Congenital radioulnar synostosis: symptom complex and surgical treatment
| Autor: | Vladimir Vasilievich Selizov, Evgeny V Prokopovich, Konstantin A. Afonichev, Aleksander B Kovzikov, Mikhail A Konev, Tatyana S Vinokurova, Maksim S. Nikitin, Ivan E Prokopovich |
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| Rok vydání: | 2016 |
| Předmět: |
medicine.medical_specialty
medicine.diagnostic_test business.industry surgical treatment medicine.medical_treatment lcsh:RJ1-570 lcsh:Pediatrics Electromyography Synostosis Osteotomy medicine.disease Functional disorder Surgery medicine.anatomical_structure Forearm Pediatrics Perinatology and Child Health medicine Orthopedics and Sports Medicine Presentation (obstetrics) upper limb congenital anomalies Complication business Radial nerve radioulnar synostosis |
| Zdroj: | Ortopediâ, Travmatologiâ i Vosstanovitelʹnaâ Hirurgiâ Detskogo Vozrasta, Vol 4, Iss 3, Pp 16-25 (2016) |
| ISSN: | 2410-8731 2309-3994 |
| DOI: | 10.17816/ptors4316-25 |
| Popis: | Background. Congenital radioulnar synostosis (CRUS) is a rare musculoskeletal disease with a wide-ranging symptom complex. Attitudes toward surgical treatment of the disease is very diverse, ranging from complete negation to acceptance. When choosing a treatment method, high recurrence and complication rates should be taken into account. Aims. To analyze the clinical implications of CRUS and to identify optimal treatment options. Materials and methods. From 2008 to 2015, 54 patients (31 boys and 23 girls; aged 1–14 years) with CRUS were examined and treated. Presenting complaints and the possible factors leading to disease development were investigated; orthopedic examination, roentgenography, electromyography, and computed tomography were performed. The treatment approach was determined on the basis of the clinicoroentgenological presentation. Results. All cases of CRUS were sporadic. In 43.7% patients, risk factors resulting in disease development were detected. Unilateral lesions were observed in 30 patients, whereas bilateral lesions were observed in 24 patients. According to the Cleary and Omer classification, the first type is the rarest; it is distinguished by the absence of bony fusion and close to average forearm positioning. In such cases, operative treatment is not necessary. For the second and third types, pronounced pronation forearm realignment requiring corrective derotational osteotomy of the radial bone is the main factor. For the fourth type, the main functional disorder is the restriction of the forearm flexion; treatment for this type involves resection of the radius head. We attempted to divide the synostosis (to achieve active movements) in five patients; however, we were unsuccessful. In three patients, synostosis recurrence occurred; and in two patients, active movements were not obtained after surgery. In four patients, radial nerve neuropathy was detected in the postoperative period after conservative therapy. In two patients, ulnar fractures occurred as a result of a fall; in one of these patients, fragment apposition was required. Conclusions. Clinicoroentgenological manifestations of CRUS determine the treatment options. The most typical and important of these manifestations is the pronation positioning of the forearm. In such cases, it is reasonable to start operative CRUS treatment after 3 years. All variants of deformation are indicators for operation, and treatment options are determined by the degree of severity of the deformation. Attempts to form the forearm bone neoarthrosis in order to get rotational movements is not effective and can result in deformation recurrence. |
| Databáze: | OpenAIRE |
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