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Case Reports in Medicine
Volume 2012 (2012), Article ID 128103, 3 pages
Overinfection by Paracoccidioides brasiliensis in Gouty Crystal Arthritis
1Rheumatology Unit, Fundación Valle del Lili, ICESI University, Cali, Colombia
2Infectious Diseases Unit, Fundación Valle del Lili, Cali, Colombia
3Internal Medicine Unit, Fundación Valle del Lili-CES University, Cali, Colombia
4Pathology Unit, Fundación Valle del Lili-ICESI University and Faculty of Health Sciences, Universidad del Valle, Cali, Colombia
5Pathology Unit, Fundación Valle del Lili-ICESI University, Cali, Colombia
6Medical Microbiology and Infectious Diseases Unit, Fundación Valle del Lili-ICESI University and Universidad del Valle, Cali, Colombia
Received 12 August 2012; Accepted 16 October 2012
Academic Editor: Christian Urban
Copyright © 2012 F. Bonilla-Abadía et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Paracoccidioidomycosis is an endemic South American systemic mycosis caused by the dimorphic fungus Paracoccidioides brasiliensis (P. brasiliensis). The main clinical form of disease is pulmonary, but all organs may be involved. We report a case of overinfection by P. brasiliensis in chronic gouty arthritis affecting the proximal phalanx of the right hallux. The patient required proximal amputation and long-term antifungal therapy.
Paracoccidioidomycosis is a systemic mycosis endemic in South America and caused by the dimorphic fungus Paracoccidioides brasiliensis (P. brasiliensis) . The infection occurs by inhalation of environmental airborne or through skin and mucosal lesions. The main clinical form of disease is pulmonary, but all organs may be involved [1, 2]. We report a case of overinfection by P. brasiliensis in chronic gouty arthritis affecting the proximal phalanx of the right hallux, confirmed by culture, histophathological specimen, and serological agar gel immunodiffusion.
2. Case Report
An 82-year-old male was admitted by one-month history of swelling and small pustules that progressed to ulcers with purulent drainage in his right hallux. Medical history includes recurrent gout attacks since 8 years ago, hypertension, diabetes mellitus, hypothyroidism, and chronic kidney failure in medical management, aortic valve replacement, and myocardial revascularization. He lived in Buga, Colombia, and worked in agriculture but had lived in Chiclayo, Peru, for six years; both are endemic areas of P. brasiliensis [3, 4].
At exam, the hallux was edematous with limited range of motion and mild pain, erythema, and two ulcers of 2 cm on the lateral and medial aspect of the foot. The patient was afebrile, and findings on general medical and pulmonary tests were unremarkable. A plain radiograph of the foot revealed a lytic lesion with cortical disruption in the proximal phalanx of the right hallux associated with soft tissue swelling (Figure 1). The chest radiograph was normal. Laboratory studies showed a PCR of 4.47 mg/dL (0–0.5 mg/dL), BUN 42 mg/dL (8–23 mg/dL), serum creatinine of 1.7 mg/dL, TSH level of 6.4 mIU/L, albumin 2.6 g/dL, white blood cell count of 8 × 103/uL with a normal differential, hemoglobin of 11.2 g/dL, hematocrit of 35%, and platelets of 390.000 K/uL. HIV test was negative. Blood and urine cultures were reported as negative. An amputation of the hallux was done. The microbiology laboratory received the sample of drainage right hallux for bacteriological study, to which Gram stain was initially performed and fungal structures were observed like a large, round, fairly thick-walled cells with single and multiple buddings. Direct examination, with KOH 10%, observed unique spherical yeast budding and also observed crystal needle-shaped structures, which observed polarized light filters with characteristic of monosodium urate crystal. At 35°–37°C on liquid medium, was obtained multiple budding “pilot wheel” morphology of P. brasiliensis. Histopathological study and bone cultures for aerobic, anaerobic, and fungal growth were done. The pathology report was consistent with osteomyelitis. Histologic examination revealed multiplebudding cells consistent with P. brasiliensis (Figure 2) and confirmed by isolation of the fungus in cultures and serological complementary diagnosis with agar gel immunodiffusion.
A diagnosis of a secondary infection by P. brasiliensis in a chronic gouty arthritis (right hallux) was made, and therapy with itraconazole was initiated without evidence of adverse effect. The patient’s clinical course was satisfactory.
Paracoccidioidomycosis is a systemic granulomatous disease caused by the dimorphic fungus P. brasiliensis. It is usually found in South America, and it is considered an endemic disease and a public health problem especially in countries as Brazil, Venezuela, Colombia, Ecuador, and Argentina [5, 6]. Paracoccidioidomycosis can be classified in acute/subacute and chronic forms . The acute/subacute form accounts for 3%–5% of all cases and is frequently seen in children and adolescents, without gender differences. It is characterized by a fast progression, lymphadenopathy, gastrointestinal manifestations, hepatosplenomegaly, osteoarticular involvement, and cutaneous lesions. The chronic form is most commonly seen in adults, predominantly in males between the third and sixth decade  and can be unifocal (affecting only the lungs) or multifocal (affecting lungs, mucosa, and skin) [5, 6]. This infection can be successfully treated with oral antifungals like itraconazole, used daily for a long period .
Paracoccidioidomycosis is more common in males, especially in the third and fourth decades of life [8, 9]. P. brasiliensis extends to the lungs by respiratory route and can infect persons exposed to the environment where the fungus survives in the saprophytic form. The host may control the primary infection, but dissemination might occur to other tissues by haematogenous and lymphatic routes.
The osteoarticular involvement in paracoccidioidomycosis can be the first or the only system involved and has a variable prevalence [10, 11]. Bone lesions have a prevalence range in the literature from 2% to 30% [12, 13], and articular and muscular lesions are very uncommon [10, 14]. A recent study of septic arthritis in monoarthritis crystals was published, but there was no evidence of fungal infection within the results .
In the disseminated form of paracoccidioidomycosis, osteoarticular involvement could reach up to 20% of cases , and some reports have found only bone involvement in the acute clinical form [16, 17]. These severe forms of this disease may be complicated to hypercalcemia and hemophagocytic syndromes .
The rates of osteoarticular involvement by P. brasiliensis are completely different between patients with acute and chronic infections, occurring almost exclusively in the acute/subacute clinical form .
The bone lesions studied with conventional radiography have been described as sharply defined osteolytic lesions without marginal sclerosis and without periosteal reaction [13, 15], and any bone can be involved [8, 9, 19].
We report a very uncommon case of septic arthritis by paracoccidioidomycosis on monosodium urate crystal arthritis with a progressive and poor evolution associated with the development of an osteomyelitic lesion, requiring proximal amputation and long-term antifungal therapy. Despite absence of clinical signs and symptoms of lung involvement, a CT scan was not performed and lung disease may not be completely roled out.
Amphotericin was contraindicated in this patient because of potential renal toxicity, and the treatment with itraconazole was closely watched by their possible cardiovascular adverse effects  and negative inotropic action . Therefore, posaconazole could become an important antifungal option.
- Z. P. Camargo, J. L. Gesztesi, E. C. O. Saraiva, C. P. Taborda, A. P. Vicentini, and J. D. Lopes, “Monoclonal antibody capture enzyme immunoassay for detection of Paracoccidioides brasiliensis antibodies in paracoccidioidomycosis,” Journal of Clinical Microbiology, vol. 32, no. 10, pp. 2377–2381, 1994.
- D. Cadavid and A. Restrepo, “Factors associated with Paracoccidiodes brasiliensis infection among permanent residents of three endemic areas in Colombia,” Epidemiology and Infection, vol. 111, no. 1, pp. 121–133, 1993.
- E. C. E. Torrado, F. de la Hoz, and A. Restrepo, “Paracoccidioidomicosis: definición de las áreas endémicas de Colombia,” Biomédica, vol. 20, pp. 327–334, 2000.
- R. Negroni, “Paracoccidioidomycosis (South American blastomycosis, Lutz's mycosis),” International Journal of Dermatology, vol. 32, no. 12, pp. 847–859, 1993.
- M. A. Shikanai-Yasuda, F. D. Q. Telles Filho, R. P. Mendes et al., “Guideliness in paracoccidioidomycosis,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 39, no. 3, pp. 297–310, 2006.
- E. Brummer, L. E. Castaneda, and A. Restrepo, “Paracoccidioidomycosis: an update,” Clinical Microbiology Reviews, vol. 6, no. 2, pp. 89–117, 1993.
- L. C. Severo, A. A. Agostini, and A. T. Londero, “Bone involvement in chronic disseminated paracoccidioidomycosis. A report on the first cases in Rio Grande do Sul,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 29, no. 3, pp. 241–244, 1996.
- M. A. B. Costa, T. N. . Carvalho, C. R. D. A. Júnior, A. O. C. Borba, and G. A. Veloso, “Extra-pulmonary manifestations of paracoccidioidomycosis,” Radiologia Brasileira, vol. 38, pp. 45–52, 2005.
- H. S. Trad, C. S. Trad, J. Elias Jr., and V. F. Muglia, “Radiological review of 173 consecutive cases of paracoccidioidomycosis,” Radiologia Brasileira, vol. 39, no. 3, pp. 175–179, 2006.
- C. H. Ferraz Picado, F. L. Garcia, and C. R. Rodrigues Marcondes, “Late outcome of Paracoccidioides brasiliensis isolated infection on the hip,” Acta Ortopedica Brasileira, vol. 14, no. 2, pp. 97–100, 2006.
- E. Miranda Aires, C. A. Costa Alves, A. V. Ferreira, I. M. Moreira, M. C. SMP, D. Peluso, et al., “Bone Paracoccidioidomycosis in an HIV-positive patient,” The Brazilian Journal of Infectious Diseases, vol. 1, pp. 260–265, 1997.
- A. Kwara, S. Roahen-Harrison, E. Prystowsky et al., “Manifestations and outcome of extra-pulmonary tuberculosis: impact of human immunodeficiency virus co-infection,” International Journal of Tuberculosis and Lung Disease, vol. 9, no. 5, pp. 485–493, 2005.
- E. M. I. Amstalden, R. Xavier, S. V. Kattapuram, M. B. Bertolo, M. N. Swartz, and A. E. Rosenberg, “Paracoccidioidomycosis of bones and joints: a clinical, radiologic, and pathologic study of 9 cases,” Medicine, vol. 75, no. 4, pp. 213–225, 1996.
- M. T. Neves, B. Livani, W. D. Belangero, A. T. Tresoldi, and R. M. Pereira, “Psoas abscesses caused by Paracoccidioides brasiliensis in an adolescent,” Mycopathologia, vol. 167, no. 2, pp. 89–93, 2009.
- L. E. Papanicolas, P. Hakendorf, and D. L. Gordon, “Concomitant septic arthritis in crystal monoarthritis,” The Journal of Rheumatology, vol. 39, pp. 157–160, 2012.
- L. M. Monsignore, R. Martinez, M. N. Simão, S. R. Teixeira, J. Elias, and M. H. Nogueira-Barbosa, “Radiologic findings of osteoarticular infection in paracoccidioidomycosis,” Skeletal Radiology, vol. 41, pp. 203–208, 2012.
- M. T. Silvestre, M. S. Ferreira, A. S. Borges, A. Rocha, G. M. de Souza, and S. A. Nishioka, “Monoarthritis of the knee as an isolated manifestation of paracoccidioidomycosis,” Revista da Sociedade Brasileira de Medicina Tropical, vol. 30, no. 5, pp. 393–395, 1997.
- A. M. Navarro, P. Pérez, A. M. Arrunategui, and C. A. Cañas, “Paracoccidioidomicosis diseminada asociada a hipercalcemia y síndrome hemofagocítico,” Acta Médica Colombiana, vol. 33, pp. 302–304, 2008.
- O. J. Castaneda, G. S. Alarcon, M. T. Garcia, and H. Lumbreras, “Paracoccidioides brasiliensis arthritis. Report of a case and review of the literature,” Journal of Rheumatology, vol. 12, no. 2, pp. 356–358, 1985.
- J. Okamoto, M. Fukunami, and H. Kioka, “Frequent premature ventricular contractions induced by itraconazole,” Circulation Journal, vol. 71, no. 8, pp. 1323–1325, 2007.
- S. R. Ahmad, S. J. Singer, and B. G. Leissa, “Congestive heart failure associated with itraconazole,” Lancet, vol. 357, no. 9270, pp. 1766–1767, 2001.