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盲肠原发性鳞状细胞癌:一例报告

Primary Squamous Cell Carcinoma of the Cecum: A Case Report.

作者信息

Albandar Mahdi, Aljarayhi Salwa

机构信息

Department of Surgery, King Saud Medical City, Riyadh, SAU.

Department of Medicine, Al Faisal University, Riyadh, SAU.

出版信息

Cureus. 2024 Feb 21;16(2):e54615. doi: 10.7759/cureus.54615. eCollection 2024 Feb.

Abstract

Primary squamous cell carcinoma (SCC) of the colon is an exceptionally rare diagnosis. The etiology and pathogenesis of this entity remain unclear. It usually presents in patients as an emergency, typically with the tumor in the advanced stage. We report a case of SCC of the cecum presenting with perforation, initially diagnosed as SCC of unknown origin. The patient underwent a limited right hemicolectomy and end ileostomy outside our center. The patient was referred to us for further workup and possible adjuvant chemotherapy. She was assessed clinically and found to have had poor appetite and anorexia for a month, with an intermittent fever documented at 39 degrees. Thus, the patient was elected to get admitted for a septic workup and re-staging by CT scan and tumor biomarkers. CT showed a phlegmon and abscess formation at the right iliac fossa that was attached to surrounding structures, including the abdominal wall. Drain placement at the site of the phlegmon was attempted but failed due to bowel overlapping. Therefore, the patient was booked for surgical exploration and drainage, where all structures were resected en bloc. Histopathological examination revealed well-differentiated keratinized SCC with lymph node metastasis. The diagnosis of primary SCC of the cecum was confirmed after investigations to rule out primary sources were negative. Surgical resection remains the mainstay of management, with a possible role for chemotherapy and radiation therapy. The prognosis in these cases is usually poor. This warrants early diagnosis and management. Studies are needed to establish a management protocol for this entity.

摘要

原发性结肠鳞状细胞癌(SCC)是一种极为罕见的诊断。该实体的病因和发病机制尚不清楚。它通常在患者中以急症形式出现,典型情况是肿瘤处于晚期。我们报告一例盲肠SCC伴穿孔的病例,最初被诊断为来源不明的SCC。该患者在我们中心以外接受了有限的右半结肠切除术和末端回肠造口术。患者被转诊至我们这里进行进一步检查及可能的辅助化疗。对她进行临床评估时发现,她食欲不佳且厌食已有一个月,有记录显示间歇性发热至39度。因此,该患者被收治以进行脓毒症检查,并通过CT扫描和肿瘤生物标志物进行重新分期。CT显示右髂窝有蜂窝织炎和脓肿形成,与包括腹壁在内的周围结构相连。尝试在蜂窝织炎部位放置引流管,但因肠道重叠而失败。因此,该患者被安排进行手术探查和引流,所有结构均被整块切除。组织病理学检查显示为高分化角化型SCC伴淋巴结转移。在排除原发性来源的检查为阴性后,确诊为原发性盲肠SCC。手术切除仍然是主要的治疗方法,化疗和放疗可能有一定作用。这些病例的预后通常较差。这就需要早期诊断和治疗。需要开展研究以建立针对该实体的治疗方案。

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