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原发性肾上腺淋巴瘤(primary adrenal lymphoma,PAL)是一种具有高度侵袭性的恶性肿瘤,由于肾上腺内无淋巴组织,因此该病极为罕见。该病的临床表现常缺乏特异性,往往容易被忽视,常由腹部影像学检查意外发现肾上腺占位性病变而发现。本文结合1例原发性双侧肾上腺淋巴瘤病例,并复习相关文献资料,对该病的临床特征、诊断要点及治疗措施进行分析讨论,旨在提高临床对该病的诊治水平。
Primary adrenal lymphoma (PAL) is a highly aggressive malignant tumor that is extremely rare due to the absence of lymphoid tissue in the adrenal glands. The clinical manifestations of the disease often lack specificity, often easily overlooked, often found by abdominal imaging studies found adrenal space-occupying lesions. In this paper, a case of primary bilateral adrenal lymphoma cases, and review the relevant literature, the clinical features of the disease, the diagnosis points and treatment measures were analyzed and discussed in order to improve the clinical diagnosis and treatment of the disease.