揭开谜底一例罕见的原发性胃鳞状细胞癌伴有侵袭性转移

Adil Aziz Khan, Sana Ahuja, Sufian Zaheer
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引用次数: 0

摘要

本报告详细介绍了一例罕见的胃鳞状细胞癌(SCC)病例,这种情况只占胃癌的一小部分。一名 46 岁的男性患者出现吞咽困难、腹痛和吐血症状,被诊断为原发性胃 SCC,并伴有侵袭性转移。原发性胃 SCC 虽然在临床上与腺癌相似,但预后较差,缺乏标准化的治疗方案。组织病理学和影像学证实了这一诊断,凸显了晚期病例的治疗难题。姑息化疗取得了部分缓解,但导致了严重的神经病变。该病例强调了医学文献中原发性胃癌 SCC 的罕见性和不良预后,凸显了研究了解其发病机制、有效管理和治疗目标的迫切性。提高临床认识和持续开展研究对于改善此类罕见病例的预后至关重要。
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Unravelling the enigma: A rare case of primary gastric squamous cell carcinoma with aggressive metastasis

This report details a rare case of squamous cell carcinoma (SCC) in the stomach, a condition accounting for only a fraction of gastric carcinomas. A 46-year-old male patient with dysphagia, abdominal pain, and haematemesis was diagnosed with primary gastric SCC displaying aggressive metastasis, an exceptionally low-incidence condition affecting mainly males in their sixth decade of life. Primary gastric SCC, though clinically similar to adenocarcinoma, involves a bleaker prognosis, lacking standardized treatment protocols. Histopathology and imaging confirmed the diagnosis, highlighting the challenges in managing advanced cases. Palliative chemotherapy showed partial remission but led to severe neuropathy. The case underscores the urgent need for research to understand the pathogenesis, effective management, and therapeutic targets for primary gastric SCC, emphasizing its scarcity and poor prognosis in medical literature. Increased clinical awareness and ongoing research are crucial for improving outcomes in such rare presentations.

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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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