Erithrophagocytic lymphohistiocytosis - Neuroradiologic findings

被引:1
作者
Caranci, F
D'Amico, A
Briganti, F
Migliorati, R
De Fusco, C
Poggi, V
Cirillo, S
Elefante, R
机构
[1] Univ Naples Federico II, Fac Med & Chirurg, Serv Neuroradiol, Dipartimento Sci Neurol, I-80132 Naples, Italy
[2] Azienda Osped Rilievo Nazl Santobono Pausilipon, Dipartimento Oncol Pediat, Naples, Italy
[3] Univ Naples 2, Fac Med & Chirurg, Serv Neuroradiol, Naples, Italy
来源
RIVISTA DI NEURORADIOLOGIA | 2003年 / 16卷 / 03期
关键词
lymphohistiocytosis; hemophagocytic syndrome;
D O I
10.1177/197140090301600307
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Erithrophagocytic lymphohistiocytosis is a rare disease characterized by exaggerated histiocytic proliferation and activation(12) and multisystem involvement including visceral organs, lymph nodes, bone marrow and central nervous system(4). Magnetic Resonance (MR) examination was performed in 10 patients with previously diagnosed Erithrophagocytic lymphohistiocytosis. This study was aimed at assessing MR accuracy in the identification and characterization of central nervous system lesions. MR findings show a good correlation with areas of parenchymal and meningeal lymphohistiocytic infiltration 5, demonstrating diffuse white matter abnormalities in the early stages and necrotic areas with parenchymal volume loss as terminal findings'. In addition, MR allows the follow-up after chemotherapy and bone marrow transplantation(2.3). Although rare, EL should be differentiated from other pediatric patchy white matter abnormalities(5).
引用
收藏
页码:365 / 372
页数:8
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