Bone and joint changes are among the most common manifestations of hemophilia. In their absence one is inclined to question the diagnosis in adult life. Roentgenologically, these changes are varied and relatively non-specific, depending to a large extent on the frequency of hemarthroses, the joints involved, and the age of the patient. During the past eight years we have had the opportunity of studying a group of hemophiliacs of various ages. In several instances x-ray examinations of involved joints were made initially prior to epiphyseal closure and periodically thereafter for several years. Thus a record of the progression of the bone and joint changes has been obtained. In addition to the serial changes, a variety of joint lesions ranging from minimal to far advanced are demonstrated in this group of patients. Clinical and Radiological Data Twelve cases are presented here, representing 6 families (Table I) . The first 5 cases have been under observation since 1945. Cases 6 through 9, from the third family, were seen in 1949. The last 3 cases, from unrelated families, were seen in 1952. In all of these cases the following laboratory criteria have been met: prolonged coagulation time of blood; positive Quick test; normal prothrombin, bleeding and clot retraction times. In 8 of the cases the prothrombin consumption was determined and found to be poor. The other 4 patients were studied prior to the development of prothrombin consumption determinations. The whole blood coagulation time in these subjects was as shown in the accompanying table. The details of the clinical course, laboratory data, and genealogical history are reported elsewhere (1). In the first family (McC.) there are 3 known hemophiliacs, the only children of their parents. Figure 1 shows the physical appearance of one of these brothers (T. McC.). Note the presence of genu valgum on the left, with posterior displacement of the tibia, associated with general atrophy of the left lower extremity. The carrying angle of the left elbow is reduced. The x-ray changes in this subject are of moderate severity. Figure 2 shows the right elbow, with enlargement and flaring of the radial head. Small rounded radiolucent defects are seen along its articular margin and along the lateral epicondyles of the humerus, indicative of cystic dissolutions. Figure 3 (HH4) shows bulging of the synovium and slight widening of the joint space due to a massive hemarthrosis in the right knee. The intercondylar fossa is slightly wider than normal, but the articular margins are smooth. Small ill-defined rarefactions are present in the subarticular portion of the tibial epiphysis, suggesting early cyst formation. During a seven-year period, x-ray studies of this knee have disclosed progressive changes. Figure 4 (1951) shows increased widening and deepening of the intercondylar fossa, decreased joint space with irregularity of articular surfaces, and slightly increased cystic changes.
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