Revista Colombia Médica Universidad del Valle - Facultad de Salud ISSN: 0120-8322 EISSN: 1657-9534 Vol. 41, Num. 4, 2010, pp. 373-376

Colombia Médica, Vol. 41, No. 4, October-December, 2010, pp. 367-372

Dysplasia epiphysealis capitis femoris. Meyer dysplasia

Displasia epifisaria de la cabeza femoral. Displasia de Meyer

Enrique Vergara-Amador, MD¹, Marcela Piña, MD²

¹Professor, Orthopaedic department, Universidad Nacional de Colombia, Bogotá, DC, Colombia. e-mail: enriquevergaraa@yahoo.com
²Orthopaedic surgeon, Universidad Nacional de Colombia, Bogotá, DC, Colombia. e-mail: marcelapina@gmail.com

Received for publication February 28, 2010
Accepted for publication   May 25,  2010

Code Number: rc10053

SUMMARY

Introduction: Epiphyseal dysplasia of the femoral head (EDFH) is defined as an alteration in the development of the child’s hip, characterized by delayed ossification of the proximal femoral epiphysis.
Methods: Herein, we present six cases of epiphyseal dysplasia of the femoral head (EDFH), seen by the principal author (EVA) within the last six years with minimum follow up at 15 months.
Results: The cases were all diagnosed as casual findings. None of the children had symptoms or clinical signs in the hip, only one had a history of hip pain for five days, two months prior, which was diagnosed at the time as transient synovitis.
Discussion: Among the differential diagnoses, the main one is Perthes disease, which is differentiated by several parameters like earlier age onset for EDFH (in children below 4 years of age), bilateralism (50% vs. 10%), and a calmer presentation in Meyer’s dysplasia. The evolution in Meyer’s dysplasia is toward improving radiographic changes. None of the patients revealed incongruence of the hip or early degenerative changes, indicating an excellent prognosis. Many authors think it is a variant of the normal ossification of the femoral head.

Keywords: Meyer dysplasia; Legg-Perthes disease; Hip.

RESUMEN

Introducción: La displasia epifisaria de la cabeza femoral (DECF) es definida como una alteración del desarrollo de la cadera en el niño, caracterizada por un retraso en la osificación con irregularidad en el núcleo de osificación de la epífisis proximal del fémur.
Métodos: Se presentan 6 casos de displasia epifisaria de la cabeza femoral (DECF), atendidos por el autor principal (EVA) en los últimos 6 años, con un seguimiento mínimo de 15 meses
Resultados: Todos los casos fueron diagnosticados como un hallazgo casual. Ninguno de los niños tenía síntomas ni signos clínicos en la cadera, solo uno tenía antecedente de dolor de cadera durante 5 días, dos meses antes, el cual fue diagnosticado en su momento como sinovitis transitoria.
Discusión: Entre los diagnósticos diferenciales, el principal es la Enfermedad de Perthes, el cual se diferencia en varios parámetros como son edad de inicio más temprano para la DECF (en niños menores de 4 años), bilateralidad (50% vs. 10%) y presentación más silente en la displasia de Meyer. La evolución en la displasia de Meyer es hacia la mejoría de los cambios radiológicos. En ningún paciente se ha observado incongruencias de la cadera o cambios degenerativos tempranos, indicando un excelente pronóstico. Muchos autores piensan que es una variante de la osificación normal de la cabeza femoral.

Palabras clave: Diplasia de Meyer; Enfermedad de Legg Perthes; Cadera.

Epiphyseal dysplasia of the femoral head (EDFH) is defined as an alteration in the development of the child’s hip, characterized by delayed ossification with irregularity in the ossification center of the proximal femoral epiphysis^1,2. Normal ossification takes place on the average at 4 months of age, although it may be considered normal up to the 11th month; however, in Meyer’s dysplasia, ossification appears around 15 to 18 months of age as multiple ossification centers, giving the femoral head a modulated epiphysis aspect¹.

The disease was first described by Pedersen in 1950³ and then by Meyer in 1964², to whom the name of the condition is attributed. Meyer estimated that close to 10% of the patients diagnosed with Perthes disease corresponded to a dysplasia and not to a necrosis, unlike Rowe who estimated a 4.4%⁴ incidence.

The etiology of EDFH, unlike Perthes disease, is not established. Several hypotheses have been postulated, among which the one formulated by Meyer² stands out announcing the theory of ischemic vascular damage as the cause of delayed and irregular ossification, the theory by Batory⁵ speaks of a congenital vascular defect, and -lastly- the congenital proximal femoral hypoplasia5; however, none of these have been supported by scientific evidence.

Epidemiologically, it has been determined that this condition involves boys in greater proportion than girls in a ratio of 5:1 and in those under 5 years of age^1,4. The bilateral commitment reported by different studies ranges from 42 to 60%^1,2,4,6, much greater than that reported for Perthes disease.

Most of these patients have no symptomatology; however, when there is also hip pain, decreased range of motion, and limp stride. Symptoms appear closet o the second year of life lasting from 1 to 3 weeks^1,5,6,7. The diagnosis is generally accidental via X-ray examination⁸.

MATERIALS AND METHODS

We present six cases of children with epiphyseal dysplasia of the femoral head, seen by the principal author (EVA) during a period of six years with minimum follow up at 15 months. The anatomical pieces were documented with digital photographs and thereafter stored. Data were analyzed through descriptive statistics in Excel 2007.

Ethical considerations. The ethical implications of the current study were minimal, given that they corresponded to a study without risk, which used information from the clinical histories, without intervention on the patients. The information obtained was kept strictly confidential and was used exclusively by the researchers. This study was approved by the Ethics Committee at the University mentioned.

RESULTS

All the cases were diagnosed as a casual finding. None of the children had symptoms or clinical signs in the hip. Only one of the children had a history of hip pain for five days, two months prior, which was diagnosed at the time as transient synovitis. One case was bilateral and the rest were unilateral, for a total of seven hips. Four patients were males and two were females. None of the patients received treatment. At the end of the follow up they continued asymptomatic. Three exemplary cases are shown:

Case 1. A 3-year-old male child, referred to consultation with diagnosis of Perthes disease. This child had not reported pain, was asymptomatic, and the physical exam of the hips was totally normal. There was no antecedent of importance, nor the taking of any medication by the patient or by the mother during gestation. The X-ray study of the right hip revealed an image of fragmenting of the epiphysis, without changes in the metaphysis. A good teardrop image and normal acetabular index, along with containment of the femoral head is noted in Figure 1. The initial diagnosis was epiphyseal dysplasia of the femoral head and only observation was recommended. Evolution was positive, remaining asymptomatic with progressive ossification of the femoral head at 5 years of age (Figure 2).

Case 2. Male child without antecedents, referred to consultation at 18 months of age with diagnosis of Perthes disease, asymptomatic and with normal physical exam. The patient had an X-ray taken at 3.5 months of age and it was considered normal. At a year and a half, the child continued asymptomatic and X-ray studies showed small and irregular nuclei. At 4 years of age, the patient was asymptomatic and the X-rays evidenced better conformation of the femoral head, good teardrop image without subluxation, lacking ossification in some sites of the epiphysis (Figures 3, 4).

Case 3. Male child 2.5 years of age sent for consultation with diagnosis of Perthes disease. The patient was found asymptomatic and with a normal physical exam. X-ray studies revealed irregularity of the right femoral head epiphysis. Because of the clinical and radiological state it was considered compatible with epiphyseal dysplasia of the femoral head or Meyer’s Dysplasia. Results at 6 years of age were promising (Figures 5, 6).

DISCUSSION

In this situation, we note delay and irregularity in ossification of the proximal femoral epiphyseal nucleus, which does not appear before two years of age⁴. The nucleus takes on an appearance with a multiple granular pattern, with an ossification center made up of multiple independent nuclei that grow and finally coalesce to form only one9; on average, around 5 years of age⁵.

The first finding is the decrease in the distance of the upper edge of the metaphysis to the Hilgenreiner line, which is generally 9.3 mm ± 1.5 at 7 months of age. In his series, Khermosh found values from 4-8 mm in 2-year-old children; from 4.5 to 9 mm in children at the third year of life, and from 5-10 mm in children at the third year of life, suggesting that the cartilaginous epiphysis is initially smaller than the normal epiphysis⁵.

Scintigraphy study reports no alterations, while magnetic resonance reveals multiple ossification centers of the femoral head with normal signal intensity and decrease in epiphysis size⁶. All the frames show normal irrigation of the epiphyseal trabecular bone, the physis articular cartilage, and of the cortical bone⁵.

Among the differential diagnoses, the main one is for Perthes disease, which is differentiated by several parameters: age of earlier onset for EDFH (in children below 4 years of age), bilateralism (50% vs. 10%)⁸, and a calmer presentation in Meyer’s dysplasia; radiological signals in Perthes disease permit staging the disease, while in dysplasia there is no fragmentation, condensation, subchondral fracture, or epiphysis collapse; hence, there are no consequences as with Perthes disease^1,4,6,7.

Other differential diagnoses point to infectious processes that in some children may be accompanied by elevated erythrocyte sedimentation rate (ESR) and leukocytosis; however, scintigraphy rules out the condition. In cases of bilateral presentation, we must rule out another type of multiple dysplasia and hypotyroidism^1,7.

Evolution in Meyer’s dysplasia is towards improvement in radiologic changes^1,2,6. None of the patients revealed incongruence of the hip or early degenerative changes, indicating excellent prognosis. Many authors consider it a variant of normal ossification of the femoral head. Because of its evolution and good prognosis, treatment has not been determined necessary for these patients. X-ray control is recommended to assess the resolution of the pathology.

All patients in this series remained asymptomatic, without clinical signs, agreeing with the literature in that most are asymptomatic. Very few patients had antecedence of synovitis^4,6.

In conclusion, it is a rare condition, with a benign clinical course, which must be kept in mind in children below five years of age with atypical onset of fragmenting of the ossification center of the femoral head^2,4-6. No treatment is required, but the evolution of the development of the femoral head should be closely watched.

Conflict of interest. None of the authors has conflicts of interest related to this study.

REFERENCES

1. Toro V, Muñoz O, Castilla JL. Displasia de la cabeza femoral (displasia de Meyer). Rev Pediatr Atencion Prim. 2007; 9: 237-43.
2. Meyer J. Dysplasta epiphysealis capitis femoris. A clinical-radiological syndrome and its relationship to Legg-Calve´-Perthes disease. Acta Orthop Scand. 1964; 34: 183-97.
3. Perdersen EK. Dysplasia epiphysialis capitis femoris. J Bone Joint Surg. 1960; 42B: 663.
4. Rowe SM, Chung JY, Moon ES, Yoon TR, Jung ST, Kim SS. Dysplasia epiphysealis capitis femoris: Meyer dysplasia. J Pediatr Orthop. 2005; 25: 18-21.
5. Khermosh O, Wientroub S. Dysplasia epiphysealis capitis femoris. J Bone Joint Surg [Br]. 1991; 73: 621-5.
6. Harel L, Kornteich L, Ashkenazi S, Rachmel A, Karmazyn B, Amir J. Meyer dysplasia in the differential diagnosis of hip disease in young children. Arch Pediatr Adolesc Med. 1999; 153: 942-5.
7. Toro A, López M. Displasia epifisaria de Meyer: un caso de diagnóstico tardío. Rev Colomb Ortop Trauma. 2005; 19: 60-4.
8. Crossan JF, Wynne-Davies R, Fulford GE. Bilateral failure of the capital femoral epiphysis: Bilateral Perthes disease, multiple epiphyseal dysplasia, pseudoachondroplasia and spondyloepiphyseal dysplasia congenital and tarda. J Pediatr Orthop. 1983; 3: 297-301.
9. Specchiuilli F, Scialpi L, Mastrorillo G. Meyer’s dysplasia epiphysealis. Chir Organi Mov. 1996; 81: 401-5.

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