The patient had multiple other bone infarcts in the long bones of the lower limbs, as well as focal areas of high signal.

Gaucher disease is a congenital storage disorder with accumulation of glucocerebroside in the reticuloendothelial system and bone marrow. The majority of patients present in childhood or as young adults - type I. Types II and III are rare, occur in neonates and young children, and carry a generally poor prognosis.

Bone marrow expansion gives rise to Erlenmeyer flask deformity of the distal femur in 50%. Ischemic necrosis of the femoral head is a common complication. Bone infarcts in the metadiaphyseal regions of long bones also occur. Bone density is decreased generally, predisposing to vertebral compression fracture. Localized lytic bone lesions may occasionally occur, which represent focal accumulations of Gaucher cells. Patients have an increased incidence of osteomyelitis.

Types I and III Gaucher disease may be treated by enzyme replacement. MRI findings include generalized low marrow signal on T1-weighted scans, focal areas of low T1 signal representing Gaucher cell accumulations, and evidence of bone infarcts.