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1.
Cerebellum ; 23(4): 1722-1726, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38117450

ABSTRACT

The present case study reported a patient diagnosed with hypertrophic olivary degeneration, a rare condition characterized by a trans-neuronal degeneration and signal enhancement in T2-weighted images on magnetic resonance imaging, usually caused by cerebral hemorrhage, cerebral infarction, and trauma. Furthermore, the relevant literature review was performed. The existing pharmacological treatment has limited clinical benefits on the patient. Since spontaneous remission hardly occurs in the disease, there are no other effective treatments. In this case, the patient was a 55-year-old Chinese male who presented progressive gait difficulty for several months due to both-sided ataxia. Neurological examination revealed upper extremity and lower limb bilateral spasticity, ataxia, slurred speech, and dysmetria. Therefore, our study treated the patient through the inventive application of cerebello-spinal transcranial direct current stimulation and body weight-supported treadmill training. After a 4-week treatment, the patient could walk independently, without aid, speeding up by 7%, as well as the ataxia symptoms, and balance has improved significantly. It was demonstrated in this case report that the combination of cerebello-spinal tDCS and body weight-supported treadmill training can be an effective treatment for patients with Hypertrophic olivary degeneration.


Subject(s)
Hypertrophy , Olivary Nucleus , Transcranial Direct Current Stimulation , Humans , Male , Middle Aged , Olivary Nucleus/pathology , Olivary Nucleus/diagnostic imaging , Transcranial Direct Current Stimulation/methods , Exercise Therapy/methods , Cerebellum/diagnostic imaging , Cerebellum/pathology , Neurodegenerative Diseases/therapy , Olivary Degeneration
3.
Clin Neuropsychol ; 38(1): 235-246, 2024 01.
Article in English | MEDLINE | ID: mdl-37021325

ABSTRACT

Objective: Hypertrophic Olivary Degeneration is a rare condition causing transneuronal degeneration of the inferior olivary nucleus. Symptoms manifest as progressively worsening palatal tremor, ataxia, and eye movement disturbances that plateau after several months. Though rarely documented in the literature of this specific condition, disconnection of the inferior olivary nucleus from the cerebellum, and cerebellar atrophy represent a pathway to developing subsequent cerebellar cognitive affective syndrome. The presented case documents the neuropsychological sequelae of a 39-year-old female with a history of hypertrophic olivary degeneration and symptoms of palatal tremor, opsoclonus myoclonus, ataxia, and delusions. Method: Review of the patient's medical records, interviews with the patient and her father, and a neuropsychological assessment battery were used to collect data. Review of currently published literature lent to case conceptualization. Results: Neuropsychological testing revealed deficits in executive functioning, attention, and language. An anomalous, fixed persecutory delusion was revealed. Conclusion: Hypertrophic olivary degeneration creates disconnection syndromes between the inferior olivary nucleus, red nucleus, and cerebellum. Late stages of the disorder cause atrophy of the inferior olivary nucleus and adjacent structures. While the motor sequela is well documented, the neuropsychological and psychiatric impact is infrequently discussed in existing literature. We present the first case to detail the neuropsychological sequelae of hypertrophic olivary degeneration and propose a mechanism for the development of cognitive impairment and psychotic features within this condition.


Subject(s)
Olivary Degeneration , Tremor , Female , Humans , Adult , Tremor/diagnosis , Tremor/etiology , Tremor/pathology , Olivary Nucleus/pathology , Neuropsychological Tests , Ataxia/complications , Ataxia/pathology , Atrophy/complications , Atrophy/pathology , Cognition , Magnetic Resonance Imaging
4.
Clin Neurol Neurosurg ; 244: 108422, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38991392

ABSTRACT

We presented a case of a 34-year-old male with postoperative brainstem cavernous malformations complicated with LGI1 encephalitis and secondary hypertrophic olivary degeneration (HOD). Due to recurrent dizziness and headache, the patient was diagnosed as brainstem cavernous malformations with recurrent hemorrhage and underwent resection. He subsequently developed unexplained abnormal mental behavior 1 month after the surgery, and diagnosed with LGI1 encephalitis. Six months later, cranial MRI showed HOD. This condition is rare in clinical practice,and a complex mechanism underlies the occurrence.


Subject(s)
Intracellular Signaling Peptides and Proteins , Humans , Male , Adult , Encephalitis/complications , Encephalitis/diagnostic imaging , Olivary Nucleus/pathology , Olivary Nucleus/diagnostic imaging , Proteins , Hemangioma, Cavernous, Central Nervous System/complications , Hemangioma, Cavernous, Central Nervous System/surgery , Hemangioma, Cavernous, Central Nervous System/diagnostic imaging , Postoperative Complications/etiology , Postoperative Complications/diagnostic imaging , Magnetic Resonance Imaging , Brain Stem/diagnostic imaging , Brain Stem/pathology , Hypertrophy , Olivary Degeneration
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