Electroconvulsive Therapy of a Depressed Patient with Septo-Optic Dysplasia

A 41-year-old man was born without perinatal injury. He had experienced persistent and obvious ataxia since he began to walk and suffered from insomnia, lack of energy, dysphoric mood, social withdrawal, and low-self-esteem since his early teenage years. He did not look for psychiatric help until he was 30 years old. He received at least three kinds of antidepressants with sufficient dosage and duration, 10 sessions of psychotherapy, as well as a single month-long hospitalization, but with limited effect. He had received a third ventriculostomy for hydrocephalus at the age of 39. Postoperative course was unremarkable despite the persistence of ataxia. He was therefore rehospitalized for ECT treatment. On admission, a mental status examination revealed a depressed man with an intact outer appearance. He experienced sleep disturbances and frequent suicidal ideations. Endocrine tests were within normal ranges. MRI of the head revealed hypogenesis of the corpus callosum, agenesis of the septum pellucidum, decreased volume of hippocampus and amygdala, and increased ventricle volume ( Figure 1 ). Hydrocephalus was not likely, based on negative findings of both CSF jet flow study and neurologic examination. No specific abnormality was found in his eyes. The patient received ECT after giving an informed consent. The MECTA SpECTrum 5000Q delivered the stimulus in a bilateral type. Eight successful ECT treatments were performed with a total motor seizure time of 346 sec. Delirium developed transiently after ECT in the first few sessions but was alleviated after the anesthetic agent pentothol was switched to propofol. His memory was mildly impaired but it gradually subsided in time. Mood status was assessed using the Hamilton Depression Rating Scale (HAM-D) at the pre- and 3-month post-ECT (scores of 22 and 23, respectively) did not show responsiveness to ECT. The only improvement was that his suicidal ideation was eliminated when he was discharged.

We present a case of refractory depression with septo-optic dysplasia who experienced transient delirium and had limited improvement of depressive symptoms in response to ECT. Unlike other septo-optic dysplasia cases, this patient only had depression and ataxia without obvious optic nerve lesions or pituitary-hypothalamic dysfunction. Several studies have found smaller hippocampal volumes in patients with major depression. 3, 4 We suggest that clinicians should incorporate a differential diagnosis of septo-optic dysplasia in refractory depression patients who were associated with neurological symptoms at early development.