Martin-Duverneuil N, Mokhtari K, Behin A, Lafitte F, Hoang-Xuan K, Chiras J
Service de Neuroradiologie Charcot, Bâtiment Babinski, Hôpital de la Salpetrière, 75013 Paris, France.
Neuroradiology. 2002 Sep;44(9):749-54. doi: 10.1007/s00234-002-0808-9. Epub 2002 Aug 10.
Intravascular malignant lymphomatosis is a rare and probably often overlooked disease characterised by massive intravascular proliferation of lymphoid cells, usually with a poor prognosis. CT and MRI appearances are nonspecific; the most suggestive finding being both asymmetrical, bilateral, contrast enhancing high-signal areas on T2 weighting and infarct-like lesions of the cortex and basal ganglia. We report two patients with previously unreported dural and spinal cord involvement.
血管内恶性淋巴瘤是一种罕见且可能常被忽视的疾病,其特征为淋巴样细胞在血管内大量增殖,通常预后较差。CT和MRI表现无特异性;最具提示性的发现是T2加权像上不对称、双侧、强化的高信号区以及皮质和基底节区类似梗死的病变。我们报告了两例先前未报道的硬脑膜和脊髓受累的患者。