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    DIAGNOSIS CHALLENGES IN A CASE OF

    PSYCHOTIC EPISODE IN CONTEXT OF

    PELLAGRA INDUCED BY ISONIAZID THERAPY

    - A CASE REPORT

    Mihaela A. Petrache1, Elena A. Nica

    1, Georgiana M. Srbu

    1, Bogdana E. Lazr

    1

    Abstract:Pellagra is a nutritional disease caused by niacin (nicotinic acid) deficiency, manifested by the

    classic triad of 3 D: dermatitis, diarrhea and dementia. This can lead to the fourth D: death (1).

    Pellagra may be caused by a series of factors that are affecting the requirement for niacin and

    among those the use of some chemotherapeutic agents, like Isoniazid for the treatment of

    tuberculosis (2). Isoniazid is known to induce adverse effects such as: dizziness, gastro-intestinal

    upset, headaches and occasionally psychosis, hepatitis, skin rash, agranulocytosis, purpura andpellagra (3). We present the case of a man with pulmonary tuberculosis treated with Isoniazid

    and Riphampicine that developed behavioral changes, confusion, insomnia, delusional thoughtsand had skin lesions, all the symptoms suggesting pellagra.

    Key words:niacin, nicotinamide, tuberculosis, mental status.

    Rezumat:Pelagra este o boal carenial datorat deficitului de niacina (acid nicotinic), manifestat

    clinic prin triada celor 3 D: dermatit, diaree, demen. Aceasta poate conduce n final la exitus(1). Pelagra poate fi cauzat de diferii factori care afecteaz necesarul de niacin si dintre

    acestia si medicamentele, ca Izoniazida folosita pentru tratamentul tuberculozei (2). Reaciile

    adverse ale tratamentului cu Izoniazida sunt: ameeli, tulburri gastro-intestinale, cefalee, iocazional psihoz, hepatit, rash, agranulocitoz, purpur i pelagr (3). Prezentm cazul unuibrbat diagnosticat cu tuberculoza pulmonar in tratament cu Izoniazid si Rifampicin, care a

    prezentat tulburri de comportament, confuzie, insomnie, ideaie delirant i de asemenealeziuni tegumentare, tablou clinic sugestiv pentru pelagr.

    Cuvinte cheie: niacin, nicotinamid, tuberculoz, status mental.

    1 Resident doctor of psychiatry, Clinical Hospital of Psychiatry Prof. Dr. Al. Obregia, Bucharest, 8th Psychiatry

    Clinic. Contact: Nica Elena : tel: 0745155226, email: [email protected].

    ReceivedApril 28, 2011,Revised August 22, 2011,AcceptedAugust 31, 2011

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    Isoniazid and a trial of antipsychotic medication. Treatment with pyridoxine and antipsychoticalone, without discontinuation of Isoniazid, may not be effective in all patients.

    4. The suggested mechanism for Isoniazid-associated psychosis involves Isoniazids alteringthe levels of catecholamines and serotonin by inhibiting monoamine oxidase or by inducing

    pyridoxine deficiency, or both (6, 7). Although pyridoxine alone has not been shown to prevent

    INH-induced psychosis, it may be partially protective. 5. Toxic psychosis due to Isoniazid has occasionally been reported in patients with previous

    history of psychiatric disturbances. However cases have been reported even in patientswithout any history of psychiatric symptoms. Prodromal symptoms in the form of anxiety,

    depression, headache, emotional outbursts, sleep disturbances, tremors usually occur

    before an acute psychotic attack. Our patient had some of these prodromal symptoms for

    about a month before he developed frank psychosis. These were somehow ignorated

    thinking to be a depression. So as a conclusion, every patient on Isoniazid, especially with

    a history of previous psychiatric symptoms, should be monitored for appearance of any of

    the prodromal symptoms (6).

    6. Isoniazid should be used with caution in patients with convulsive disorders, a history of

    psychosis, or hepatic or renal impairment. Patients who are at risk of neuropathy orpyridoxine deficiency, including those who are diabetic, alcoholic, malnourished,

    uraemic, pregnant, or infected with HIV, should be given pyridoxine, usually in a dose of10 mg daily, although up to 5,0 mg daily may be used.

    CONCLUSION

    Even it is a disappearing disease, pellagra should be suspected in patients who developmental and neurological symptoms without any evident cause and who have an increased

    necessary requirement for niacin, in or in absence of typical pellagra dermatitis.

    REFERENCES

    1. World Health Organization (WHO). Pellagra. In: Nutrition in preventive medicine. The major deficiencysyndromes, epidemiology and approaches to control. Geneva: WHO Monograph Series 1976; 62:126-135.

    2. Stratigos JD, Katsambas A. Pellagra: a still existing disease.British Journal of Dermatology1977; 96:99-106.3. McConnell RB, Cheetham HD. Acute pellagra during isoniazid therapy.Lancet1952; 2:959-960.

    4. Aspinall. D. L. Multiple deficiency state associated with Isoniazid therapy. Brit med J 1964; 2:1177.

    5. Ishii N, Nishihara Y. Pellagra encephalopathy among tuberculous patients: its relation to isoniazid therapy.

    Journal of Neurology, Neurosurgery and Psychiatry1985; 48:628-634.6. Still CN. Nicotinic acid and nicotinamide deficiency: Pellagra and related disorders of the nervous system. In:

    Vinken PJ, Bruyn GW( eds.). Handbook of Clinical Neurology. Amsterdam: North-Holand, 1975, 59-104.7. Schrestha S,Alao A. Isoniazid-induced psychosis.Psychosomatics 2009; 50:640-641.