表现为皮下结节和皮肤斑块的里克特综合征

Melissa Nickles, Samantha Hunt, Saul Turcios-Escobar, Amaara Babwah, Nisreen Mobayed, Carlos Murga-Zamalloa, Michelle Bain, John Quigley, Paul Rubinstein, Carlos Galvez
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引用次数: 0

摘要

里克特综合征(RS)描述了一种慢性淋巴细胞白血病(CLL)患者罹患侵袭性淋巴瘤(最常见的是弥漫性大 B 细胞淋巴瘤(DLBCL))的现象。皮肤 RS 的报告仍然极为罕见。我们报告了一名 61 岁的复发性/难治性 CLL 女性患者,她的手臂和腿部出现多个皮下结节,腹部有一个真皮斑块。皮肤活检显示她被诊断为 ABC 型 DLBCL,确诊后她的临床状况迅速恶化。我们回顾了皮肤 RS 的各种临床表现、其与 CLL 的关联、CLL 患者发生 RS 的风险因素以及 DLBCL 独特的组织病理学和免疫表型特征。我们希望强调对出现进行性皮肤病变的 CLL 患者及时进行皮肤活检的重要性,并提高人们对这种侵袭性临床综合征的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Richter Syndrome Presenting as Subcutaneous Nodules and a Dermal Plaque.
Richter syndrome (RS) describes a phenomenon in which a patient with chronic lymphocytic leukemia (CLL) develops an aggressive lymphoma, most commonly diffuse large B-cell lymphoma (DLBCL). Reports of cutaneous RS remain exceedingly rare. We report a 61-year-old woman with relapsed/refractory CLL presenting with several subcutaneous nodules on her arms and legs and a single dermal plaque on her abdomen. Skin biopsy revealed a diagnosis of DLBCL, ABC-type, and her clinical status rapidly deteriorated following diagnosis. We review the variety of clinical presentations of cutaneous RS, its association with CLL, risk factors for RS development in CLL patients, and the distinctive histopathologic and immunophenotypic features of DLBCL. We hope to highlight the importance of prompt skin biopsy in patients with CLL presenting with progressive skin lesions and increase awareness of this aggressive clinical syndrome.
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