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Dive into the research topics where Arielle Salon is active.

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Featured researches published by Arielle Salon.


Journal of Hand Surgery (European Volume) | 2000

Long-Term Follow-Up of Surgical Correction of Madelung’s Deformity with Conservation of the Distal Radioulnar Joint in Teenagers:

Arielle Salon; M. Serra; J. C. Pouliquen

Eleven wrists with painful Madelung deformity in seven patients were corrected during adolescence by a closing wedge osteotomy of the radius and a shortening osteotomy of the ulna, with conservation of the distal radioulnar joint. At late follow-up (9.7 years) function was considerably improved. When the ulnar head was correctly relocated during operation, a new distal radioulnar space developed. Shortening of the ulna must be generous and combined with slight flexion at the osteotomy.


Journal of Hand Surgery (European Volume) | 2012

Recurrence of Radial Bowing After Soft Tissue Distraction and Subsequent Radialization for Radial Longitudinal Deficiency

Caroline Dana; Jean-Charles Aurégan; Arielle Salon; Stéphane Guéro; Christophe Glorion; Stéphanie Pannier

PURPOSE Centralization and radialization are the most widely reported surgical treatments for Bayne and Klug Type III and IV radial longitudinal deficiency. Prior soft tissue distraction has been introduced to improve reducibility of the deformity without skeletal resection. Satisfying long-term effects have been reported with centralization but are still unclear with radialization. METHODS This is a retrospective study of 8 consecutive children with Bayne and Klug Type III or IV radial longitudinal deficiency treated with preliminary soft tissue distraction followed by radialization between 2003 and 2008. All children underwent the same surgical protocol. End points of the study were clinical appearance, the hand-forearm angle, and mean angular correction at last follow-up. RESULTS The mean preoperative hand-forearm angle was 61° (26°-91°). The average duration of distraction was 1.9 month (1-3 mo). The initial postoperative angle averaged 12° (-14°-40°). There were 3 postoperative complications: 2 cases of pin loosening and 1 case of fracture of the base of the small finger metacarpal. Mean follow-up duration was 2.6 years (1-4 y). At last follow-up, 7 of the 8 patients had visible recurrence of the deformity, the hand-forearm angle had deteriorated to 44° (20°-69°), and the mean angular correction was 18° (-43°-59°). CONCLUSIONS Preoperative distraction allows a gradual realignment of the hand on the forearm without skeletal resection, but the recurrence rate after radialization is high. Tendon transfers and soft tissue tensioning were unable to maintain hand-forearm alignment following soft tissue distraction. TYPE OF STUDY/LEVEL OF EVIDENCE Therapeutic IV.


Journal of Hand Surgery (European Volume) | 2017

Metacarpal lengthening in children: comparison of three different techniques in 15 consecutive cases

Caroline Dana; Jean-Charles Aurégan; Arielle Salon; Stéphane Guéro; Christophe Glorion; Stéphanie Pannier

Metacarpal lengthening is a useful procedure to address hand deficiencies in children. In this study, we aimed to compare the results of three different techniques from one consecutive clinical series of hand deficiencies. A total of 15 metacarpal lengthenings have been performed in 12 children aged from 9 to 14 years. The callotasis technique was used in seven cases, the two-stage distraction-graft technique in four cases and the single-stage lengthening in four cases. All the metacarpals healed with bone. The lengthening obtained was a mean of 13 mm (range 8–21 mm), a mean of 22 mm (range 13–32 mm) and a mean of 12 mm (range 9–15 mm), respectively, in the three different techniques. The healing index was longer for callotasis (81 days/cm) compared with the other techniques (41 days/cm and 46 days/cm, respectively). We observed one case of fracture after callotasis and one after distraction-graft. One patient underwent tenolysis of the extensor mechanism after single-stage lengthening. In conclusion, distraction graft and single-stage lengthening may be valuable alternatives to callotasis. Level of evidence: IV; therapeutic study; multi-case series


Journal of Pediatric Orthopaedics B | 2005

Post-traumatic distal interphalangeal finger joint reconstruction using a free hemi-joint transfer from the fifth toe middle phalanx.

Arielle Salon; Pierre Journeau; Jean Luc Drape

We present three cases of finger distal interphalangeal joint reconstruction in children using a new donor site, the middle phalanx of the fifth toe, transferred as a non-vascularized graft. The patients were followed a minimum of 36 months with serial radiographs, magnetic resonance imaging and photographs. Alignment was improved and persisting growth was demonstrated in all cases. Postoperative magnetic resonance imaging of the grafted phalanx and control toe showed comparable signals. The absence of a proximal epiphysis of these toe phalanges may have an important role in their survival after free transplantation, and may promote continued growth.


Journal of Hand Surgery (European Volume) | 2018

Surgical Treatment of Enchondromas of the Hand During Childhood in Ollier Disease

Céline Klein; Tiphanie Delcourt; Arielle Salon; G. Finidori; Christophe Glorion; Stéphanie Pannier

PURPOSE The objective of the present study was to evaluate the outcome of surgical treatment of hand lesions in Ollier disease (OD) carried out during childhood. METHODS A retrospective review was carried out of 10 pediatric patients with hand involvement of OD, who had undergone surgery for metacarpal or phalangeal enchondromas. The technique comprised curettage and cortical bone reconstruction with corticoplasty, to restore a near-normal phalangeal volume. The range of finger motion (pulp-to-palm distance), the shortened Disabilities of the Arm, Shoulder, and Hand (QuickDASH) questionnaire score, cosmetic improvement, radiological findings (according to Tordais classification), and recurrence were recorded after a mean follow-up of 7.5 years (range, 4-11.3 years). RESULTS The mean age at surgery was 10.7 years (range, 6-14 years). Curettage was performed on 35 enchondromas, and 9 cavities were filled with a bone graft. The mean pulp-to-palm distance was significantly lower after surgery (from 1.5 cm to 0.25 cm; P < .05). The mean QuickDASH score was 3.84 (range, 0-11.4). A marked cosmetic improvement was noted for 83% of the hands. Three enchondromas recurred in 1 patient, requiring a second curettage. Fifty-seven percent of the cavities were completely filled with bone (Tordai stage 1) at last follow-up. The outcome did not depend on the presence or absence of a bone graft. CONCLUSIONS Our results suggest that early surgical treatment comprising curettage and corticoplasty leads to good clinical, cosmetic, and radiological outcomes. Early surgical treatment of well-developed and/or symptomatic enchondromas of the hand in OD should be considered. TYPE OF STUDY/LEVEL OF EVIDENCE Therapeutic V.


Chirurgie De La Main | 2013

Ostéotomie en roseau du radius chez l’enfant dans la paralysie de la pronation du plexus brachial obstétrical

F. Alkar; Caroline Dana; Arielle Salon; Christophe Glorion


Hand surgery and rehabilitation | 2017

Chirurgie des clinodactylies dans le syndrome de Rubinstein et Taybi – apport du transfert non vascularisé de phalange d’orteil

Marie Le Mapihan; Stéphane Guéro; Alina Badina; Arielle Salon; Stéphanie Pannier


Hand surgery and rehabilitation | 2017

Physiolyse selon Vickers pour le traitement de la clinodactylie par phalange delta–efficacité précoce

Laila El Sayed; Arielle Salon; Christophe Glorion; Stéphane Guéro


Chirurgie De La Main | 2014

Main de Poland et symbrachydactylie avec instabilité osseuse : stratégie thérapeutique en deux temps

Arielle Salon; Caroline Dana


Revue de Chirurgie Orthopédique et Traumatologique | 2012

Résultats cliniques et radiologiques des transferts épiphysaires de fibula après résection d’une tumeur osseuse chez sept enfants

Manon Bachy; Stéphanie Pannier; Caroline Dana; Arielle Salon; Eric Mascard; Christophe Glorion

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Christophe Glorion

Necker-Enfants Malades Hospital

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Stéphanie Pannier

Necker-Enfants Malades Hospital

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Caroline Dana

Necker-Enfants Malades Hospital

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Stéphane Guéro

Necker-Enfants Malades Hospital

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Pouliquen Jc

Necker-Enfants Malades Hospital

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Pierre Journeau

Boston Children's Hospital

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Jean-Charles Aurégan

Necker-Enfants Malades Hospital

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Alina Badina

Necker-Enfants Malades Hospital

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C. Delaroche

Necker-Enfants Malades Hospital

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Céline Klein

Necker-Enfants Malades Hospital

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