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Nasopharyngeal Mantle Cell Lymphoma: An Extremely Rare Entity

机译:鼻咽套细胞淋巴瘤:极为罕见的实体。

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摘要

Mantle cell lymphoma (MCL) is a rare, aggressive subtype of non-Hodgkin lymphoma with a poor prognosis and high recurrence rate. It seldom affects the Waldeyer’s ring let alone the nasopharynx. Patients usually present at late stages of the disease leading to poor failure-free and overall survival rates. Intensive chemotherapy regimes and autologous stem cell transplantation have reported increased survival rates. We report a relapsed case of nasopharyngeal MCL, which previously occurred in the gastrointestinal tract. The patient had undergone a hemicolectomy for colon intussusception secondary to the intraluminal lymphoma mass. He was unable to complete the treatment regime for MCL due to the adverse side effects. Oropharyngeal mass was discovered during routine outpatient follow-up, which was confirmed as nasopharyngeal MCL. We discuss the prognosis, disease progression, and possible treatments.
机译:套细胞淋巴瘤(MCL)是一种非霍奇金淋巴瘤的罕见,侵袭性亚型,预后差且复发率高。它很少影响Waldeyer的环,更不用说鼻咽了。患者通常出现在疾病的晚期,导致不良的无故障生存率和总生存率。强化化疗方案和自体干细胞移植已报告了提高的存活率。我们报告了以前发生在胃肠道的鼻咽MCL复发病例。该患者因腔内淋巴瘤肿块继发结肠切除术。由于不良副作用,他无法完成MCL的治疗方案。在常规门诊期间发现口咽部肿块,证实为鼻咽部MCL。我们讨论了预后,疾病进展和可能的治疗方法。

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