Saleem Umair, Ansari Tayyaba
Medical Oncology, Peterborough City Hospital, Peterborough, GBR.
Cureus. 2024 Sep 7;16(9):e68850. doi: 10.7759/cureus.68850. eCollection 2024 Sep.
Sarcomatoid carcinoma of the gastrointestinal tract is an extremely rare and aggressive tumor with both epithelial and mesenchymal characteristics, and it typically has a poor prognosis. We report the case of a 74-year-old male diagnosed with sarcomatoid carcinoma of the duodenum. The patient presented with gastrointestinal bleeding and was found to have a vascular tumor in the third part of the duodenum. Initial duodenal biopsies, repeat biopsies, and extensive immunohistochemical analysis confirmed a diagnosis of sarcomatoid carcinoma. Despite radical surgery and multiple lines of chemotherapy, including carboplatin and paclitaxel, the disease demonstrated aggressive progression, ultimately leading to the patient's death two years post-diagnosis. This report highlights the challenges in diagnosing and treating sarcomatoid carcinoma of the small intestine, the limited efficacy of current therapeutic options, and the need for further research to establish effective treatment protocols.
胃肠道肉瘤样癌是一种极其罕见且具有侵袭性的肿瘤,兼具上皮和间充质特征,预后通常较差。我们报告一例74岁男性十二指肠肉瘤样癌病例。该患者因胃肠道出血就诊,十二指肠第三段发现血管性肿瘤。最初的十二指肠活检、重复活检及广泛的免疫组化分析确诊为肉瘤样癌。尽管进行了根治性手术及包括卡铂和紫杉醇在内的多线化疗,疾病仍呈侵袭性进展,最终在确诊两年后导致患者死亡。本报告强调了小肠肉瘤样癌诊断和治疗中的挑战、当前治疗方案疗效有限以及需要进一步研究以建立有效的治疗方案。