Pelvis: Ischium and Pubic Bones
Diagnosis | Findings | Comments |
Trauma | Separation of the medial ends of the pubic bones. | A second pelvic fracture is usually present to complete a break through the pelvic ring. |
Osteitis pubis | Lysis of the pubic symphysis and marginal sclerosis during healing phase. Bone marrow edema in the pubis about the pubic symphysis. Increased uptake on bone scan. | Typically occurs in athletes. |
Bladder exstrophy Fig. 5.24, p. 512 | Tilted iliac bone with horizontal acetabular roof. True widening of the symphysis. | DD: variants of exstrophy (cloacal, superior vesicle fissure, duplicated exstrophy), epispadias, anorectal anomalies, and urogenital anomalies. |
Metabolic Fig. 5.25, p. 512 Fig. 5.26, p. 512 | Margins may appear eroded. | Hyperparathyroidism/renal osteodystrophy. |
Infection/inflammation | Lysis and erosions. Widening may be asymmetric. | DD: bacterial, tuberculosis, JIA, reactive arthritis. |
Connective tissue disorders | Marfan and Ehlers-Danlos syndromes, for example. | |
Campomelic dysplasia Fig. 5.14, p. 501 | (see Table 5.12 ) | |
Prune belly syndrome (Eagle-Barrett syndrome) | Flared iliac wings and wide interpubic distance. | Spectrum of congenital anomalies of the gastrointestinal and genitourinary systems. Associated with other syndromes. |
Cleidocranial dysplasia Fig. 5.15a-d, p. 501 | Delayed ossification of the pubis. | (see Table 5.15 ) |
Spondyloepiphyseal dysplasia Fig. 5.27, p. 512 | Absent ossification of the pubis during infancy. | Bone dysplasia with premature osteoarthritis (OA) of the hips. Platyspondyly, short stature. No ossification of the epiphyses of the knees, talus, and calcaneus. Ovoid pear-shaped vertebra in infancy progressing to platyspondyly. |
Diagnosis | Findings | Comments |
Trisomy 21 | Flattened, broad pelvis with flared iliac wings, and decreased acetabular and iliac angles. | An enlarged iliac angle may be seen by fetal US in the second trimester of fetal life. |
Exstrophy-epispadias complex | Wide pubic symphysis. | Spectrum of anomalies of the lower abdominal wall, bladder, anterior bony pelvis, and e xternal genitalia. |
Sacral agenesis and hypoplasia | Associated abnormalities include deformities of the lower extremities and anomalies of the genitourinary tract, lower gastrointestinal tract, and spine. |
Diagnosis | Comments |
Achondroplasia | (see Table 5.20 ) |
Pseudoachondroplasia | (see Table 5.20 ) |
Thanatophoric dysplasia and variants | (see Table 5.20 ) |
Short rib-polydactyly syndrome, type I (Saldino-Noonan type) | (see Table 5.20 ) |
Chondroectodermal dysplasia (Ellis-van Creveld syndrome) | Short limbs, short ribs, postaxial polydactyly, and dysplastic nails and teeth. Sixty percent have congenital heart disease. |
Spondyloepimetaphyseal dysplasia | |
A narrow sacrosciatic notch may be seen in almost all the bone dysplasias with a small iliac bone (see Fig. 5.23 ). |