Penicilliosis: Difference between revisions

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==Overview==


'''Penicilliosis''' is an [[infection]] caused by ''[[Penicillium marneffei]]''. Once considered rare, its occurrence has increased due to [[AIDS]]. It is now the third most common opportunistic infection (after extrapulmonary [[tuberculosis]] and [[cryptococcosis]]) in HIV-positive individuals within the [[Endemic (epidemiology)|endemic]] area of [[Southeast Asia]].
'''Penicilliosis''' is an [[infection]] caused by ''[[Penicillium marneffei]]''. Once considered rare, its occurrence has increased due to [[AIDS]]. It is now the third most common opportunistic infection (after extrapulmonary [[tuberculosis]] and [[cryptococcosis]]) in HIV-positive individuals within the [[Endemic (epidemiology)|endemic]] area of [[Southeast Asia]].

Revision as of 20:22, 10 August 2015

This page is about clinical aspects of the disease.  For microbiologic aspects of the causative organism(s), see Penicillium marneffei.

For patient information click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Penicilliosis is an infection caused by Penicillium marneffei. Once considered rare, its occurrence has increased due to AIDS. It is now the third most common opportunistic infection (after extrapulmonary tuberculosis and cryptococcosis) in HIV-positive individuals within the endemic area of Southeast Asia.

Diagnosis is usually made by identification of the fungi from clinical specimens. Biopsies of skin lesions, lymph nodes, and bone marrow demonstrate the presence of organisms on histopathology.

The most common symptoms are fever, skin lesions, anemia, generalized lymphadenopathy, and hepatomegaly.

Penicillium marneffei demonstrates in vitro susceptibility to multiple antifungal agents including ketoconazole, itraconazole, miconazole, flucytosine, and amphotericin B. Without treatment patients have a poor prognosis.

Treatment

Antimicrobial Regimen

  • 1. Mild disease
  • Preferred regimen: Itraconazole 200 mg PO bid for 8 to 12 weeks without amphotericin B induction therapy[1]
  • Alternative regimen: Voriconazole 400 mg PO bid on day 1 THEN 200 mg PO bid for 12 weeks[2]
  • 2. Moderate-severe disease
  • 3. Maintenance therapy[4]

References

  1. Supparatpinyo K, Chiewchanvit S, Hirunsri P, Baosoung V, Uthammachai C, Chaimongkol B; et al. (1992). "An efficacy study of itraconazole in the treatment of Penicillium marneffei infection". J Med Assoc Thai. 75 (12): 688–91. PMID 1339213.
  2. 2.0 2.1 Supparatpinyo K, Schlamm HT (2007). "Voriconazole as therapy for systemic Penicillium marneffei infections in AIDS patients". Am J Trop Med Hyg. 77 (2): 350–3. PMID 17690411.
  3. Sirisanthana T, Supparatpinyo K (1998). "Epidemiology and management of penicilliosis in human immunodeficiency virus-infected patients". Int J Infect Dis. 3 (1): 48–53. PMID 9831676.
  4. Supparatpinyo K, Perriens J, Nelson KE, Sirisanthana T (1998). "A controlled trial of itraconazole to prevent relapse of Penicillium marneffei infection in patients infected with the human immunodeficiency virus". N Engl J Med. 339 (24): 1739–43. doi:10.1056/NEJM199812103392403. PMID 9845708.



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