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The most common causes are psychiatric illnesses such as bipolar I disorder and schizoaffective disorder, but mania can also occur secondary to neurological illnesses, brain injury, or neurosurgical procedures.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>For this narrative review, we searched Medline for articles on the association of mania with stroke, brain tumors, traumatic brain injury, multiple sclerosis, neurodegenerative disorders, epilepsy, and neurosurgical interventions. We discuss the epidemiology, features, and treatment of these cases. We also review the anatomy of the lesions, in light of what is known about the neurobiology of bipolar disorder.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>The prevalence of mania in patients with brain lesions varies widely by condition, from &lt;2% in stroke to 31% in basal ganglia calcification. Mania occurs most commonly with lesions affecting frontal, temporal, and subcortical limbic brain areas. Right\u2010sided lesions causing hypo\u2010functionality or disconnection (e.g., stroke; neoplasms) and left\u2010sided excitatory lesions (e.g., epileptogenic foci) are frequently observed.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Secondary mania should be suspected in patients with neurological deficits, histories atypical for classic bipolar disorder, and first manic episodes after the age of 40 years. Treatment with antimanic medications, along with specific treatment for the underlying neurologic condition, is typically required. Typical lesion locations fit with current models of bipolar disorder, which implicate hyperactivity of left\u2010hemisphere reward\u2010processing brain areas and hypoactivity of bilateral prefrontal emotion\u2010modulating regions. Lesion studies complement these models by suggesting that right\u2010hemisphere limbic\u2010brain hypoactivity, or a left\/right imbalance, may be relevant to the pathophysiology of mania.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bdi.12387","type":"journal-article","created":{"date-parts":[[2016,4,26]],"date-time":"2016-04-26T19:17:04Z","timestamp":1461698224000},"page":"205-220","source":"Crossref","is-referenced-by-count":86,"title":["Mania secondary to focal brain lesions: implications for understanding the functional neuroanatomy of bipolar disorder"],"prefix":"10.1111","volume":"18","author":[{"given":"David","family":"Satzer","sequence":"first","affiliation":[{"name":"Medical School University of Minnesota Minneapolis MN USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David J","family":"Bond","sequence":"additional","affiliation":[{"name":"Department of Psychiatry University of Minnesota Minneapolis MN 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