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 Table of Contents    
LETTERS TO EDITOR  
Year : 2021  |  Volume : 63  |  Issue : 5  |  Page : 517-519
Chronic psychiatric illness masquerading as bipolar disorder in a family secondary to familial systemic lupus erythematosus with limbic encephalitis


Department of Neurology, Princess Esra Hospital, Deccan College of Medical Sciences, Hyderabad, Telangana, India

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Date of Submission04-Mar-2021
Date of Decision19-May-2021
Date of Acceptance15-Aug-2021
Date of Web Publication12-Oct-2021
 

How to cite this article:
Manorenj S, Shaik RS. Chronic psychiatric illness masquerading as bipolar disorder in a family secondary to familial systemic lupus erythematosus with limbic encephalitis. Indian J Psychiatry 2021;63:517-9

How to cite this URL:
Manorenj S, Shaik RS. Chronic psychiatric illness masquerading as bipolar disorder in a family secondary to familial systemic lupus erythematosus with limbic encephalitis. Indian J Psychiatry [serial online] 2021 [cited 2021 Oct 23];63:517-9. Available from: https://www.indianjpsychiatry.org/text.asp?2021/63/5/517/328102




Systemic lupus erythematosus (SLE) is an autoimmune disease which has an evidence of multifactorial etiopathogenesis. Neuropsychiatric SLE (NPSLE) can have variable presentation ranging from nonspecific vague symptoms like headache to the most devastating CNS manifestations like limbic encephalitis (LE).[1],[2] Limbic encephalitis in SLE, remains poorly understood, with a prevalence ranging between 12% to 95% . Stroke, seizure disorder, acute confusional state, cognitive decline and neuropathies encompass the diverse features in NPSLE. It has been reported that 10% of lupus patients have a first or second degree relative with SLE. Here we describe, chronic psychiatric illness masquerading as bipolar disorder in a family secondary to familial SLE and limbic encephalitis.

A 26-year-old lady presented with insidious onset, progressive behavioral disturbances for 4 years, in the form of excessive irritability, decreased self-care, and inability to communicate and maintain attention and inability to perform all the activities of daily living. She also had episodes of mood elation and depression. She was diagnosed as bipolar disorder with 2 episodes of mania per year. She was on olanzapine 7.5 mg and lamotrigine 100 mg daily. She was bed bound for the previous 2 months. She was brought in an unconscious state.

Examination revealed Glasgow Coma Scale; E3M1V1, and the patient was stuporous. Her blood pressure was 80/60 mmHg, pulse rate was 110/min, temperature of 100 F. Her oral hygiene was poor, she had anasarca, sacral region showed Grade 4 bedsore. She was unable to comprehend verbally, and there was no speech output. Pupils were normal, with bilateral horizontal gaze palsy indicating pontine brain lesion. There were stereotypical movements of perioral region and both upper limbs which were arrhythmic, irregular, involving only distal upper limb in the form of flexion extension of the digits. She remained in an akinetic rigid state with minimal movements of upper limbs. Deep tendon reflexes were brisk and plantar's were extensors. Provisional diagnosis of delirium with septic shock secondary to bedsore on a background of chronic encephalitis was considered. Investigation is shown in [Table 1].
Table 1: Investigation profile of the case study


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MRI brain showed trident sign in pons [Figure 1], temporal atrophy [Figure 2], and claustrum atrophy [Figure 3]. She improved subsequently with care of bedsore and antibiotics. Antiepileptic drugs were initiated for involuntary movements typical of faciobrachial dystonic seizures. Steroids for systemic lupus erythematosus (SLE) encephalitis could not be initiated in view of bedsore positive for methicillin-resistant Staphylococcus aureus. She was discharged in a stable condition with improvement in her movements. On further interview with relatives, it was found that her mother and elder sister had behavioral disturbances and were also on antipsychotic medications. Serological markers asked for these relatives were positive for SLE.
Figure 1: Magnetic resonance imaging brain showing diffusion restriction as seen in diffusion and apparent diffusion coefficient sequence. Lesion in pons is characteristic of trident sign indicating osmotic demyelination in pons

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Figure 2: Magnetic resonance imaging brain flair sequences showing marked temporal atrophy for age as marked with arrow sign

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Figure 3: Magnetic resonance imaging brain flair sequence showing claustral atrophy marked with arrow

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SLE can mimic like limbic encephalitis (LE) thus making the diagnosis even more challenging.[1] It has been reported that 20% of SLE patients develop a chronic mild psychotic disorder.[2] SLE is found to be independently associated with bipolar disorder.[3] Familial SLE has been described and it indicates a basis of genetic influences in its pathophysiology.[4] It has been observed that familial SLE had a female preponderance, a concordance in the age of presentation and clinical features was observed and a role for HLA DR2 was found.[4] Pontine lesion in MRI brain in our case was consistent with osmotic demyelination secondary to sepsis and hypotension while claustral and temporal atrophy clued to chronic limbic involvement of brain due to SLE. As most of the autoimmune diseases are amenable to treatment, hence early recognition remains the key.

This case throws light on the following aspects. SLE can masquerade as LE with bipolar disorder features. Misdiagnosis of neuropsychiatric systemic lupus erythematosus (NPSLE) can have catastrophic adverse events and inappropriate management. NPSLE can have a familial presentation. There is a need for the evaluation of reversible and systemic causes of psychiatric presentations.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the legal guardian has given his consent for images and other clinical information to be reported in the journal. The guardian understands that names and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Angst DB, de Figueiredo NS, Passarelli V, Baldocchi MA, Rocha MS, Brucki SM. Autoimmune limbic encephalitis: A manifestation of systemic lupus erythematosus in the central nervous system. Dement Neuropsychol 2015;9:189-95.  Back to cited text no. 1
    
2.
Bertsias GK, Ioannidis JP, Aringer M, Bollen E, Bombardieri S, Bruce IN, et al. EULAR recommendations for the management of systemic lupus erythematosus with neuropsychiatric manifestations: Report of a task force of the EULAR standing committee for clinical affairs. Ann Rheum Dis 2010;69:2074-82.  Back to cited text no. 2
    
3.
Tiosano S, Nir Z, Gendelman O, Comaneshter D, Amital H, Cohen AD, et al. The association between systemic lupus erythematosus and bipolar disorder - A big data analysis. Eur Psychiatry 2017;43:116-9.  Back to cited text no. 3
    
4.
Eroglu GE, Kohler PF. Familial systemic lupus erythematosus: The role of genetic and environmental factors. Ann Rheum Dis 2002;61:29-31.  Back to cited text no. 4
    

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Correspondence Address:
Sandhya Manorenj
Department of Neurology, Princess Esra Hospital, Deccan College of Medical Sciences, Hyderabad, Telangana
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/indianjpsychiatry.indianjpsychiatry_178_21

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    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
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