腮腺Warthin肿瘤引起的涎腺癌:一例罕见病例报告,并附文献复习和PD-L1表达。

IF 3.2 Q2 PATHOLOGY
Head & Neck Pathology Pub Date : 2023-12-01 Epub Date: 2023-10-13 DOI:10.1007/s12105-023-01587-1
Kaitlyn J Nielson, Gamaliel Lorenzo, Shweta Agarwal
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引用次数: 0

摘要

Warthin肿瘤是腮腺第二常见的肿瘤,由两个组成部分组成,包括淋巴基质和腺上皮。这种肿瘤的恶性转化主要见于淋巴成分;然而,上皮成分的癌性转化是极为罕见的。文献中报道的后者包括鳞状细胞癌、腺癌、粘液表皮样癌、嗜酸细胞癌、Merkel细胞癌和未分化癌。我们描述了一例极为罕见的唾液管癌,发生在64岁男性的Warthin肿瘤中。患者左侧腮腺肿块增大,活检显示为唾液管癌。随后,他接受了左侧腮腺切除术和左侧II-IV级淋巴结清扫术。组织学显示Warthin肿瘤引起的原位和侵袭性唾液管癌。免疫组织化学显示肿瘤细胞CK7、AR和GATA3阳性,而p63在原位组分中突出了肌上皮细胞层。Her2是2+ 通过免疫组织化学。此外,PD-L1 IHC显示阳性表达,综合阳性评分为20%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Salivary Duct Carcinoma Arising in a Warthin Tumor of the Parotid Gland: A Rare Case Report with Review of Literature and PD-L1 Expression.

Warthin's tumor is the second most common neoplasm of the parotid gland and consists of 2 components, including lymphoid stroma and glandular epithelium. Malignant transformation in this tumor is mostly seen in the lymphoid component; however, the carcinomatous transformation of the epithelial component is extremely rare. Cases of latter reported in the literature include squamous cell carcinoma, adenocarcinoma, mucoepidermoid carcinoma, oncocytic carcinoma, Merkel cell carcinoma, and undifferentiated carcinoma. We describe an extremely rare case of salivary duct carcinoma arising in a Warthin tumor in a 64-year-old male. Patient presented with an enlarging left parotid mass, biopsy of which showed salivary duct carcinoma. He subsequently underwent left parotidectomy along with left level II-IV lymph node dissection. Histology revealed both in situ as well as invasive salivary duct carcinoma arising from Warthin tumor. Immunohistochemistry showed tumor cells positive for CK7, AR, and GATA3, while p63 highlighted the myoepithelial cell layer in the in situ component. Her2 was 2+ by immunohistochemistry. In addition, PD-L1 IHC revealed positive expression with a combined positive score of 20%.

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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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