Dong Ming, Liu Jinghao, Song Zuoqing, Li Xin, Shi Tao, Wang Dan, Ren Dian, Chen Jun
From the Department of Lung Cancer Surgery, Tianjin Lung Cancer Institute (MD, JL, ZS, XL, DR, JC); Department of Pathology; Tianjin Medical University General Hospital, Heping District, Tianjin, China (TS, DW).
Medicine (Baltimore). 2015 Jul;94(27):e1136. doi: 10.1097/MD.0000000000001136.
Primitive neuroectodermal tumors (PNETs) arising directly from the lung are extremely rare but particularly aggressive neoplasms. Although thoracic PNET usually develops on the chest wall, there have been reports of primary Ewing sarcoma/PNET of the lung.We present the case of a 16-year-old male with PNET diagnosed following histologic and immunohistochemical examination of a video-assisted thoracic surgical biopsy. As typically occurring for these tumors, the diagnosis was initially delayed in our patient and prognosis was poor despite aggressive surgical resection and postoperative chemotherapy. We attempted to explore the use of targeted pharmacotherapy through high-throughput sequencing in this case. We found that this treatment using Avastin and Cetuximab could provide a new therapeutic direction for PNET.PNENTs arising from the lung parenchyma without pleural or chest wall involvement are extremely rare. Although uncommon, if the pathological features are similar to Ewing sarcoma, PNENTs should be kept in mind, and the target therapy may be a potent treatment for this disease.
直接起源于肺的原始神经外胚层肿瘤(PNETs)极为罕见,但却是侵袭性很强的肿瘤。尽管胸段PNET通常发生于胸壁,但也有原发性肺尤因肉瘤/PNET的报道。我们报告一例16岁男性患者,经电视辅助胸腔镜手术活检的组织学和免疫组化检查后诊断为PNET。正如这些肿瘤的典型情况,我们这位患者的诊断起初被延误,尽管进行了积极的手术切除和术后化疗,预后仍很差。我们试图在该病例中通过高通量测序探索靶向药物治疗的应用。我们发现使用阿瓦斯汀和西妥昔单抗的这种治疗可为PNET提供新的治疗方向。起源于肺实质而无胸膜或胸壁受累的PNENTs极为罕见。虽然不常见,但如果病理特征与尤因肉瘤相似,应考虑到PNENTs,靶向治疗可能是这种疾病的有效治疗方法。