Chapter 6 - Paracoccidioidomycosis

Abstracts

A paracoccidioidomicose é uma micose sistêmica causada pelo fungo dimórfico Paracoccidioides brasiliensis. A doença é restrita à América Latina. É a principal micose sistêmica no Brasil, com maior frequência nas regiões sul, sudeste e centro-oeste. A doença é adquirida através da inalação de propágulos do fungo. Nas áreas endêmicas, a infecção primária ocorre durante a infância e envolve o sistema imunológico. A forma crônica do adulto mais frequente é de disseminação multifocal, com envolvimento dos pulmões, linfonodos, pele e mucosas. Essa forma tem evolução crônica com diagnóstico tardio. Tosse, dispneia e perda de peso associada a lesões cutâneas e das mucosas são evidentes e constituem as queixas principais da doença. A radiografia simples de tórax apresenta infiltrado reticulonodular difuso mais evidente nos lobos superiores. O diagnóstico etiológico se baseia na achado de P. brasiliensis no exame microscópico direto de espécimes clínicos, tais como aspirado de gânglios ou material de LBA, complementado pelo crescimento do fungo em cultura. O exame histopatológico de amostra de tecidos evidencia a parede espessa e birrefringente do fungo, assim como o aspecto típico de multibrotamento na célula-mãe. A imunodifusão em duplo gel de ágar é muito útil no diagnóstico quando o fungo não é encontrado nos exames micológicos. O tratamento de escolha é realizado com sulfametoxazol e trimetoprima, mas o itraconazol é a melhor droga. A anfotericina B é usada nos casos graves da doença.

Paracoccidioidomicose; Micoses; Pneumopatias fúngicas

CONTINUING EDUCATION COURSE

MYCOSES

Chapter 6 - Paracoccidioidomycosis^*

Bodo Wanke^I; Miguel Abidon Aidê^II

^IPhysician Researcher in the Department of Mycology. Evandro Chagas Hospital Research Center, Fundação Oswaldo Cruz - Fiocruz, Oswaldo Cruz Foundation - Rio de Janeiro, Brazil

^IICoordinator of the Specialization in Pulmonology Course. Universidade Federal Fluminense - UFF, Fluminense Federal University - Niterói, Brazil

Correspondence to

ABSTRACT

Paracoccidioidomycosis is a systemic mycosis caused by the dimorphic fungus Paracoccidioides brasiliensis. The disease is restricted to Latin America. It is the principal systemic mycosis in Brazil, with higher incidences in the southern, southeastern and central regions. The disease is acquired by inhaling fungal propagules. In endemic areas, the primary infection occurs during childhood and involves the immune system. The most common chronic form of paracoccidioidomycosis in adults is the multifocal form, in which there is dissemination to the lungs, lymph nodes, skin and mucosae. This form of the disease has a chronic progression, and the diagnosis is typically delayed. Cough, dyspnea and weight loss due to cutaneous and mucosal lesions are evident and are the principal complaints reported by paracoccidioidomycosis patients. Chest X-rays reveal diffuse reticulonodular infiltrates, which are more evident in the upper lobes. The etiologic diagnosis is based on the identification of P. brasiliensis in clinical specimens, such as lymph node aspirates or BAL fluid, by direct microscopy and culture. Histopathological testing of tissue samples reveals the thick birefringent cell wall of the fungus and the typical pattern of multiple budding around the mother cell. Double agar gel immunodiffusion is useful for the diagnosis when the fungus cannot be detected through mycological tests. Although paracoccidioidomycosis is most often treated with the sulfamethoxazole-trimethoprim combination, itraconazole is preferable. Amphotericin B is used in severe cases.

Keywords: Paracoccidioidomycosis; Mycosis; Lung diseases, fungal.

Introduction

Paracoccidioidomycosis is a systemic mycosis originally described by Adolfo Lutz in 1908. Paracoccidioidomycosis is autochthonous to Latin America, and the highest incidence of the disease was registered in South American countries (Brazil, Argentina, Colombia and Venezuela). In Brazil, most cases have been reported in the southern, southeastern and central-west regions. Paracoccidioidomycosis is endemic among rural area populations and affects male individuals in their economically productive years (30-60 years of age); the disease is related to agricultural activities. The etiologic agent is a thermally dimorphic fungus (Paracoccidioides brasiliensis).^(1,2)

Paracoccidioidomycosis constitutes a serious public health problem because it is quite potentially disabling and causes premature deaths.

Epidemiology

Paracoccidioidomycosis is a disease for which reporting is not compulsory, and there is a lack of precise data regarding its incidence in Brazil.

It is believed that the annual incidence of paracoccidioidomycosis in endemic rural areas ranges from 3-4 new cases/1,000,000 population to 1-3 new cases/100,000 population. Paracoccidioidomycosis is considered to be the third leading cause of death from chronic infectious disease, and the mortality rate for paracoccidioidomycosis is 1.65 cases/1,000,000 population.⁽³⁾

The incidence of paracoccidioidomycosis is higher among males (1:10-15 males) in the 30-50 year age bracket. In individuals younger than 14 years of age, paracoccidioidomycosis affects both genders equally but is, in general, uncommon.⁽⁴⁾

Pathophysiology (natural history of paracoccidioidomycosis)

The disease is acquired through inhalation of the fungus, and younger individuals are the most commonly affected. Infective propagules (microconidia) reach the lower airway, where a primary complex is formed, and the fungus can spread to other organs through lymphohematogenous dissemination, depending on the following: the number of inoculates; the pathogenicity of the fungus; the virulence of the fungus; the immune status of the patient; and possible genetic factors. In immunocompetent individuals, the infection does not progress, and the disease resolves. The fungus remains in those sites, amid fibrotic lesions, in a latent but viable state. After a prolonged period of time, the infection might progress and give rise to the chronic forms in adults (endogenous reactivation). Less commonly, the disease might progress from the primary focus (or even due to re-exposure to inoculates in endemic areas), giving rise to the acute form in children or to the subacute form in adolescents.^(1-3,5)

Classification

According to the 1986 International Colloquium on Paracoccidioidomycosis, cited by the Brazilian Consensus on Paracoccidioidomycosis, paracoccidioidomycosis is classified according to the clinical data and natural history of the disease⁽³⁾:

1) infection

2) disease

3) acute form in children/subacute form in adolescents

4) chronic form in adults: unifocal or multifocal

5) residual form

Clinical forms

Acute/subacute (children/adolescents)

The acute/subacute form of paracoccidioidomycosis is the clinical form of the disease in children, adolescents and adults up to 35 years of age. This form accounts for 3-5% of the cases of paracoccidioidomycosis. The principal manifestations of the disease are as follows: superficial lymph node enlargement; deep lymph node enlargement; digestive symptoms; cutaneous symptoms; and osteoarticular symptoms. Other manifestations include anemia, fever and weight loss, the overall health of children deteriorating rapidly. Pulmonary involvement is rare.⁽³⁾

Chronic unifocal/multifocal form in adults

The chronic unifocal/multifocal form is the most common form of paracoccidioidomycosis, accounting for 90% of the cases; males are predominantly affected. The unifocal form is characterized by a chronic progression, predominantly accompanied by weakness, weight loss, cough, dyspnea, reticulonodular infiltrate (generally in the two upper thirds of the lungs) and distal hypertransparent areas at both lung bases.

The multifocal form is characterized by the involvement of extrapulmonary sites, such as the skin, the oral mucosa (mulberry-like stomatitis), the pharyngeal mucosa or the laryngeal mucosa (or a combination of the two) and the apices of teeth. The symptoms of the multifocal form include pain during mastication, sialorrhea and odynophagia. Wasting is common due to a delay in seeking medical assistance. A chest X-ray reveals the same lesions as those observed in the unifocal form.

Other sites affected by paracoccidioidomycosis include the adrenal glands, the central nervous system, the cervical lymph nodes, the submandibular lymph nodes, the intestines, the osteoarticular system, the epididymis, the liver and the spleen.^(3-5)

Differential diagnosis

The principal differential diagnosis is pulmonary tuberculosis, which is quite similar to paracoccidioidomycosis with regard to the radiological alterations and clinical manifestations (Chart 1). The diagnosis is confirmed by the presence of the fungus (paracoccidioidomycosis) or of Koch's bacillus (tuberculosis) in the specimens analyzed. Tuberculosis and paracoccidioidomycosis can affect the same individual, and this association occurs in 5.5-19% of the cases, which makes the diagnosis of the two diseases more difficult.^(4,6)

Initial investigation

The initial investigation should include the following⁽³⁾:

• history taking focusing on the clinical forms in adults and in children

• chest X-ray

• blood workup

• ESR

• liver function tests

• urea, creatinine, sodium and potassium

Specific investigation

The definitive diagnosis (gold standard) is based on the identification of the fungus in clinical specimens or in tissue biopsy specimens.

The 10% potassium hydroxide test applied to smear samples (on slides coverslipped for direct examination) is a highly effective and inexpensive method of screening for the fungus. This method can be used for various specimens, such as sputum, scrapings (from cutaneous lesions or from mucosae) and lymph node aspirate, as well as for material obtained through fiberoptic bronchoscopy. The Grocott-Gomori methenamine-silver stain technique and the periodic acid-Schiff staining of tissue biopsy specimens are imperative to visualize the fungus. Culture on Sabouraud agar can aid in the diagnosis of paracoccidioidomycosis and therefore should always be ordered, although it does not yield rapid results.^(1-3,5)

In addition to aiding in the diagnosis, serologic tests can evaluate treatment response and disease recurrence. In these cases, elevated antibody titers usually precede clinical recurrence. Agar gel double immunodiffusion is the test that is most readily available in clinical practice, and its sensitivity and specificity are greater than 80% and 90%, respectively. Agar gel double immunodiffusion should always be titrated so that the interpretation of the therapeutic response is more accurate.⁽⁷⁾

Radiological findings

A simple chest X-ray (Figure 1) can reveal asymmetric reticulonodular infiltrate, predominantly in the two upper thirds of both lungs, accompanied by hypertransparent areas at the lung bases.^(1,2,4)

A HRCT scan (Figure 2) can reveal nodules, ground-glass opacities, tree-in-bud pattern, acinar lesions, parenchymal bands, peribronchovascular interstitial thickening, cavities, reticular pattern, "reversed halo" sign, scar-related emphysema and traction bronchiectasis.^(8,9)

Treatment

General considerations

The following points should be observed:

a) Support measures should be adopted in cases of clinical complications.

b) Itraconazole is the best option for mild/moderate forms.

c) The sulfamethoxazole-trimethoprim combination is the alternative that is most widely used in the outpatient treatment of paracoccidioidomycosis.

d) The consumption of cigarettes and alcohol should be limited.

e) Intestinal parasitosis (particularly strongyloidiasis), quite common in paracoccidioidomycosis patients, should be treated.

f) Long-term treatment is required.

g) Patients should be monitored until the criteria for cure are met.

Severe disease

In severe cases, the following can occur⁽¹⁾:

a) reduction of more than 10% in the body mass index

b) difficulty in swallowing

c) respiratory failure: PaO₂/FiO₂ < 250

d) neurological manifestations and central nervous system involvement

e) adrenal gland involvement

Treatment regimens: mild/moderate forms

The following regimens have been used^(1,2,10):

1) sulfamethoxazole-trimethoprim combination, capsules of 80-400 mg and of 160-800 mg

• initial dose: 3 capsules (80-400 mg) every 12 h for 21 days

• 2 capsules every 12 h for 21 days

• 1 capsule every 12 h for 2 years

• Children: 8-10 mg • kg^-1 • day^-1 of trimethoprim or 40-50 mg • kg^-1 • day^-1 of sulfamethoxazole every 12 h

• > 80% of cure

2) Ketoconazole, capsules of 200 mg

• dose: 400 mg/day for 3 months, followed by 200 mg/day for 9 months

• taken with a full meal

• side effects: gynecomastia, decreased libido, liver disease, teratogenesis

3) Itraconazole, capsules of 100 mg

• dose: 200 mg/day at large meals for 6-9 months

• side effects: digestive disorders, teratogenesis

• children < 30 kg of weight or > 5 years of age: 5-10 mg • kg^-1 • day^-1

4) Fluconazole, capsules of 50 mg; 100 mg; 150 mg

• dose: 400 mg/day for 3-6 months

• maintenance: 100 to 200 mg/day for 6-12 months

• children: 3-6 mg • kg^-1 • day^-1

5) Voriconazole⁽¹⁰⁾

• dose: 200 mg every 12 h

• side effects: decreased visual acuity and blurred vision

6) Amphotericin B, 50 mg/bottle

• indication: severe forms; allergy, resistance or intolerance to sulfonamides

• dose: 1 mg • kg^-1 • day^-1; total of 25-35 mg/kg (until 1-2 g)

• maintenance with a sulfonamide for 1-3 years

• side effects: azotemia, ↑↓ potassium, anemia, fever, chills and phlebitis

• other forms of presentation:

• amphotericin B in colloidal dispersion: 1 mg • kg^-1 • day^-1

• liposomal amphotericin B: 3-5 mg • kg^-1 • day^-1

• amphotericin B lipid complex: 5 mg • kg^-1 • day^-1

7) Rifampin (severe, disseminated forms; used in combination with amphotericin B)

• dose: 600 mg/day + amphotericin B, 25 mg • kg^-1 • day^-1, three times a week

Drug interaction between azoles and sulfonamides

The interaction between azoles and sulfonamides increases the concentration of the following drugs: aminophylline; calcium channel blockers; coumarins; hypoglycemic agents; and protease inhibitors.^(3,10)

It should be highlighted that voriconazole cannot be combined with rifampin or with rifabutin.

Sulfonamides decrease the effect of contraceptives and increase methotrexate-induced bone marrow suppression.^(3,10)

Sequelae of paracoccidioidomycosis

The principal sequelae of paracoccidioidomycosis are as follows⁽¹⁰⁾:

• worsening of COPD

• adrenal gland dysfunction (15-50% of the cases)

• dysphonia or laryngeal obstruction, or a combination of the two

• reduced mouth opening

• epilepsy or hydrocephalus, or a combination of the two (6-25% of the cases)

Criteria for cure⁽¹⁰⁾

The criteria for cure are as follows⁽¹⁰⁾:

• clinical, radiological and mycological improvement

• stabilization of agar gel double immunodiffusion results at 1:2 or negative conversion of two samples within a 6-month interval after the treatment

• protein electrophoresis, ESR and mucoproteins showing normal results for 3 consecutive months, as an alternative to agar gel double immunodiffusion

References

• 1. Tarantino AB, Gonçalves AJR, Capone D, Aide MA, Lazera MS, Wanke B. Micoses Pulmonares. In: Tarantino AB, editor. Doenças Pulmonares. Rio de Janeiro: Guanabara Koogan; 2002. p. 416-50.
• 2. Wanke B, Lazer MS, Capone D. Paracoccidioidomicose. In: Sociedade de Pneumologia e Tisiologia do Estado do Rio de Janeiro, Aidé MA, editors. Pneumologia aspectos práticos e atuais. Rio de Janeiro: Revinter; 2001. p. 147-52.
• 3. Shikanai-Yasuda MA, Telles Filho FQ, Mendes RP, Colombo AR, Moretti MA. Consenso de paracoccidioidomicose. Rev Soc Bras Med Trop. 2006;39:297-310.
• 4. Paniago AM, Aguiar JI, Aguiar ES, Cunha RV, Pereira GR, Londero AT, et al. Paracoccidioidomicose: estudo clínico e epidemiológico de 422 casos observados no Estado do Mato Grosso do Sul. Rev Soc Bras Med Trop. 2003;36(4):455-459.
• 5. Londero AT. Paracoccidioidomicose: patogenia, formas clínicas, manifestações pulmonares e diagnóstico. J Pneumol. 1986;(12):41-60.
• 6. Quagliato Júnior R, Grangeia Tde A, Massucio RA, De Capitani EM, Rezende Sde M, Balthazar AB. Association between paracoccidioidomycosis and tuberculosis: reality and misdiagnosis. J Bras Pneumol. 2007;33(3):295-300.
• 7. Valle AC, Costa RL, Monteiro PC. Interpretation and clinical correction of serological test in paracoccidioidomycosis. Medical Mycology. 2001;39:373-7.
• 8. Muniz MAS, Machiori E, Magnago M, Moreira LB, Almeida Jr JG. Paracoccidioidomicose pulmonar: aspectos na tomografia computadorizada de alta resolução. Radiol Bras. 2002;35:147-54.
• 9. Souza AS Jr, Gasparetto EL, Davaus T, Escuissato DL, Marchiori E. High-resolution CT findings of 77 patients with untreated pulmonary paracoccidioidomycosis. AJR Am J Roentgenol. 2006;187(5):1248-52.
• 10. Yasuda MA. Pharmacological management of paracoccidioidomycosis. Expert Opin Pharmacother. 2005;6(3):385-97.

*

Trabalho realizado na Universidade Federal Fluminense - UFF - Niterói (RJ) Brasil.

Publication Dates

• Publication in this collection
  20 Jan 2010
• Date of issue
  Dec 2009

History

• Accepted
  05 Aug 2009
• Received
  05 Aug 2009