Department of Pathology, University of Pittsburgh School of Medicine, University of Pittsburgh Medical Center, 200 Lothrop Street, A616 Scaife Hall, Pittsburgh, PA, USA.
Head Neck Pathol. 2023 Sep;17(3):883-885. doi: 10.1007/s12105-023-01578-2. Epub 2023 Aug 4.
A 67-year-old female with a history of chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) presented with right sided otalgia and a 2-3 cm firm, tender right posterior parotid mass. Fine needle aspiration biopsy (FNAB) established a diagnosis of acinic cell carcinoma (AciCC). Further workup demonstrated lung nodules which were confirmed by FNAB to represent metastatic AciCC. A right radical parotidectomy with sacrifice of the facial nerve, segmental mandibulectomy, and selective neck dissection (levels II-IV) was performed. Microscopically, the tumor displayed an infiltrative border with a solid multinodular growth pattern and fibrosclerotic septation. The tumor was composed mainly of uniform cells with abundant eosinophilic granular cytoplasm with round nuclei with prominent nucleoli. Nuclei were fairly monomorphic, mitotic counts were 3-4 per 2mm and there was no necrosis despite the aggressive growth pattern. An anti-mitochondrial immunohistochemical stain showed strong reactivity in the tumor cells, with an internal positive control of adjacent striated ducts. An immunohistochemical stain for NR4A3 demonstrated strong nuclear reactivity in the tumor cells. Electron microscopy highlighted the tumor cells with numerous mitochondria and distinctive electron dense intramitochondrial inclusions. Concurrent CLL/SLL was identified on histologic examination of the lymph nodes, but they were free of AciCC. After eight weeks of follow-up, she tolerated the surgery well and is currently receiving radiation therapy to the parotid and neck. In this illustrative case, we justify the oncocytic designation of AciCC by morphology, immunohistochemistry, and electron microscopy.
一位 67 岁女性,患有慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL),表现为右侧耳痛和 2-3 厘米大小的右侧腮腺后份质硬、触痛性肿块。细针穿刺活检(FNAB)确立了涎腺腺泡细胞癌(AciCC)的诊断。进一步检查显示肺部结节,FNAB 证实这些结节为转移性 AciCC。行右侧根治性腮腺切除术,牺牲面神经,节段性下颌骨切除术,选择性颈部淋巴结清扫术(II-IV 区)。显微镜下,肿瘤边界浸润性,呈实性多结节生长模式,纤维硬化性分隔。肿瘤主要由均匀一致的细胞组成,细胞胞质丰富嗜酸性颗粒状,细胞核圆形,核仁明显。核形态较为单一,每 2mm 有 3-4 个有丝分裂象,尽管生长方式具有侵袭性,但无坏死。抗线粒体免疫组化染色显示肿瘤细胞强阳性反应,相邻纹状管的内部阳性对照。肿瘤细胞中 NR4A3 的免疫组化染色显示强核反应性。电子显微镜突出显示肿瘤细胞具有大量线粒体和独特的电子致密性线粒体内含物。淋巴结组织学检查同时发现 CLL/SLL,但无 AciCC。随访 8 周后,患者手术耐受良好,目前正在接受腮腺和颈部放射治疗。在这个说明性病例中,我们通过形态学、免疫组化和电子显微镜证实了 AciCC 的嗜酸细胞性肿瘤的命名。