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1.
Neuropsychologia ; 130: 78-91, 2019 07.
Article de Anglais | MEDLINE | ID: mdl-30098328

RÉSUMÉ

Neuroimaging studies have identified the superior parietal lobules bilaterally as the neural substrates of reduced visual attention (VA) span in developmental dyslexia. It remains however unclear whether the VA span deficit and the deficits in temporal and spatial attention shifting also reported in dyslexic children reflect a unitary spatio-temporal deficit of attention - probably linked to general posterior parietal dysfunction- or the dysfunction of distinct attentional systems that relate to different neural substrates. We explored this issue by testing an adult patient, IG, with a specific damage of the bilateral superior parietal lobules after stroke, on tasks assessing the VA span as well as temporal and spatial attention shifting. IG demonstrated a very severe VA span deficit, but preserved temporal attention shifting. Exogenous spatial orientation shifting was spared but her performance was impaired in endogenous attention. The overall findings show that distinct sub-systems of visual attention can be dissociated within the parietal lobe, suggesting that different attentional systems associated with specific neural networks can be selectively impaired in developmental dyslexia.


Sujet(s)
Trouble déficitaire de l'attention avec hyperactivité/imagerie diagnostique , Trouble déficitaire de l'attention avec hyperactivité/psychologie , Dyslexie/imagerie diagnostique , Dyslexie/psychologie , Lobe pariétal/imagerie diagnostique , Lobe pariétal/traumatismes , Adulte , Attention , Clignement , Souffrance cérébrale chronique/imagerie diagnostique , Souffrance cérébrale chronique/psychologie , Encéphalopathie ischémique/imagerie diagnostique , Encéphalopathie ischémique/psychologie , Femelle , Humains , Tests d'intelligence , Mâle , Neuroimagerie , Tests neuropsychologiques , Stimulation lumineuse , Lecture , Accident vasculaire cérébral/imagerie diagnostique , Accident vasculaire cérébral/psychologie
2.
Sci Rep ; 7(1): 14563, 2017 11 06.
Article de Anglais | MEDLINE | ID: mdl-29109424

RÉSUMÉ

Recent studies reported that Action Video Game-AVG training improves not only certain attentional components, but also reading fluency in children with dyslexia. We aimed to investigate the shared attentional components of AVG playing and reading, by studying whether the Visual Attention (VA) span, a component of visual attention that has previously been linked to both reading development and dyslexia, is improved in frequent players of AVGs. Thirty-six French fluent adult readers, matched on chronological age and text reading proficiency, composed two groups: frequent AVG players and non-players. Participants performed behavioural tasks measuring the VA span, and a challenging reading task (reading of briefly presented pseudo-words). AVG players performed better on both tasks and performance on these tasks was correlated. These results further support the transfer of the attentional benefits of playing AVGs to reading, and indicate that the VA span could be a core component mediating this transfer. The correlation between VA span and pseudo-word reading also supports the involvement of VA span even in adult reading. Future studies could combine VA span training with defining features of AVGs, in order to build a new generation of remediation software.


Sujet(s)
Attention , Lecture , Jeux vidéo , Adolescent , Adulte , Femelle , Humains , Mâle , Adulte d'âge moyen , Jeux vidéo/psychologie , Perception visuelle , Jeune adulte
3.
Pediatr Transplant ; 18(5): E146-51, 2014 Aug.
Article de Anglais | MEDLINE | ID: mdl-24815678

RÉSUMÉ

We describe here a two-yr-old boy with biliary RMS successfully treated by chemotherapy and LT. The child presented with obstructive jaundice at 20 months of age. A mildly vascularized, non-calcified, partially cystic lesion was visualized in the left hepatic lobe. Solid infiltration of the common bile duct and of both left and right hepatic ducts was suspected. Liver biopsy suggested a botryoid-type embryonal RMS originating from the biliary tract. After extrahepatic spread of the tumor was excluded, a biliary drain was applied and neoadjuvant chemotherapy was started. After the treatment, although reduced in volume, the mass was still unresectable without aggressive surgery and gross residual disease. LT with a reduced segment II/III graft was performed four months after diagnosis. The patient received six cycles of adjuvant chemotherapy, and he is alive and recurrence-free 48 months post-transplantation. A posteriori, the transplant might have possibly been avoided with an aggressive resection with biliary reconstruction. Nevertheless, although the risk of the transplant has to be balanced against the chemoresponsiveness of the tumor, the four-yr disease-free survival of this patient suggests that, when coupled with effective chemotherapy, transplantation might be considered a potential treatment for unresectable biliary RMS.


Sujet(s)
Tumeurs des voies biliaires/thérapie , Transplantation hépatique , Rhabdomyosarcome/thérapie , Antinéoplasiques/usage thérapeutique , Tumeurs des voies biliaires/imagerie diagnostique , Biopsie , Traitement médicamenteux adjuvant/méthodes , Enfant d'âge préscolaire , Survie sans rechute , Survie du greffon , Humains , Immunosuppression thérapeutique , Foie/anatomopathologie , Mâle , Traitement néoadjuvant/méthodes , Récidive tumorale locale , Rhabdomyosarcome/imagerie diagnostique , Tomodensitométrie , Résultat thérapeutique
4.
Brain Lang ; 120(3): 381-94, 2012 Mar.
Article de Anglais | MEDLINE | ID: mdl-22285025

RÉSUMÉ

A dissociation between phonological and visual attention (VA) span disorders has been reported in dyslexic children. This study investigates whether this cognitively-based dissociation has a neurobiological counterpart through the investigation of two cases of developmental dyslexia. LL showed a phonological disorder but preserved VA span whereas FG exhibited the reverse pattern. During a phonological rhyme judgement task, LL showed decreased activation of the left inferior frontal gyrus whereas this region was activated at the level of the controls in FG. Conversely, during a visual categorization task, FG demonstrated decreased activation of the parietal lobules whereas these regions were activated in LL as in the controls. These contrasted patterns of brain activation thus mirror the cognitive disorders' dissociation. These findings provide the first evidence for an association between distinct brain mechanisms and distinct cognitive deficits in developmental dyslexia, emphasizing the importance of taking into account the heterogeneity of the reading disorder.


Sujet(s)
Trouble déficitaire de l'attention avec hyperactivité/physiopathologie , Attention/physiologie , Dyslexie/physiopathologie , Imagerie par résonance magnétique , Phonétique , Stimulation acoustique , Adulte , Troubles de la cognition/physiopathologie , Femelle , Lobe frontal/physiopathologie , Humains , Mâle , Tests neuropsychologiques , Lobe pariétal/physiopathologie , Reconnaissance visuelle des formes/physiologie , Stimulation lumineuse , Lecture , Jeune adulte
5.
Transplant Proc ; 41(8): 3284-9, 2009 Oct.
Article de Anglais | MEDLINE | ID: mdl-19857731

RÉSUMÉ

Because lung transplantation is the only effective therapy for terminal respiratory failure, the demand for donor lungs has increased steadily. However, the number of donors has remained fairly constant over the years, which results in an increasing duration of waiting for lung transplantation. To overcome the lack of organs, various strategies have been developed by transplant centers including use of marginal donors. To increase the lung utilization rate in multiorgan donors, we implemented a simple lung recruitment protocol involving a brief period of controlled sustained inflation. In 2005, the lung utilization rate in the transplant program at our institution was only 20% in multiorgan donors. With the lung recruitment protocol, the rate of lung utilization for transplantation increased to 33%, in 2006, 24% in 2007, and 24% in 2008. Following the lung recruitment protocol, the arterial oxygen tension/fraction of inspired oxygen ratio increased to greater than 15% in more than 40% of donors. We were able to improve gas exchange sufficiently that as many as two-thirds of the lungs were suitable for transplantation. During the protocol, no complications were reported, and no patient became hemodynamically unstable, precluding organ procurement. We believe that optimization of multiorgan donor management with simple interventions may improve oxygenation, reducing the number of inadequate donor lungs and increasing the overall donor pool and organ availability.


Sujet(s)
Transplantation pulmonaire/statistiques et données numériques , Donneurs de tissus/statistiques et données numériques , Listes d'attente , Mort cérébrale , Bronchoscopie , Cadavre , Humains , Adulte d'âge moyen , Consommation d'oxygène , Sélection de patients , Québec , Radiographie thoracique , Fumer/épidémiologie , Acquisition d'organes et de tissus/méthodes , Acquisition d'organes et de tissus/statistiques et données numériques , États-Unis
6.
Eur J Pediatr Surg ; 18(6): 410-4, 2008 Dec.
Article de Anglais | MEDLINE | ID: mdl-19012235

RÉSUMÉ

BACKGROUND: Surgery is the first line treatment for low-grade neuroblastomas. In stage I tumors, the presence of MYCN amplification is rarely detected and the Shimada histology is not always taken into consideration when deciding on the treatment. This study concerns the significance of these two factors in the evolution of children with low-grade neuroblastomas. METHODS: We analyzed the assessment and follow-up of children with low-grade neuroblastomas (stages I and II) with or without MYCN amplification, with either a favorable or unfavorable histology and with or without tumor cell diploidy. Favorable histology was defined as stroma-poor tumors with more than 5 % differentiating neuroblasts and a mitosis karyorrhexis index (MKI) of less than 100/5000 cells. RESULTS: From 1995 to 2006, out of 114 neuroblastomas, nine (7.9 %) were stage I and 21 (18.4 %) stage II. Of these 30 patients, 27 underwent surgery alone and three received chemotherapy after surgery. The combination of MYCN amplification, unfavorable histology and diploidy was noted in one patient who developed metastases within two months. MYCN amplification alone was noted in two cases who are still tumor-free after two years. Unfavorable histology alone was noted in four patients, of whom one suffered a recurrence of the tumor (previously stage I) and three are tumor-free after six years. Tumor cell diploidy alone was present in 11 patients whose evolution is satisfactory. CONCLUSION: Because MYCN amplification and unfavorable histology are rare in early stage neuroblastomas, these tumors may be misclassified if they are not investigated further. It seems that no single clinical or biological feature can be considered a significant factor in establishing a prognosis or determining whether additional treatment is required.


Sujet(s)
ADN tumoral/métabolisme , Diploïdie , Amplification de gène , Marqueurs génétiques , Neuroblastome/anatomopathologie , Protéines nucléaires/génétique , Protéines oncogènes/génétique , Enfant d'âge préscolaire , Femelle , Humains , Nourrisson , Mâle , Protéine du proto-oncogène N-Myc , Neuroblastome/thérapie , Pronostic , Études rétrospectives
7.
J Pharm Biomed Anal ; 45(1): 70-81, 2007 Sep 21.
Article de Anglais | MEDLINE | ID: mdl-17646076

RÉSUMÉ

As reported in a previous paper, the main objective of the new commission of the Société Française des Sciences et Techniques Pharmaceutiques (SFSTP) was the harmonisation of approaches for the validation of quantitative analytical procedures. In a series of meetings, members of this Commission have first tried to review the objectives of analytical methods and the objectives of validation methods and to recommend the use of two-sided beta-expectation tolerance intervals for total error of validation samples (accuracy profile) in the acceptance/rejection of analytical method in validation phase. In the context of the harmonization, the other objectives were: (i) to propose a consensus on the norms usually recognized, while widely incorporating the ISO terminology; (ii) to recommend to validate the analytical procedure accordingly to the way it will be used in routine; (iii) to elaborate a rational, practical and statistically reliable strategy to assure the quality of the analytical results generated. This strategy has been formalised in a guide and the three latter objectives made by the Commission are summarised in the present paper which is the second part of summary report of the SFSTP commission. The SFSTP guide has been produced to help analysts to validate their analytical methods. It is the result of a consensus between professionals having expertise in analytical and/or statistical fields. The suggestions presented in this paper should therefore help the analyst to design and perform the minimum number validation experiments needed to obtain all the required information to establish and demonstrate the reliability of its analytical procedure.


Sujet(s)
Techniques de chimie analytique , Chimie pharmaceutique , Sociétés médicales , Calibrage , Techniques de chimie analytique/méthodes , Techniques de chimie analytique/normes , Chimie pharmaceutique/méthodes , Chimie pharmaceutique/normes , Techniques de laboratoire clinique/méthodes , Techniques de laboratoire clinique/normes , France , Normes de référence , Reproductibilité des résultats
8.
Can J Gastroenterol ; 20(7): 475-8, 2006 Jul.
Article de Anglais | MEDLINE | ID: mdl-16858500

RÉSUMÉ

BACKGROUND: Liver disease is the third most common cause of death in children with cystic fibrosis (CF). Liver transplantation is an effective treatment in children with hepatic failure. AIMS: The objective of the present study was to review the indications and postoperative course of hepatic transplantation in a cystic fibrosis population. PATIENTS: Five children with CF, at a mean age of 16.5 years, underwent liver transplantation. RESULTS: All patients showed cirrhosis, portal hypertension and hepatic failure. The main postoperative complication was ascites refractory to treatment in two patients. No significant deterioration of the pulmonary function was noted. Two patients died, one of Hodgkin lymphoma and the other of progressive pulmonary failure. CONCLUSION: Liver transplantation was indicated in children with CF when hepatic failure and/or severe portal hypertension was present with well-preserved pulmonary function.


Sujet(s)
Mucoviscidose/complications , Cirrhose du foie/chirurgie , Transplantation hépatique , Mucoviscidose/physiopathologie , Femelle , Humains , Hypertension portale/étiologie , Immunosuppresseurs/usage thérapeutique , Nourrisson , Nouveau-né , Durée du séjour , Cirrhose du foie/étiologie , Mâle , Complications postopératoires/épidémiologie , Tests de la fonction respiratoire
9.
J Pharm Biomed Anal ; 36(3): 579-86, 2004 Nov 15.
Article de Anglais | MEDLINE | ID: mdl-15522533

RÉSUMÉ

This paper is the first part of a summary report of a new commission of the Société Française des Sciences et Techniques Pharmaceutiques (SFSTP). The main objective of this commission was the harmonization of approaches for the validation of quantitative analytical procedures. Indeed, the principle of the validation of theses procedures is today widely spread in all the domains of activities where measurements are made. Nevertheless, this simple question of acceptability or not of an analytical procedure for a given application, remains incompletely determined in several cases despite the various regulations relating to the good practices (GLP, GMP, ...) and other documents of normative character (ISO, ICH, FDA, ...). There are many official documents describing the criteria of validation to be tested, but they do not propose any experimental protocol and limit themselves most often to the general concepts. For those reasons, two previous SFSTP commissions elaborated validation guides to concretely help the industrial scientists in charge of drug development to apply those regulatory recommendations. If these two first guides widely contributed to the use and progress of analytical validations, they present, nevertheless, weaknesses regarding the conclusions of the performed statistical tests and the decisions to be made with respect to the acceptance limits defined by the use of an analytical procedure. The present paper proposes to review even the bases of the analytical validation for developing harmonized approach, by distinguishing notably the diagnosis rules and the decision rules. This latter rule is based on the use of the accuracy profile, uses the notion of total error and allows to simplify the approach of the validation of an analytical procedure while checking the associated risk to its usage. Thanks to this novel validation approach, it is possible to unambiguously demonstrate the fitness for purpose of a new method as stated in all regulatory documents.


Sujet(s)
Techniques de chimie analytique/méthodes , Techniques de chimie analytique/normes , Chimie pharmaceutique/méthodes , Chimie pharmaceutique/normes , Sociétés médicales/normes , Techniques de laboratoire clinique/méthodes , Techniques de laboratoire clinique/normes , France , Reproductibilité des résultats
10.
Transplant Proc ; 36(2 Suppl): 448S-450S, 2004 Mar.
Article de Anglais | MEDLINE | ID: mdl-15041384

RÉSUMÉ

The aim of this study was to assess the relationship between cyclosporine (CyA) trough level (C0) and 2-hour postdose (C2) and total cholesterol (TC) in kidney transplant (KT) recipients on Neoral maintenance immunosuppression. In KT recipients who had more than 5 years of follow-up, stable graft function, and stable Neoral dose, we measured C2 and C0 blood levels, serum creatinine, mean total cholesterol (TC) over the last 5 years, prednisone dose, use of beta-blockers and thiazides. Correlations between C0 and C2 levels and TC were performed with the Pearson coefficient. Receiver operating characteristics (ROCs) were used to define the threshold with greater accuracy for significant variables at the correlation test. Statistical tests were performed with SPSS 9.5 The C2 correlated with TC (0.31; P=.008) whereas C0 did not. The C2 level was an independent predictor for TC after adjusting for recipient age, gender, dose of prednisone, creatinine clearance, and use of beta-blockers and thiazides (B coefficient=1.124(E-3); P=.009). A threshold C2 value of 700 microg/L yielded to a TC level of 5.2 mmol/L. This is the first study to report a correlation between C2 levels and TC. Although C2 explained a small fraction of TC variability, it is an independent predictor of TC in KT recipients on Neoral maintenance immunosuppression. A long-term C2 value under 700 microg correlates with better control of hypercholesterolemia.


Sujet(s)
Cholestérol/sang , Ciclosporine/sang , Ciclosporine/usage thérapeutique , Transplantation rénale/physiologie , Ciclosporine/pharmacocinétique , Femelle , Études de suivi , Humains , Transplantation rénale/immunologie , Mâle , Adulte d'âge moyen , Courbe ROC , Études rétrospectives
12.
Ann Dermatol Venereol ; 128(6-7): 715-8, 2001.
Article de Français | MEDLINE | ID: mdl-11460032

RÉSUMÉ

BACKGROUND: The association between mucosal oncogenic human papillomaviruses (HPV) and bowenoid papulosis or genital Bowen's disease is well documented. In contrast this association with extra-genital Bowen's disease is poorly studied. The aim of this study was to detect oncogenic (16/18, 31/33/51) and non oncogenic (8/11) mucosal HPV using a in situ hybridization method in 28 skin biopsy specimens of extra-genital Bowen's disease. PATIENTS AND METHODS: Twenty-eight cases of extra-genital Bowen's disease seen in the period 1990-96 in the Dermatology department were included: 19 women and 9 men (mean age: 72 years). Bowen's disease locations were: hands and feet (8 cases), limbs (11 cases), face (8 cases), trunk (1 case). Blinded histopathologic examination confirmed the diagnosis of Bowen's disease and signs of HPV infection (koilocytosis). In situ hybridization was performed using three biotinylated probes detecting HPV types 6/11, 16/18, 31/33/51. RESULTS: Oncogenic HPV genoma was detected in 8 skin samples (28.6 p. 100). In all these cases, 16/18 probe was positive and in two cases, both 16/18 and 31/33/51 probes were positive; 4/8 Bowen's diseases of the extremities were positive for HPV. Koilocytes were found in 6/8 of skin samples with positive HPV detection. DISCUSSION: Mucosal oncogenic HPV are detected by in situ hybridization in 28.6 p. 100 of extra-genital Bowen's disease. In situ hybridization is an easier technique than Southern-Blot hybridization which is the gold standard. Five studies reported similar results and three studies reported different results that we discuss. A precise understanding of oncogenic HPV implication in the development of extra-genital Bowen's disease could lead to the development of new therapeutic strategies (topical cidofovir or imiquimod).


Sujet(s)
Maladie de Bowen/virologie , Hybridation in situ , Papillomaviridae/pathogénicité , Infections à papillomavirus/virologie , Tumeurs cutanées/virologie , Infections à virus oncogènes/virologie , Sujet âgé , Maladie de Bowen/anatomopathologie , Femelle , Tumeurs de l'appareil génital féminin/anatomopathologie , Tumeurs de l'appareil génital féminin/virologie , Tumeurs de l'appareil génital mâle/anatomopathologie , Tumeurs de l'appareil génital mâle/virologie , Humains , Mâle , Papillomaviridae/isolement et purification , Infections à papillomavirus/anatomopathologie , Sensibilité et spécificité , Peau/anatomopathologie , Peau/virologie , Tumeurs cutanées/anatomopathologie , Infections à virus oncogènes/anatomopathologie , Virulence
14.
J Pediatr Surg ; 36(5): 760-2, 2001 May.
Article de Anglais | MEDLINE | ID: mdl-11329583

RÉSUMÉ

PURPOSE: The goal of the current study was to evaluate the risk of intraabdominal injury in children who sustained spinal fractures in a motor vehicle collision (MVC). METHODS: Between 1980 and 1999, 48 patients, 24 girls and 24 boys, with a mean age of 12.8 years (range, 4 to 17) were reviewed. Twenty-nine were rear seat passengers, 12 front seat, and 7 unknown. Fifty-eight percent wore a seat belt. Thirty fractures involved the lumbar spine, 12 the thoracic, and 6 combined. Computed tomography (CT) scan, abdominal ultrasound, and peritoneal lavage were used to screen for abdominal injuries. RESULTS: Twenty-two of 48 patients had an intraabdominal injury. Eighteen (38%) required an early (<24 hours; n = 12) or delayed (n = 6) therapeutic laparotomy. Fourteen patients were rear seat passengers, 15 wore a seat belt, and 13 had an abdominal wall ecchymoses (AWE). They were 17 lumbar fractures (13 Chance) and one thoracic. The most common findings at laparotomy were hollow viscus injury (n = 12), mesenteric tear (n = 9), and solid organ injury (n = 8). Seventy-two percent of patients presenting with a lumbar fracture and AWE needed a therapeutic laparotomy. The overall survival rate was 98% with only 1 death. The mean hospital stay was 22.4 days. In this study, 38% of patients presenting with a spinal fracture required laparotomy, 68% of whom had simultaneous lumbar fracture and AWE. CONCLUSION: In light of these results, the authors propose that laparoscopy or laparotomy should be strongly considered in patients sustaining lumbar fracture and AWE after MVC. J Pediatr Surg 36:760-762.


Sujet(s)
Traumatismes de l'abdomen/étiologie , Accidents de la route , Vertèbres lombales/traumatismes , Polytraumatisme/étiologie , Fractures du rachis/étiologie , Vertèbres thoraciques/traumatismes , Traumatismes de l'abdomen/diagnostic , Traumatismes de l'abdomen/chirurgie , Adolescent , Phénomènes biomécaniques , Enfant , Enfant d'âge préscolaire , Femelle , Humains , Durée du séjour/statistiques et données numériques , Mâle , Dépistage de masse/méthodes , Polytraumatisme/diagnostic , Polytraumatisme/chirurgie , Lavage péritonéal , Études rétrospectives , Facteurs de risque , Ceintures de sécurité/statistiques et données numériques , Fractures du rachis/diagnostic , Fractures du rachis/chirurgie , Analyse de survie , Tomodensitométrie , Centres de traumatologie
15.
Can J Anaesth ; 46(10): 970-4, 1999 Oct.
Article de Anglais | MEDLINE | ID: mdl-10522585

RÉSUMÉ

PURPOSE: To describe the anesthetic and ventilatory management of an infant with diffuse pulmonary bullous lesions. CLINICAL FEATURES: Four successive operations were scheduled for an infant with diffuse pulmonary bullous lesions. At the age of seven weeks, conventional positive pressure ventilation during laparotomy for intestinal occlusion led to arterial desaturation. This was corrected by returning to spontaneous respiration and deep inhalation anesthesia with halothane. Based on our ICU experience and due to a potential impaired oxygenation during conventional ventilation, we chose high-frequency oscillatory ventilation (HFOV) for bilateral sequential thoracotomies for bullectomies at the age of five months. We elected the same ventilatory mode for laparotomy for intestinal obstruction secondary to a polyp at the age of six months. This ventilatory mode was combined with total intravenous anesthesia and epidural analgesia and provided optimal oxygenation and ventilation as well as vital signs stability. CONCLUSION: High frequency oscillatory ventilation is a safe technique that may be used in the operating room in cases where conventional ventilation failed to provide satisfactory gas exchange.


Sujet(s)
Ventilation à haute fréquence , Maladies pulmonaires/thérapie , Anesthésie péridurale , Anesthésie intraveineuse , Gazométrie sanguine , Dioxyde de carbone/sang , Femelle , Hémodynamique , Humains , Nourrisson , Poumon/imagerie diagnostique , Maladies pulmonaires/imagerie diagnostique , Maladies pulmonaires/chirurgie , Oxygène/sang , Radiographie , Thoracotomie
16.
J Pediatr Surg ; 34(7): 1057-9, 1999 Jul.
Article de Anglais | MEDLINE | ID: mdl-10442587

RÉSUMÉ

BACKGROUND: Pleuropulmonary blastoma is among the rarest tumors of childhood. Three types have been described: cystic, solid, and mixed. To date, bilateral disease has not been documented. METHODS AND RESULTS: A 5-week-old girl presented with a history of fever. Chest x-ray showed bilateral diffuse cystic lesions. Bowel obstruction developed that required laparotomy. Multiple small bowel polyps were resected. The patient was readmitted 4 months later with deteriorating respiratory status. She underwent sequential thoracotomies for resection of multiple bullae under high-frequency oscillatory ventilation. Small bowel polypectomies were again required because of obstruction. Lung lesions were compatible with pulmonary blastoma but could not be correlated with intestinal polyposis. Bilateral cystic renal lesions were seen on ultrasound scan. Her disease progressed, despite chemotherapy, with the appearance of metastatic iris lesions. She again underwent laparotomies for multiple recurrent generalized small bowel polyps that were causing obstruction. Expanding renal cysts affected kidney function, and she died at 14 months of age. CONCLUSIONS: The rare association between pleuropulmonary blastoma and Wilms' tumor or nephroblastomatosis is known but rarely reported. Lacking pathological evidence, we can only speculate that this was the case. We have been unable to demonstrate any histological association between the renopulmonary and digestive lesions. Despite many unanswered questions, we are likely dealing with a "syndrome" of sorts with a dire outcome, despite aggressive treatments.


Sujet(s)
Tumeurs du poumon/diagnostic , Blastome pulmonaire/diagnostic , Protocoles de polychimiothérapie antinéoplasique/usage thérapeutique , Ponction-biopsie à l'aiguille , Issue fatale , Femelle , Humains , Nourrisson , Tumeurs du poumon/traitement médicamenteux , Tumeurs du poumon/anatomopathologie , Blastome pulmonaire/traitement médicamenteux , Blastome pulmonaire/anatomopathologie , Tomodensitométrie
17.
J Pediatr Surg ; 34(7): 1053-6, 1999 Jul.
Article de Anglais | MEDLINE | ID: mdl-10442586

RÉSUMÉ

PURPOSE: The aim of this study was to evaluate the pertinence of pH studies for persistent ear, nose, and throat (ENT) symptoms and their eventual relationship to gastroesophageal reflux (GER). METHODS: Retrospective analysis was performed of age, reason for referral, pH study, treatment, and follow-up of patients with ENT symptoms suspected to have GER. RESULTS: Of 3,000 esophageal pH studies performed over 16 years, 105 children were referred for ENT symptoms by an otorhinolaryngologist to rule out GER. Mean age was 33 months; 65% were boys. Reasons for referral included (number and mean age): stridor (n = 31, 8 months), laryngomalacia (n = 18, 13 months), recurrent otitis (n = 12, 42 months), laryngitis (n = 16, 50 months), dysphonia (n = 14, 59 months), laryngeal papillomatosis (n = 8, 62 months), sinusitis (n = 5, 56 months), and dysphagia (n = 1). Overall, 41% of study results were positive: stridor (58%), laryngomalacia (61%), laryngitis (56%) and sinusitis (40%). Patients with otitis, dysphonia and laryngeal papillomatosis had GER in 1%, 14%, and 25%, respectively. Follow-up in the three larger groups of patients showed resolution of the ENT symptoms after medical treatment of the reflux in 83% of patients with stridor and reflux, 86% with laryngitis and reflux, and 80% with laryngomalacia and reflux. Four fundoplications were performed: one neurologically impaired patient, and four nonresponders. CONCLUSIONS: The authors recommend that a pH study be performed in children with stridor, laryngomalacia, laryngitis, and sinusitis when faced with failure of the usual treatment. However, a pH study does not seem as beneficial for recurrent otitis, dysphonia, or laryngeal papillomatosis.


Sujet(s)
Oesophage/métabolisme , Reflux gastro-oesophagien/complications , Reflux gastro-oesophagien/diagnostic , Maladies oto-rhino-laryngologiques/étiologie , Enfant , Enfant d'âge préscolaire , Femelle , Études de suivi , Reflux gastro-oesophagien/thérapie , Humains , Concentration en ions d'hydrogène , Incidence , Mâle , Monitorage physiologique/méthodes , Maladies oto-rhino-laryngologiques/diagnostic , Études rétrospectives , Facteurs de risque , Sensibilité et spécificité
18.
J Pediatr Surg ; 34(7): 1060-3, 1999 Jul.
Article de Anglais | MEDLINE | ID: mdl-10442588

RÉSUMÉ

BACKGROUND: Falls are a major cause of emergency room visits and admissions in pediatric hospitals. METHODS: To better understand the epidemiology of falls from height and develop prevention strategies, the authors reviewed all admissions after a fall at a single institution from 1994 to 1997. Inclusion criteria are falls from a minimum height of 10 feet. RESULTS: Of 1,410 patients admitted after a fall, 64 patients including 45 boys and 19 girls with a mean age of 7.4 years (range, 1 to 18) are included in this study. Fifty (78%) children fell from 20 feet or less (two stories) and 14 (22%) from height greater than 20 feet. Patients mainly fell from balconies (n = 15), windows (n = 13), trees (n = 9), roofs (n = 6), stairs (n = 6), diving board (n = 3) and miscellaneous (n = 12). Over 60% of falls occurred in private houses and during the summer months. Fifty-five patients (86%) sustained only one system injury, two patients had no significant injury, and seven patients had multisystem injury. Major injuries included head trauma (39%), musculoskeletal (34%), abdominal (12%), maxillofacial (8%), and spine (6%). A surgical intervention was required for 43% of intracranial trauma, 39% of musculoskeletal injuries, 60% of facial trauma, and 50% of spine fractures. Mean length of stay in hospital varied according to the injured system. The overall survival rate is 98% with only one death after a fall greater than 50 feet. CONCLUSIONS: Although rarely mortal, falls from height carry a significant morbidity and are costly to the health care system. To decrease the occurrence of injuries caused by falls, strategies should include awareness campaigns, parent's education about the mechanisms of falls, increase parenteral supervision during playing activities, and legislative measures to ensure the safety of windows and balconies before the onset of summer.


Sujet(s)
Chutes accidentelles/statistiques et données numériques , Polytraumatisme/épidémiologie , Chutes accidentelles/prévention et contrôle , Adolescent , Répartition par âge , Enfant , Enfant d'âge préscolaire , Service hospitalier d'urgences , Femelle , Humains , Incidence , Score de gravité des lésions traumatiques , Mâle , Polytraumatisme/étiologie , Polytraumatisme/thérapie , Québec/épidémiologie , Études rétrospectives , Facteurs de risque , Répartition par sexe , Taux de survie , Population urbaine
19.
J Pediatr Surg ; 34(7): 1133-5, 1999 Jul.
Article de Anglais | MEDLINE | ID: mdl-10442608

RÉSUMÉ

Two patients presented as full-term baby girls with anorectal and genital malformations with extensive perineal hemangiomas. The first patient had a vestibular anus with a perineal hemangioma involving the bladder, rectal, and vaginal walls. Skin ulcerations required a transverse loop colostomy for wound care. The vulva, urethral opening, and clitoris were deviated to the left, labia minora were absent, and the labia majora were abnormal. The second patient had an anus displaced anteriorly and deviated to the right. The external anal sphincter was hypertrophic on the left and atrophic on the right. Rectal examination showed agenesis of the right levator ani and a dentate line located at the skin level. She had a large perineal, sacral, vaginal, pararectal and retroperitoneal hemangioma and developed extensive skin ulcerations. She had only a hemiclitoris located to the left of the midline, near absence of labia minora, and hypertrophied labia majora. The urethra was displaced to the left and opened in the vestibule. Both patients had a spinal malformation (one with tethered cord and one with spina bifida) and a normal karyotype. Steroids and interferon allowed near-complete resolution of hemangiomas in both patients. The authors were impressed by the similarity of these two cases and could not find any previous description of this association.


Sujet(s)
Malformations multiples/thérapie , Imperforation anale/chirurgie , Système génital de la femme/malformations , Hémangiome/traitement médicamenteux , Périnée , Tumeurs des tissus mous/chirurgie , Malformations multiples/diagnostic , Imperforation anale/diagnostic , Association thérapeutique , Femelle , Études de suivi , Hémangiome/diagnostic , Humains , Nouveau-né , Interférons/usage thérapeutique , Rectum/malformations , Rectum/chirurgie , Tumeurs des tissus mous/diagnostic , Stéroïdes/usage thérapeutique , Résultat thérapeutique
20.
J Pediatr Surg ; 33(6): 846-8, 1998 Jun.
Article de Anglais | MEDLINE | ID: mdl-9660211

RÉSUMÉ

BACKGROUND/PURPOSE: Although medullary thyroid carcinoma (MTC) can occur sporadically, in the pediatric population it is most often associated with the multiple endocrine neoplasia syndrome (MEN type 2). Traditional screening was based on evaluation of basal and stimulated serum calcitonin levels. The recent cloning of the MEN2 gene on the RET proto-oncogene of chromosome 10 now allows for testing of gene carrier status in individuals at risk who could benefit from prophylactic treatment. The current study was undertaken to determine the appropriate age for safe total prophylactic thyroidectomy. METHODS: Over a 16-year period, 12 patients with a family history of MEN2A and one with a MEN2B underwent total thyroidectomy and central neck dissection without parathyroid autotransplantation. Four patients (31%) were treated previously for Hirschsprung's disease. RESULTS: In seven patients (mean age, 11.8 years) undergoing biochemical screening for diagnosis, multifocal MTC and C cell hyperplasia (CCH) were found in all the resected specimens. Of six patients identified with genetic screening (mean age, 9.1 years), two had elevated stimulated calcitonin levels, one (age 14) had evidence of MTC, and one (age 6) had CCH. Four patients with normal calcitonin levels had no evidence of MTC (ages 6, 8, 10) but there was one occurrence of CCH (age 11). No permanent postoperative hypoparathyroidism or recurrent laryngeal nerve damage occurred in this series. With a mean follow-up of 4 years (range, 1 to 14 years), the overall disease-free survival is 100%. CONCLUSIONS: From this study the authors conclude that total thyroidectomy can be performed safely in children and should be the treatment of choice in patients with a family history of MEN2A carrying a germinal RET mutation even if the serum basal or stimulated serum calcitonin level is normal. Total thyroidectomy should be performed as early as 5 years of age before the occurrence of CCH or MTC.


Sujet(s)
Néoplasie endocrinienne multiple de type 2a/génétique , Néoplasie endocrinienne multiple de type 2a/prévention et contrôle , Tumeurs de la thyroïde/prévention et contrôle , Thyroïdectomie , Adolescent , Enfant , Enfant d'âge préscolaire , Femelle , Hétérozygote , Humains , Nourrisson , Mâle , Proto-oncogène Mas , Études rétrospectives
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