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Optimization of the Longa Middle Cerebral Artery Occlusion Method for Complete Reperfusion
Published on: November 22, 2024
[Conjugate deviation in ischemia of medial medullary oblongata--report of three cases]
Yoshimasa Kinoshita1, Hideoki Yasukouchi, Atsukuni Harada
1Department of Neurosurgery, Munakata Suikokai General Hospital, Fukutsu-shi, Fukuoka, Japan.
Abstract:
Medial medullary infarct (MMI) is a rare type of brain stem infarction. Its clinical picture was characterized by contralateral hemiparesis, deep sensory disturbance, and ipsilateral hypoglossal paresis, but conjugate deviation or nystagmus is uncommon as initial symptom. Case 1: A 73-year-old man developed vomiting and vertigo. Examination revealed right conjugate deviation and horizontal nystagmus beating toward the left side, and numbness on his right upper limb,but no hypoglossal nerve palsy. Cranial MRI demonstrated an infarction in the left paramedian region of the upper medulla and thrombus of the left vertebral artery. Case 2: A 74-year-old man suffered from dizziness and nausea. He showed left conjugate deviation and right-beating horizontal nystagmus without Horner syndrome or hypoglossal nerve palsy. MRI disclosed an infarction in the right upper medial medulla. MRA revealed the right dissecting vertebral artery. Case 3: A 71-year-old man developed vertigo when watching at TV. He showed transient left conjugate deviation and transient motor paresis on the left upper limb. MRI showed the thickened wall of the right vertebral artery but no abnormal ischemic lesion. Digital subtraction angiograms revealed the dissecting right vertebral artery. All ischemic events limited to the upper third of the medulla were caused by the vertebral artery lesions, and prognosis was good. The unilateral MMI lesion in the nucleus prepositus hypoglossi and/or the medullary reticular formation caused contralesional shift of the eyes and ipsilesional nystagmus. The upper MMI will be characterized by a triad of contralateral hemiparesis, deep sensory disturbance and abnormal ocular motor findings.
Insights
Medial medullary infarct (MMI), a rare brain stem stroke, can present with eye movement abnormalities and limb weakness. Early diagnosis of vertebral artery issues is key for good prognosis.
Area of Science:
- Neurology
- Vascular Neurology
- Neuroimaging
Background:
- Medial medullary infarct (MMI) is an uncommon stroke affecting the brainstem.
- Typical MMI symptoms include contralateral hemiparesis, sensory loss, and ipsilateral hypoglossal nerve palsy.
- Ocular motor disturbances like conjugate deviation or nystagmus are less common initial MMI symptoms.
Observation:
- Three cases of medial medullary infarction are presented, all linked to vertebral artery pathologies.
- Patients experienced vertigo, vomiting, dizziness, and abnormal eye movements (conjugate deviation, nystagmus).
- Neurological deficits varied, with some cases lacking typical hypoglossal nerve palsy but showing distinct ocular motor findings.
Findings:
- Cranial MRI and MRA revealed infarcts in the upper medial medulla, associated with vertebral artery thrombosis or dissection.
- Lesions involved the nucleus prepositus hypoglossi and/or medullary reticular formation, explaining the observed ocular motor abnormalities.
- All cases, despite initial atypical presentations, showed good prognosis due to prompt identification and management of vertebral artery disease.
Implications:
- Upper medial medullary infarcts, particularly those involving the vertebral artery, may present with a triad of contralateral hemiparesis, sensory disturbance, and abnormal ocular motor findings.
- Recognizing these specific clinical and imaging features is crucial for accurate diagnosis and timely intervention in MMI.
- This study highlights the importance of evaluating vertebral artery status in patients with suspected medial medullary infarction.
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