RESUMO
Histoplasmosis is a mycosis caused by Histoplasma capsulatum, a dimorphic fungus endemic to areas with nitrogen-rich soil, like the one contaminated with bird and bat excrement. Patients with a deficient immune response are especially at risk for developing invasive infections, such as disseminated histoplasmosis, and secondary immunodeficiency can be a consequence of malnutrition. This case report presents a 15-month-old male infant with malnutrition who presented with signs and symptoms of disseminated histoplasmosis, including fever, malaise, weight loss, cough, and diarrhea. The infant came from a geographic area where histoplasmosis is endemic, and he was a member of a cultural group with a higher prevalence of histoplasmosis than the general population. On physical examination, hepatosplenomegaly, lymphadenopathy, and lung crackles were found, which are common in most patients with histoplasmosis. The keystone of diagnosis of H. capsulatum infection is antigen detection, but the criterion standard is isolation of the organism from body specimens through laboratory culture. Histological diagnosis is especially useful for rapid diagnosis. Treatment of disseminated histoplasmosis in the pediatric population consists of deoxycholate amphotericin B for four to six weeks followed by itraconazole to complete a total of three months of treatment. Despite the involvement of multiple organ systems, the patient recovered satisfactorily after the completion of amphotericin B treatment for one month and the resolution of his malnourishment.
RESUMO
In the following case review, we present a 49-year-old male without a history of injection drug (IDU) use nor any known structural heart disease, who developed left-sided pseudomonal infectious endocarditis. The only known risk factors were urinary tract infection (UTI) with secondary bacteremia and prolonged healthcare contact with admission to the intensive care unit. Infectious endocarditis (IE) is the infection of the endocardium. The official diagnosis can only be established after histological and microbiological studies confirm microorganism-colonized vegetations in the heart valves, but a clinical suspicion with high sensitivity and specificity can be approached with modified Duke's criteria. Even though structural heart disease is the major predisposing factor for IE, healthcare-associated IE has risen with the new therapeutic interventions. Transient bacteremia, which might result after various procedures, forms part of the factors causing healthcare-associated IE. Although both, community-acquired and hospital-acquired infections by Pseudomonas aeruginosa have been reported, pure community-acquired infections without previous exposure to the hospital or healthcare environment are extremely rare. Intensive care unit (ICU) patients are at special risk for this microbe. It is considered an important causative agent in ventilator/associated pneumonia, catheter-associated urinary tract infection (UTI), and catheter-associated bloodstream infections. IE by P. aeruginosa remains a rare form of IE. Though 95% of cases are associated with injection drug use (IDU), healthcare contact is becoming more important each day as the primary risk factor. The most common complications include abscesses in the ring and annulus, congestive heart failure (CHF), embolisms, inability to sterilize valves, splenic abscesses, recurrent bacteremia, and neurologic complications. This condition is highly fatal, with a mortality rate of over 73% for patients older than 30 years. Recommended antibiotic treatment for IE caused by P. aeruginosa consists of high-dose tobramycin in combination with antipseudomonal penicillin or high-dose ceftazidime, cefepime, or imipenem.
