An unexpected encounter and outcome between endobronchial lipoma and carcinoma: a case report and literature review.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-01-01 DOI:10.1177/17534666231208575
Yang Yang, Jun Liu, Songkuan Chen, Guangzhao Yang, Guoqun Mao, Xiaoyu Han, Jian Wang
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Abstract

Bronchial lipoma is a rare benign tumor of the lung, which is often misdiagnosed due to concomitant pulmonary diseases. In addition, the coexistence of endobronchial lipoma and lung cancer is extremely unusual. To date, no related computed tomography (CT) images have been reported. The patient was a 53-year-old man, who was admitted to our hospital with cough, yellow phlegm, and fever for 1 week. The CT image showed an irregular mass in the medial segment of the right middle lobe (B4a) with surrounding ground glass opacity, and another solid nodule in the right lower lobe (B6b). Unfortunately, after 2 weeks of anti-inflammatory treatment, the bronchial invasion of the B4a nodule did not decrease significantly, so further bronchoscopy was carried out and tumor resection was performed using endoscopic mucosal resection with a ligation device (EMR-L). During the follow-up 4 months, it was found that the B6b nodule was marked enlargement and then removed. The lesions of the B4a and B6b were confirmed as endobronchial lipoma and squamous cell carcinoma (T1aN0M0) by histopathology and immunohistochemical staining, respectively, and no postoperative radiotherapy or chemotherapy was performed. Regrettably, after 29 months of follow-up, we observed recurrence and slow enlargement of the lipoma in its original location, progressive emphysema in both lungs, and solitary chest wall metastasis from the B6b squamous cell carcinoma that had been resected. Therefore, endobronchial endoscopy resection should be carefully selected for larger endobronchial lipoma. If it is accompanied by early squamous cell carcinoma (T1aN0M0), we still recommend active postoperative chemoradiotherapy.

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支气管内膜脂肪瘤和癌症的意外相遇和结局:一例病例报告和文献综述。
支气管脂肪瘤是一种罕见的肺部良性肿瘤,常因合并肺部疾病而被误诊。此外,支气管内脂肪瘤和癌症并存是极不寻常的。到目前为止,还没有相关的计算机断层扫描(CT)图像的报道。患者是一名53岁的男子,他因咳嗽、黄痰和发烧入院1天 周CT图像显示,右中叶内侧段有一个不规则肿块(B4a),周围有毛玻璃样混浊,右下叶有另一个实性结节(B6b)。不幸的是,在2之后 经过数周的抗炎治疗,B4a结节的支气管侵袭没有显著减少,因此进行了进一步的支气管镜检查,并使用带结扎装置的内镜粘膜切除术(EMR-L)进行了肿瘤切除。随访期间4 几个月后,发现B6b结节明显增大,然后切除。B4a和B6b的病变分别通过组织病理学和免疫组织化学染色确认为支气管内膜脂肪瘤和鳞状细胞癌(T1aN0M0),并且没有进行术后放疗或化疗。令人遗憾的是,29 在几个月的随访中,我们观察到脂肪瘤在原位复发和缓慢增大,两肺进行性肺气肿,以及已切除的B6b鳞状细胞癌的孤立性胸壁转移。因此,对于较大的支气管内脂肪瘤,应仔细选择支气管内窥镜切除术。如果伴有早期鳞状细胞癌(T1aN0M0),我们仍然建议术后积极放化疗。
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7.20
自引率
4.30%
发文量
567
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