Chaudhry Ammar A, Gul Maryam, Chaudhry Abbas A, Dunkin Jared
From the *Department of Radiology, Stony Brook University Medical Center, Stony Brook; and †Department of Internal Medicine, Winthrop University Hospital, Mineola, NY.
J Comput Assist Tomogr. 2016 Jan-Feb;40(1):61-6. doi: 10.1097/RCT.0000000000000337.
Myeloid sarcoma is a rare form of extramedullary leukemia, which can present with or without systemic leukemia. The purpose of this study was to evaluate characteristic computed tomography (CT) and magnetic resonance imaging (MRI) findings (including diffusion weighted imaging and susceptibility weighted imaging) of myeloid sarcoma involving the brain.
One hundred nine patients with pathologically proven myeloid sarcoma underwent pretreatment CT and MRI, which were retrospectively reviewed. Computed tomography and MRI characteristics reviewed include lesion location, shape, size, architecture, margins, ± multiplicity, ± bone destruction, pattern and degree of enhancement, ± restricted diffusion, and ± susceptibility artifact.
Twenty-five patients (14 men, 11 women; mean age, 55 years; range, 9-80 years) met the inclusion criteria. Acute myeloid leukemia with subtypes M3 (44.4%) and M5 (22.2%) were the most common. On unenhanced CT, mean lesion size was 1.9 ± 0.4 cm; 60% were intra-axial hyperdense masses, 8% were intraventricular hyperdense masses, 12% were isodense intra-axial masses, and 20% of cases were extra-axial hyperdense nodular masses. There was no observable intralesional or perilesional calcium. On MRI, mean lesion size was 2.1 ± 0.6 cm. The lesions were isointense (80%) or hypointense (20%) on T1-weighted images with homogeneous (88%) or heterogeneous (12%) enhancement. On fluid-attenuated inversion recovery and T2-weighted images, lesions were hyperintense (96%) or isointense (4%) with mild vasogenic edema. Majority (96%) of cases demonstrated restricted diffusion, whereas only a few (16%) demonstrated susceptibility artifact.
In patients with history of leukemia or myeloproliferative disorder, identification of homogenous mass hyperdense on unenhanced CT, T1 isointense, and T2/fluid-attenuated inversion recovery hyperintense with restricted diffusion and homogenous postcontrast enhancement without significant susceptibility artifact is suggestive of myeloid sarcoma.
髓系肉瘤是一种罕见的髓外白血病形式,可伴有或不伴有全身性白血病。本研究的目的是评估累及脑部的髓系肉瘤的特征性计算机断层扫描(CT)和磁共振成像(MRI)表现(包括扩散加权成像和磁敏感加权成像)。
对109例经病理证实的髓系肉瘤患者进行了治疗前的CT和MRI检查,并进行回顾性分析。回顾的CT和MRI特征包括病变位置、形状、大小、结构、边缘、是否多发、是否有骨质破坏、强化方式和程度、是否有扩散受限以及是否有磁敏感伪影。
25例患者(14例男性,11例女性;平均年龄55岁;范围9 - 80岁)符合纳入标准。急性髓系白血病伴M3(44.4%)和M5(22.2%)亚型最为常见。平扫CT上,病变平均大小为1.9±0.4 cm;60%为脑内高密度肿块,8%为脑室内高密度肿块,12%为脑内等密度肿块,20%为脑外高密度结节状肿块。病灶内及病灶周围未见明显钙化。MRI上,病变平均大小为2.1±0.6 cm。在T1加权像上,病变呈等信号(80%)或低信号(20%),强化均匀(88%)或不均匀(12%)。在液体衰减反转恢复序列和T2加权像上,病变呈高信号(96%)或等信号(4%),伴有轻度血管源性水肿。大多数病例(96%)表现为扩散受限,而只有少数(16%)表现为磁敏感伪影。
在有白血病或骨髓增殖性疾病病史的患者中,平扫CT上发现均匀的高密度肿块、T1等信号、T2/液体衰减反转恢复序列高信号伴扩散受限以及均匀的强化后无明显磁敏感伪影提示为髓系肉瘤。