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骶管髓系肉瘤作为粒细胞白血病的首发表现:MRI特征及鉴别诊断(附病例报告)

Sacral canal myeloid sarcoma as initial manifestation of granulocytic leukemia: MRI features and differential diagnosis (with a case report).

作者信息

Anqi Xiao, Siqing Huang, Zhenlin Li, Chao You

机构信息

Sichuan University, West China Hospital, Department of Neurosurgery, Chengdu, P. R. China.

出版信息

Turk Neurosurg. 2014;24(2):281-3. doi: 10.5137/1019-5149.JTN.7125-12.1.

Abstract

Myeloid sarcoma initially occurring in the sacral canal is often misdiagnosed as other pathological tumors on MRI due to the lack of a definite history or clinical evidence of granulocytic leukemia. Here, we report a case of 24-year-old male patient with myeloid sarcoma misdiagnosed radiologically. On MRI, sacral myeloid sarcoma is characterized by homogeneous signal intensity, marked enhancement, and the lack of cystic degeneration, calcification and necrosis. Based on our study of this patient and review of the relevant literature, we believe that these MRI features in the sacral region may help us differentiate it from other pathological tumors, which could prompt further clinical examinations to confirm the diagnosis of granulocytic leukemia.

摘要

由于缺乏明确的粒细胞白血病病史或临床证据,最初发生于骶管的髓系肉瘤在磁共振成像(MRI)上常被误诊为其他病理性肿瘤。在此,我们报告一例24岁男性髓系肉瘤患者的影像学误诊病例。在MRI上,骶骨髓系肉瘤的特征为信号强度均匀、强化明显,且无囊性变、钙化及坏死。基于对该患者的研究及相关文献回顾,我们认为骶骨区域的这些MRI特征可能有助于我们将其与其他病理性肿瘤相鉴别,从而促使进一步的临床检查以确诊粒细胞白血病。

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