Scognamiglio Theresa, Joshi Rohan, Kuhel William I, Tabbara Sana O, Rezaei M Katayoon, Hoda Rana S
Address: Department of Pathology and Laboratory Medicine, New York-Presbyterian Hospital, New York, NY 10065, USA.
Department of Otorhinolaryngology, New York-Presbyterian Hospital, New York, NY 10065, USA.
Cytojournal. 2015 Apr 29;12:7. doi: 10.4103/1742-6413.156080. eCollection 2015.
Carcinoma ex pleomorphic adenoma (CXPA) is a rare epithelial malignancy that arises from a primary or recurrent pleomorphic adenoma (PA). It may be noninvasive (NI) or invasive. NI CXPA is extremely rare. Preoperative diagnosis on fine needle aspiration (FNA) of CXPA may be difficult and poses a diagnostic challenge to clinicians and pathologists. Herein, we describe the FNA findings of a case of NI-CXPA. A 69-year-old woman presented with rapid enlargement of a stable parotid mass of 25 years. Cytologically, malignant cells were focally associated with metachromatic fibromyxoid matrix that was homogeneous and dense with a vague fibrillary quality. There were cell groups, papillary-like clusters and single malignant cells. The nuclei were pleomorphic with irregularly dispersed chromatin, and the cytoplasm was ill-defined and granular. Nucleoli were small to inconspicuous. Mitoses and necrosis were not seen. Cytological features were not specific for any type of salivary gland carcinoma. The FNA diagnosis was primary high-grade adenocarcinoma of the parotid gland, not otherwise specified. Facial nerve-sparing total parotidectomy was performed, which histologically showed PA interspersed with ducts and nests composed of pleomorphic atypical nuclei surrounded by extensive hyalinization. Single cells were also noted. No capsular infiltration was seen in the entirely sampled tumor. Immunohistochemistry for Ki-67 showed a higher proliferation rate in the malignant ducts and p63 positive cells focally surrounded some of the malignant ducts. Histological diagnosis was NI-CXPA. Accurate diagnosis is important for proper surgical management; however, the preoperative diagnosis of NI-CXPA is difficult to make on FNA.
多形性腺瘤恶变(CXPA)是一种罕见的上皮性恶性肿瘤,起源于原发性或复发性多形性腺瘤(PA)。它可以是非侵袭性(NI)或侵袭性的。NI CXPA极为罕见。术前通过细针穿刺抽吸(FNA)对CXPA进行诊断可能很困难,给临床医生和病理学家带来诊断挑战。在此,我们描述一例NI-CXPA的FNA检查结果。一名69岁女性,其稳定存在25年的腮腺肿块迅速增大。细胞学上,恶性细胞局灶性地与异染性纤维黏液样基质相关,该基质均匀且致密,具有模糊的纤维状特征。有细胞团、乳头状簇和单个恶性细胞。细胞核多形性,染色质不规则分布,细胞质界限不清且呈颗粒状。核仁小至不明显。未见有丝分裂和坏死。细胞学特征对任何类型的涎腺癌均无特异性。FNA诊断为腮腺原发性高级别腺癌,未另行特指。实施了保留面神经的全腮腺切除术,组织学显示PA中散在分布着由多形性非典型核组成的导管和巢,周围有广泛的玻璃样变。也可见单个细胞。在整个取样的肿瘤中未见包膜浸润。Ki-67免疫组化显示恶性导管中的增殖率较高,p63阳性细胞局灶性地围绕一些恶性导管。组织学诊断为NI-CXPA。准确诊断对于正确的手术管理很重要;然而,术前通过FNA对NI-CXPA进行诊断很困难。