原发性肺滑膜肉瘤伴血气胸:病例报告。

Abdullah Abdulaziz AlQatari, Ayesha Ahmed, Fatima AlHije, Mohammed Sabry, Hatem Elbawab
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摘要

背景:滑膜肉瘤是一种罕见的侵袭性软组织恶性肿瘤:滑膜肉瘤是一种罕见的侵袭性软组织恶性肿瘤,最常见于四肢的关节周围组织。虽然文献中的一些病例报告了不同的起源,但原发性肺滑膜肉瘤(PPSS)是一种极为罕见且未得到充分认识的实体肿瘤,占所有肺部恶性肿瘤的 0.5%。临床表现包括胸痛、呼吸困难、咳嗽和咯血。发现血气胸是一种罕见的表现,文献中几乎没有报道。由于其罕见性和侵袭性,最佳治疗方法尚不明确,目前仍以手术切除加化疗和/或放疗为主:目的:报告一例出血性积液后诊断为原发性肺滑膜肉瘤的病例,主要目的是丰富有关这种罕见恶性肿瘤的文献:我院接诊了一名 52 岁的男性吸烟者,他患有冠心病、高血压和糖尿病。患者有胸痛、呼吸困难和右侧大量胸腔积液病史。除贫血外,实验室检查无异常。胸部X光片显示右下区完全不透明,右侧胸腔积液。胸腔穿刺术显示出血性渗出性积液。计算机断层扫描(CT)显示,右侧异质性肺肿块压迫中叶内侧段。随后,患者接受了支气管镜检查,结果显示右侧中叶支气管受压和水肿,右侧下叶有血迹。患者接受了右侧后外侧开胸手术,切除了侵蚀中叶内侧段的发霉肿块,诊断为高级别原发性肺滑膜肉瘤。患者接受了放疗。患者两年后因复发死亡:结论:原发性肺滑膜肉瘤是一种侵袭性疾病,预后较差,其表现与其他肺部恶性肿瘤几乎相似。结论:PPSS 是一种侵袭性疾病,预后较差,其表现几乎与其他肺部恶性肿瘤相似,目前尚无明确的治疗指南,大多数治疗方法是在可行的情况下进行手术切除,并辅以化疗和放疗。
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Primary Pulmonary Synovial Sarcoma with Hemothorax: a Case Report.

Background: Synovial sarcoma is a rare and aggressive soft tissue malignancy most commonly arises from periarticular tissue of the extremities. Although several cases in the literature have reported different origins, primary pulmonary synovial sarcoma (PPSS) is an exceedingly rare and underrecognized entity, accounting for 0.5% of all lung malignancies. Clinical presentation includes chest pain, dyspnea, cough, and hemoptysis. The finding of hemothorax is a rare presentation and was barely reported in the literature. Due to its rarity and aggressive nature, the optimal treatment is unclear, while the mainstay remains surgical resection with chemo- and/or radiation therapy.

Objective: To report a case of hemorrhagic effusion subsequently diagnosed with primary pulmonary synovial sarcoma with the main objective of enriching the literature regarding this rare malignancy.

Case report: A 52-year-old male smoker with a background of coronary artery disease, hypertension, and diabetes mellitus was referred to our hospital. The patient presented with a history of chest pain, dyspnea, and massive right-sided pleural effusion. Laboratory investigations were unremarkable except for anemia. Chest x-ray showed a complete opacity on the right lower zone with right-sided pleural effusion. Thoracentesis was done and revealed hemorrhagic exudative effusion. Computed tomography (CT) scan showed a right heterogeneous lung mass compressing the medial segment of the middle lobe. Subsequently, the patient underwent bronchoscopy, which showed compression and edema on the right middle lobe bronchus with traces of blood coming from the right lower lobe. The patient underwent a right posterolateral thoracotomy, a fungating mass eroding the medial segment of the middle lobe was resected that was diagnosed as high-grade primary pulmonary synovial sarcoma. Radiotherapy was instituted. The patient died after two years due to recurrence.

Conclusion: PPSS is an aggressive disease with poor prognostic outcomes, and Its presentation is almost similar to other lung malignancies. Meanwhile, there is no definitive management guideline, and most management depends on surgical resection if feasible with adjuvant chemo-radiation therapy.

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