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1.
Orthop Traumatol Surg Res ; 102(1): 117-20, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26751973

RESUMO

We present a new bone suture anchor technique for fractures of the medial epicondyle. The hypothesis was that the results would be similar to those with the divergent K-wire fixation. This retrospective study included 40 patients who presented with displaced fractures of the medial epicondyle: one group was treated with a Mitek(®) non-resorbable bone suture anchor (group A: n=21), the other by K-wire fixation (group B: n=19). A medial approach was taken with an anchor placed above the olecranon fossa. The epicondyle was then repositioned by bone suture. After a mean follow-up of 18.6 months, union was obtained in all epicondyles. There was no difference in flexion-extension of the elbow. The rate of hypertrophy of the medial epicondyle was similar in both groups (57%). The bone suture anchor of the medial epicondyle is an effective technique that does not require hardware removal and is an alternative treatment option to divergent K-wire fixation.


Assuntos
Articulação do Cotovelo/cirurgia , Fraturas do Úmero/cirurgia , Âncoras de Sutura , Fios Ortopédicos , Criança , Feminino , Fixação Interna de Fraturas , Consolidação da Fratura , Humanos , Masculino , Estudos Retrospectivos
2.
Ann Fr Anesth Reanim ; 30(1): 73-6, 2011 Jan.
Artigo em Francês | MEDLINE | ID: mdl-21190809

RESUMO

We report the case of an unexpected respiratory complication after a surgical treatment of scoliosis during postoperative period in an adolescent patient. This complication results of a vascular compression of the left main bronchus between the aorta and the pulmonary artery, which induces severe atelectasis of left lower lobe. Prolonged non-invasive ventilation with high level of positive end-expiratory pressure prevents aorto-pulmonary compression, allows a pulmonary recruitment associated with a favorable prognostic for the adolescent.


Assuntos
Complicações Pós-Operatórias/terapia , Doenças Respiratórias/etiologia , Doenças Respiratórias/terapia , Escoliose/complicações , Escoliose/cirurgia , Adulto , Humanos , Pneumopatias/etiologia , Pneumopatias/terapia , Masculino , Procedimentos Ortopédicos , Consumo de Oxigênio , Respiração com Pressão Positiva , Atelectasia Pulmonar/diagnóstico por imagem , Atelectasia Pulmonar/etiologia , Atelectasia Pulmonar/terapia , Radiografia Torácica , Respiração Artificial , Tomografia Computadorizada por Raios X
3.
Acta Orthop Belg ; 66(2): 190-3, 2000 Apr.
Artigo em Francês | MEDLINE | ID: mdl-10842882

RESUMO

We report the case of a teenager who was involved in a road traffic accident. She presented a flexion-distraction type of vertebral injury, (Chance fracture). This fracture was associated with an intra-abdominal injury. The child was a passenger in a rear seat using a shoulder seatbelt restraint.


Assuntos
Traumatismos Abdominais/etiologia , Vértebras Lombares/lesões , Fraturas da Coluna Vertebral/patologia , Traumatismos Abdominais/patologia , Acidentes de Trânsito , Adolescente , Feminino , Humanos , Vértebras Lombares/diagnóstico por imagem , Vértebras Lombares/patologia , Radiografia , Cintos de Segurança , Fraturas da Coluna Vertebral/complicações , Fraturas da Coluna Vertebral/diagnóstico por imagem
4.
Pediatrie ; 48(4): 301-4, 1993.
Artigo em Francês | MEDLINE | ID: mdl-8397381

RESUMO

Cervical tumors of thymic origin are considered to be uncommon lesions in the differential diagnosis of neck masses. They can be either cystic or solid. The authors present one case of solid cervical thymic tumor in a 2 month-old baby. The embryogenesis of the thymus explains the cervical location of these tumors. Theories of physiopathology are presented. The clinical presentation is variable and their nature is often recognized only upon surgery and preoperative pathologic examination. Some cases of thymoma and respiratory complications resulting from ectopic thymus have been described in the literature, so that total excision of the mass must be performed. This lesion may be more common than suggested in the literature.


Assuntos
Coristoma/diagnóstico , Neoplasias de Cabeça e Pescoço/diagnóstico , Timo , Coristoma/fisiopatologia , Coristoma/cirurgia , Neoplasias de Cabeça e Pescoço/fisiopatologia , Neoplasias de Cabeça e Pescoço/cirurgia , Humanos , Lactente , Masculino , Timo/embriologia , Timo/fisiopatologia , Timo/cirurgia
5.
Artigo em Francês | MEDLINE | ID: mdl-1955658

RESUMO

The authors report eight cases of antenatal diagnosis of sacro-coccygeal teratoma (SCT) in five girls and three boys in whom the diagnosis was made between the 19th and 34th week of amenorrhea (mean = 27 weeks). The ultrasound pictures taken antenatally of the SCT assist in the discovery of a mass that is usually heterogenous, attached to the distal end of the sacrum, and the discovery is usually made fortuitously or because the height of the uterus is too great. A different series of antenatal diagnoses for SCT have made it possible to work out certain criteria of seriousness to be able to predict intra-uterine death: the presence of anasarca or of hydramnios, the discovery of the lesion before the 30th week of amenorrhoea, the relative weight of the teratoma as against the weight of the fetus being above 50%. We think from our experience that it is important to add the scale of the antenatal growth of the teratoma. A rapid growth of the SCT will lead to a tumour mass which is great as compared to the size of the fetus. Similarly in certain cases the vascular bed will increase in size, and intratumour haemorrhages can occur and give rise to fetal heart failure and also to fetal anaemia, hypoproteinaemia and the appearance of anasarca or of hydramnios. The child dies in utero or immediately after birth because of prematurity from the haemorrhagic state or from cardiac insufficiency. Furthermore accelerated growth of the tumour is nearly always in the immature tumour cells and that means that the child, if it is born alive, should be followed up for a long time because there is a risk of it becoming locally malignant. In practice the monitoring of SCT and the antenatal discovery of the condition should be carried out very seriously in order, in some cases, if it is viable to produce a living child in conditions where the rapid growth of tumour would make it likely that the child would die in utero.


Assuntos
Doenças Fetais/diagnóstico por imagem , Região Sacrococcígea , Teratoma/diagnóstico por imagem , Ultrassonografia Pré-Natal/normas , Estudos de Avaliação como Assunto , Feminino , Doenças Fetais/classificação , Doenças Fetais/patologia , Idade Gestacional , Humanos , Masculino , Tamanho do Órgão , Valor Preditivo dos Testes , Gravidez , Prognóstico , Índice de Gravidade de Doença , Teratoma/classificação , Teratoma/patologia
6.
Chir Pediatr ; 31(2): 73-8, 1990.
Artigo em Francês | MEDLINE | ID: mdl-2268955

RESUMO

The authors report the case of an 3 months old caucasian boy which had an extrahepatic biliary atresia associate with a congenital biliary cyst and an anomalous pancreaticobiliary junction. The patency between gallbladder and duodenum permits the operative opacification of this long common pancreaticobiliary channel. The congenital biliary cyst was located on the upper part of the common bile duct and was obstructed by biliary concretions. Unfortunately, no patency between intrahepatic bile ducts and this cyst was found. Because this long common pancreaticobiliary channel may cause biliary dilatation or biliary cancer, we performed an hepatic portoenterostomy rather an hepatic portocholecystostomy. A few weeks later, the bile flow was restored and the jaundice decreased. With a follow up of 18 months, this boy is currently anicteric, despite the hepatic fibrosis found on the operative biopsy. The association extrahepatic biliary atresia-long common pancreaticobiliary channel is uncommon and only 20 cases were reported. In our case, the pancreatic juice reflux into the biliary tract might have caused the dilatation of the common bile duct and the biliary atresia by chronic obstructive cholangiopathy.


Assuntos
Atresia Biliar/patologia , Ducto Colédoco/anormalidades , Ductos Pancreáticos/anormalidades , Cisto do Colédoco/patologia , Cálculos Biliares/patologia , Humanos , Lactente , Masculino
7.
Ann Pediatr (Paris) ; 36(2): 141-7, 1989 Feb.
Artigo em Francês | MEDLINE | ID: mdl-2784653

RESUMO

We report seven cases of complete volvulus of the small bowel without malrotation seen from 1973 through 1986. The clinical setting is always the same in this condition: the infant exhibits no clinical anomalies during the symptom-free interval between birth and the volvulus (4 h to 35 d, m = 7 d in our series). Onset is extremely sudden, with a complete, proximal obstruction, early and abundant passage of blood per rectum, and above all a severe shock that fails to respond to resuscitation. Roentgenograms contribute little to the diagnosis and surgery should never be delayed to perform complementary investigations of any kind. Indeed, the only effective treatment is unwinding the volvulus within the first six hours following onset, for beyond that time irreversible necrosis of the entire small bowel and occasionally colon occurs. Five infants died because they were seen too late and operated on 36 hours on average after the onset of symptoms. The two survivors had an early operation that prevented total necrosis of the small bowel. However, this pattern seems to vary according to the degree of cecum anchorage: a fixed cecum results in a very tight volvulus with complete, early ischemia and usually irreversible necrosis of the small bowel beyond the sixth hour (9/9 published cases); an even slightly mobile cecum results in a looser volvulus, with less severe ischemia, more delayed necrosis, and a possibility of complete recovery (5/6 published cases).(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Obstrução Intestinal/patologia , Intestino Delgado , Feminino , Hemorragia Gastrointestinal/patologia , Humanos , Recém-Nascido , Intestino Delgado/irrigação sanguínea , Intestino Delgado/patologia , Isquemia/patologia , Masculino , Necrose , Anormalidade Torcional , Vômito/patologia
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