Meyer's dysplasia : delayed ossification of the femoral head as a differential diagnosis in perthes' disease.

نویسندگان

  • Nasir Muzaffar
  • Hae-Ryong Song
  • Kamlesh Devmurari
  • Hitesh Modi
چکیده

Meyer's dysplasia strongly mimics Legg-Calve-Perthes' disease despite differing markedly in eventual outcome. This study presents the clinicoradiologi-cal features which differentiate it from Perthes' disease in a group of 178 children with a preliminary diagnosis of Perthes' disease, of whom nine were subsequently diagnosed with Meyer's dysplasia. All had a near normal development of the femoral head; mild flattening was seen in two cases. Clinical initial presentation often resembles Perthes' disease. However, the presence of a granular aspect of the femoral head, often bilateral, in a male child with a preliminary diagnosis of Perthes' disease should alert the clinician to the possibility of Meyer's dysplasia. Restitution of normal capital architecture is usual; there may however be a mild residual hypoplasia.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Evolution in diagnosis and treatment of Legg-Calve-Perthes disease

Legg-Calvé-Perthes disease (LCPD) is an idiopathic osteonecrosis of the femoral head with variable complications and resultant deformity of the femoral head and osteoarthritis. Suggested risk factors are acetabular retroversion, obesity, latitude, hyperactivity, and coagulopathy. The most commonly applied classification is based on radiolucency in the lateral pillar of the femoral head, which i...

متن کامل

Clinical Outcome of Femoral Osteotomy in Patients with Legg-Calve´-Perthes Disease

  Background: Legg-Calve´-Perthes disease is a juvenile idiopathic osteonecrosis in which the blood supply of femoral head is not sufficient and the bone dies provisionally. The aim of this study is to evaluate outcome of Femoral osteotomy in children with LCPD in our University Hospital.   Methods: In a descriptive analytic study, between 2008 and 2013, patients with the diagnosis of Legg-Calv...

متن کامل

Delayed ossification of the proximal capital femoral epiphysis in Legg-Calvé-Perthes' disease.

We studied radiographs of 125 children (105 boys, 20 girls) with unilateral Legg-Calvé-Perthes' disease to examine the epiphyseal development of the femoral head in the contralateral (unaffected) hip. The epiphyseal height (EH) and width (EW) of the unaffected hip were measured on the initial anteroposterior pelvic radiograph. In 109 of the patients (87.2%) the EH was below the mean for normal ...

متن کامل

Familial Cleidocranial Dysplasia in a Neonate: A Case Report

Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence of 1 case per 1000,000 individuals. It is a form of predominantly autosomal dominant inheritance and is associated with a mutation in runt related transcription factor-2 gene mapped on chromosome 6p21. This disease primarily affects the bones formed by intramembranous ossification and is characte...

متن کامل

Legg-Calvé-Perthes disease and slipped femoral capital epiphysis in the skeletal remains of the Mediaeval Necropolis of Santa Maria (Sintra, Portugal)

This paper discusses the differential diagnosis of unusual and distinct pathological changes in two left femurs and one left pelvic bone fragment from the Necropolis of Santa Maria, Sintra (Portugal), dated from the 14-17 centuries. The differential diagnosis of the lesions gave rise to several possible pathological conditions, namely, slipped femoral capital epiphysis, Legg-CalvéPerthes diseas...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Acta orthopaedica Belgica

دوره 76 5  شماره 

صفحات  -

تاریخ انتشار 2010