Webb-Detiege Tamika, Sasken Harvey, Kaur Primal
Division of Rheumatology, Department of Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
J Clin Rheumatol. 2009 Feb;15(1):25-6. doi: 10.1097/RHU.0b013e31817d1197.
Multicentric reticulohistiocytosis (MRH) is a rare multisystem disease characterized by skin nodules and a destructive polyarthritis. We describe cardiac disease in a 42-year-old African American female with a history of MRH for 29 years and dilated cardiomyopathy for 5 years. During a congestive heart failure flare, the patient was slow to respond to standard treatment. A left/right heart catheterization and endomyocardial biopsy were performed, and the patient was found to have evidence of myocardial MRH infiltration.
多中心网状组织细胞增多症(MRH)是一种罕见的多系统疾病,其特征为皮肤结节和破坏性多关节炎。我们描述了一名42岁非裔美国女性的心脏疾病,该患者有29年的MRH病史和5年的扩张型心肌病病史。在充血性心力衰竭发作期间,患者对标准治疗反应迟缓。进行了左右心导管检查和心内膜心肌活检,发现该患者有心肌MRH浸润的证据。