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涎腺导管癌中的嗜酸细胞特征,在细针抽吸标本中误诊为沃辛瘤的潜在陷阱:14 例细胞形态学分析。

Oncocytic features in salivary duct carcinoma, a potential pitfall for misdiagnosis as Warthin tumor in fine needle aspiration specimens: A cytomorphologic analysis of 14 cases.

机构信息

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, US.

出版信息

Diagn Cytopathol. 2020 Jul;48(7):604-609. doi: 10.1002/dc.24426. Epub 2020 Apr 9.

Abstract

BACKGROUND

Salivary duct carcinoma (SDC) is an uncommon and highly aggressive primary salivary gland neoplasm. Cytomorphologic features of SDC include cellular smears, nuclear atypia, prominent nucleoli, cribriform and papillary architecture, and background necrosis. The presence of oncocytic features has been described but not adequately characterized in the current literature.

METHOD

This study cohort consisted of 14 cases of histologically proven SDC with previous salivary gland fine needle aspiration (FNA). The cytologic material of each case was semi-quantitatively analyzed and evaluated for various cytomorphologic, architectural, and background features.

RESULTS

Twelve SDCs were located in the parotid gland and two in the submandibular gland. In two cases the initial cytologic diagnoses was Warthin tumor or favor Warthin tumor. Moderate to marked degree of oncocytic changes were noted in all cases except one case. Nuclear atypia was variable with most cases exhibiting moderate to high-grade nuclear features, while four cases demonstrated low-grade nuclear cytomorphology. Cytoplasmic vacuolation was seen in nine cases and variable amount of background necrosis was observed in eight cases. Cribriform and papillary architecture was recognized in only six cases. Background lymphocytes were absent in all but one case.

CONCLUSIONS

Precise diagnosis of SDC based on cytomorphologic features alone can be challenging. Oncocytic change is one of the most consistent features observed in this case series and when associated with less pronounced cytologic atypia, can potentially lead to misdiagnosis as Warthin tumor. SDC should be considered in the differential diagnosis of oncocytic salivary gland neoplasms where precise diagnosis is not possible.

摘要

背景

涎腺导管癌(SDC)是一种罕见且高度侵袭性的原发性涎腺肿瘤。SDC 的细胞学特征包括细胞涂片、核异型性、明显的核仁、筛状和乳头状结构以及背景坏死。目前文献中已经描述了存在嗜酸性细胞特征,但未充分描述其特征。

方法

本研究队列包括 14 例经组织学证实的 SDC 患者,均有先前的涎腺细针抽吸(FNA)。对每个病例的细胞学材料进行半定量分析,并评估各种细胞学形态、结构和背景特征。

结果

12 例 SDC 位于腮腺,2 例位于颌下腺。在 2 例病例中,最初的细胞学诊断为沃辛瘤或倾向于沃辛瘤。除 1 例外,所有病例均有中度至明显的嗜酸性细胞变化。核异型性不同,大多数病例表现为中至高核特征,而 4 例表现为低核细胞学形态。9 例可见细胞质空泡,8 例可见不同程度的背景坏死。仅在 6 例中观察到筛状和乳头状结构。除 1 例外,所有病例均未见背景淋巴细胞。

结论

仅基于细胞学形态特征精确诊断 SDC 具有挑战性。在本病例系列中,嗜酸性细胞变化是最常见的特征之一,当与不明显的细胞学异型性相关时,可能导致误诊为沃辛瘤。在无法明确诊断的情况下,应考虑将 SDC 作为嗜酸细胞性涎腺肿瘤的鉴别诊断。

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