Sialadenoma Papilliferum of the Bronchus: An Unrecognized Bronchial Counterpart of the Salivary Gland Tumor With Frequent BRAF V600E Mutations.

Autor:	Nakaguro M; Department of Pathology and Laboratory Medicine, Nagoya University Graduate School of Medicine, Nagoya.; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA., Mino-Kenudson M; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA., Urano M; Department of Diagnostic Pathology, School of Medicine, Fujita Health University, Toyoake., Ogawa I; Center of Oral Clinical Examination, Hiroshima University Hospital, Hiroshima., Honda Y; Department of Diagnostic Pathology, Kumamoto University Hospital, Kumamoto., Hirai H; Departments of Anatomic Pathology., Tanigawa M; Departments of Anatomic Pathology., Sukeda A; Departments of Anatomic Pathology., Kajiwara N; Surgery, Tokyo Medical University., Ohira T; Surgery, Tokyo Medical University., Ikeda N; Surgery, Tokyo Medical University., Mikami Y; Department of Diagnostic Pathology, Kumamoto University Hospital, Kumamoto., Tada Y; Department of Head and Neck Oncology and Surgery, International University of Health and Welfare Mita Hospital, Tokyo., Ikeda JI; Department of Diagnostic Pathology, Chiba University Graduate School of Medicine, Chiba, Japan., Matsubayashi J; Departments of Anatomic Pathology., Faquin WC; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA., Sadow PM; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA., Nagao T; Departments of Anatomic Pathology.
Jazyk:	angličtina
Zdroj:	The American journal of surgical pathology [Am J Surg Pathol] 2021 May 01; Vol. 45 (5), pp. 662-671.
DOI:	10.1097/PAS.0000000000001657
Abstrakt:	Sialadenoma papilliferum (SP) is a rare benign tumor of the salivary glands, and only 3 unequivocal cases of SP arising in the bronchus have been reported. We herein describe the histomorphologic and molecular features of 4 bronchial SP cases and discuss the differential diagnosis of this entity and the relationship with its clinicopathologic mimics, in particular, glandular papilloma and mixed squamous cell and glandular papilloma (GP/MP). We encountered 2 male and 2 female patients with bronchial SP (mean: 66.8 y old). All 4 tumors arose in the central bronchus and were characterized by a combination of surface exophytic endobronchial papillary proliferation and a submucosal multicystic component with complex architecture. The neoplastic epithelium consisted predominantly of nonciliated stratified columnar cells with ciliated, squamous, and mucinous cells present focally. While 2 tumors (50%) harbored a BRAF V600E mutation by molecular and immunohistochemical analysis, similar to GP/MP, no KRAS, HRAS, AKT1, or PIK3CA mutations were detected in any of the cases. Two patients were treated with limited resection, while 2 patients underwent lobectomy based on the diagnosis of adenocarcinoma or possible squamous cell carcinoma in situ in the preoperative biopsy. All survived without recurrence or metastasis for 23 to 122 months after treatment. SP can develop in the central bronchus as the bronchial counterpart of the salivary gland tumor and should be considered in the differential diagnosis of endobronchial tumors. In addition, some histologic resemblance and frequent BRAF V600E mutation raise the possibility of SP and GP/MP being on the same disease spectrum. Competing Interests: Conflicts of Interest and Source of Funding: The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article. (Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.)
Databáze:	MEDLINE
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