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Primary pulmonary glomus tumor of uncertain malignant potential: A case report with literature review focusing on current concepts of malignancy grade estimation

机译:恶性潜能不确定的原发性肺glomus肿瘤:病例报告并结合当前恶性程度估计的概念进行文献复习

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摘要

We report a 38-year-old woman with a left lung tumor presenting as obstructive pneumonia. Bronchoscopic examination revealed a polypoid tumor filling the left main bronchus. The tumor was partially resected by a snaring procedure for diagnostic purposes. Microscopic examination revealed a submucosal tumor located underneath normal bronchial epithelium. The tumor was composed of sheets of uniform oval to cuboidal cells encompassing numerous blood vessels. Immunohistochemically, the tumor cells exhibited smooth muscle markers, but were negative for neuroendocrine markers. The diagnosis of primary pulmonary glomus tumor was therefore made. Subsequent bronchoscopic intervention allowed us to pin-point the origin of the tumor: superior segmental B6a/b. She underwent a left lower lobe superior segmental resection successfully. Glomus tumors are relatively rare soft tissue tumors, and those of bronchopulmonary origin are exceedingly rare clinical condition. Among primary lung tumors, the carcinoid tumor is a mimic of the glomus tumor, and differentiating these tumors is known to be difficult, especially using small biopsy samples. In the present case, a large tissue sample obtained by bronchoscopic snaring was quite useful for the correct preoperative diagnosis. Because of the disease rarity, malignancy grade estimation of visceral glomus tumors has not been clearly addressed. Recently, the histopathological diagnostic criteria for malignant glomus tumors was defined in the WHO classification of soft tissue and bone tumors 4th edition. Here we also reviewed the literature on primary bronchopulmonary glomus tumors with special attention to the current concept of malignancy grade estimation.
机译:我们报告了一名38岁的左肺肿瘤阻塞性肺炎患者。支气管镜检查发现息肉样肿瘤充满左主支气管。为了诊断目的,通过诱捕程序部分切除了肿瘤。镜检发现位于正常支气管上皮下的粘膜下肿瘤。肿瘤由覆盖许多血管的均匀卵圆形到长方体细胞片组成。在免疫组织化学上,肿瘤细胞表现出平滑肌标志物,但对神经内分泌标志物呈阴性。因此作出了原发性肺血管球肿瘤的诊断。随后的支气管镜干预使我们能够查明肿瘤的起源:上段B 6a / b 。她成功地进行了左下叶上段切除术。 Glomus肿瘤是相对罕见的软组织肿瘤,而支气管肺源性肿瘤则极为罕见。在原发性肺部肿瘤中,类癌肿瘤是球囊肿瘤的模仿者,并且区分这些肿瘤是困难的,尤其是使用小型活检样本时。在本例中,通过支气管镜声纳获得的大量组织样本对于正确的术前诊断非常有用。由于疾病的稀有性,内脏球蛋白肿瘤的恶性程度评估尚未明确解决。最近,在WHO软组织和骨肿瘤分类第4版中定义了恶性球蛋白肿瘤的组织病理学诊断标准。在这里,我们还回顾了有关原发性支气管肺球肿瘤的文献,特别关注当前恶性程度评估的概念。

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