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Symmetric palatal swelling as the first clinical manifestation of a mantle cell non-Hodgkin's lymphoma: A case report and review of literature

机译:对称性lat肿是套细胞非霍奇金淋巴瘤的首例临床表现:一例病例并文献复习

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摘要

The mantle cell lymphoma (MCL) is a rare (3.7%) low-grade non-Hodgkin lymphoma originating from the B-cell precursor-subpopulation. The clinical appearance in the oral cavity is rare. Since 1980, nine cases have been reported. A 41-year-old patient showed a MCL presenting with a symmetric, painless palatal swelling without any other clinical symptoms. Histological sections revealed malignant monotonous lymphoid cells (CD20+, CD43+, Ki67+) and the typical cyclinD1 over-expression by the chromosomal translocation t(11;14)(q13;q32). The proliferating cells weekly expressed CD5, kappa-and lambda-light chains and no EMA, CD10, bcl-6, CD30, and CD23. The patient was treated according to the European MCL younger study, and the MCL is regressive. The high incidence of dento-alveolar abscesses, inflammations, or benign tumor-formations leads to associate any maxillary or palatal swelling with this clinical condition. Considering the serious consequences of a missed therapy a histological examination of any untypical “swelling” is demanded.
机译:套细胞淋巴瘤(MCL)是一种罕见的(3.7%)低级非霍奇金淋巴瘤,起源于B细胞前体亚群。在口腔中的临床外观很少见。自1980年以来,已报告9例。一名41岁的患者显示MCL呈对称性,无痛性pa肿,无任何其他临床症状。组织学切片显示,恶性单调淋巴样细胞(CD20 +,CD43 +,Ki67 +)和典型的cyclinD1通过染色体易位t(11; 14)(q13; q32)过度表达。增殖细胞每周表达CD5,κ和λ轻链,而没有EMA,CD10,bcl-6,CD30和CD23。根据欧洲MCL较年轻的研究对患者进行了治疗,并且MCL呈退行性。牙槽泡脓肿,炎症或良性肿瘤形成的高发生率导致任何上颌或pa肿与该临床状况相关。考虑到错过治疗的严重后果,需要对任何不典型的“肿胀”进行组织学检查。

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