Pulighe Fabio, Paliogiannis Panagiotis, Cossu Antonio, Palmieri Giuseppe, Colombino Maria, Scognamillo Fabrizio, Trignano Mario
Department of Surgical, Microsurgical and Medical Sciences, University of Sassari, Viale San Pietro 43B, 07100 Sassari, Italy.
J Med Case Rep. 2013 Jun 28;7:170. doi: 10.1186/1752-1947-7-170.
In this report, we present the case of a patient affected by appendiceal cystadenoma, a colorectal adenocarcinoma, and a concomitant bladder carcinoma, as well as the results of the molecular study of the most relevant mutational pathways involved in these tumors.
A 68-year-old Italian man was admitted to our unit complaining of macrohematuria, rectorrhagia, and rectal tenesmus for about 2 months. A colonoscopy showed the presence of a rectal lesion at 11cm from the anal margin; multiple biopsies were performed and a diagnosis of moderately differentiated adenocarcinoma was made. Abdominal ultrasonography and total body computed tomography performed subsequently to stage the rectal cancer showed the presence of two round nodules, interpreted as swollen lymph nodes of neoplastic origin, at the anterior aspect of the iliopsoas muscle and a budding lesion affecting the bladder. The patient underwent transurethral biopsy of the lesion in the right retrotrigonal region; the diagnosis was grade II urothelial carcinoma. The patient underwent an open anterior rectal resection with loco-regional lymphadenectomy. An enlarged appendix and a voluminous whitish soft-tissue lesion requiring an appendicectomy were detected perioperatively. Transurethral resection of the bladder lesion was also performed. The histological examination revealed that the nodular lesions in the appendix were due to a cystadenoma. For mutation analysis, genomic deoxyribonucleic acid was isolated from tumor tissue samples; for PIK3CA mutations, screening revealed that all three samples analyzed carried mutations in exon 9.
Appendiceal mucoceles are rare but require adequate surgical treatment, given their malignant potential and the possibility of causing peritoneal pseudomyxoma. It is essential to make a correct preoperative evaluation based on a colonoscopy rather than ultrasound and computed tomography to exclude synchronous neoplasias often associated with mucoceles and to plan the optimum surgical strategy. The association between appendiceal mucoceles and other neoplasias is relatively frequent, especially with colorectal cancer. Oncogenic activation in the PIK3CA-depending pathway may contribute substantially to the pathogenesis of the different solid tumors in the same patient.
在本报告中,我们介绍了一例患有阑尾囊腺瘤、结肠直肠癌和同时存在的膀胱癌的患者病例,以及对这些肿瘤中最相关突变途径的分子研究结果。
一名68岁的意大利男子因大约2个月的肉眼血尿、直肠出血和直肠坠胀感入住我院。结肠镜检查显示距肛门边缘11cm处有直肠病变;进行了多次活检,诊断为中分化腺癌。随后为直肠癌分期进行的腹部超声检查和全身计算机断层扫描显示,在髂腰肌前方有两个圆形结节,被解释为肿瘤来源的肿大淋巴结,以及一个累及膀胱的芽状病变。患者接受了右侧膀胱三角区病变的经尿道活检;诊断为II级尿路上皮癌。患者接受了开放性直肠前切除术及局部区域淋巴结清扫术。术中发现阑尾肿大以及一个需要进行阑尾切除术的大量白色软组织病变。还进行了膀胱病变的经尿道切除术。组织学检查显示阑尾中的结节性病变是由囊腺瘤引起的。为进行突变分析,从肿瘤组织样本中分离出基因组脱氧核糖核酸;对于PIK3CA突变,筛查显示所分析的所有三个样本在第9外显子中都携带突变。
阑尾黏液囊肿虽然罕见,但鉴于其恶性潜能和导致腹膜假黏液瘤的可能性,需要进行充分的手术治疗。基于结肠镜检查而非超声和计算机断层扫描进行正确的术前评估至关重要,以排除常与黏液囊肿相关的同步肿瘤,并规划最佳的手术策略。阑尾黏液囊肿与其他肿瘤的关联相对常见,尤其是与结肠直肠癌。依赖PIK3CA的途径中的致癌激活可能在很大程度上促成同一患者中不同实体瘤的发病机制。