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口腔皮肤CD4阳性T细胞淋巴瘤:两例患者的研究

Oral-cutaneous CD4-positive T-cell lymphoma: a study of two patients.

作者信息

May Steve A, Jones Dan, Medeiros L Jeffrey, Duvic Madeleine, Prieto Victor G, Lazar Alexander J F

机构信息

Department of Pathology, The University of Texas, MD Anderson Cancer Center, Houston, TX 77030-4009, USA.

出版信息

Am J Dermatopathol. 2007 Feb;29(1):62-7. doi: 10.1097/01.dad.0000246949.49071.17.

Abstract

We describe two slowly progressive cases of T-cell lymphoma that involved both acral skin and oral cavity. One patient presented with a tongue nodule, completely responded to chemotherapy and then developed recurrent lymphoma involving tongue and skin a few months later that also responded to therapy. The second patient presented with a skin nodule that spontaneously resolved without therapy, and subsequently recurred in tongue and skin a few years later. In both cases, the neoplasms were composed of atypical lymphoid cells with epidermotropism and were of T-helper cell lineage (CD4+). The initial lesions were also negative for CD30. Identical T-cell receptor gene rearrangements were detected in the initial and recurrent lesions of one case. Although these neoplasms were classified as unspecified peripheral T-cell lymphoma because of the unusual distribution of disease, both cases also had histopathologic features of mycosis fungoides. These cases are strikingly similar, and may represent an unusual clinicopathologic type of T-cell lymphoma that can hone to cutaneous and oral mucosal sites with a slowly progressive natural history.

摘要

我们描述了两例累及手足皮肤和口腔的缓慢进展性T细胞淋巴瘤病例。一名患者表现为舌部结节,对化疗完全缓解,数月后复发,累及舌部和皮肤,再次治疗仍有反应。第二名患者表现为皮肤结节,未经治疗自行消退,数年后在舌部和皮肤复发。两例病例中的肿瘤均由具有亲表皮性的非典型淋巴细胞组成,为辅助性T细胞谱系(CD4+)。初始病变CD30也为阴性。在其中一例的初始病变和复发病变中检测到相同的T细胞受体基因重排。尽管由于疾病分布异常,这些肿瘤被归类为未特指的外周T细胞淋巴瘤,但两例病例均具有蕈样肉芽肿的组织病理学特征。这些病例极为相似,可能代表一种不寻常的临床病理类型的T细胞淋巴瘤,其自然病程缓慢进展,可累及皮肤和口腔黏膜部位。

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