A Case of Late-Onset Bipolar Disorder With Severely Abnormal Behavior and Neuroimaging Observations Very Similar to Those of Frontotemporal Dementia

The patient was a 52-year-old-man. There was no definite family or past history of mental or neurological diseases. At 42 years of age, he began to show depressive symptoms, including depressive mood and psychomotor retardation. At age 46, he gradually began to show hypomanic symptoms, including hyperactivity and hypersexual talk. He appeared stark naked in an orthopedic hospital and was thus admitted to our hospital at age 47. He sometimes stripped himself to the waist and masturbated in front of others. Valproate (800 mg/day) was immediately prescribed, instead of clomipramine (225 mg/day). Thereafter, his abnormal behaviors were gradually ameliorated; however, he became apathetic and had difficulty in doing his daily activities. Medical examinations, including complete blood count, liver, renal and thyroid function tests, and electroencephalography showed no definite abnormalities. Neuroimaging observations (SPECT) showed predominant frontal hypoperfusion, as well as predominant frontal brain atrophy shown by MRI. A Wisconsin Card-Sorting Test also demonstrated frontal lobe hypofunction. He was thus diagnosed with FTD. However, lithium (600 mg/day) was prescribed instead of valproate because of the possible diagnosis of bipolar disorder. Thereafter, his apathetic symptoms were gradually ameliorated, and he was discharged from our hospital about 22 months after the admission. The abnormalities shown by neuroimaging studies described above were ameliorated after the lithium treatment for BP for about 2 years. He has been euthymic for about 4 years, until the present time.

Woolley et al. demonstrated that patients with FTD were more likely to initially present to a psychiatrist than to a neurologist and often receive erroneous psychiatric diagnoses before FTD was correctly diagnosed.^2,3 On the contrary, in the present case, the diagnosis of FTD was temporarily made because of severely abnormal behaviors and neuroimaging observations. To the best of our knowledge, there have been no reports describing late-onset BP preceding the diagnosis of FTD. Ng et al. suggested that the clinician should keep bipolar spectrum disorders in the differential diagnosis of late-onset affective dysregulation in the setting of dementia.⁴ Mendez et al. have demonstrated that consensus criteria and neuropsychological measures lacked sensitivity for FTD and that clinical diagnosis of FTD needs to combine neuropsychiatric features with SPECT or PET findings.⁵ We clinicians should bear the present case in mind and diagnose carefully in the clinical setting of dementia.