- Case report
- Open Access
Attempted infanticide and suicide inaugurating catatonia associated with Hashimoto’s encephalopathy: a case report
BMC Psychiatry volume 16, Article number: 13 (2016)
Catatonia is a neuropsychiatric syndrome with motor and behavioural symptoms. Though usually occuring in patients with schizophrenia and mood disorders, this syndrome may also be associated with neurological diseases or general medical conditions. Few cases of catatonia associated with autoimmune disorders have been described.
Here, we report the case of a 27-year-old woman diagnosed with Hashimoto’s encephalitis (HE) who attempted suicide and infanticide by defenestration. As she presented risk factors for postpartum psychosis, she was treated principally with antipsychotics. Despite adequate treatment for psychosis, symptoms worsened and she developed catatonia. Complementary investigations showed elevated titres of anti-thyroglobulin and anti-thyroperoxidase antibodies (200 and 10 times, respectively, as compared to normal levels) and electroencephalography were suggestive of encephalopathy. In the presence of an otherwise unexplained neuropsychiatric condition, HE was suspected and oral prednisolone was introduced. Psychiatric symptoms improved dramatically within 72 h and the patient was still free of any symptom 3 years later.
Catatonia of organic aetiology should always be considered before a psychiatric aetiology especially in case of clinical worsening in spite of adequate psychotropic treatment. To our knowledge, this is the first description of catatonia associated with HE.
Catatonia is a neuropsychiatric syndrome with motor and behavioural symptoms occurring in approximately 8 % of patients admitted for psychiatric illness such as schizophrenia or mood disorders . Seven to 45 % of catatonias are “organic catatonias” that is, catatonia secondary to a general medical condition [1–4]. Among them, some cases of catatonia associated with autoimmune diseases have been described in systemic lupus erythematosus, anti-NMDAR (N-methyl-d-aspartate receptor) encephalitis [5–8], paraneoplasic syndrome [7, 9, 10], PANDAS (Pediatric Autoimmune Neuropsychiatric Disorder)  and in other rare syndromes like Wilson disease . First line recommended treatementr in catatonia are benzodiazepine and ECT  but, in case of SLE and anti-NMDAR encephalitis in adults, etiological treatment, respectively plasma exchange and immunoglobulin perfusion associated with corticosteroid, is an efficient option avoiding using ECT and psychotropic drugs [14, 15]. Here we present a case highlighting that, as psychiatric symptoms can be prominent in encephalopathy, the presence of catatonia associated with psychotic features can be a misleading presentation for an underlying organic aetiology.
In 2009, a 27-year-old woman was admitted to our psychiatric department. She had been found by emergency response firemen, sitting with her 8-month-old twin babies on the window ledge of her 9th floor apartment tossing personal effects into the air.
The patient had no prior personal or family psychiatric history. She was of Algerian origin and had arrived in France 18 months earlier. Her husband was unemployed, drug-dependent, and was rarely present at home. It had been her first pregnancy, and she had given birth to two girls via caesarean section, due to uterine haemorrhage during the 35th week of amenorrhoea.
Upon admission, an examination found fluctuating psychomotor agitation, anxiety, emotional lability, and impulsivity. The patient had incoherent speech, persecutory delusions, auditory hallucinations, and was disoriented in time and space. According to her family, symptoms had appeared three months earlier and had progressively worsened. She was not known to be taking any medications nor did she suffer from substance abuse. Considering the clinical picture and because of the presence of classical risk factors (first-time mother with multiple births associated with obstetrical complications, recent immigration, father of the children barely present), post-partum psychosis was firstly suspected even though the delayed onset of psychiatric symptoms 5 to 8 months after birth was longer than what is usually admitted for such a diagnosis . As a consequence, oral risperidone 2 mg daily and cyamemazine 30 mg daily were introduced. Forty-eight hours later, symptoms worsened, and the patient presented with permanent auditory hallucinations, psychomotor instability, as well as aggressive behaviour alternating with mutism, negativism, stereotypic gestures and diffuse rigidity with catalepsy. A vesperal aggravation was noted. According to DSM-IV  and DSM-5  criteria, catatonia was diagnosed. Oral lorazepam was introduced and progressively increased until 12.5 mg daily. Because the clinical picture worsened and to avoid an evolution towards malignant catatonia, antipsychotics were stopped and complementary investigations were conducted.
Electroencephalography (EEG) showed a widespread slowing of background activity without sharp-waves, suggestive of encephalopathy. Brain imaging including CT-scan, magnetic resonance imaging (MRI) scan, and single photon emission computed tomography (SPECT-scan) were all normal. The patient was euthyroid but had elevated titres of anti-thyroglobulin (TGAB) and anti-thyroperoxidase (TPOAB) antibodies (200 and 10 times compared to normal, respectively). Cerebrospinal fluid (CSF) examination revealed normal cell count, protein, and glucose levels. CSF cultures were negative and TGAB and TPOAB titres in the CSF were normal. Thyroid echography showed a heterogeneous gland without any sign of inflammation. No other abnormality was found from further testing, including blood tests for regular auto-immune disorders, serological tests for herpes simplex virus, cytomegalovirus, viral hepatitis B and C, human immunodeficiency virus, syphilis, as well as blood sampling for vitamins B 12, PP, and ceruloplasmin.
Hashimoto’s encephalopathy (HE) was suspected given the association of high concentrations of anti-thyroid antibodies and the presence of an otherwise unexplained neuropsychiatric condition. Although medication with risperidone 2 mg daily, cyamemazine 30 mg daily, and eventually lorazepam 12.5 mg daily, was ongoing, no clinical amelioration was observed. Therefore, oral prednisolone was introduced at 60 mg daily. It was quickly followed by a dramatic improvement of the clinical picture; within 72 h, the patient was again oriented in time and space, and auditory hallucinations, as well as catatonia, disappeared. A follow-up EEG returned normal. Corticosteroid treatment was maintained at a dosage of 60 mg daily for a month before being progressively decreased and stopped within a year. In 2013, after three years of follow up, the patient still remained free of any psychiatric symptom.
Here, we describe a case of attempted infanticide and suicide at the onset of catatonia. The literature report increased risk of suicide and infanticide in catatonia especially of psychiatric origin [19, 20]. Due to the predominance of psychiatric symptoms and the presence of multiple risk factors, our initial diagnosis was post-partum psychosis. However, treatment resistance made us suspect a catatonia of organic origin. In catatonia, a causality assessment score (CAUS) has been proposed by Consoli et al. (2012) . This score takes into account the presence of similar cases described in the literature, the presence of clinical, biological and paraclinical symptoms, and the response of the patient to the specific treatment related to the suspected medical condition. When applied to our clinical case, the score is 7/10, clearly favoring an organic origin. HE is very probable in our patient given high titers of anti-thyroid antibodies and the rapid normalization of her clinical symptoms and EEG once prednisolone was introduced [22–27]. It must be noted that neither abnormal brain imaging nor the presence of anti-thyroid antibodies in the CSF are necessarily required for HE diagnosis . Additionally, the thyroid status may vary from normal to pathological among patients with HE [23–25].
Hashimotos’encephalopathy is a rare syndrome, first described by Brain et al. in 1966 . It is suspected whenever symptoms of acute or subacute encephalopathy are associated with high serum levels of anti-thyroid antibodies [18–21]. Because it lacks specific markers and is a clinically heterogeneous syndrome, HE remains an elusive nosologic entity [18–21]. Clinical manifestations include confusion, coma, stroke-like episodes, seizures, psychosis, dementia, myoclonus and myelopathy [22–26]. The pathophysiology of HE remains poorly understood: proposed mechanisms include cerebral vasculitis and neuronal reaction mediated by antibodies . Recent publications suggested that an insufficiency of cerebral blood flow, especially the in left prefrontal cortex and anterior cingulate areas, due to vasculitis causes the neuropsychiatric symptoms in HE, like psychosis, consciousness disturbance  and mood disorders . Besides, the litterature showed a link between depression and antithyroid antibodies regardless of thyroid status, even after adjustment of psycho-social determinants of depression . However, it is still not known whether antibodies in HE may play a direct role in brain dysfunction especially as the level of circulating autoantibodies is not correlated with the severity of clinical manifestations or with response to treatment. Moreover, antithyroid antibodies can be elevated in a significant percentage of the normal population and in other thyroid disorders . Laske et al (2005) reported a case of severe depression associated with HE  and Babtain (2010) reported a case of HE as late onset depression with psychotic features . Both interpretated psychiatric symptoms as resulting from encephalopathy associated with autoimmune thyroid disease. Both of cases rapidly and dramatically improved under prednisolone, just as was seen with our clincial case. Favorable response to corticosteroids and association with other autoimmune diseases in HE point to inflammatory or autoimmune dysfunction [26, 29, 32–34] that may also underlie the pathophysiology of associated psychiatric symptoms such as depression, psychosis and catatonia. It is consistent with the current hypothesis of autoimmune and inflammatory pathophysiology of mood and psychotic disorders [34, 35].
As psychiatric symptoms can be prominent in encephalopathy, they could potentially be misleading and point to catatonia of psychiatric origin. However, an organic aetiology should be always considered, especially in the absence of any mental disorder history. Hashimoto’s encephalopathy is a difficult diagnosis, especially when the thyroid hormonal status is normal. Clinicians should therefore think about dosing thyroid antibodies when confronted with catatonia. More generally, a multidisciplinary diagnosis approach with psychiatrists, internists and neurologists is recommended in any case of catatonia .
Written informed consent was obtained from the patients for publication of their case reports and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
Pommepuy N, Januel D. Catatonia: resurgence of a concept. A review of the international literature. Encéphale. 2002;28:481–92.
Gelenberg AJ. The catatonic syndrome. Lancet. 1976;1:1339–41.
Huang TL, Ree SC, Huang YC, Liu HY, Yang YY. Catatonic features: differential diagnosis and treatments at an emergency unit. Psychiatry Clin Neurosci. 1999;53:63–6.
Carroll BT, Spetie L. Catatonia on the consultation-liaison service: a replication study. Int J Psychiatry Med. 1994;24:329–37.
Brelinski L, Cottencin O, Guardia D, Anguill JD, Queyrel V, Hatron PY. Catatonia and systemic lupus erythematosus: a clinical study of three cases. Gen Hosp Psychiatry. 1999;31:90–2. doi:10.1016/j.genhosppsych.2008.06.010.
Grover S, Parakh P, Sharma A, Rao P, Modi M, Kumar A. Catatonia in systemic lupus erythematosus: a case report and review of literature. Lupus. 2013;22:634–8. doi:10.1177/0961203313486951.
Rosenfeld MR, Dalmau J. Anti-NMDA-Receptor Encephalitis and Other Synaptic Autoimmune Disorders. Curr Treat Options Neurol. 2011;13(3):324–32. doi:10.1007/s11940-011-0116-y.
Mann A, Machado NM, Liu N, Mazin AH, Silver K, Afzal KI. A multidisciplinary approach to the treatment of anti-NMDA-receptor antibody encephalitis: a case and review of the literature. J Neuropsychiatry Clin Neurosci. 2012;24:247–54. doi:10.1176/appi.neuropsych.11070151.
Akil M, Schwartz JA, Dutchak D, Yuzbasiyan-Gurkan V, Brewer GJ. The psychiatric presentations of Wilson’s disease. J Neuropsychiatry Clin Neurosci. 1991;3(4):377–82.
Davis EJ, Borde M. Wilson’s disease and catatonia. Br J Psychiatry. 1993;162:256–9.
Elia J1, Dell ML, Friedman DF, Zimmerman RA, Balamuth N, Ahmed AA, et al. PANDAS with catatonia: a case report. Therapeutic response to lorazepam and plasmapheresis. J Am Acad Child Adolesc Psychiatry. 2005;44(11):1145–50.
Nayak RB, Shetageri VN, Bhogale GS, Patil NM, Chate SS, Chattopadhyay S. Catatonia: a rare presenting symptom of Wilson’s disease. J Neuropsychiatry Clin Neurosci. 2012;24(3):E34–5. doi:10.1176/appi.neuropsych.11070169.
Taylor MA, Fink M. Catatonia in psychiatric classification: a home of its own. Am J Psychiatry. 2003;160:1233–41.
Marra D, Amoura Z, Soussan N, Haroche J, Consoli A, Ghillami-Dalbin P, et al. Plasma exchange in patients with stuporous catatonia and systemic lupus erythematosus. Psychother Psychosom. 2008;77(3):195–6. doi:10.1159/000120280.
Lalanne L, Jantzi C, Gorse A, Zimmermann MA, Danion JM, Foucher J. Melancholia Associated With Severe Cognitive Disorders as the Expression of Late-Onset Postpartum Anti-N-Methyl-d-Aspartic Acid Receptor Limbic Encephalitis. J Neuropsychiatry Clin Neurosci. 2015;27(2):e168–9. doi:10.1176/appi.neuropsych.14040079.
Valdimarsdóttir U, Hultman CM, Harlow B, Cnattingius S, Sparén P. Psychotic illness in first-time mothers with no previous psychiatric hospitalizations: a population-based study. PLoS Med. 2009;6(2), e13. doi:10.1371/journal.pmed.1000013.
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV). Washington, DC: American Psychiatric Association; 1994.
Tandon R, Heckers S, Bustillo J, Barch DM, Gaebel W, Gur RE, et al. Catatonia in DSM-5. Schizophr Res. 2013;150:26–30. doi:10.1016/j.schres.2013.04.034.
Yanagawa Y, Ohshita T, Takemoto M, Matsumoto N, Sakamoto T, Okada Y. A case of catatonia associated with the ingestion of hydroxyzine. No To Shinkei. 2005;57(1):45–9. Review.
Godfroid IO. Violence, desire and death. Reflections on 3 taboos in psychiatry. Encéphale. 2001;27(1):22–7.
Consoli A, Raffin M, Laurent C, Bodeau N, Campion D, Amoura Z, et al. Medical and developmental risk factors of catatonia in children and adolescents: a prospective case-control study. Schizophr Res. 2012;137(1-3):151–8. doi:10.1016/j.schres.2012.02.012.
Chong JY, Rowland LP, Utiger RD. Hashimoto encephalopathy: syndrome or myth? Arch Neurol. 2003;60:164–71.
Chaudhuri A, Behan PO. The clinical spectrum, diagnosis, pathogenesis and treatment of Hashimoto’s encephalopathy (reccurent acute disseminated encephalomyelitis). Curr Med Chem. 2003;10(19):1945–53.
Rodriguez AJ, Jicha GA, Steeves TD, Benarroch EE, Westmoreland BF. EEG changes in a patient with steroid-responsive encephalopathy associated with antibodies to thyroperoxidase (SREAT, Hashimoto’s encephalopathy). J Clin Neurophysiol. 2006;23:371–3.
Ferraci F, Carnevale A. The neurological disorder associated with thyroid autoimmunity. J Neurol. 2006;253:975–84.
Laske C, Leyhe T, Buchkremer G, Wormstall H. Depression in Hashimoto’s encephalopathy. Successful treatment of a severe depressive episode with a glucocorticoid as an add-on therapy. Nervenarzt. 2005;76(5):617–22.
Shaw PJ, Walls TJ, Newman PK, Cleland PG, Cartlidge NE. Hashimoto’s encephalopathy: a steroid-responsive disorder associated with high anti-thyroid antibody titer--report of 5 cases. Neurology. 1991;41:228–33.
Brain L, Jellinek EH, Ball K. Hashimoto’s disease and encephalopathy. Lancet. 1966;2:512–4.
de Holanda NC, de Lima DD, Cavalcanti TB, Lucena CS, Bandeira F. Hashimoto’s encephalopathy: systematic review of the literature and an additional case. J Neuropsychiatry Clin Neurosci. 2011;23(4):384–90. doi:10.1176/appi.neuropsych.23.4.384.
Muramatsu T, Ikawa M, Yoneda M, Sugimoto K, Matsunaga A, Yamamura O, et al. Pathophysiological decrease in the regional cerebral blood flow in Hashimoto’s encephalopathy: a multiple-case SPECT study. Eur Neurol. 2014;72(1-2):13–9. doi:10.1159/000358220.
Bocchetta A, Tamburini G, Cavolina P, Serra A, Loviselli A, Piga M. Affective psychosis, Hashimoto’s thyroiditis, and brain perfusion abnormalities: case report. Clin Pract Epidemiol Mental Health. 2007;3:31. doi:10.1186/1745-0179-3-31.
Rolland F, Chevrollier JP. Depression, anti-thyroid antibodies and Hashimoto encephalopathy. Encéphale. 2001;27(2):137–42.
Babtain FA. Steroid responsive encephalopathy associated with autoimmune thyroiditis presenting with late onset depression. Neurosci (Riyadh). 2010;15(3):196–9.
Fond G, Hamdani N, Kapczinski F, Boukouaci W, Drancourt N, Dargel A, et al. Effectiveness and tolerance of anti-inflammatory drugs’ add-on therapy in major mental disorders: a systematic qualitative review. Acta Psychiatr Scand. 2014;129(3):163–79. doi:10.1111/acps.12211.
Hamdani N, Doukhan R, Kurtlucan O, Tamouza R, Leboyer M. Immunity, inflammation, and bipolar disorder: diagnostic and therapeutic implications. Curr Psychiatry Rep. 2013;15(9):387. doi:10.1007/s11920-013-0387-y. Review.
Lahutte B, Cornic F, Bonnot O, Consoli A, An-Gourfinkel I, Amoura Z, et al. Multidisciplinary approach of organic catatonia in children and adolescents may improve treatment decision making. Prog Neuropsychopharmacol Biol Psychiatry. 2008;32(6):1393–8. doi:10.1016/j.pnpbp.2008.02.015.
Special acknowledgement goes to the Centre Hospitalier Régional Universitaire in Strasbourg for its contribution. We wish to thank sincerely Cecilia Paasche for her proofreading of English.
We have no competing interests. We have no conflict of interest to declare with respect to the manuscript, including no financial, consultant, institutional, political, personal, religious, ideological, academic, intellectual, commercial or other relationships that could lead to any bias or a conflict of interest. We have no financial disclosure to make. We have no financial gain or loss from the publication of the manuscript. We received no support from any pharmaceutical company or other industry.
All the authors were involved in psychiatric care. The article was written by LL, MEM, ER. PV, MAZ and JMD has made substantial contributions to the analysis and interpretation of data and has been involved in revising the article critically for important intellectual content. LL, MEM, ER, PV, MAZ and JMD have given final approval of the version to be published and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
About this article
Cite this article
Lalanne, L., Meriot, ME., Ruppert, E. et al. Attempted infanticide and suicide inaugurating catatonia associated with Hashimoto’s encephalopathy: a case report. BMC Psychiatry 16, 13 (2016). https://0-doi-org.brum.beds.ac.uk/10.1186/s12888-016-0719-7
- Hashimoto’s encephalopathy
- Post-partum auto-immune disease