Shishido Yutaka, Aoyama Akihiro, Hara Shigeo, Hamakawa Hiroshi, Takahashi Yutaka
Department of General Thoracic Surgery, Kobe City Medical Centre General Hospital, Kobe, Hyogo, Japan.
Department of Diagnostic Pathology, Kobe City Medical Centre General Hospital, Kobe, Hyogo, Japan.
Am J Case Rep. 2019 Aug 15;20:1205-1209. doi: 10.12659/AJCR.917139.
BACKGROUND Tumor-to-tumor metastasis is an uncommon phenomenon in which a primary tumor metastasizes into another tumor. CASE REPORT An 81-year-old Asian woman was referred to our hospital for evaluation and treatment of a solid mass in the right middle lung lobe that had rapidly enlarged for 1.5 years compared to that observed over the last 5 years. On computed tomography (CT), the mass was 68×60 mm, and 2 different tumors appeared to exist in the upper portion of the mass. Blood examination findings revealed high serum levels of progastrin-releasing peptide and neuron-specific enolase. Based on the radiographic course of the tumor and elevated levels of tumor markers, we suspected that a new malignant tumor, such as a neuroendocrine tumor, had developed dorsally adjacent to the benign tumor. CT-guided percutaneous needle biopsy of the lung indicated a solitary fibrous tumor (SFT), which did not lead to the diagnosis of another tumor adjacent to the original tumor. Therefore, a right middle lobectomy was performed. The resected specimen contained 2 different tumors: an SFT and a typical carcinoid without mitosis or necrosis. On microscopic examination, they were separated from each other by normal alveolar tissue. In addition, a typical carcinoid was also observed inside the SFT lesion, completely enclosed by the SFT tissue. These findings suggested that the carcinoid metastasized to the SFT in the same lung lobe. CONCLUSIONS To the best of our knowledge, this is the first case of a pulmonary typical carcinoid metastasizing to an intraparenchymal SFT.
背景 肿瘤-to-肿瘤转移是一种罕见现象,即原发性肿瘤转移至另一肿瘤。
病例报告 一名81岁亚洲女性因右肺中叶实性肿块前来我院评估和治疗,该肿块在1.5年内迅速增大,而过去5年观察到的情况相对稳定。计算机断层扫描(CT)显示,肿块大小为68×60 mm,肿块上部似乎存在两种不同的肿瘤。血液检查结果显示血清促胃泌素释放肽和神经元特异性烯醇化酶水平升高。基于肿瘤的影像学表现及肿瘤标志物水平升高,我们怀疑在良性肿瘤背侧出现了一种新的恶性肿瘤,如神经内分泌肿瘤。肺部CT引导下经皮穿刺针吸活检提示为孤立性纤维瘤(SFT),但未明确诊断出与原肿瘤相邻的另一种肿瘤。因此,进行了右肺中叶切除术。切除标本包含两种不同的肿瘤:一个SFT和一个无有丝分裂或坏死的典型类癌。显微镜检查发现,它们被正常肺泡组织分隔开。此外,在SFT病灶内也观察到一个典型类癌,完全被SFT组织包绕。这些发现提示类癌转移至同一肺叶内的SFT。
结论 据我们所知,这是首例肺典型类癌转移至肺实质内SFT的病例。