盲肠结外粘膜相关淋巴组织非霍奇金淋巴瘤及急性阑尾炎。个案报告

Nicolas Hdj, Hector Br, Luis Zrj, Antonio Rql, Fernando Gcc, Roberto Msj, Andres Efc, Teresa Vgt, Brenda Dc, I. Vsa, Emmanuel Mpj, Yamil Tog, Noemi Bbn, Mario Gs, Cayetano Pdlr, Adrian Thc
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摘要

目的:报告一例急性阑尾炎伴非霍奇金淋巴瘤伴盲肠结外粘膜的临床病例。简介:非霍奇金淋巴瘤(NHL)可以通过肿瘤的扩展而影响盲肠阑尾;然而原发性阑尾淋巴细胞增生性病变并不常见。粘膜相关淋巴组织(MALT)的NHL是例外。为了确定MALT的诊断,需要形态学、分子和免疫组织化学诊断,包括反映B细胞克隆的分子技术、PCR分析或染色体异常的鉴定。方法:男性,40岁,右下腹腹痛(RLQ)发展15天,伴有食欲下降、恶心、乏力等症状,首次诊断为尿路感染,门诊治疗;在他再次入院时,他进行了CT扫描,证明肠系膜膜炎和阑尾壁增厚;手术干预发现蚓状阑尾水肿充血伴下三穿孔,盲肠硬化伴盲肠底部2 cm穿孔,行右半结肠切除术伴回肠-横断面机械吻合;术后7 d出院;组织病理学和免疫组化检查符合malt型淋巴瘤,边缘无病变。扩展CT扫描未发现远处病变。他被送到肿瘤科做后续检查。结论:对于这种罕见的病理,重要的是要得到一个明确的诊断与分子技术,而不仅仅是组织病理切口,因为30%的患者复发。
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Non-hodgkin Lymphoma of Lymphoid Tissue Associated with Extranodal Mucosa of the Cecum and Acute Appendicitis. Report of a Case
Objective: Presentation of an acute appendicitis and non-Hodgkin lymphoma of lymphoid tissue associated with extranodal mucosa from the cecum clinical case. Introduction: The cecal appendix can be affected by Non-Hodgkin Lymphomas (NHL) by extension of the neoplasm; however primary appendicular lymphoproliferative processes are uncommon. The NHL of Mucosal-Associated Lymphoid Tissue (MALT) is exceptional. To establish the diagnosis of MALT, a morphological, molecular and immunohistochemical diagnosis is required, including molecular techniques that reflect B cell clones, PCR analysis or the identification of chromosomal abnormalities. Methods: 40 year old male, with 15 days of evolution of abdominal pain located in Right Lower Quadrant (RLQ) and associated symptoms like decreased appetite, nausea, and adynamia, who was firstly diagnosticated as an urinary tract infection treated as outpatient; upon his readmission, he was performed CT scan evidencing mesenteric panniculitis and thickening of the appendicular wall; he was surgically intervened finding edematous and congestive vermiform appendix with lower third perforation, and indurated cecum with 2 cm perforation from the appendicular base, performing right hemicolectomy with ileo-transverse mechanical anastomosis; he was discharged home 7 days after the postoperative period; the histopathological study and immunohistochemistry panel was compatible with MALT-type lymphoma, with lesion-free edges. Extension CT scans with no evidence of distant disease. He was sent to oncology for follow-up. Conclusion: It is important to get an established diagnosis in this rare pathology with molecular techniques and not only with histopathological cuts, since 30% of patients relapse.
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