and positive immunohistochemical markers, including CD31, D2-40, Vimentin, and Factor VIII. Tragically, the patient developed a hospital-acquired infection and passed away before any definitive treatment for the angiosarcoma could be initiated. This case underscores the diagnostic complexities of PPA and highlights the utility of MT in identifying this rare malignancy.

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来源期刊
Respirology Case Reports
Respirology Case Reports RESPIRATORY SYSTEM-
CiteScore
1.40
自引率
0.00%
发文量
178
审稿时长
8 weeks
期刊介绍: Respirology Case Reports is an open-access online journal dedicated to the publication of original clinical case reports, case series, clinical images and clinical videos in all fields of respiratory medicine. The Journal encourages the international exchange between clinicians and researchers of experiences in diagnosing and treating uncommon diseases or diseases with unusual presentations. All manuscripts are peer-reviewed through a streamlined process that aims at providing a rapid turnaround time from submission to publication.
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