Abstract

BackgroundPrimary gastric adenosquamous carcinoma (ASC) is a rare subset of ASC. This study aims to investigate the clinicopathological features, diagnosis, treatment, and outcomes of primary gastric ASC.MethodsThe medical records of 13 consecutive patients with primary gastric ASC between January 2010 and July 2014 from a single institutional database were reviewed.ResultsMale predominance was observed (M/F = 10/3) among the patients, and their median age was 62 years (range: 43 to 79 years). The primary lesions were most often found in the upper third of the stomach, with a median tumor size of 5 cm (range: 2.25 cm to 10.5 cm). Ten patients underwent radical resections (R0 resection, 76.9%), while three patients had palliative resections (R1/R2 resection, 23.1%). Twelve patients had lymph node metastasis at the time of surgery. Adenocarcinoma and squamous cell carcinoma components in lymph node were found in eight and two cases, respectively, while two patients had both squamous cell carcinoma and adenocarcinoma components. In terms of the TNM staging system, stages IIB, IIIA, IIIB, IIIC, and IV were detected in 2 (15.4%), 2 (15.4%), 1 (7.7%), 5 (38.5%), and 3 (23.1%) patients, respectively. The median follow-up period was 22 months (range: 5 to 52 months); during which, four patients were still alive and eight patients died because of tumor progression. The 1-, 2-, and 3-year survival rates were 76.9%, 46.2%, and 15.4%, respectively.ConclusionsPrimary gastric ASC has a very poor prognosis, and both squamous cell carcinoma and adenocarcinoma components have distant metastasis potential.

Highlights

  • Primary gastric adenosquamous carcinoma (ASC) is a rare subset of ASC

  • We investigated the clinicopathological features, diagnosis, treatment, and survival outcomes of these patients to contribute to deeper knowledge on this tumor and provide additional assistance for ASC management

  • Patient characteristics The clinicopathological data of the ASC patients are summarized in Tables 1 and 2

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Summary

Introduction

This study aims to investigate the clinicopathological features, diagnosis, treatment, and outcomes of primary gastric ASC. Given the rarity of these carcinomas, most literatures are based on case reports [2,4,5,7,8,9,10,11] The histogenesis of these tumors has been debated considerably, and clinical therapies and prognosis of ASC have not been well established to date [12]. In the current study, we incorporated the data of 13 consecutive patients with primary gastric ASC who underwent surgery at a single medical institution. We investigated the clinicopathological features, diagnosis, treatment, and survival outcomes of these patients to contribute to deeper knowledge on this tumor and provide additional assistance for ASC management

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