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原发性泪腺导管原位腺癌

Primary De novo ductal adenocarcinoma of the lacrimal gland.

作者信息

Tripathy Devjyoti, Agarwal Sunil, Biala Abhinav, Rath Suryasnata, Mittal Ruchi

机构信息

Ophthalmic Plastic Surgery, Orbit and Ocular Oncology Services, LV Prasad Eye Institute, Mithu Tulsi Chanrai Campus, Bhubaneswar, India.

Department of Pathology, Hi-Tech Medical College and Hospital, Odisha, India.

出版信息

Ann Diagn Pathol. 2021 Feb;50:151651. doi: 10.1016/j.anndiagpath.2020.151651. Epub 2020 Oct 23.

Abstract

BACKGROUND

Primary ductal adenocarcinoma of the lacrimal gland is a rare and aggressive malignant epithelial lacrimal gland neoplasm, morphologically and phenotypically resembles salivary duct carcinoma, and both strongly resemble infiltrating ductal carcinoma of breast.

METHOD

Retrospective Chart review of cases of malignant lacrimal gland tumors from 2013 July to 2020 July. Authors describe the clinico radiological, morphological and immunohistochemical features of primary ductal adenocarcinoma (PDA) of lacrimal gland. Extensive review of literature of PDA of lacrimal gland and salivary gland ductal carcinoma has been performed.

RESULTS

Retrospective chart review of the last 7 years yielded 22 malignant lacrimal gland neoplasms of which 4 cases demonstrated features of primary ductal adenocarcinoma of lacrimal gland, 2/4 cases showed an evidence of a pre existing pleomorphic adenoma and 2 were found to be de novo ductal adenocarcinomas. PDA of lacrimal gland showed expression of CK7, CK19, AR, HER2, cyclin D1 and were negative for CK5/14, CK 20, ER, PR, PSA, TTF-1, S-100 and SMA. Expression of GCDFP-15 was noted in one case. The presence of multiple events of loco-regional recurrences and/or distant metastasis necessitated a multidisciplinary approach.

CONCLUSIONS

Authors have expressed the need of clinical correlation; thorough tissue sampling and extensive immunohistochemical work up in identification of de novo PDA's and their molecular subtypes. A multi-institutional study might help in formulating the diagnostic criteria, identification of actionable targets, and thus study the role of targeted therapy in this rare and aggressive tumor which may result in better patient outcomes.

摘要

背景

泪腺原发性导管腺癌是一种罕见且侵袭性强的恶性上皮性泪腺肿瘤,在形态学和表型上类似于涎腺导管癌,且二者都与乳腺浸润性导管癌极为相似。

方法

对2013年7月至2020年7月期间的恶性泪腺肿瘤病例进行回顾性病历审查。作者描述了泪腺原发性导管腺癌(PDA)的临床放射学、形态学和免疫组化特征。对泪腺PDA和涎腺导管癌的文献进行了广泛回顾。

结果

对过去7年的回顾性病历审查发现了22例恶性泪腺肿瘤,其中4例表现出泪腺原发性导管腺癌的特征,4例中有2例显示存在先前的多形性腺瘤,另外2例为新发导管腺癌。泪腺PDA表达CK7、CK19、AR、HER2、细胞周期蛋白D1,而CK5/14、CK20、ER、PR、PSA、TTF-1、S-100和SMA均为阴性。1例中观察到GCDFP-15的表达。局部区域复发和/或远处转移的多次发生需要多学科方法。

结论

作者表示需要进行临床关联;在识别新发PDA及其分子亚型时进行彻底的组织采样和广泛的免疫组化检查。多机构研究可能有助于制定诊断标准、识别可操作靶点,从而研究靶向治疗在这种罕见且侵袭性肿瘤中的作用,这可能会带来更好的患者预后。

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