晚期结肠癌与儿童的多重骨质状骨质瘤共存;巧合还是因果关系? - 一个案例报告报告
Ramon Andres Ramírez Calas1, Tania González Millán2, Sheriff Mohammed1
1Department of Surgery, Tamale Teaching Hospital, Box TL 16, Tamale, Ghana; Department of Surgery, School of Medicine and Health Science, University for Development Studies, Box TL 1350, Tamale, Ghana.
International journal of surgery case reports
|June 24, 2023
概括
本案例报告详细介绍了一例罕见的儿童结直肠癌与多重骨髓瘤同时发生的罕见病例. 这次独特的演讲强调了对罕见的儿科癌症和遗传疾病的进一步调查的需要.
科学领域:
- 在瘤学瘤学.
- 儿科瘤学 儿科瘤学
- 遗传学 遗传学是一种遗传学.
背景情况:
- 儿童结肠直肠癌 (CRC) 和多重骨髓瘤是个别罕见的疾病.
- 非洲人群中这些疾病的流行病学数据很少.
- 在儿童中,CRC和多重骨髓瘤的同时存在是非常罕见的,之前没有记录的病例.
研究的目的:
- 报告一个独特的儿科病人的病例,诊断出患有结直肠癌和多重骨髓瘤.
- 贡献到关于这两种罕见疾病同时发生的有限文献.
主要方法:
- 一个临床病例的介绍,涉及一个12岁的男孩.
- 手术干预:急需的左侧半结肠切除术和转向横向结肠切除术.
- 辅助化疗,然后在8个月的随访后进行结肠静脉逆转.
主要成果:
- 这位患者因晚期下降结肠癌 (IIIB阶段) 而出现大肠阻塞.
- 诊断出多种骨质瘤,影响了各种骨部位.
- 成功的手术管理和辅助化疗导致在8个月的随访中没有瘤复发或转移的迹象.
结论:
- 一个孩子同时患有结直肠癌和多重骨髓瘤是一个非凡的发现,在现有文献中没有先例.
- 进一步的基因组测序可能是必要的,以阐明导致这种罕见共存的潜在机制.
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