Li Guangxing, Han Chuanji, Cao Jin, Zhu Yongcun, Sun Shengbo
Department of Gastrointestinal Surgery, Weihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Weihai, PR China.
Department of Pathology, Weihai Municipal Hospital, Cheeloo College of Medicine, Shandong University, Weihai, PR China.
Case Rep Oncol. 2025 Apr 24;18(1):582-592. doi: 10.1159/000545101. eCollection 2025 Jan-Dec.
Primary squamous cell carcinoma (SCC) of the small intestine is an exceptionally rare malignancy, with limited cases reported in the literature. The rarity of this condition, combined with nonspecific clinical manifestations, poses significant diagnostic and therapeutic challenges.
We report the case of a 47-year-old woman who presented with a 2-month history of left lower abdominal pain and discomfort. Imaging studies, including enhanced abdominal CT and PET-CT, revealed a suspicious mass in the jejunum. Comprehensive diagnostic evaluations excluded metastatic origins, and a diagnosis of primary small intestinal SCC was confirmed by histopathology and immunohistochemistry. The patient underwent radical surgical resection, which revealed a poorly differentiated SCC invading the serosa and regional lymph nodes. Postoperative management included infection prevention and fluid rehydration, with recommendations for adjuvant chemotherapy and immunotherapy based on multidisciplinary consultation. Despite the advanced disease stage, the patient recovered well post-surgery and is undergoing regular follow-up.
This case underscores the importance of thorough diagnostic evaluation to distinguish primary SCC from metastatic lesions. Early surgical intervention is critical for improving prognosis of this rare malignancy. The findings contribute to the limited knowledge of the primary SCC of the small intestine and emphasize the need for further research to guide optimal management strategies.
原发性小肠鳞状细胞癌(SCC)是一种极为罕见的恶性肿瘤,文献报道的病例有限。这种疾病的罕见性,加上非特异性的临床表现,带来了重大的诊断和治疗挑战。
我们报告了一例47岁女性患者,她有2个月的左下腹痛和不适病史。包括增强腹部CT和PET-CT在内的影像学检查显示空肠有一个可疑肿块。综合诊断评估排除了转移来源,组织病理学和免疫组织化学确诊为原发性小肠SCC。患者接受了根治性手术切除,结果显示为低分化SCC侵犯浆膜和区域淋巴结。术后管理包括预防感染和补液,并根据多学科会诊建议进行辅助化疗和免疫治疗。尽管疾病分期较晚,但患者术后恢复良好,正在接受定期随访。
该病例强调了进行全面诊断评估以区分原发性SCC与转移瘤的重要性。早期手术干预对于改善这种罕见恶性肿瘤的预后至关重要。这些发现有助于增加对原发性小肠SCC的有限认识,并强调需要进一步研究以指导最佳管理策略。