ABSTRACT
BACKGROUND: Congenital muscular torticollis is the postural deformity of the head and of the neck. The purpose of the present study is to evaluate the results of bipolar sternocleidomastoid (SCM) muscle tenotomy in children. METHODS: The present prospective study was conducted at the Department of Orthopedic Surgery from December 2010 to December 2014. A total of 34 children with congenital muscular torticollis and a mean age of 4.8 years (range: 114 years) were recruited from the Outpatient Department. They were treated with bipolar SCM muscle release under general anesthesia. The functional and cosmetic results were rated on a scoring system modified from Lim et al (2014). All of the children were followed-up for 2 years. RESULTS: At the final follow-up, the neck range of movement and head tilt improved and their appearance were cosmetically improved despite the long-standing nature of the deformity. The results were excellent in 30 patients (88.23%) and good in 4 patients (11.76%). No postoperative complications were found in any of the 34 patients. CONCLUSION: Bipolar tenotomy of the SCM muscle is a good method for correcting difficult cases of congenital muscular torticollis. It is a safe, effective and complicationfree method for these patients.
INTRODUCCIÓN: La tortícolis muscular congénita es la deformidad postural de la cabeza y del cuello. El propósito de este estudio es evaluar los resultados de la tenotomía del músculo esternocleidomastoideo bipolar en niños. MÉTODOS: Este estudio prospectivo, se realizó en el departamento de Cirugía Ortopédica a partir de diciembre de 2010 a diciembre de 2014. Treinta y cuatro niños con tortícolis muscular congénita con una edad media de 4,8 años (rango: 1 a 14 años) fueron reclutados del ambulatorio. Fueron tratados con liberación de músculo esternocleidomustoide bipolar bajo anestesia general. Los resultados funcionales y cosméticos se evaluaron en un sistema de puntuación modificado de Lim y col (2014). Todos los niños recibieron acompañamiento durante dos años. RESULTADOS: En el acompañamiento final, el rango del cuello del movimiento, la inclinación y su apariencia fueron cosméticamente mejorados a pesar de la permanente naturaleza de la deformidad. Los resultados fueron excelentes en treinta pacientes (88,23%) y bueno en cuatro pacientes (11,76%).. No se encontraron complicaciones en el post-operatorio de esos 34 pacientes. CONCLUSIÓN: La tenotomía bipolar de los esternocleidomastoideos es un buen método para corregir los casos de tortícolis muscular congénita.. Para los pacientes, es un método seguro, efectivo y sin complicaciones.
Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Torticollis/surgery , Torticollis/congenital , Tenotomy/methods , Torticollis/physiopathology , Torticollis/rehabilitation , Prospective Studies , Surveys and Questionnaires , Treatment Outcome , Patient Satisfaction , Orthopedic Procedures/methodsABSTRACT
Objective : Describe the functional, clinical and quality of life (QoL) profiles in patients with cervical dystonia (CD) with residual effect or without effect of botulinum toxin (BTX), as well as verify the existence of correlation between the level of motor impairment, pain and QoL. Method : Seventy patients were assessed through the Craniocervical dystonia questionnaire-24 (CDQ-24) and the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS). Results : The greater the disability, pain and severity of dystonia, the worse the QoL (p<0.0001). Greater severity relates to greater disability (p<0.0001). Pain was present in 84% of the sample, being source of disability in 41%. The most frequent complaints were: difficulty in keeping up with professional and personal demands (74.3%), feeling uneasy in public (72.9%), hindered by pain (68.6%), depressed, annoyed or bitter (47.1%), lonely or isolated (32.9%). Conclusion : The physical, social and emotional aspects are the most affected in the QoL of these patients. .
Objetivo : Descrever o perfil funcional, clínico e de qualidade de vida (QV) de pacientes com distonia cervical (DC) com efeito residual ou sem efeito da toxina botulínica (BTX), bem como verificar a existência de correlação entre o nível de comprometimento motor, dor e QV. Método : Setenta pacientes foram avaliados através do Craniocervical dystonia questionnaire-24 (CDQ 24) e Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS). Resultados : Quanto maior a incapacidade, dor e gravidade da distonia pior a QV (p<0,0001). A maior gravidade está relacionada à maior incapacidade (p<0,0001). A dor esteve presente em 84% da amostra sendo fonte de incapacidade em 41%. Dificuldade em manter-se com as demandas profissionais e pessoais (74,3%), sentir-se desconfortável em público (72,9%), prejudicado pela dor (68,6%), deprimido, irritado ou amargurado (47,1%), solitário ou isolado (32,9%) foram as queixas mais frequentes. Conclusão : Os domínios físico, social e emocional são os mais prejudicados na QV desses pacientes. .
Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Activities of Daily Living , Quality of Life/psychology , Torticollis/physiopathology , Torticollis/psychology , Botulinum Toxins/therapeutic use , Motor Activity/physiology , Neck Pain/physiopathology , Neck Pain/psychology , Neurotoxins/therapeutic use , Severity of Illness Index , Socioeconomic Factors , Surveys and Questionnaires , Time Factors , Treatment Outcome , Torticollis/drug therapyABSTRACT
BACKGROUND AND PURPOSE: Few studies have attempted to develop clinical predictors for cervical dystonia (CD) aiming at progression of the dystonic movement. METHOD: We retrospectively evaluated 73 patients with primary CD who underwent treatment with Botulinum toxin type-A (BTX-A). The patients were assembled in two groups according to the spread of dystonia during follow-up: spreading and non-spreading CD. We performed a binary logistic regression model using spreading of cervical dystonia as dependent variable aiming to find covariates which increase the risk of spreading. RESULTS: Our logistic regression model found the following covariates and their respective risk ratios: time of disease >18.5 months=2.4, retrocollis=1.9, anterocollis=1.8, head tremor=1.6. CONCLUSION: Time of disease >18.5 months, retrocollis, anterocollis and head tremor may predict spreading of dystonic movement to other regions of the body in CD patients.
INTRODUÇÃO: Poucos estudos avaliam preditores clínicos de progressão dos movimentos distônicos, para além da região cervical, em pacientes com distonia cervical (DC) primária. MÉTODO: Avaliamos, retrospectivamente, 73 pacientes com DC primária, que tinham sido submetidos ao tratamento com a toxina botulínica tipo A (BTX-A). Estes pacientes foram divididos em dois grupos de acordo com a progressão ou não da DC para outras áreas do corpo. Aplicamos um modelo de regressão logística binária usando a progressão da distonia como variável dependente com o objetivo de identificar co-variáveis que aumentassem o risco de progressão. RESULTADOS: O modelo de regressão logístico identificou as seguintes co-variáveis como preditoras de progressão e seus respectivos índices de risco: tempo de doença >18,5 meses=2,4, retrocolis=1,9, anterocolis=1,8, tremor cefálico=1,6. CONCLUSÃO: Tempo de doença >18,5 meses, retrocolis, anterocolis, e tremor cefálico podem predizer a progressão do movimento distônico para outras regiões do corpo em pacientes com DC primária.
Subject(s)
Adult , Female , Humans , Male , Torticollis/physiopathology , Tremor/physiopathology , Botulinum Toxins, Type A/therapeutic use , Disease Progression , Neuromuscular Agents/therapeutic use , Retrospective Studies , Torticollis/complications , Torticollis/drug therapyABSTRACT
OBJECTIVE: To evaluate the effect of low-frequency repetitive transcranial magnetic stimulation (rTMS) on the symptoms of a patient with primary segmental dystonia (PSD). METHOD: 1200 TMS pulses at a frequency of 1Hz, over the premotor cortex, with an intensity of 90 percent of the motor threshold (MT), using an eight-shaped coil; a total of 5 sessions were carried out. RESULTS: A reduction of 50 percent in the neck subset of the Burke, Fahn and Marsden torsion dystonia scale (BFM) was observed in our patient. CONCLUSION: The reduction in the BFM scale supports the concept that rTMS of the premotor cortex may reduce specific motor symptoms in PSD.
OBJETIVO: Investigar o efeito da estimulação magnética transcraniana repetitiva (EMTr) de baixa freqüência nos sintomas de um paciente com distonia segmentar primária (DSP). MÉTODO: 1200 pulsos a uma freqüência de 1Hz, sobre o córtex pré-motor, a uma intensidade de 90 por cento do limiar motor (LM), usando uma bobina em forma de 8. Foram realizadas 5 sessões. RESULTADOS: Uma redução de 50 por cento no sub-item "pescoço" na escala de distonia de torção de Burke, Fahn e Marsden (BFM) foi observada no paciente em questão. CONCLUSÃO: A redução na escala BFM corrobora a idéia de que a EMTr sobre o córtex pré-motor pode reduzir sintomas motores específicos na DSP.
Subject(s)
Adult , Humans , Male , Motor Cortex/physiology , Transcranial Magnetic Stimulation , Torticollis/physiopathology , Evoked Potentials, Motor/physiology , Neck Muscles/physiopathology , Torticollis/pathologyABSTRACT
Objetivo: Conocer los resultados de nuestra cirugía correctora del tortícolis (T) horizontal por nistagmus ocular congénito sin estrabismo. Material y Métodos: Estudio retrospectivo de 31 casos operados con diferentes procedimientos según las características del bloqueo y magnitud del T. Según esto último, los casos se clasificaron en 5 grupos. Resultados: La corrección del T fue exitosa (T residual del 12° o menos) en 80.7 por ciento del total de casos. En dos grupos obtuvimos curación del 100 por ciento de los casos, en otros 2,77 por ciento y 75 por ciento, respectivamente. En el 5° grupo la cirugía no fue uniforme y no es posible extraer normas de sus resultados. Como complicaciones tuvimos la aparición de un pequeño estrabismo en 3 casos y 4 pacientes debieron ser reintervenidos por tortícolis residual. Conclusiones: Las publicaciones con procedimientos comparables a los nuestros son escasas o con resultados vagos. Este estudio permite sacar guías quirúrgicas cuantitativas recomendables para 4 de los 5 grupos.
Purpose: To evaluate our surgical results in horizontal ocular torticollis present in congenital nystagmus without strabismus. Methods: A retrospective review was made in 31 consecutive patients, undergoing different surgical procedures considering the so called null zone and quantity of torticollis. Cases were classified in five groups. Results: In 80.7 percent of cases a successful result was obtained, defined as a residual torticollis not greater than 12°. Two groups obtained 100 percent correction. Two other groups obtained 77 and 75 percent correction respectively. The surgery indicated in group five was too heterogeneous and therefore non conclusive. After surgery a small strabismus presented in 3 cases. Four other patients were reoperated due to remaining torticollis. Conclusions: Papers with comparable procedures are few and don't show exact or detailed results. Our review allows us to obtain guide lines at least in 4 of the 5 groups.
Subject(s)
Humans , Male , Adolescent , Adult , Female , Infant , Child, Preschool , Child , Young Adult , Nystagmus, Congenital/surgery , Nystagmus, Congenital/physiopathology , Ophthalmologic Surgical Procedures/methods , Torticollis/surgery , Follow-Up Studies , Oculomotor Muscles/surgery , Nystagmus, Congenital/complications , Posture , Retrospective Studies , Torticollis/etiology , Torticollis/physiopathologySubject(s)
Female , Humans , Infant , Recurrence , Remission, Spontaneous , Torticollis/physiopathologyABSTRACT
La fibromatosis colli es una patología rara caracterizada por fibrosis del músculo esternocleidomastoideo, que se presenta clínicamente como una casa en el cuello. Aparece por lo general en el recién nacido, y debe reconocerse de manera temprana para proporcionar un tratamiento adecuado y oportuno. Se presenta el caso de un niño con fibromatosis colli bilateral, y se discuten aspectos de fisiopatogenia, diagnóstico y tratamiento de esta entidad