胸膜单发纤维瘤破裂伴血气胸:病例报告。

IF 0.7 Q4 SURGERY
Hiroaki Komatsu, Nao Furukawa, Kosuke Imamoto, Kazunori Okabe
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引用次数: 0

摘要

背景:胸膜单发纤维性肿瘤(SFT)患者大多无症状,SFT破裂并伴有血气胸的情况非常罕见:一名 48 岁男子因突发左胸痛被救护车送往我院。转诊前两个月,他在另一家医院接受计算机断层扫描筛查时发现左肺上叶有一肿瘤,因怀疑肿瘤为良性,建议进一步观察。我们的胸部对比增强计算机断层扫描分析显示,左胸腔内有一个实体瘤(直径 5 厘米),靠近心包处有不规则的增强效应和胸腔积液。之前的成像分析未发现胸腔积液。胸腔积液的CT值为40 HU,怀疑是血源性胸腔积液。因此,由于胸腔积液发生突然,怀疑是肿瘤破裂出血所致。术前诊断为纵隔肿瘤,如畸胎瘤,因为肿瘤靠近心包。患者取右侧卧位,进行了胸腔镜手术;观察并引流了血性胸腔积液。肿瘤源于左肺上叶的内脏胸膜,用手术器械切除。切除肿瘤的宏观分析表明,出血是肿瘤在囊壁缺损处破裂所致。手术耗时 63 分钟。术后病理诊断为良性 SFT。出血点位于肿瘤囊壁下方。患者术后恢复顺利,术后两天就出院了:结论:即使 SFT 既非巨大也非恶性,也可能发生破裂,因此无论肿瘤大小或恶性特征如何,都应考虑进行切除。SFT破裂后需要仔细随访,监测肿瘤是否在胸腔内复发或扩散。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ruptured solitary fibrous tumor of the pleura with hemothorax: a case report.

Background: The majority of the patients with a solitary fibrous tumor (SFT) of the pleura are asymptomatic, and rupture of an SFT with hemothorax is rare.

Case presentation: A 48-year-old man was taken by ambulance to our hospital because of sudden onset of left chest pain. Two months before the referral, a tumor was detected in the left upper lobe of the lung by screening computed tomography at another hospital, and further observation was recommended, because the tumor was suspected to be benign. Our contrast-enhanced computed tomography analysis of the chest revealed a solid tumor (5 cm in diameter) with an irregular enhancement effect close to the pericardium and pleural effusion in the left thoracic cavity. Pleural effusion was not detected in the previous imaging analysis. CT number of the pleural effusion was 40 HU, and the pleural effusion was suspected to be hematogenous. Therefore, rupture of the tumor with bleeding was suspected as the cause of the effusion because of the sudden onset. Preoperative diagnosis was a mediastinal tumor, such as a teratoma, because the tumor was close to the pericardium. Thoracoscopic surgery was performed with the patient in the right lateral decubitus position; bloody pleural effusion was observed and drained. The tumor originated from the visceral pleura of the left upper lobe of the lung and was resected with a surgical stapler. Macroscopic analyses of the resected tumor indicated that bleeding were caused by the rupture of the tumor at the defect of the capsule wall. The operation took 63 min. The postoperative pathological diagnosis was a benign SFT. Hemorrhage was observed just under the capsule wall of the tumor. The postoperative course of the patient was uneventful, and he was discharged 2 days after surgery.

Conclusions: Even when an SFT is neither huge nor malignant, rupture can occur, and resection should be considered regardless of the size or malignant characteristics. After an SFT rupture, careful follow-up is needed to monitor for the intrathoracic recurrence or dissemination of the tumor.

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