慢性淋巴细胞白血病(CLL)患者肝、甲状腺出现Richter综合征的罕见病例报告及文献。

Ewa Wąsik-Szczepanek, Agnieszka Szymczyk, Dariusz Szczepanek, Ewelina Grywalska, Justyna Szumiło, Piotr Trojanowski, Olga Czabak, Marek Hus
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引用次数: 0

摘要

里希特综合征(RS)是一种罕见的并发症,慢性淋巴细胞性白血病(CLL)或小淋巴细胞性淋巴瘤(SLL)转变为更具侵袭性的淋巴瘤-弥漫性大B细胞淋巴瘤(DLBCL)或霍奇金淋巴瘤(HL)。本文报道1例慢性淋巴细胞白血病合并RS诊断的临床病例。腹腔的计算机断层扫描(CT)在肝脏中发现了许多正常密度的区域。同时,甲状腺超声检查(USG)显示一个实性低回声肿块的存在。这两例患者的肝脏和甲状腺闭合活检均诊断为弥漫大B细胞淋巴瘤(DLBCL)。肝脏和甲状腺是特别罕见的RS部位。然而,这些病例表明,RS甚至可能发生在一个非常意外和不太可能发生的部位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare case of Richter's syndrome localization in liver and thyroid of a patient with a chronic lymphocytic leukemia (CLL) - Case report and literature.

Richter's syndrome (RS) is a rare complication in which chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL) transforms into a more aggressive type of lymphoma - diffuse large B cell lymphoma (DLBCL), or Hodgkin's lymphoma (HL). The review describes the clinical case of a patient with CLL and RS diagnosis. A computed tomography (CT) scan of the abdominal cavity detected numerous normodense areas in the liver. Simultaneously, ultrasound examination (USG) of the thyroid revealed the presence of a solid hypoechogenic lump. The material sampled from closed biopsies of liver and thyroid in both cases allowed the diagnosis of diffuse large B cell lymphoma (DLBCL). The liver and the thyroid are particularly rare locations of RS. However, those cases allowed the conclusion that RS may occur even in a very unexpected and less probable location.

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