Periampullary Mass as an Unusual Manifestation of Coccidioidomycosis. Case Report and Literature Review

In Colombia, coccidioidomycosis is a rare entity, and the intestinal manifestation is infrequent, with around a dozen cases reported in the world literature. This article reports the case of a 29-year-old male Venezuelan immigrant with a 4-month history of abdominal pain, jaundice, nausea, and vomiting. The tomography and the endoscopic study revealed a circumferential exophytic mass in the second portion of the duodenum. The biopsy revealed multiple spherules filled with round fungal endospores with a final diagnosis of disseminated coccidioidomycosis. The patient was discharged before the final pathology report with fluconazole doses of 200 mg every other day and an order for outpatient magnetic resonance cholangiography for outpatient follow-up, which he has not attended.

La coccidioidomicosis en Colombia es una entidad infrecuente y la presentación intestinal es extremadamente rara, con alrededor de una docena de casos reportados en la literatura mundial. En el presente artículo se reporta el caso de un paciente inmigrante venezolano masculino de 29 años con historia de dolor abdominal, ictericia, náuseas y vómito de 4 meses de evolución. La tomografía y el estudio endoscópico evidenciaron una masa exofítica circunferencial en la segunda porción del duodeno. La biopsia reveló múltiples esférulas llenas de endosporas fúngicas redondas con diagnóstico final de coccidioidomicosis diseminada. El paciente fue dado de alta antes del reporte final anatomopatológico con dosis de fluconazol de 200 mg interdiario y orden de colangiorresonancia ambulatoria para control ambulatorio, mismo al cual no ha asistido.

Antifungal activity of liriodenine on agents of systemic mycoses, with emphasis on the genus Paracoccidioides

Endemic systemic mycoses remain a health challenge, since these opportunistic diseases are increasingly infecting immunosuppressed patients. The simultaneous use of antifungal compounds and other drugs to treat infectious or non-infectious diseases has led to several interactions and undesirable effects. Thus, new antifungal compounds should be investigated. The present study aimed to evaluate the activity of liriodenine extracted from Annona macroprophyllata on agents of systemic mycoses, with emphasis on the genus Paracoccidioides. Methods: The minimum inhibitory concentration (MIC) and minimum fungicide concentration (MFC) were determined by the microdilution method. The cellular alterations caused by liriodenine on a standard P. brasiliensis (Pb18) strain were evaluated by transmission and scanning electron microscopy. Results: Liriodenine was effective only in 3 of the 8 strains of the genus Paracoccidioides and in the Histoplasma capsulatum strain, in a very low concentration (MIC of 1.95 µg.mL-1); on yeasts of Candida spp. (MIC of 125 to 250 µg.mL-1), including C. krusei (250 µg.mL-1), which has intrinsic resistance to fluconazole; and in Cryptococcus neoformans and Cryptococcus gattii (MIC of 62.5 µg.mL-1). However, liriodenine was not effective against Aspergillus fumigatus at the studied concentrations. Liriodenine exhibited fungicidal activity against all standard strains and clinical isolates that showed to be susceptible by in vitro tests. Electron microscopy revealed cytoplasmic alterations and damage to the cell wall of P. brasiliensis (Pb18). Conclusion: Our results indicate that liriodenine is a promising fungicidal compound that should undergo further investigation with some chemical modifications.(AU)

Paracoccidioidomicosis: características clínicas de 94 casos / Paracoccidioidomycosis: Clinical Characteristics of 94 Cases

Paraguay es considerado una zona afectada por esta micosis endémica en gran parte de Sudamérica. No existe trabajo analítico en nuestro país que evalúe las formas de presentación y los desenlaces de la forma crónica de la paracoccidioidomicosis. Objetivo: Descripción de las características clínicas de casos de paracoccidioidomicosis con compromiso pulmonar. Material y métodos: Estudio observacional descriptivo de fichas clínicas de pacientes con diagnóstico de paracoccidioidomicosis internados en el INERAM durante el período de enero 1980-diciembre 2003. El análisis estadístico consistió en un análisis bivariado (X2 y ANOVA), considerando significativa una p < 0,05. Resultados: Se identificaron 94 casos diagnosticados durante el periodo de estudio. La edad de presentación fue de 49±11 años y un notorio bajo índice de masa corporal promedio (16,6) sumado a la alta prevalencia de tabaquismo (77%) caracterizaron a la serie. A pesar de la preponderancia de síntomas respiratorios, se consignaron además lesiones mucosas en 33% y adenopatías cervicales en 19% de los registros médicos. Se describen hallazgos en la analítica sanguínea y en los análisis radiográficos asentados. El análisis de las variables entre el grupo de los fallecidos y de los sobrevivientes mostró una diferencia significativa en la frecuencia respiratoria y en la distribución radiográfica de las lesiones al momento de la internación. Utilizando imidazólicos en 97% de los casos, la mejoría sintomática fue constatada a las 1.6 semanas en promedio, aunque se ha registrado una mortalidad intrahospitalaria del 11.7%. Los pacientes quedaban internados durante 63±58 días para poder recibir tratamiento, pero una vez en condiciones ambulatoriales, el 88% discontinuaba los fármacos. Conclusión: Pese a los síntomas inespecíficos, se debería considerar el diagnóstico de esta micosis en cuadros respiratorios subagudos o crónicos concomitantes a lesiones mucosas y/o adenopatías. Urgen medidas generales que puedan paliar la alta tasa de abandono terapéutico.

Paraguay is an endemic country for paracoccidiomycosis. There is no analytical work in our country evaluating the clinical presentation and the outcomes of the chronic form of paracoccidioidomycosis. Objective: To describe the clinical characteristics of paracoccidioidomycosis cases with pulmonary involvement. Material and Methods: Observational study of clinical records of patients admitted with a diagnosis of paracoccidioidomycosis during the period of January 1980 - December 2003 in INERAM, a reference medical center. Statistical analysis consisted of a bivariate analysis (X2 and ANOVA), considering significant a p < 0.05. Results: 94 cases diagnosed during the study period were identified. The mean age of presentation was 49 ± 11 years old. The patients had notorious low average body mass index (16.6) and a high prevalence of smoking habit (77%). Respiratory symptoms, mucosal lesions (33%) and cervical lymphadenopathy (19%) were noted. Blood testing and radiographic results are described. The analysis of the variables between the group who died and the survival group showed significant difference in the respiratory rate and the radiographic images at admission. Most patients (97%) were treated with imidazole antifungal drugs; clinical improvement was observed after on average 1.6 weeks of treatment. Lethality among hospitalized patients was 11.7%. Patients were hospitalized for 63 ± 58 days, in order to receive treatment but once at home, 88% discontinued the drugs . Conclusion: Despite the nonspecific symptoms, diagnosis should be suspected in patients with subacute or chronic respiratory symptoms which are concomitant with mucosal lesions and lymphadenopathy. General measures should be taken to decrease the high rate of treatment default at home.

Paracoccidioidomycosis in southern Rio Grande do Sul: a retrospective study of histopathologically diagnosed cases

Paracoccidioidomycosis (PCM) is a systemic mycosis caused by the fungus Paracoccidioides brasiliensis and is endemic to Brazil. The aim of this study was to perform a retrospective analysis of the PCM cases in the countryside south of Rio Grande do Sul, Brazil. The files from four histopathology laboratories located in the city of Pelotas were obtained, and all of the epidemiological and clinical data from the PCM diagnosed cases were collected for analysis. A total of 123 PCM cases diagnosed between 1966 and 2009 were selected. Of these patients, 104 (84.5%) were male, and 17 were female. The patients ranged from 02 to 92 years of age. Fifty-two cases (41.9%) were obtained from the oral pathology laboratory, and the remaining 71 cases (58.1%) were obtained from the three general pathology laboratories. Of all of the patients studied, 65.2% lived in rural zones and worked in agriculture or other related fields. Data on the evolution of this disease was available for 43 cases, and the time frame ranged from 20 to 2920 days (mean = 572.3 days). An accurate diagnosis performed in less than 30 days only occurred in 21% of the cases. PCM is endemic to the countryside of Rio Grande do Sul. Therefore, it is recommended that PCM be included as a differential diagnosis, mainly for individuals between 30 and 60 years of age, living in rural zones and who have respiratory signs and associated-oropharyngeal lesions.

Estudio de casos de paracoccidioidomicosis infantil diagnosticados en el área de la Gran Caracas Venezuela / Study paracoccidioidomycosis diagnosed cases of childhood in the area of Greater Caracas Venezuela

La paracoccidioidomicosis pocas veces afecta niños y no es de denuncia obligatoria. Su verdadero impacto en la población infantil es desconocido. El objetivo fue determinar en número de casos de paracoccidioidomicosis infantil diagnosticados en centros de salud de la Gran Caracas, en niños con edades entre 0-15 años. Se evaluaron historias de niños con paracoccidioidomicosis, provenientes de hospitales de la Gran Caracas. Se revisaron 420 historias con diagnóstico de paracoccidioidomicosis, de las cuales 33 (7,9%) fueron niños menores de 15 años, siendo la media de edad 7,97 años. El género masculino predominó (69,7%), la razón masculino-femenino fue 1,5:1 en niños con edades de 0-7 años y 5,5:1 entre 8-15 años. La mayoría procedían del estado Miranda, 11 (35,5%) seguido del Distrito Capital 9 (29,1%). En 26 casos se clasificó la enfermedad, encontrando que 24 (92,3%) desarrollaron la forma aguda. Las principales manifestaciones clínicas precisadas en 25 historias fueron: fiebre 18 (72%) adenomegalias 16 (64%), hepatomegalia 12 (48,0%) y esplenomegalia 11 (44%). De 24 casos que tenían datos de laboratorio se observó que la eosinofilia y la anemia fueron los principales hallazgos. El diagnóstico micológico se realizó por serología en 24 (72,7%) casos, biopsia 11 (45,8%), examen directo 3 (12,5%) y cultivo 1 (4,2%). La paracoccidioidomicosis infantil es una entidad infrecuente, la cual se observa en 7,9% de los casos. Las manifestaciones más frecuentes son fiebre, adenomegalias y hepatoesplenomegalia. El diagnóstico de la paracoccidioidomicosis aguda infantil, siempre debe ser considerado en niños con edades de 0-15 años, en Venezuela.

Paracoccidioidomycosis rarely affects children, and it is not a notifiable disease. Its real impact in the child population is unknown. The aim of the study was to determine the number of paracoccidioidomycosis cases diagnosed in various health centers in Great Caracas, in children between 0-15 years. We reviewed 420 records with diagnosis of paracoccidioidomycosis from Hospital of Caracas. 33 (7,9%) were from children less than 15 years old. Age average 7,97 years. Male gender accounted for 69.7%, with a male: female relation of 1.5:1 in children between 0-7 years and 5,5:1 between 8-15 years. Most of the patients 11 (35,5%) came from Miranda state, followed bu Distrito Capital 9 (29,1%). In 26 patients the disease could be classified, from which 24 (92,3%) developed the acute form. Clinical manifestations, recorded in 25 cases were: fever 18 (72%), enlarged lymph nodes 16 (64%), hepatomegaly 12 (48,0%) and splenomegaly 11 (44%). From 24 cases in which laboratory data was recorded, eosinophilia and anemia were the most relevent findings. Mycological diagnosis was performed by serology in 24 (72,7%) cases, biopsy 11 (45,8%), direct examination 3 (12,5%) and culture 1 (4,2%). Child paracoccidioidomycosis is a rare disease, observed in 7, )% of cases. Most relevant clinical manifestations are fever, enlarged lymph nodes and hepatosplenomegaly. Acute paracoccidioidomycosis must be considered as a possible diagnosis in children between 0-15 years, in endemic countries such as Venezuela.

Paracoccidioidomycosis: description of two cases autochthonous in Ceará

Paracoccidioidomycosis is endemic in most countries of Latin America. Brazil has the greatest number of cases, with no autochthonous case registered in the state of Ceará. The cases of two patients that had never gone outside the State of Ceará and lived at least some years in the municipality of Palmácia.

Micoses sistêmicas: fatores associados ao óbito em pacientes com infecção pelo vírus da imunodeficiência humana, Cuiabá, Estado de Mato Grosso, 2005-2008 / Systemic mycosis: factors associated with death among patients infected with the human immunodeficiency virus, Cuiabá, State of Mato Grosso, Brazil, 2005-2008

A prevalência de micose sistêmica entre 1.300 pacientes portadores de HIV/Aids de Cuiabá, Mato Grosso foi de 4,6 por cento, no período de 2005-2008. As espécies de fungos isoladas foram o Cryptococcus neoformans (50 por cento), Cryptococcus gattii (1,6 por cento), Cryptococcus spp (6,6 por cento), Histoplasma capsulatum (38,3 por cento) e Paracoccidioides brasiliensis (3,3 por cento). Óbito foi registrado em 32 (53,3 por cento) pacientes, sendo a criptococose a principal causa. A contagem de linfócitos T CD4+ foi baixa e semelhante entre os pacientes que sobreviveram ou faleceram por micose sistêmica. O etilismo (OR:8,2; IC95 por cento: 1,4-62,1; p=0,005) e o nível médio de desidrogenase lática [758 (182) U/L vs 416 (268) U/L; p<0,001] foram as características independentemente associadas ao óbito dos pacientes do estudo. Os resultados mostram alta letalidade por micoses sistêmicas em pacientes portadores de HIV/Aids de Cuiabá e sugerem que características clínico-laboratoriais tais como o etilismo e a elevação precoce da desidrogenase lática podem ser fatores relacionados ao pior prognóstico nessas condições.

Between 2005 and 2008, the prevalence of systemic mycosis among 1,300 HIV/AIDS patients in Cuiabá, Mato Grosso, was 4.6 percent. The fungus species isolated were Cryptococcus neoformans in 50 percent, Cryptococcus gattii in 1.6 percent, Cryptococcus spp in 6.6 percent, Histoplasma capsulatum in 38.3 percent and Paracoccidioides brasiliensis in 3.3 percent. Death was recorded in the cases of 32 patients (53.3 percent), and cryptococcosis was the main cause. The CD4+ T lymphocyte count was low and similar among patients who survived or died due to systemic mycosis. The factors independently associated with the deaths of these patients were alcoholism (OR: 8.2; 95 percent CI: 1.4-62.1; p = 0005) and the mean level of lactate dehydrogenase [758 (182) U/l vs. 416 (268) U/l; p < 0001]. The findings showed that systemic mycosis was highly lethal among the patients with HIV/AIDS in Cuiabá and suggested that clinical-laboratory characteristics such as alcoholism and early elevation of lactate dehydrogenase may be factors relating to worse prognosis under these conditions.

Histoplasmose: [revisão] / Histoplasmosis: [review]

A histoplasmose é uma micose causada por fungo dimórfico, o Histoplasma capsulatum. É considerada classicamente uma micose endêmica, embora o fungo tenha um comportamento oportunístico em pacientes com depressão da imunidade celular. O homem adquire a infecção através da inalação de conídeos presentes na natureza (cavernas com morcegos, galinheiros, etc). O quadro clínico pode variar, desde infecções assintomáticas até quadros graves disseminados, que acometem pacientes com Aids, transplantados ou com neoplasias hematológicas. O diagnóstico baseia-se no encontro do fungo em fluidos orgânicos (escarro, sangue, líquor) ou tecidos (histopatologia), na cultura de materiais biológicos e na sorologia. O tratamento das formas agudas graves, respiratória crônica ou de formas localizadas pode ser feito com azólicos orais (itraconazol) e nas disseminadas, a Anfotericina B (preferencialmente as formulações lipídicas) constitui a droga da eleição para iniciar a terapia. A histoplasmose representa, hoje uma das micoses sistêmicas mais importantes nas Américas, com ampla distribuição em todas as regiões do Brasil.

Histoplasmosis is a fungal infection caused by the dimorphic fungus Histoplasma capsulatum. It is classically considered an endemic mycosis, even though the fungus has an opportunistic behavior in immunocompromised patients. People acquired the infection through the inhalation of conidial forms present in the environmental, such as caves dwelling bats and soils inhabited by chickens. The clinical features may vary from asymptomatic infections to disseminated severe forms that affect patients with acquired immunodeficiency syndrome or hematological malignancies and allograft recipients. The diagnosis is based on the detection of the fungus in organic fluids (sputum, blood, liquor) or tissues (histopathological assays), in the culture of biological samples and serological assays. The treatment of severe chronic respiratory acute or localized forms can be performed with oral azolic (itraconazol) and in the disseminated forms, the amphotericin B (preferentially the lipidic formulations) consists in the elected drug to initiate the therapy. Nowadays, histoplasmosis represents one of the most important systemic mycosis in the Americas, with broad distribution in all regions of Brazil.

Sistemic mycosis associated to tuberculosis in Bolívar state Venezuela

Se determinó la frecuencia y características clínicas de las micosis sistémicas endémicas asociadas a tuberculosis en el estado Bolívar. Se revisaron las historias clínicas de los casos con diagnóstico confirmado de micosis sistémicas y tuberculosis en un período de cinco años. Se detectaron 7 casos de las micosis sistémicas endémicas en la región, Paracoccidioidomicosis e Histoplasmosis, asociadas a tuberculosis. Todos los pacientes procedían del estado Bolívar, sólo uno era del sexo femenino y ninguno tenía serología positiva para la infección por el Virus de Inmunodeficiencia Humana. Todos presentaron manifestaciones pulmonares, la mayoría sintomáticos y con pérdida de peso (6 de 7). En todos los casos, se evidenciaron alteraciones en el estudio radiológico del tórax, con diferentes patrones, predominando el compromiso alveolar difuso bilateral. En 6 de los 7 pacientes, se observaron bacilos ácidos resistentes en muestras de esputo. La micosis más frecuentemente asociada a tuberculosis fue Paracoccidioidomicosis (6 de 7). Todos los pacientes recibieron tratamiento antimicótico y tratamiento antituberculoso con cuatro drogas y todos mostraron mejoría. La asociación de micosis sistémicas endémicas con tuberculosis no es rara en el estado Bolívar, por tanto, la asociación de estas infecciones deberían investigarse sistemáticamente.

The frequency and clinical characteristics of endemic systemic mycosis associated with tuberculosis were determined in Bolívar State. Clinical case records with confirmed diagnoses of systemic mycosis and tuberculosis were reviewed for a 5-year period. Seven cases of systemic mycoses endemic to the region were detected: Paracoccidioidomycosis and Histoplasmosis, associated with tuberculosis. All patients came from Bolívar state; only one was feminine and no one was seropositive for the Human Immunodeficiency Virus. All presented pulmonary compromise, mostly symptomatic, accompanied by weight loss (6 of 7). In all cases, alterations appeared on the radiological study of the thorax, mainly diffuse bilateral alveolar compromise. In 6 of the 7 patients, acid-resistant bacilli were observed in sputum samples. The mycosis most frequently associated with tuberculosis was Paracoccidioidomycosis (6 of 7); the other associated mycosis was Histoplasmosis (1 of 7). All patients received antimycotic and 4-drug anti-tuberculosis treatments and all of them improved. The association of endemic systemic mycosis with tuberculosis is not unusual in Bolívar state and therefore, the association of these infections should be systematically investigated.

Paracoccidioidomicose aguda/subaguda disseminada. Primeiro caso no Rio Grande do sul / Acute/subacute disseminated paracoccidioidomycoses. First case in Rio Grande do Sul

The first autochthonous case of acute/subacute disseminated paracoccidioidomycosis observed in a child in Rio Grande do Sul (Brazil) is reported. The disease started with widespread superficial lymphadenopathy six months before the patient was admitted to the hospital. The diagnosis was made through a cervical lymph node biopsy. The spectrum of the clinical forms of the mycosis observed in this State is commented upon.

É relatado o primeiro caso autóctone de paracoccidioidomicose disseminada aguda/subaguda ocorrido em criança no Rio Grande do Sul. A doença iniciou com adenomegalias superficiais generalizadas, seis meses antes da internação hospitalar. O diagnóstico foi feito através de biópsia de gânglio cervical. É comentado o espectro de formas clínicas da micose observado nesse Estado.