Department of Pathology, RWJBH/Saint Barnabas Medical Center, Livingston, NJ, USA.
Department of Pathology, RWJBH/Monmouth Medical Center, Long Branch, NJ, USA.
Am J Case Rep. 2021 Dec 22;22:e932904. doi: 10.12659/AJCR.932904.
BACKGROUND Richter transformation (RT) is an uncommon clinicopathological condition referring to the development of aggressive lymphoma from chronic lymphocytic lymphoma/small lymphocytic lymphoma (CLL/SLL) and characterized by sudden clinical deterioration with marked multifocal lymphadenopathy. Transformation of CLL/SLL to diffuse large B-cell lymphoma is the most common (2-9%), but T-cell and Hodgkin transformation (HL) (0.4%) occur, although less frequently. CASE REPORT A 68-year-old woman initially diagnosed with CLL/SLL presented to the hospital with fever, weakness, abdominal pain, and vomiting. The physical examination showed hepatosplenomegaly and extensive abdominal lymphadenopathy on radiological imaging. The laboratory work-up revealed pancytopenia and a markedly increased alkaline phosphatase. In the setting of extensive granulomatous hepatitis, the development of aggressive Hodgkin lymphoma Richter transformation with multi-organ involvement within a few months led to the patient's sudden death. Autopsy findings led to the post-mortem diagnosis of Richter's transformation of CLL. CONCLUSIONS Here, we describe a rare case of Hodgkin lymphoma RT from progressive CLL, with transformation occurring at approximately 12 years after initial diagnosis, despite treatment. Our case report underscores the diagnostic challenges and pitfalls associated with the granulomatous presentation masking RT transformation of CLL to Hodgkin lymphoma. The purpose of this report is to raise suspicion for the clinicopathological signs of Richter transformation in the presence of an atypical granulomatous presentation.
Richter 转化(RT)是一种罕见的临床病理状况,指慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)发展为侵袭性淋巴瘤,其特征是突然出现临床恶化,并伴有明显的多灶性淋巴结病。CLL/SLL 向弥漫性大 B 细胞淋巴瘤的转化最为常见(2-9%),但也会发生 T 细胞和霍奇金淋巴瘤(HL)(0.4%)转化,尽管较少见。
一名 68 岁女性最初被诊断为 CLL/SLL,因发热、乏力、腹痛和呕吐就诊。体格检查显示肝脾肿大和影像学检查广泛的腹部淋巴结病。实验室检查发现全血细胞减少和碱性磷酸酶明显升高。在广泛的肉芽肿性肝炎的背景下,在几个月内迅速发展为侵袭性霍奇金淋巴瘤 RT,累及多个器官,导致患者突然死亡。尸检结果导致死后诊断为 CLL 的 Richter 转化。
在这里,我们描述了一例罕见的进行性 CLL 发生的霍奇金淋巴瘤 RT 病例,尽管进行了治疗,但在初始诊断后约 12 年发生转化。我们的病例报告强调了与肉芽肿表现掩盖 CLL 向霍奇金淋巴瘤 RT 转化相关的诊断挑战和陷阱。本报告的目的是在存在非典型肉芽肿表现的情况下,对 Richter 转化的临床病理特征提高警惕。