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具有广泛腺附件样分化的囊性多形性腺瘤的细针穿刺活检:与黏液表皮样癌的鉴别诊断陷阱

Fine-needle aspiration biopsy of a cystic pleomorphic adenoma with extensive adnexa-like differentiation: differential diagnostic pitfall with mucoepidermoid carcinoma.

作者信息

Brachtel Elena F, Pilch Ben Z, Khettry Urmila, Zembowicz Artur, Faquin William C

机构信息

Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.

出版信息

Diagn Cytopathol. 2003 Feb;28(2):100-3. doi: 10.1002/dc.10240.

Abstract

Although fine-needle aspiration biopsy (FNAB) is a highly accurate tool for the diagnosis of pleomorphic adenomas, even this common salivary gland neoplasm can be diagnostically challenging and cause pitfalls in cytodiagnosis. In particular, the presence of either cystic degeneration or squamous and mucinous metaplasia can lead to a false positive diagnosis of malignancy. Here we present the case of a 16-year-old female who presented with a painless, slowly growing mass in the superficial lobe of the right parotid gland. Magnetic resonance imaging of the parotid demonstrated a mass with heterogeneous postcontrast enhancement and a central, nonenhancing area suggestive of necrosis. FNAB of the lesion yielded proteinaceous debris and numerous whorls of keratin, small cohesive clusters of basaloid and squamoid epithelial cells, and many vacuolated and foamy cells. Initially and after consultation at an outside institution, the FNAB was reported as an "atypical neoplasm, cannot exclude mucoepidermoid carcinoma." A total, nerve-sparing parotidectomy and level II neck dissection revealed a pleomorphic adenoma with central cystic degeneration and extensive mixed appendageal differentiation. While foci of squamous metaplastic changes may occur in pleomorphic adenomas, the combination of cystic degeneration and extensive appendageal differentiation with numerous keratotic cysts is rare, and it presents the potential for misinterpretation of the FNAB as indicative of malignancy in general, and mucoepidermoid carcinoma in particular.

摘要

尽管细针穿刺活检(FNAB)是诊断多形性腺瘤的一种高度准确的工具,但即使是这种常见的涎腺肿瘤在诊断上也可能具有挑战性,并在细胞诊断中造成陷阱。特别是,出现囊性退变或鳞状及黏液化生可导致恶性肿瘤的假阳性诊断。在此,我们报告一例16岁女性患者,其右侧腮腺浅叶出现无痛性、生长缓慢的肿块。腮腺的磁共振成像显示一个肿块,增强后呈不均匀强化,中央有一个无强化区域提示坏死。对该病变进行FNAB检查,结果显示有含蛋白质的碎屑和大量角质层涡、基底样和鳞状上皮细胞的小黏附性细胞团,以及许多空泡状和泡沫细胞。最初及在外部机构会诊后,FNAB报告为“非典型肿瘤,不能排除黏液表皮样癌”。完整的、保留面神经的腮腺切除术及II区颈部淋巴结清扫术显示为一个伴有中央囊性退变和广泛混合性附件分化的多形性腺瘤。虽然多形性腺瘤中可能出现鳞状化生灶,但囊性退变、广泛的附件分化以及大量角化囊肿同时存在的情况较为罕见,这总体上存在FNAB被误诊为恶性肿瘤的可能性,尤其是误诊为黏液表皮样癌的可能性。

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