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Medial medullary syndrome
From Wikipedia, the free encyclopedia
Medial medullary syndrome (also known as Dejerine syndrome) is a set of clinical features resulting from an infarction in the brainstem. The vessel usually involved is the anterior spinal artery which supplies the medial part of the medulla oblongata.
The condition usually consists of a weakened tongue on the affected side of the brainstem (due to involvement of the hypoglossal nerve), weakness of the limbs on the contralateral (opposite) side (caused by pyramidal tract damage), and a loss discriminative sensation on the contralateral side (from medial lemniscus involvement).
Sensation of pain and temperature from the body is preserved, as this travels up the spinothalamic tract which is more lateral in this part of the brainstem, and supplied by the vertebral or the posterior inferior cerebellar artery. Sensation on the face is usually intact, as this travels mostly by the trigeminal nucleus; most of this nucleus is higher up in the pons, and the spinal part (responsible for pain sensation) is lateral to the infarct.
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