Misdiagnosis of Inclusion Body Myositis: Two Case Reports and a Retrospective Chart Review

Amaiak Chilingaryan; Richard A. Rison; Said R. Beydoun

Disclosures

J Med Case Reports. 2015;9(169) 

In This Article

Retrospective Chart Review

Table 1 shows 20 patients (16 men, 4 women) seen at our neuromuscular division between 2004 and 2014 (including patients 1 and 2 in the present report listed as patients 8 and 9, respectively). The patients' average age at initial evaluation at our clinic was 67.8 years (standard deviation, 11.5; range, 43–85). The average number of months from symptom onset to diagnosis was 70.0 (standard deviation, 54.8; range, 6–240). One patient did not follow up to confirm the diagnosis but was clinically diagnosed with s-IBM. Our clinic population had characteristics of s-IBM similar to those described in previous reports. The topography was proximal leg weakness presenting as difficulty with ambulation and rising from chairs, in addition to finger flexor weakness presenting as difficulty handling objects and opening jars and bottles. Four patients had dysphagia.

Several patients were misdiagnosed before evaluation at our institute: two patients (patients 9 and 17) diagnosed with PM who were given immunosuppressive medications; three (patients 8, 18, and 19) who were diagnosed with ALS; one (patient 5) diagnosed with entrapment neuropathy who underwent cubital tunnel release with no improvement; one (patient 14) who was diagnosed with extrapyramidal symptoms of Parkinson's disease versus radiculopathy; and one (patient 16) who was diagnosed with s-IBM and given etanercept. The remaining 12 patients were referred without diagnosis or for second opinions for myopathy.

(Please note the standard deviations given above for time until the final correct diagnosis, and see below for discussion of trends and how our findings coincide with the existing published literature.)

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