首页> 美国卫生研究院文献>Case Reports in Hematology >Peripheral T-Cell Lymphoma of the Submandibular Salivary Gland as an Unusual Manifestation of Richters Syndrome: A Case Report and Literature Review
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Peripheral T-Cell Lymphoma of the Submandibular Salivary Gland as an Unusual Manifestation of Richters Syndrome: A Case Report and Literature Review

机译:下颌下唾液腺的外周T细胞淋巴瘤是Richter综合征的异常表现:一例病例并文献复习

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摘要

Richter's syndrome is the development of high-grade non-Hodgkin lymphoma (NHL) or Hodgkin lymphoma in patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). In most patients with Richter's syndrome, the high-grade NHL is diffuse large B-cell lymphoma. Only a small minority of CLL/SLL patients develop T-cell malignancies. Herein, we describe a 40-year-old male patient presenting with peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) in the submandibular salivary gland, two years after the diagnosis of CLL/SLL. The PTCL-NOS consisted of small lymphocytes, which complicated diagnosis. Immunohistochemical, cytological, and molecular studies allowed the correct diagnosis of composite lymphoma (SLL/PTCL-NOS) of the submandibular salivary gland. The PTCL-NOS had a cytotoxic phenotype and aberrant expression of CD79a. There was no evidence to suggest that the PTCL-NOS of the submandibular salivary gland developed from an intimately associated submandibular lymph node or by PTCL-NOS dissemination. A review of the literature and presented case suppose that the PTCLs developed following CLL/SLL have the cytotoxic phenotype and can clinically mimic typical Richter's syndrome.
机译:里氏综合症是慢性淋巴细胞性白血病(CLL)/小淋巴细胞性淋巴瘤(SLL)患者的高级别非霍奇金淋巴瘤(NHL)或霍奇金淋巴瘤的发展。在大多数患有Richter综合征的患者中,高度NHL是弥漫性大B细胞淋巴瘤。只有一小部分CLL / SLL患者发展为T细胞恶性肿瘤。本文中,我们描述了一名40岁的男性患者,在诊断为CLL / SLL两年后,在颌下颌唾液腺中出现了未另作说明的外周T细胞淋巴瘤(PTCL-NOS)。 PTCL-NOS由小淋巴细胞组成,这使诊断变得复杂。免疫组织化学,细胞学和分子学研究可以正确诊断下颌下唾液腺复合淋巴瘤(SLL / PTCL-NOS)。 PTCL-NOS具有细胞毒性表型和CD79a的异常表达。没有证据表明下颌下唾液腺的PTCL-NOS是由紧密相关的下颌下淋巴结或PTCL-NOS扩散形成的。对文献和病例的回顾认为,CLL / SLL后发展的PTCL具有细胞毒性表型,并且可以在临床上模拟典型的Richter综合征。

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