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1.
J Perinatol ; 21(8): 553-5, 2001 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11774019

RESUMO

Pneumatoceles due to acquired localized overinflation as a form of pulmonary interstitial emphysema are complications of advanced bronchopulmonary dysplasia. Different ventilation modes, selective bronchial intubation, balloon obstruction of the affected bronchus and steroids have been reported with success. Lobectomy has also been used. We present a premature infant with multiple large pneumatoceles causing respiratory compromise. In our case percutaneous decompression under fluoroscopy guidance resulted in a permanent cure.


Assuntos
Descompressão Cirúrgica , Doenças do Prematuro/cirurgia , Pneumopatias/cirurgia , Idoso , Descompressão Cirúrgica/métodos , Drenagem , Fluoroscopia , Hérnia/complicações , Herniorrafia , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Pneumopatias/complicações , Masculino , Síndrome do Desconforto Respiratório do Recém-Nascido/etiologia
3.
J Pediatr Surg ; 24(10): 1068-70, 1989 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2681656

RESUMO

A case of isolated complete transection of the common bile duct due to blunt abdominal trauma in a 3-year-old child is presented. The rarity of this injury and its initial presentation as a pancreatic pseudocyst warrant its description. This patient, the fifteenth child to be reported in the literature, was diagnosed as having a biliary injury following ultrasound-guided percutaneous drainage. Choledochal transection was documented at laparotomy and was successfully treated by proximal cholecystostomy and choledochojejunostomy with Roux-en-Y reconstruction. Delayed diagnosis is common, but this injury should always be kept in mind. Early diagnosis is feasible with the use of the HIDA scan. A review of the literature, modes of diagnosis, and techniques for surgical repair are described.


Assuntos
Ducto Colédoco/lesões , Ferimentos não Penetrantes/cirurgia , Pré-Escolar , Ducto Colédoco/diagnóstico por imagem , Ducto Colédoco/cirurgia , Diagnóstico Diferencial , Humanos , Masculino , Pseudocisto Pancreático/diagnóstico por imagem , Tomografia Computadorizada por Raios X , Ferimentos não Penetrantes/diagnóstico por imagem
4.
J Pediatr Surg ; 24(10): 1103-7, 1989 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2681658

RESUMO

Leiomyoma of the esophagus is not uncommon in the adult population but is rarely seen in children; only 20 cases have been reported in the pediatric population. In this paper we describe two cases of esophageal leiomyoma in female patients aged 6 and 13 years and review previous reports. Several differences were noted between the pediatric and adult population. The mean age in children is 14 years (range, 4 to 20 years). Leiomyoma appears 1.71 times more often in females than in males. Localized lesions are found in only 9%, whereas the diffuse form predominates in 91%. The entire esophagus may be involved 35% of the time, and encroachment on the cardia or upper stomach occurs in 70%. Leiomyomas associated with familial syndromes (familial leiomyoma and Alport's syndrome) occur in 22% of the cases. Major symptoms include dysphagia (86%), dyspnea (36%), vomiting (27%), retrosternal pain (27%), and coughing (22%). The initial diagnosis following contrast studies is most often achalasia. The diagnosis of leiomyoma is made only with subsequent endoscopy. Enucleation was performed in only 11% of the cases; surgical resection (including part of the stomach) was necessary in 78% with a 21% postoperative mortality. Esophageal leiomyoma should be considered in the differential diagnosis of mediastinal masses and esophageal obstruction. Accurate preoperative diagnosis is desirable in order to plan proper surgical treatment.


Assuntos
Neoplasias Esofágicas/cirurgia , Leiomioma/cirurgia , Adolescente , Criança , Neoplasias Esofágicas/diagnóstico , Feminino , Humanos , Leiomioma/diagnóstico
5.
J Pediatr Surg ; 24(10): 1079-83, 1989 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2553909

RESUMO

Malignant small-cell tumor of the thoracopulmonary region (MSCT) is an uncommon neoplasm in children. We describe five cases diagnosed since 1981 that fulfill the criteria put forth by Askin et al. Surgery was performed for diagnosis or therapy in all patients. Two patients underwent open lung biopsy, only because of tumor extent. The other three had chest wall resections. All patients received radiotherapy and chemotherapy. Three patients presenting initially with extensive disease died at intervals of 2.5 to 7 months after diagnosis. Two patients are alive and disease-free at 16 and 24 months postdiagnosis. All five cases were reviewed for standard histology and differential immunohistochemistry. Electronmicroscopy and tissue cultures were done in 3 of the 5 patients. All five patients were neuron-specific enolase-positive. MSCT is an exclusion diagnosis not always readily made. Clinical course and pathologic expertise may point to the correct diagnosis.


Assuntos
Carcinoma de Células Pequenas/cirurgia , Neoplasias Pulmonares/cirurgia , Neoplasias Torácicas/cirurgia , Adolescente , Carcinoma de Células Pequenas/patologia , Criança , Pré-Escolar , Feminino , Humanos , Neoplasias Pulmonares/patologia , Masculino , Neoplasias Embrionárias de Células Germinativas/patologia , Neoplasias Embrionárias de Células Germinativas/cirurgia , Neoplasias Torácicas/patologia
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