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1.
Orthop Traumatol Surg Res ; 102(1): 117-20, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26751973

ABSTRACT

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.


Subject(s)
Elbow Joint/surgery , Humeral Fractures/surgery , Suture Anchors , Bone Wires , Child , Female , Fracture Fixation, Internal , Fracture Healing , Humans , Male , Retrospective Studies
2.
Ann Fr Anesth Reanim ; 30(1): 73-6, 2011 Jan.
Article in French | MEDLINE | ID: mdl-21190809

ABSTRACT

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.


Subject(s)
Postoperative Complications/therapy , Respiratory Tract Diseases/etiology , Respiratory Tract Diseases/therapy , Scoliosis/complications , Scoliosis/surgery , Adult , Humans , Lung Diseases/etiology , Lung Diseases/therapy , Male , Orthopedic Procedures , Oxygen Consumption , Positive-Pressure Respiration , Pulmonary Atelectasis/diagnostic imaging , Pulmonary Atelectasis/etiology , Pulmonary Atelectasis/therapy , Radiography, Thoracic , Respiration, Artificial , Tomography, X-Ray Computed
3.
Acta Orthop Belg ; 66(2): 190-3, 2000 Apr.
Article in French | MEDLINE | ID: mdl-10842882

ABSTRACT

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.


Subject(s)
Abdominal Injuries/etiology , Lumbar Vertebrae/injuries , Spinal Fractures/pathology , Abdominal Injuries/pathology , Accidents, Traffic , Adolescent , Female , Humans , Lumbar Vertebrae/diagnostic imaging , Lumbar Vertebrae/pathology , Radiography , Seat Belts , Spinal Fractures/complications , Spinal Fractures/diagnostic imaging
4.
Pediatrie ; 48(4): 301-4, 1993.
Article in French | MEDLINE | ID: mdl-8397381

ABSTRACT

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.


Subject(s)
Choristoma/diagnosis , Head and Neck Neoplasms/diagnosis , Thymus Gland , Choristoma/physiopathology , Choristoma/surgery , Head and Neck Neoplasms/physiopathology , Head and Neck Neoplasms/surgery , Humans , Infant , Male , Thymus Gland/embryology , Thymus Gland/physiopathology , Thymus Gland/surgery
5.
Article in French | MEDLINE | ID: mdl-1955658

ABSTRACT

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.


Subject(s)
Fetal Diseases/diagnostic imaging , Sacrococcygeal Region , Teratoma/diagnostic imaging , Ultrasonography, Prenatal/standards , Evaluation Studies as Topic , Female , Fetal Diseases/classification , Fetal Diseases/pathology , Gestational Age , Humans , Male , Organ Size , Predictive Value of Tests , Pregnancy , Prognosis , Severity of Illness Index , Teratoma/classification , Teratoma/pathology
6.
Chir Pediatr ; 31(2): 73-8, 1990.
Article in French | MEDLINE | ID: mdl-2268955

ABSTRACT

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.


Subject(s)
Biliary Atresia/pathology , Common Bile Duct/abnormalities , Pancreatic Ducts/abnormalities , Choledochal Cyst/pathology , Gallstones/pathology , Humans , Infant , Male
7.
Ann Pediatr (Paris) ; 36(2): 141-7, 1989 Feb.
Article in French | MEDLINE | ID: mdl-2784653

ABSTRACT

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)


Subject(s)
Intestinal Obstruction/pathology , Intestine, Small , Female , Gastrointestinal Hemorrhage/pathology , Humans , Infant, Newborn , Intestine, Small/blood supply , Intestine, Small/pathology , Ischemia/pathology , Male , Necrosis , Torsion Abnormality , Vomiting/pathology
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