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Slipped capital femoral epiphysis (SCFE) is a condition which affects mostly obese children in their prepubertal years.
It is generally not preceded by any trauma to the hip, though a minority of cases are an acute sequel to a fall or minor injury.
In children, it is thought that a combination of physiological weakness of the growth plate in the proximal femur and excessive mechanical loading are responsible for the SCFE. It occurs invariably before the growth plate closes, between 10-14 years in girls and 12-16 years in boys.
The risk factors for SCFE in children are linked to reduced shear resistance and increased mechanical stress on the growth plate, and include:
In children, the left hip is affected more often than the right. The contralateral hip is affected within 18 months of the first in 40% of younger children with this condition (below the age of 10 years). Treatment involves pinning the femoral head through the growth plate.
SCFE in adults is rare with only a handful of cases having been published so far. Most are sporadic but a few seem to show a familial inheritance. In adult SCFE, growth hormone deficiency leading to prolonged growth plate persistence seems to be a common factor.
These patients may have hypogonadotropic hypogonadism and a eunuchoid constitution, with long arms and legs as a result of an excessive period of growth at the epiphyses of the long bones. The growth plate fuses in the third decade instead of the second in this case.
The pituitary deficiency is occasionally iatrogenic, such as following the excision of a benign pituitary tumor without pituitary hormone replacement. It is necessary to consider the differential diagnosis of endocrinopathies, in order to initiate and continue appropriate hormonal management in addition to surgical fixation of the hip by in situ pinning or other techniques as indicated. A dult patients were found to have the following associated endocrine disorders :