主要尾MALT淋巴瘤临床伪装为慢性尾炎:一个病例报告
Tilahun H Nureta1, Wongel T Shale2, Mohammed A Abadura2
1Jimma University College of Public Health and Medical Sciences, Department of Surgery, Ethiopia; Jimma University College of Public Health and Medical Sciences, Department of Surgery, GI Oncology Surgery Unit, Ethiopia.
International journal of surgery case reports
|August 9, 2023
概括
尾的原发性MALT淋巴瘤是一种罕见的,惰的癌症. 诊断需要组织学,尾切除术可能是足够的治疗这种不常见的尾淋巴瘤.
科学领域:
- 在瘤学瘤学.
- 胃肠病学 胃肠病学
- 病理学 病理学 病理学
背景情况:
- 粘膜关联淋巴组织 (MALT) 淋巴瘤是额外的淋巴瘤.
- 它们通常发生在没有正常淋巴细胞存在的组织中,通常是由于慢性刺激.
- 尾的初级MALT淋巴瘤是非常罕见的.
研究的目的:
- 报告一种罕见的尾原发性MALT淋巴瘤病例.
- 讨论这种罕见疾病的临床表现,诊断和管理.
主要方法:
- 一个22岁男性的病例介绍,他患有反复出现的腹痛.
- 诊断成像 (CT扫描) 显示尾壁加厚和淋巴腺病变.
- 通过右半球切除术进行手术管理,然后进行组织病理学检查.
主要成果:
- 组织病理学证实了尾的MALT淋巴瘤.
- 患者出现了模仿慢性尾炎的症状.
- 尾MALTomas很少见,诊断依赖于组织学分析.
结论:
- 尾的初级MALT淋巴瘤是极其罕见的和惰的.
- 临床表现可以模仿慢性尾炎.
- 尾切除和监测可能是局部疾病的适当管理,预后很好.
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