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截瘫作为既往未诊断的慢性粒细胞白血病髓外巨核细胞转化的首发表现。

Paraplegia as the presenting manifestation of extramedullary megakaryoblastic transformation of previously undiagnosed chronic myelogenous leukemia.

作者信息

Bryant Barbara J, Alperin Jack B, Elghetany M Tarek

机构信息

Department of Pathology, The University of Texas Medical Branch, Galveston, Texas, USA.

出版信息

Am J Hematol. 2007 Feb;82(2):150-4. doi: 10.1002/ajh.20777.

Abstract

Extramedullary tumors, also known as granulocytic sarcomas (GS), occur most frequently in acute myelogenous leukemia (AML). They may signal the onset of the accelerated phase of chronic myelogenous leukemia (CML) or the blastic transformation of a myeloproliferative disorder. Occasionally, a GS may be the presenting sign of undiagnosed AML, and rarely the presenting sign of undiagnosed CML or aleukemic leukemia. Paraplegia due to a spinal cord GS is an extremely rare presentation of undiagnosed leukemia. This is the first case report of paraplegia as the presenting manifestation of extramedullary megakaryoblastic transformation of previously undiagnosed CML. A 53-year-old woman reported back pain for 6 days, rapidly progressing to paraplegia. Physical examination noted a large abdominal mass and flaccid paralysis in both lower extremities. Spinal MRI revealed a T4-T6 vertebral mass causing spinal stenosis and cord compression. Tumor debulking and laminectomy were performed emergently. The tumor consisted of noncohesive blast cells. The CBC revealed a leukocyte count of 238,300/microl and a differential consistent with CML. Reexamination of the patient found that the abdominal mass was a giant spleen. Further immunohistochemical studies of the tumor were consistent with extramedullary acute megakaryoblastic blast transformation of CML. Although extramedullary blast crises herald the accelerated phases in approximately 10% of CML cases, megakaryoblastic blast transformation of CML accounts for less than 3% of these cases. The combination of acute paraplegia and megakaryoblastic transformation in a previously undiagnosed patient with CML is extremely rare and may pose a diagnostic dilemma.

摘要

髓外肿瘤,也称为粒细胞肉瘤(GS),最常发生于急性髓系白血病(AML)。它们可能预示慢性髓系白血病(CML)加速期的开始或骨髓增殖性疾病的原始细胞转化。偶尔,GS可能是未诊断出的AML的首发症状,很少是未诊断出的CML或无白血病性白血病的首发症状。脊髓GS导致的截瘫是未诊断出的白血病极为罕见的表现。这是首例以截瘫为首发表现的既往未诊断出的CML髓外巨核母细胞转化的病例报告。一名53岁女性报告背痛6天,迅速发展为截瘫。体格检查发现腹部有巨大肿块,双下肢弛缓性瘫痪。脊柱MRI显示T4 - T6椎体有肿块,导致椎管狭窄和脊髓受压。紧急进行了肿瘤减瘤和椎板切除术。肿瘤由非黏附性原始细胞组成。血常规显示白细胞计数为238,300/微升,分类结果与CML一致。对患者复查发现腹部肿块是巨大脾脏。对肿瘤进一步进行免疫组化研究,结果与CML的髓外急性巨核母细胞原始细胞转化一致。虽然髓外原始细胞危象在约10%的CML病例中预示加速期,但CML的巨核母细胞原始细胞转化在这些病例中占比不到3%。在既往未诊断出的CML患者中,急性截瘫与巨核母细胞转化同时出现极为罕见,可能会造成诊断困境。

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