Panda Tribikram, Aggarwal Mukul, Mallick Saumyaranjan, Dass Jasmita
Hematology, All India Institute of Medical Sciences, New Delhi, Delhi, India.
Hematology, All India Institute of Medical Sciences, New Delhi, Delhi, India
BMJ Case Rep. 2021 Mar 2;14(3):e238864. doi: 10.1136/bcr-2020-238864.
Classical CRAB features (hypercalcaemia, renal failure, anaemia, osteolytic lesions) have been traditionally defined in patients with plasma cell dyscrasia. But these can be rare and uncommon presentations of other chronic lymphoproliferative disorders (CLPD). The pathophysiological basis of CRAB features in other CLPD need to be explored further for better outcomes and therapeutic interventions. These can present a diagnostic dilemma and requires extensive workup to rule out coexisting malignancy and myeloma. Here, we report an unusual case of B CLPD in a middle-aged male who presented with classical CRAB features along with a brief literature review. After detailed investigations, he was diagnosed as chronic lymphocytic leukaemia, without any second malignancy and responded well to ibrutinib-based therapy.
经典的CRAB特征(高钙血症、肾衰竭、贫血、溶骨性病变)传统上是在浆细胞异常增生症患者中定义的。但这些特征在其他慢性淋巴细胞增殖性疾病(CLPD)中可能是罕见的表现。其他CLPD中CRAB特征的病理生理基础需要进一步探索,以获得更好的治疗效果和治疗干预措施。这些特征可能会带来诊断难题,需要进行广泛的检查以排除并存的恶性肿瘤和骨髓瘤。在此,我们报告一例中年男性B CLPD的罕见病例,该患者具有经典的CRAB特征,并进行简要的文献复习。经过详细检查,他被诊断为慢性淋巴细胞白血病,无任何第二恶性肿瘤,对基于伊布替尼的治疗反应良好。