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. 2020 Mar 30;10(4):521. doi: 10.3390/biom10040521

Table 1.

Sporadic inclusion body myositis (IBM) patient characteristics.

Patient Gender/Age Clinical Features Muscle Pathology Autoantibodies
IBM1 M/63 Forearm, finger, and quadriceps weakness. Several non-necrotic invaded fibers and fibers with rimmed vacuoles and inclusions. cNIA+
IBM2 M/71 Forearm and finger flexor weakness. Several muscle fibers with rimmed vacuoles and inclusions, rare inflammation. cNIA-
IBM3 M/72 Forearm, finger, and quadriceps weakness. Some fibers with rimmed vacuoles and with inclusions. cNIA-
IBM4 M/70 Quadriceps muscle weakness. Severe inflammation and fibrosis, many fibers with inclusions. ND
IBM5 M/65 Forearm flexor and quadriceps weakness. Severe inflammation, many fibers with inclusions. ND
IBM6 F/59 Proximal leg and distal finger flexor muscle weakness. Many non-necrotic invaded fibers, some fibers with inclusions, mild fibrosis. ND
IBM7 M/83 Forearm flexor and quadriceps weakness. Several non-necrotic invaded fibers and fibers with rimmed vacuoles and inclusions. cNIA-
IBM8 F/59 Dysphagia, forearm finger flexor, and quadriceps weakness. Rare non-necrotic invaded fibers, few inclusions, mild fibrosis. cNIA-
IBM9 M/72 Quadriceps muscle weakness. Many fibers with rimmed vacuoles and inclusions, scarce inflammation. cNIA+

cytosolic 5′-nucleotidase 1A autoantibody seropositive (cNIA+); seronegative (cNIA-); not determined (ND).