Secondary Schizophrenia



Secondary Schizophrenia







“From error to error one discovers the entire truth.”

Sigmund Freud, 1856-1939

Many medical disorders can potentially mimic schizophrenia. For those schizophrenia like psychoses that are the result of medical illness, I follow the suggestion of Spitzer et al. (1992) to abandon the old term, “organic mental disorder,” and use “secondary schizophrenia” instead. The distinction between primary and secondary disorders is familiar to most physicians, and it does not imply that schizophrenia is not brain based (a wrong conclusion fostered by calling it a “functional” disorder). This leaves four possibilities when faced with schizophrenic symptoms: primary schizophrenia; secondary schizophrenia (i.e., symptoms are secondary to a nonpsychiatric medical disorder, either a systemic disorder
that affects the brain or demonstrable neuropathology in the brain); substance-induced psychosis (see previous chapter); and psychiatric disorders with psychotic symptoms (see following chapter). For brevity’s sake, I still occasionally use the adjective “organic” to indicate nonpsychiatric causes.


Johnstone et al. (1987) found organic disease (judged to be etiologically relevant for the psychiatric presentation) in 15 out of 268 (less than 6%) patients with first-episode schizophrenia. Specific conditions identified were syphilis, sarcoidosis, alcohol excess, drug abuse, lung cancer, autoimmune multisystem disease, cerebral cysticercosis, thyroid disease, and previous head injury.




DIAGNOSIS

There is no generally agreed-upon workup that every patient with psychosis must have. Follow these principles to exclude secondary schizophrenia:



  • Order a screening test battery to exclude common and a few selected yet very treatable disorders (Table 5.1).


  • An MRI will provide reassurance that a silent brain tumor (e.g., frontal lobe meningioma) is not missed, although the clinical yield of ordering an MRI will be low (Lubman et al., 2002). Expect to detect the mostly innocuous, incidental MRI abnormalities seen in 20% of the normal population (Katzman et al., 1999).


  • Electroencephalograms (EEGs) can be difficult to interpret since almost half of patients with first-episode schizophrenia will have EEG abnormalities of unclear significance (Manchanda et al., 2005). Moreover, a normal EEG does not exclude medial brain abnormalities and interictal psychosis (schizophrenia like psychosis of epilepsy; see below under Neurologic Conditions).


  • More tests are not necessarily better: Indiscriminate screening for rare disorders is inadvisable because of false-positive and false-negative test results. Order specific tests to rule in or out a disorder you suspect clinically.



  • Order the correct tests; for example, to exclude neurosyphilis, your patient needs to have the highly sensitive serum fluorescent treponemal antibody absorption test (FTA-Abs) and a lumbar puncture (LP), not the commonly ordered rapid plasma reagin (RPR).


  • In poorly responsive psychosis, expand your search to exclude a paraneoplastic syndrome, epilepsy, and sarcoidosis.


  • Expand your search for medical etiologies in atypical presentations (atypical with regard to age or symptoms).








TABLE 5.1. Initial Workup for First-Episode Schizophreniaa













Imaging studiesb




  • MRI to rule out demyelinating disease, brain tumor (e.g., meningioma)


EEGc


Laboratory studies




  • Complete blood count



  • Electrolytes



  • BUN/creatinine



  • Glucose



  • Calcium and phosphorus



  • TSH



  • Liver function tests



  • Erythrocyte sedimentation rate (ESR)



  • Antinuclear antibodies



  • Ceruloplasmin



  • HIV screeningc



  • FTA-Abs for syphilis (RPR not sufficient)



  • Vitamin B12 and folate



  • Urinalysis



  • Urine drug screen


BUN blood urea nitrogen, CXR chest X-ray


aThis list of tests is not exhaustive but represents merely one possible initial workup.

Other tests should be considered if the clinical history and the clinical picture suggest that they might be useful diagnostically (e.g., EEG, CXR, lumbar puncture, karyotype).

b Controversial, as yield is low.

c Recommended as part of routine care for psychotic patients (Branson et al., 2006).

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Sep 12, 2016 | Posted by in PSYCHIATRY | Comments Off on Secondary Schizophrenia

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