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Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

An. Bras. Dermatol. vol.86 no.4 supl.1 Rio de Janeiro July/Aug. 2011

http://dx.doi.org/10.1590/S0365-05962011000700037 

CASE REPORT

 

Erythrodermic psoriasis with regression after prophylaxis with isoniazid and antidepressant therapy - case report*

 

 

Isabella Portela RedighieriI; Tatiana de Carvalho MaiaI Millena Accetta NadalII; Tatiana Romeu Lorenzon CalimanII; Maria de Fátima Maklouf Amorim RuizIII; Valeria PetriIV

ITrainee Physician of the Dermatology Service of the Hospital Ipiranga (HI) - Ipiranga (SP), Brasil
IIDermatologist of the Psoriasis Unit of the Escola Paulista de Medicina of the Universidade Federal de São Paulo (UNIFESP) - São Paulo (SP), Brasil
IIIDermatologist, Tutor at the Psoriasis Unit of the Escola Paulista de Medicina of the Universidade Federal de São Paulo (UNIFESP) - São Paulo (SP), Brasil
IVFull Professor of the Dermatology Department of the Escola Paulista de Medicina - Universidade Federal de São Paulo (UNIFESP) - São Paulo (SP), Brasil

Mailing address

 

 


ABSTRACT

An 83 year old woman, exhibiting severe psoriasis, was treated conventionally (phototherapy, acitretin, and cyclosporine). After poor clinical results and significant changes in laboratory procedures, those treatments were suspended. She was then being prepared to be submitted to biological treatment, when preliminary results disclosed a 30mm PPD. Complete improvement occurred [only] after introducing prophylactic therapy for tuberculosis and anti-depressive medication.

Keywords: Acitretin; Antidepressive agents; Cyclosporine; Isoniazid; Psoriasis; Tuberculosis


 

 

INTRODUCTION

Psoriasis is a chronic immunologic disease, with genetic background and inflammatory changes, which affects the skin, the cutaneous appendages and the joints. It afflicts approximately 2% of the world population and it causes significant psychosocial damage. 1,2 Bacterial infections, medications and emotional stress are among the triggering factors. Patients resistant to the classical treatment can be offered immune biological treatment, which can lead to the control of the process. 3-8 Tuberculosis is an infection that contraindicates the use of immune biological drugs and chemoprophylaxis can work by eliminating the probable triggering agent.

 

CASE REPORT

White female, 83 years old, original from Ururai (SP), living in São Paulo, capital city, presented with disseminated erythematous-desquamative lesions (PASI = 7,2) for 18 months. The histopathological examination was compatible with psoriasis. She underwent phototherapy (PUVA and, afterwards, narrow band UVB, two sessions a week for 18 months), without significant improvement. She was then treated with acitretin (10mg/day), with marked improvement of the disease but with significant alterations of the hepatic enzymes. The drug was discontinued and she was treated with topical emollients and phototherapy (narrow band UVB). There was worsening of the clinical status and rise of the PASI to 14.6 (Figures 1 and 2). Besides, she had a PPD of 16 mm, which prompted a pneumologic evaluation that did not disclose active tuberculosis. Eight months after the laboratory tests normalized treatment with cyclosporine (200mg/day) started and after five months there was an improvement of the PASI (4.8). Recurrence developed slowly with the gradual reduction of the cyclosporine (50mg/week), and the initial dose was reintroduced. The dermatosis was under control for ten months when there was an alteration of the renal function. Biological treatment was indicated and the preconised screening tests revealed a PPD test of 30mm.

 

 

 

 

Active tuberculosis was excluded and prophylaxis with isoniazid, 300mg/day for six months began.1 Simultaneously the patient's depressive status was treated with sertraline (50mg/day). After 90 days of treatment there was a complete regression of the disease (Figures 3 and 4), without recurrence over the subsequent months.

 

 

 

 

DISCUSSION

Psoriasis is a common disease, with a world prevalence of around 2 to 3% and genetic predisposition, ambient aspects (traumas, lifestyle habits, and medications), infections and psychological stress are implicated on the development of the disease.9, 10,11 Treatment is individualized and should be based on the clinical presentation and severity of each case. Elimination of probable causative agents is essential and preliminary when planning the therapeutic options. Because of resistance and intolerance to conventional therapy of psoriasis, the immune biological drugs area an option capable of promoting the control of the disease, the social reinsertion and an improvement on the quality of life of the patients. 12 Tumor necrosis factor-alpha (TNF-alpha) has a central role on the physiopathology of cutaneous and arthropathic psoriasis and, at the same time, it is able to prevent primary infection of tuberculosis, avoid its reactivation and keep the causal agent latent. 13-17 There is sufficient evidence that inhibitors of TNF-alpha are related to increased numbers of active tuberculosis. 18,19 The possibility of reactivation of latent tuberculosis and rigorous screening on endemic areas should be considered.19-24 Besides, tuberculinic turning is observed with treatment with cyclosporine, a drug capable of suppressing immunity and facilitating the reactivation of latent foci or even primary infection. 22

On the present case the previous treatment with cyclosporine might have been responsible for the relative immunosupression capable of reactivating a latent focus or facilitating the development of primary tuberculosis infection. The control of the latent infectious process with chemoprophylaxis thus resulted in an improvement of the severe psoriasis, and the control of the depressive status with medication might have had an additional impact.

 

REFERENCES

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15. Tobin AM, Kirby B. TNF alpha inhibitors in the treatment of psoriasis and psoriatic arthritis. BioDrugs. 2005;19:47-57.         [ Links ] 16. Kircik LH, Del Rosso JQ. Anti-TNF agents for the treatment of psoriasis. J Drugs Dermatol. 2009;8:546-59.         [ Links ]

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24. Arruda LHF, Rodriguez SYSD, Gladys AM. Tratamento sistêmico da psoríase - Parte II: imunomoduladores biológicos. An Bras Dermatol. 2004;79:393-408.         [ Links ]

 

 

Mailing address:
Isabella Portela Redighieri
Instituto da Pele (Escola Paulista de Medicina - Universidade Federal de São Paulo)
Rua Borges Lagoa, 783 - 9º Andar Vila Clementino
04038 901 São Paulo SP, Brazil
E-mail: isabellapr@hotmail.com

Received on 20.10.2010.
Approved by the Advisory Board and accepted for publication on 08.12.2011.
Conflict of interest: None
Financial funding: None

 

 

* Work performed at: Instituto da Pele - Escola Paulista de Medicina - Universidade Federal de São Paulo (UNIFESP) - São Paulo (SP), Brasil.