RESUMEN
The prognosis of tuberculous meningitis, a rare form of extrapulmonary tuberculosis, depends on the stage of treatment initiation. We report a fatal case of tuberculous meningitis. The patient had received successive tumor necrosis factor (TNF) antagonists and abatacept to treat juvenile idiopathic arthritis, with negative results for polymerase chain reaction and acid-fast bacilli on smear, had normal cerebrospinal fluid (CSF) adenosine deaminase and glucose levels. Six weeks post-admission, the CSF culture demonstrated Mycobacterium tuberculosis. The altered immunological responses caused by anti-TNF treatment made the diagnosis challenging. Clinicians should bear this in mind and, if suspected, treatment should be initiated immediately.
Asunto(s)
Antituberculosos/efectos adversos , Artritis Juvenil/complicaciones , Artritis Juvenil/tratamiento farmacológico , Tuberculosis Meníngea/diagnóstico , Tuberculosis Meníngea/etiología , Inhibidores del Factor de Necrosis Tumoral , Adolescente , Resultado Fatal , Humanos , Imagen por Resonancia Magnética , Masculino , Mycobacterium tuberculosis/aislamiento & purificación , Reacción en Cadena de la Polimerasa , Tuberculosis Meníngea/líquido cefalorraquídeoRESUMEN
Abstract The prognosis of tuberculous meningitis, a rare form of extrapulmonary tuberculosis, depends on the stage of treatment initiation. We report a fatal case of tuberculous meningitis. The patient had received successive tumor necrosis factor (TNF) antagonists and abatacept to treat juvenile idiopathic arthritis, with negative results for polymerase chain reaction and acid-fast bacilli on smear, had normal cerebrospinal fluid (CSF) adenosine deaminase and glucose levels. Six weeks post-admission, the CSF culture demonstrated Mycobacterium tuberculosis. The altered immunological responses caused by anti-TNF treatment made the diagnosis challenging. Clinicians should bear this in mind and, if suspected, treatment should be initiated immediately.
Asunto(s)
Humanos , Masculino , Adolescente , Artritis Juvenil/complicaciones , Artritis Juvenil/tratamiento farmacológico , Tuberculosis Meníngea/diagnóstico , Tuberculosis Meníngea/etiología , Inhibidores del Factor de Necrosis Tumoral , Antituberculosos/efectos adversos , Tuberculosis Meníngea/líquido cefalorraquídeo , Imagen por Resonancia Magnética , Reacción en Cadena de la Polimerasa , Resultado Fatal , Mycobacterium tuberculosis/aislamiento & purificaciónRESUMEN
Brevibacterium spp. are catalase-positive, non-spore-forming, non motile, aerobic Gram- positive rods that were considered apathogenic until a few reports of infections in immunocompromised patients had been published. To the best of our knowledge, this is the first report of B. casei catheter-related bloodstream infection in a child with acute leukemia. We aim to enhance the awareness of pediatric hematology and infectious disease specialists about this pathogen and review of the literature.
Asunto(s)
Humanos , Masculino , Niño , Infecciones por Actinomycetales/microbiología , Brevibacterium/aislamiento & purificación , Infecciones Relacionadas con Catéteres/microbiología , Leucemia-Linfoma Linfoblástico de Células Precursoras B/complicaciones , Brevibacterium/clasificaciónRESUMEN
Brevibacterium spp. are catalase-positive, non-spore-forming, non motile, aerobic Gram-positive rods that were considered apathogenic until a few reports of infections in immunocompromised patients had been published. To the best of our knowledge, this is the first report of B. casei catheter-related bloodstream infection in a child with acute leukemia. We aim to enhance the awareness of pediatric hematology and infectious disease specialists about this pathogen and review of the literature.
Asunto(s)
Infecciones por Actinomycetales/microbiología , Brevibacterium/aislamiento & purificación , Infecciones Relacionadas con Catéteres/microbiología , Leucemia-Linfoma Linfoblástico de Células Precursoras B/complicaciones , Brevibacterium/clasificación , Niño , Humanos , MasculinoRESUMEN
We present a case of a 4.5-month-old boy from Turkey with hemophagocytic lymphohistiocytosis (HLH) associated with H1N1 virus and Leishmania spp. coinfection. Because visceral leishmaniasis can mimic hematologic disorders like HLH, it is important to rule out this clinical condition before starting immunosuppressive therapy. In our case, treatment with liposomal amphotericin B resulted in a dramatic resolution of clinical and laboratory abnormalities.
Asunto(s)
Subtipo H1N1 del Virus de la Influenza A , Gripe Humana/complicaciones , Leishmaniasis Visceral/complicaciones , Linfohistiocitosis Hemofagocítica/complicaciones , Anfotericina B/uso terapéutico , Antiprotozoarios/uso terapéutico , Preescolar , Humanos , Gripe Humana/diagnóstico , Gripe Humana/tratamiento farmacológico , Leishmaniasis Visceral/diagnóstico , Leishmaniasis Visceral/tratamiento farmacológico , Linfohistiocitosis Hemofagocítica/diagnóstico , MasculinoRESUMEN
We present a case of a 4.5-month-old boy from Turkey with hemophagocytic lymphohistiocytosis (HLH) associated with H1N1 virus and Leishmania spp. coinfection. Because visceral leishmaniasis can mimic hematologic disorders like HLH, it is important to rule out this clinical condition before starting immunosuppressive therapy. In our case, treatment with liposomal amphotericin B resulted in a dramatic resolution of clinical and laboratory abnormalities.
É relatado um caso de um menino de 4,5 meses de idade, da Turquia, com linfohistiocitose hemofagocítica (HLH) associado à coinfecção com o vírus H1N1 e leishmaniose visceral. Como a leishmaniose visceral pode imitar doenças hematológicas como HLH, é importante afastar essa condição clínica antes de iniciar a terapia imunossupressora. No caso relatado, o tratamento com anfotericina B lipossomal resultou em uma resolução dramática das anomalias clínicas e laboratoriais.