Helton Matthew, Abu-Rmaileh Muhammad, Thomas Kevin, Gokden Murat, Kanaan Alissa, Rodriguez Analiz
Department of Neurosurgery, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Division of Neuropathology, Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Case Rep Oncol Med. 2020 Jul 21;2020:5073236. doi: 10.1155/2020/5073236. eCollection 2020.
While pituitary tumors are well understood, little research has been done on metastasis from primary tumors into pituitary adenomas, also known as composite tumors. Because only 34 cases of composite tumors have been reported to date, we hope to better characterize these tumors by reviewing cases reported in the literature and reviewed our own documented case, which includes next-generation sequencing. . A 74-year-old man presented to the emergency department with left vision loss for 3 months. He had a history of colon cancer treated with colectomy and clear cell renal carcinoma treated with left nephrectomy. A preoperative MRI demonstrated growth of a peripherally enhancing, centrally necrotic mass with sellar expansion measuring 5.7 × 3.1 × 3.0 cm. Given these findings, an endoscopic endonasal transsphenoidal resection was performed. Histological assessment revealed a composite tumor: one neoplasm was a nonfunctioning pituitary adenoma, and another neoplasm was a clear cell carcinoma. Next-generation sequencing demonstrated that the tumors shared mutations in and 2. The patient died 2 months later from systemic metastatic cancer.
From our literature review, most metastatic lesions in these composite tumors originated from neoplasms of the lung and kidney. Approximately 63% patients presented with ophthalmoplegia as the initial symptom while 23% displayed hormonal abnormalities. Postoperative mortality had a median of 3.5 months. In our patient, the presence of and 2 mutations in both tumors highlights the possibility of using next-generation sequencing to help identify therapeutic targets even in complex composite neoplasms.
虽然垂体瘤已为人熟知,但对于原发性肿瘤转移至垂体腺瘤(也称为复合性肿瘤)的研究却很少。由于迄今为止仅报道了34例复合性肿瘤病例,我们希望通过回顾文献中报道的病例并审视我们自己记录的病例(包括二代测序)来更好地描述这些肿瘤。一名74岁男性因左眼视力丧失3个月就诊于急诊科。他有结肠癌行结肠切除术及透明细胞肾癌行左肾切除术的病史。术前MRI显示一个周边强化、中央坏死的肿块生长,蝶鞍扩大,大小为5.7×3.1×3.0厘米。鉴于这些发现,进行了内镜鼻内蝶窦切除术。组织学评估显示为复合性肿瘤:一种肿瘤为无功能性垂体腺瘤,另一种肿瘤为透明细胞癌。二代测序显示肿瘤在 和2中有共同突变。患者2个月后死于全身转移性癌症。
通过我们的文献回顾,这些复合性肿瘤中的大多数转移灶起源于肺和肾的肿瘤。约63%的患者以眼肌麻痹为首发症状,而23%表现为激素异常。术后死亡率中位数为3.5个月。在我们的患者中,两种肿瘤中均存在 和2突变,这凸显了即使在复杂的复合性肿瘤中使用二代测序来帮助识别治疗靶点的可能性。