Vollmann Henning, Hagemann Georg, Mentzel Hans-Joachim, Witte Otto W, Redecker Christoph
Department of Neurology, Friedrich-Schiller-University, Erlanger Allee 101, 07747 Jena, Germany.
Clin Neurol Neurosurg. 2011 Jun;113(5):430-3. doi: 10.1016/j.clineuro.2011.01.010. Epub 2011 Mar 2.
Here, we demonstrate a first case of tick-borne encephalitis (TBE) associated with an isolated reversible splenial corpus callosum lesion (IRSL) and highlight the wide range of different clinical entities in which such alterations have been observed. A 42-year-old man showed fever, cephalgia and mild disturbance of coordination and gait. Diagnosis was ascertained by slight CSF-pleiocytosis and positive TBE-IgG as well as by positive intrathekal specific antibody index on follow-up. MRI demonstrated a single ovoid hyperintensity in T2 and DWI with reduction in ADC in the splenium of corpus callosum which was abrogated in follow-up after 6 weeks. Most entities of IRSL presented with excellent prognosis, including our novel case of TBE. We discuss different possible pathomechanisms and the so far unexplained propensity of the splenium for such alterations. Clinicians should be familiar with this phenomenon to avoid unnecessary diagnostic or therapeutic efforts.
在此,我们展示了首例与孤立性可逆性胼胝体压部病变(IRSL)相关的蜱传脑炎(TBE)病例,并强调了观察到此类改变的广泛不同临床实体。一名42岁男性出现发热、头痛以及轻度协调和步态障碍。通过轻微的脑脊液淋巴细胞增多和TBE-IgG阳性,以及随访时鞘内特异性抗体指数阳性确诊。MRI显示胼胝体压部在T2和DWI上有单个椭圆形高信号,ADC降低,6周后的随访中该表现消失。大多数IRSL实体预后良好,包括我们的新型TBE病例。我们讨论了不同的可能发病机制以及迄今为止胼胝体压部对此类改变的不明倾向。临床医生应熟悉这一现象,以避免不必要的诊断或治疗措施。