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Disoriented and forgetful

Current Psychiatry. 2011 December;10(12):59-65
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Ms. P, age 53, was diagnosed with Fabry’s disease 5 years ago and now presents with memory problems, disorientation, and delusions. Is her medical disorder causing these mental status changes?

The authors’ observations

Ms. P presented with an interesting manifestation of neuropsychiatric symptoms in the context of FD; however, common cardiac and cerebrovascular features of the disease were not fully developed. Ms. P experienced progressive cognitive and behavioral changes for 2 years before her admission (Table 2), which may represent a prodromal period leading up to what appeared to be a frontally mediated dementia syndrome. Müller et al15 described a patient with FD who displayed a behavioral profile similar to Ms. P’s that included increasingly unstable mood for at least 3 years, borderline personality disorder features, and rapidly fluctuating mood. A case study reported that risperidone, 1 mg/d, used to treat psychosis in a male FD patient caused extrapyramidal symptoms.16

Ms. P presented with no evidence of stroke or transient ischemic attacks, which is atypical for FD patients with cognitive impairment. However, neuroimaging did reveal frontal atrophy that may be associated with her impulse control deficits, risk-taking behavior, emotional instability, and poor judgment. Her cognitive testing was notable for impairment and exaggeration of symptoms consistent with personality disorder symptoms. Possible reasons for exaggeration include a desire to maintain the sick role or secondary gain related to obtaining disability income.

Ms. P’s behavior pattern could be caused by dementia with frontal features, possibly secondary to FD, in combination with personality and psychiatric pathology.

The mainstay of FD treatment is enzyme replacement therapy (ERT), which addresses the underlying enzyme deficiency. Available research indicates that ERT may reduce symptom severity and slow disease progression; however, further studies are needed to determine if it will reduce outcomes such as stroke, ischemic heart disease, or renal disease.2

Table 2

Symptoms that preceded Ms. P’s admission

Time frameSymptoms
24 months before admissionDepressed mood
Decreased ability to manage independent activities of daily living (eg, finances, cooking)
Minimal objective cognitive impairment
12 months before admissionIncreased depression
Mild to moderate decline in cognitive functioning
Visual and auditory hallucinations
Impulsivity/poor impulse control
Irrational decision-making
Increased risky behavior
6 months before admissionSevere cognitive decline with cognitive symptom exaggeration
Psychiatric symptom exaggeration
Disorganized thinking
Continued risky behavior and poor decision-making

TREATMENT: Persistent deficits

Ms. P is started on risperidone rapidly titrated to 4 mg/d for delusional thinking and behavioral disturbance. After initially improving, she develops delirium when risperidone is increased to 4 mg/d. She has visual hallucinations, marked confusion with disorientation, worsened short-term memory, and an unsteady, shuffling gait. Risperidone is tapered and discontinued and Ms. P’s motor symptoms resolve within 2 days; however, she remains confused and delusional. We start her on quetiapine, 25 mg/d titrated to 50 mg/d, and her agitation and delusional thinking progressively decline. Memantine, titrated to 20 mg/d, and rivastigmine, started at 3 mg/d titrated to 9 mg/d, are added to address her cognitive symptoms.

Over several weeks, Ms. P’s mental status slowly improves and her drug-induced delirium completely resolves. However, she has persistent cognitive impairment characterized by compromised short-term memory and poor insight into her medical and psychological condition. She maintains unrealistic expectations about her ability to live independently and return to the workforce. The treatment team recommends that Ms. P’s daughter pursue guardianship and that she receive around-the-clock supervision after discharge from the hospital.

Table

Ms. P’s neuropsychological assessment results

 JuneNovember
Intellectual functioning
Wechsler Adult Intelligence Scale-III  
  FSIQ60 
  VIQ68 
  PIQ56 
Ravens Colored Progressive Matrices 70
Premorbid intellectual functioning estimates
Peabody Picture Vocabulary Test-2 89
Barona Demographic Estimate104104
North American Adult Reading Test99 
Memory functioning
Wechsler Memory Scale-III  
  Immediate memory45 
  General delay memory47 
  Auditory recognition delay55 
California Verbal Learning Test-II  
  Trial 1 (immediate recall)<60 (raw = 3) 
  Trial 5<60 (raw = 3) 
  Total Words Learned<60 (raw = 15) 
  Short Delay Free Recall<60 (raw = 2) 
  Long Delay Free Recall<60 (raw = 4) 
Executive functioning
Trail Making Test A8888
Trail Making Test Bfailed to understandfailed to understand
Wisconsin Card Sort-64  
  Number of categories<60 (raw = 0) 
  Errors81 
  Percent conceptual level responses74 
  Perseverative responses107 
  Perseverative errors108 
COWAT FAS6569
Category exemplar6980
Motor functioning
Finger Tapping Dominant Hand68 
Finger Tapping Non-Dominant Hand62 
Invalidity/effort
TOMM  
  Trial 1raw = 34raw = 37
  Trial 2raw = 42raw = 45
  Recognitionraw = 44 
MSVT verbal fail
MSVT nonverbal fail
Scores provided are standardized (mean = 100; SD = 15). Raw scores are also provided when indicated.
COWAT: Controlled oral word association test; FSIQ: Full Scale IQ; MSVT: Medical Symptom Validity Test; PIQ: Performance IQ; TOMM: Test of Memory Malingering; VIQ: Verbal IQ

Related Resources

  • National Institute of Neurological Disorders and Stroke. Fabry disease information page. www.ninds.nih.gov/disorders/fabrys/fabrys.htm.
  • National Fabry Disease Foundation. www.thenfdf.org.
  • Rozenfeld P, Neumann PM. Treatment of Fabry disease: current and emerging strategies. Curr Pharm Biotechnol. 2011;12(6):916-922.

Drug Brand Names

  • Donepezil • Aricept
  • Memantine • Namenda
  • Quetiapine • Seroquel
  • Risperidone • Risperdal
  • Rivastigmine • Exelon