Lee V S, Martinez S, Coleman R E
Department of Radiology, Duke University Medical Center, Durham, NC 27710, USA.
Radiology. 1997 Apr;203(1):237-44. doi: 10.1148/radiology.203.1.9122401.
To assess the clinical and imaging findings in primary muscle lymphoma.
Seven patients with biopsy-proved primary muscle lymphoma without evidence of systemic disease underwent imaging with plain radiography or computed tomography (CT) and magnetic resonance (MR) imaging. Four underwent bone scintigraphy, and two underwent gallium scintigraphy and fluorine-18 fluorodeoxyglucose (FDG) positron emission tomography (PET) before and after therapy.
Plain radiographs at initial examination (n = 5) showed no bone abnormalities. Soft-tissue masses and bone marrow involvement showed isoattenuation at CT (n = 3), but at MR imaging (n = 7), all masses demonstrated increased signal intensity on T2-weighted images that involved multiple muscle compartments and typically spanned a long segment of the extremity. Adjacent bone disease was less extensive than muscle disease, and, in most cases, subcutaneous stranding or extension was observed adjacent to the masses. Good size correlation was observed between findings at MR imaging, gallium scintigraphy, and FDG PET. Two patients developed recurrent multifocal muscle lymphoma several years after initial examination.
The presence of an extensive soft-tissue mass with infiltration of adjacent subcutaneous fat and minimal or no extension into the bone marrow cavity at MR imaging and normal plain radiographic findings may suggest primary muscle lymphoma.
评估原发性肌肉淋巴瘤的临床及影像学表现。
7例经活检证实为原发性肌肉淋巴瘤且无全身疾病证据的患者接受了X线平片、计算机断层扫描(CT)及磁共振成像(MR)检查。4例接受了骨闪烁显像,2例在治疗前后接受了镓闪烁显像及氟-18氟脱氧葡萄糖(FDG)正电子发射断层显像(PET)。
初次检查时的X线平片(n = 5)显示无骨质异常。软组织肿块及骨髓受累在CT上表现为等密度(n = 3),但在MR成像(n = 7)上,所有肿块在T2加权像上均表现为信号强度增加,累及多个肌间隙,通常跨越肢体的较长节段。相邻骨质病变不如肌肉病变广泛,且在大多数情况下,肿块旁可见皮下条索状影或皮下延伸。MR成像、镓闪烁显像及FDG PET的表现之间存在良好的大小相关性。2例患者在初次检查数年后出现复发性多灶性肌肉淋巴瘤。
MR成像显示存在广泛的软组织肿块,伴有相邻皮下脂肪浸润,且极少或无骨髓腔受累,同时X线平片表现正常,可能提示原发性肌肉淋巴瘤。