Wang Huiying, Liang Jiancong, Yong William H, Sullivan Peggy
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA, USA.
Acta Cytol. 2017;61(3):242-246. doi: 10.1159/000467384. Epub 2017 Apr 12.
Pituitary carcinomas are rare neoplasms whose designation requires demonstration of metastatic disease. No specific morphologic features can reliably distinguish pituitary carcinomas from pituitary adenomas, rendering the diagnosis particularly challenging. Furthermore, as reports of pituitary carcinoma on fine needle aspiration (FNA) biopsy are exceedingly rare in the literature, the cytological features of pituitary carcinoma are poorly characterized.
Here we describe a case of pituitary carcinoma in a 67-year-old woman with history of recurrent adrenocorticotropic hormone (ACTH)-producing pituitary adenoma who presented with a persistent left cervical nodule for 2 years. Ultrasound-guided FNA of the nodule consisted of loosely cohesive clusters of epithelioid cells with marked cytologic atypia, intermediate to large nuclei, relatively irregular nuclear contour, coarse granular chromatin, prominent nucleoli, and delicate finely granular cytoplasm. Immunohistochemical stains performed on the cell block revealed positivity for synaptophysin, chromogranin and ACTH with an increased Ki-67 proliferation index (approximately 25%). Review of the patient's previously resected pituitary tumor showed similar cytomorphologic features.
Given the similar cytologic features of pituitary carcinomas compared to other neuroendocrine tumors, it is important to obtain a complete clinical history and maintain a high index of suspicion in order to make a correct diagnosis of pituitary carcinoma on FNA.
垂体癌是罕见的肿瘤,其诊断需要证明存在转移性疾病。没有特定的形态学特征能够可靠地将垂体癌与垂体腺瘤区分开来,这使得诊断极具挑战性。此外,由于文献中关于垂体癌细针穿刺(FNA)活检的报道极为罕见,垂体癌的细胞学特征尚不明确。
在此,我们描述了一例67岁女性垂体癌病例,该患者有复发性促肾上腺皮质激素(ACTH)分泌型垂体腺瘤病史,出现左侧颈部持续性肿块2年。对该肿块进行超声引导下FNA,结果显示为松散聚集的上皮样细胞团,具有明显的细胞异型性,细胞核中等至大,核轮廓相对不规则,染色质粗糙呈颗粒状,核仁突出,细胞质细腻呈细颗粒状。对细胞块进行免疫组织化学染色,结果显示突触素、嗜铬粒蛋白和ACTH呈阳性,Ki-67增殖指数增加(约25%)。回顾患者先前切除的垂体肿瘤,显示出相似的细胞形态学特征。
鉴于垂体癌与其他神经内分泌肿瘤具有相似的细胞学特征,重要的是获取完整的临床病史并保持高度怀疑,以便在FNA时正确诊断垂体癌。