Xu Danyi, Xu Guanhua, Xu Liqin, Cao Heng, Xu Bei, Chen Weiqian, Sun Chuanyin, Yue Lihuan, Lin Jin
Department of Rheumatology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China.
Oncol Lett. 2016 Feb;11(2):1143-1145. doi: 10.3892/ol.2015.4026. Epub 2015 Dec 11.
The present study describes the case of an 18-year-old adolescent male exhibiting acute lymphocytic leukemia (ALL), complicated by the onset of the symptom of sacroiliitis mimicking spondyloarthritis. Atypical features including an enlarged spleen, poor effects of non-steroidal anti-inflammatory drug therapy, low levels of hemoglobin, a low platelet count, a low neutrophil count and increased levels of monocytes, indicated the possibility of hematological malignancy. Bone marrow examination confirmed the diagnosis of ALL. The patient received chemotherapy and the symptoms were dramatically relieved. To the best of our knowledge, the current study reports the second published case of a patient with ALL presenting with sacroiliitis. Sacroiliitis as an onset manifestation of ALL may result in misdiagnosis, therefore, a differential diagnosis is essential when atypical features are present.
本研究描述了一名18岁青少年男性的病例,该患者患有急性淋巴细胞白血病(ALL),并伴有类似脊柱关节炎的骶髂炎症状。非典型特征包括脾脏肿大、非甾体抗炎药治疗效果不佳、血红蛋白水平低、血小板计数低、中性粒细胞计数低以及单核细胞水平升高,提示血液系统恶性肿瘤的可能性。骨髓检查确诊为ALL。患者接受了化疗,症状得到显著缓解。据我们所知,本研究报告了第二例已发表的ALL患者出现骶髂炎的病例。骶髂炎作为ALL的首发表现可能导致误诊,因此,当出现非典型特征时,进行鉴别诊断至关重要。