Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Pediatr Surg Int ; 40(1): 124, 2024 May 07.
Artigo em Inglês | MEDLINE | ID: mdl-38713441

RESUMO

PURPOSE: Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a well described clinical condition, but reports are focused on microcolon and intestinal hypoperistalsis, while data on bladder management are scant. Aim of the study is to present urological concerns in MMIHS. METHODS: Retrospective evaluation of clinical data on urological management of MMIHS patients treated in the last 10 years. RESULTS: Six patients were enrolled (3 male, 3 female). Three girls had prenatal diagnosis of megacystis (1 vesicoamniotic shunt was placed). All patients had genetic diagnosis: 5 had ACTG2 gene mutations and 1 MYH11 mutation. All patients were addressed to our attention for urinary symptoms, such as urinary retention, urinary tract infections, acute renal injury. Two patients presented frequent stoma prolapses. All children underwent a complete urological evaluation, and then started a bladder management protocol (clean intermittent catheterization, via urethra or cystostomy-tube placement), with improvement of urinary infections, upper urinary tract dilation and stoma prolapses, if present. All patients had good renal function at last follow-up. CONCLUSION: We believe that MMIHS patients must be addressed soon and before onset of symptoms for a multidisciplinary evaluation, including an early assessment by a pediatric urologist expert in functional disorder, to preserve renal function at its best.


Assuntos
Anormalidades Múltiplas , Colo , Colo/anormalidades , Pseudo-Obstrução Intestinal , Bexiga Urinária , Bexiga Urinária/anormalidades , Humanos , Feminino , Estudos Retrospectivos , Masculino , Anormalidades Múltiplas/cirurgia , Colo/cirurgia , Bexiga Urinária/cirurgia , Lactente , Pseudo-Obstrução Intestinal/cirurgia , Pseudo-Obstrução Intestinal/diagnóstico , Recém-Nascido , Pré-Escolar , Mutação
2.
Pediatr Surg Int ; 40(1): 116, 2024 May 02.
Artigo em Inglês | MEDLINE | ID: mdl-38695977

RESUMO

PURPOSE: Existing guidelines provide weak recommendations on the surgical management of nutritional problems in children. The objective was to design a management pathway to address the best nutritional surgery (NS) procedure in a given patient. METHODS: Retrospective analysis of children treated at our department from January 2015 to December 2019. The sample was divided into two groups according to presence or absence of neurological impairment (NI). Patients with NI (Group 1) were classified in three subgroups based on presenting symptoms: A-Dysphagia without gastroesophageal reflux (GER); B-GER with or without dysphagia; C-Symptoms associated with a delayed gastric emptying. RESULTS: A total of 154 patients were included, 111 with NI. One-hundred-twenty-eight patients underwent only one procedure. Complications and mortality were superior in Group 1. In subgroup A, isolated gastrostomy was the first NS in all patients. In subgroup B most of patients were subjected to a Nissen fundoplication, while in 5 cases total esophagogastric dissociation (TEGD) was the first intervention. Considering the entire sample, 92.3% patients who underwent a TEGD did not require further procedures. CONCLUSION: NS encompasses various procedures depending on presenting symptoms and neurological status. A management flowchart for these patients is proposed.


Assuntos
Transtornos de Deglutição , Humanos , Estudos Retrospectivos , Feminino , Masculino , Criança , Pré-Escolar , Lactente , Transtornos de Deglutição/etiologia , Refluxo Gastroesofágico/cirurgia , Gastrostomia/métodos , Adolescente , Doenças do Sistema Nervoso , Fundoplicatura/métodos , Complicações Pós-Operatórias/epidemiologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...