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1.
Orbit ; 39(3): 209-211, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-31509038

RESUMO

Retrobulbar orbital abscess in children is a rare condition, and diagnosis and management can be challenging. We report the case of a 5-week-old male infant with retrobulbar orbital abscess secondary to acute dacryocystitis developed from a dacryocystocele. The patient presented with respiratory difficulty, sepsis and progressive clinical findings suggestive of post-septal cellulitis. He was successfully treated with endonasal incision of subturbinate dacryocystoceles followed by probing of the lacrimal ducts. Congenital dacryocystocele must be considered a differential diagnosis in infants with respiratory difficulty and may develop into a vision- and life-threatening condition requiring immediate intervention.


Assuntos
Abscesso/etiologia , Dacriocistite/complicações , Infecções Oculares Bacterianas/etiologia , Doenças Orbitárias/etiologia , Infecções Estafilocócicas/etiologia , Antibacterianos/uso terapêutico , Terapia Combinada , Dacriocistite/congênito , Dacriocistite/diagnóstico por imagem , Dacriocistite/terapia , Infecções Oculares Bacterianas/diagnóstico por imagem , Infecções Oculares Bacterianas/terapia , Humanos , Lactente , Masculino , Doenças Orbitárias/diagnóstico por imagem , Doenças Orbitárias/terapia , Infecções Estafilocócicas/diagnóstico por imagem , Infecções Estafilocócicas/terapia
2.
Acta Paediatr ; 101(5): e232-4, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22211919

RESUMO

AIM: To inform that Actinobaculum schaalii can colonize the urine and cause urinary tract infection in children. METHODS: Urine samples were examined by wet smear microscopy, incubated in 5% CO(2) for 1-2 days, and species-specific real-time polymerase chain reaction (PCR) for A. schaalii was performed. RESULTS: In 5 of the 29 screened urines, A. schaalii was found only by real-time PCR in quantities equivalent to ≥ 10(4) -10(5) CFU/mL. In addition, A. schaalii was found in quantities equivalent to ≥ 10(6) CFU/mL by both culture and PCR in two children with a urinary tract infection and large numbers of leucocytes in the urine. CONCLUSION: Actinobaculum schaalii is CO(2)-dependent. Therefore, if there are clinical symptoms and/or a negative culture despite the presence of leucocytes in the urine, Gram staining and incubation in 5% CO(2) or species-specific real-time PCR should be performed to identify A. schaalii.


Assuntos
Bactérias Gram-Positivas/isolamento & purificação , Infecções por Bactérias Gram-Positivas/microbiologia , Infecções por Bactérias Gram-Positivas/urina , Infecções Urinárias/microbiologia , Infecções Urinárias/urina , Adolescente , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Estudos Retrospectivos
3.
Ugeskr Laeger ; 171(23): 1919-22, 2009 Jun 01.
Artigo em Dinamarquês | MEDLINE | ID: mdl-19500514

RESUMO

Improving the diabetes metabolic regulation decreases the risk of microvascular diabetic complications. Insulin treatment in children therefore tends to be intensified to multiple-dose insulin (MDI) or continuous subcutaneous insulin injection (CSII). Further, insulin analogues are increasingly used. The pharmacokinetics of human and analogue insulin are summarised. It is concluded that pharmacokinetic studies on analogue insulin in children are required. Yet, no clear evidence of improved glycaemic control of the intensified treatment regimes has been shown in children. Long-term randomised studies are needed.


Assuntos
Diabetes Mellitus Tipo 1/tratamento farmacológico , Hipoglicemiantes/administração & dosagem , Insulina/administração & dosagem , Adolescente , Criança , Diabetes Mellitus Tipo 1/sangue , Medicina Baseada em Evidências , Humanos , Hipoglicemiantes/farmacocinética , Insulina/farmacocinética , Sistemas de Infusão de Insulina , Insulina Isófana/administração & dosagem , Insulina Isófana/farmacocinética , Insulina de Ação Prolongada/administração & dosagem , Insulina de Ação Prolongada/farmacocinética , Resultado do Tratamento
4.
Ugeskr Laeger ; 171(23): 1923-4, 2009 Jun 01.
Artigo em Dinamarquês | MEDLINE | ID: mdl-19500515

RESUMO

A two-month-old Danish girl was admitted to the hospital in diabetic ketoacidosis and diagnosed with permanent neonatal diabetes mellitus (PNDM). She received continuous insulin treatment until she was genetically tested at the Steno Diabetes Centre. She carried a KCNJ11 Arg201His mutation, an activating mutation in the KCNJ11-gene which encodes the ATP-sensitive potassium subunit Kir6.2 in the beta cell which is responsible for insulin secretion. As recommended in the literature, she was successfully shifted from insulin therapy to sulfonylurea tablets at the age of three years and nine months. PNDM-patients should be screened for gene mutations regardless of current age.


Assuntos
Diabetes Mellitus Tipo 1/tratamento farmacológico , Cetoacidose Diabética/tratamento farmacológico , Glibureto/uso terapêutico , Hipoglicemiantes/uso terapêutico , Pré-Escolar , Diabetes Mellitus Tipo 1/genética , Cetoacidose Diabética/genética , Feminino , Humanos , Lactente , Insulina/uso terapêutico , Mutação , Canais de Potássio Corretores do Fluxo de Internalização/genética , Resultado do Tratamento
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