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Manic Episode after Ventricular-Peritoneal Shunt Replacement in a Patient with Radiation-Induced Hydrocephalus: The Role of Lifetime Subthreshold Bipolar Features

DOI: 10.1155/2014/953728

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Abstract:

We present a case report of a woman hospitalized for a ventricular-peritoneal shunting replacement, who developed a manic episode with psychotic symptoms after hydrocephalus resolution. We have no knowledge of cases of manic episodes due to hydrocephalus resolution by ventricular-peritoneal shunt replacement, although previous case reports have suggested that hydrocephalus might induce rapid-onset affective episodes or mood cycles. The patient’s history revealed the lifetime presence of signs and features belonging to the subthreshold bipolar spectrum, in absence of previous full-blown episodes of a bipolar disorder. Our hypothesis is that such lifetime sub-threshold bipolar features represented precursors of the subsequent full-blown manic episode, triggered by an upregulated binding of striatum D2 receptors after the ventricular-peritoneal shunt replacement. 1. Introduction Neuropsychiatric manifestations, although uncommon, have been described in association with hydrocephalus (a condition caused by obstruction in drainage, decreased absorption or excess production of cerebrospinal fluid). Normal Pressure Hydrocephalus (NPH) may present with its classic progressive triad (abnormal gait, ataxic/apractic dementia and urinary incontinence) [1], as paranoid psychosis [2, 3] or as a mood disorder, such as depressive episodes, manic episodes [4–6], or mood cycling [7, 8]. As far as we know, there is no knowledge of mood episodes with the onset after hydrocephalus resolution. We present the case of a woman hospitalized for a ventricular-peritoneal shunt replacement after a radiation-induced hydrocephalus, who developed a manic episode with psychotic symptoms when hydrocephalus remitted. The patient was treated with antipsychotics and completely recovered. Apparently no previous mood episodes had been manifested in her lifetime history. However, the information collected during hospitalization revealed a lifetime history characterized by several indicators of a bipolar spectrum diathesis. We hypothesized that the ventricular-peritoneal shunting might be associated with an increased dopaminergic tone and that this condition was able to trigger the manic episode in a patient with a lifetime history of subthreshold bipolar manifestations. This hypothesis derived from two recent positron emission tomography studies that found a reduced binding of striatum D2 receptors in normal pressure hydrocephalus [9] and an upregulated binding after the ventricular-peritoneal shunting [10]. Moreover, both studies showed that changes in striatum D2 receptors were correlated

References

[1]  U. Schneider, A. Malmadier, R. Dengler, W.-P. Sollmann, and H. M. Emrich, “Mood cycles associated with normal pressure hydrocephalus,” American Journal of Psychiatry, vol. 153, no. 10, pp. 1366–1367, 1996.
[2]  S. Hakim and R. D. Adams, “The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure. Observations on cerebrospinal fluid hydrodynamics,” Journal of the Neurological Sciences, vol. 2, no. 4, pp. 307–327, 1965.
[3]  U. Lying-Tunell, “Psychotic symptoms in normal-pressure hydrocephalus,” Acta Psychiatrica Scandinavica, vol. 59, no. 4, pp. 415–419, 1979.
[4]  G. Pinner, H. Johnson, W. P. Bouman, and J. Isaacs, “Psychiatric manifestations of normal-pressure hydrocephalus: a short review and unusual case,” International Psychogeriatrics, vol. 9, no. 4, pp. 465–470, 1997.
[5]  J. A. Kwentus and R. P. Hart, “Normal pressure hydrocephalus presenting as mania,” Journal of Nervous and Mental Disease, vol. 175, no. 8, pp. 500–502, 1987.
[6]  A. Yusim, D. Anbarasan, C. Bernstein et al., “Normal pressure hydrocephalus presenting as othello syndrome: case presentation and review of the literature,” American Journal of Psychiatry, vol. 165, no. 9, pp. 1119–1125, 2008.
[7]  C.-Y. Lee and Y.-H. Chou, “Aripiprazole in treating a manic episode associated with hydrocephalus: a case report,” The Primary Care Companion to the Journal of Clinical Psychiatry, vol. 13, no. 1, p. e1, 2011.
[8]  T. Reisch, C. Brekenfeld, and A. Barth, “A case of hydrocephalus occlusus presenting as bipolar disorder,” Acta Psychiatrica Scandinavica, vol. 112, no. 2, pp. 159–162, 2005.
[9]  Y. Ouchi, T. Nakayama, T. Kanno, E. Yoshikawa, T. Shinke, and T. Torizuka, “In vivo presynaptic and postsynaptic striatal dopamine functions in idiopathic normal pressure hydrocephalus,” Journal of Cerebral Blood Flow and Metabolism, vol. 27, no. 4, pp. 803–810, 2007.
[10]  T. Nakayama, Y. Ouchi, E. Yoshikawa, G. Sugihara, T. Torizuka, and K. Tanaka, “Striatal D2 receptor availability after shunting in idiopathic normal pressure hydrocephalus,” The Journal of Nuclear Medicine, vol. 48, no. 12, pp. 1981–1986, 2007.

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