双表达阑尾伯基特淋巴瘤1例报告及文献复习

IF 0.7 Q4 HEMATOLOGY
Osama N. Dukmak, Hamzeh M. I. Abugharbieh, Mohammad Emar, Iman Khamayseh, Salem M. Tos, Rafiq Salhab
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引用次数: 1

摘要

阑尾淋巴瘤是一种非常罕见的疾病,占胃肠道淋巴瘤病例的0.015%。急性阑尾炎是原发性阑尾肿瘤最常见的表现。Burkitt淋巴瘤表现为急性阑尾炎是一种罕见的实体,约21%的病例表现为下髂窝肿块。案例演示。一例23岁男性患者因急性阑尾炎,右髂窝局部压痛,反跳压痛阳性,rosing征阳性,超声检查疑似复杂阑尾炎而入院。行阑尾切除术。阑尾切除标本的组织病理学检查显示为双表达非霍奇金弥漫性大细胞淋巴瘤,具有伯基特样形态。他被送去接受化疗。结论仅34例伯基特淋巴瘤被报道为急性阑尾炎。阑尾炎切除术后的组织学检查是必要的。此外,全血细胞计数和计算机断层扫描有助于淋巴瘤的诊断。双表达性淋巴瘤的预后较差。因此,及时和积极的治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Double-Expressor Appendiceal Burkitt's Lymphoma: A Case Report and Literature Review
Background Appendiceal lymphoma is a very rare entity accounting for 0.015% of all gastrointestinal lymphoma cases. Acute appendicitis is the most common presentation of primary appendix neoplasms. Burkitt's lymphoma presenting as an acute appendicitis is a rare entity with around 21% of the cases presenting as a lower iliac fossa mass. Case Presentation. A 23-year-old male was admitted to the surgical ward as a case of acute appendicitis with localized tenderness in the right iliac fossa, positive rebound tenderness, a positive Rovsing's sign, and ultrasound findings of suspected complicated appendicitis. Appendectomy was performed. Histopathological examination of the appendectomy specimen revealed a double-expressor non-Hodgkin diffuse large cell lymphoma with Burkitt's-like morphology. He was sent for chemotherapy treatment. Conclusion Only 34 cases of Burkitt's lymphoma have been reported to present as acute appendicitis. Histological examination following appendectomy for an apparent appendicitis is essential. Furthermore, complete blood count and a computed tomography scan aid the diagnosis of lymphoma. Double-expressor lymphoma has been shown to have poor outcomes. Therefore, prompt and aggressive treatment is vital.
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