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涎腺分泌性癌:儿童中的罕见病例。

Secretory Carcinoma of the Salivary Gland: A Rarity in Children.

作者信息

Kelly Gillean A, Venkatramani Rajkumar, Quintanilla Norma M, Chelius Daniel C, Roy Angshumoy, Mahajan Priya

机构信息

Baylor College of Medicine.

Division of Hematology/Oncology, Department of Pediatrics, Texas Children's Cancer Center.

出版信息

J Pediatr Hematol Oncol. 2022 May 1;44(4):167-172. doi: 10.1097/MPH.0000000000002304. Epub 2021 Sep 6.

Abstract

Originally described as mammary analog secretory carcinoma (SC), SC of the salivary gland is a rare malignancy with morphologic and molecular similarities to SC of the breast. We present 2 children with salivary gland SC with the classic ETV6-NTRK3 gene fusion, including 1 with lymph node metastases. Both patients underwent surgical resection and were in remission 24 months postsurgery. One patient was additionally found to have synchronous papillary thyroid carcinoma with a TFG-MET fusion. A review of published cases highlights the expanding molecular profile and confirms the favorable course of salivary gland SC after surgical resection.

摘要

涎腺分泌性癌最初被描述为乳腺类似物分泌性癌(SC),是一种罕见的恶性肿瘤,在形态学和分子水平上与乳腺SC相似。我们报告了2例患有涎腺SC且具有经典ETV6-NTRK3基因融合的儿童,其中1例有淋巴结转移。两名患者均接受了手术切除,术后24个月病情缓解。另外发现1例患者同时患有伴TFG-MET融合的甲状腺乳头状癌。对已发表病例的回顾突出了不断扩大的分子特征,并证实了涎腺SC手术切除后的良好病程。

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