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110 Possible Causes for Muscle Biopsy showing Inclusion Bodies

  • Inclusion Body Myositis

    We performed a muscle biopsy that showed inclusion body myositis (IBM).[ncbi.nlm.nih.gov] A review of the previously performed muscle biopsy showed most of the cardinal myopathologic features of sporadic inclusion body myositis, in addition to the granuloma.[ncbi.nlm.nih.gov] The muscle biopsy of inclusion body myositis shows mild to moderate inflammation, atrophic denervated fibers, and most characteristically "rimmed vacuoles" as well as some[bcm.edu]

  • Radiculomyelopathy

    Electromyography (EMG) and occasionally muscle biopsy are needed to confirm the diagnosis. Inclusion body myositis has a more benign prognosis than MND.[patient.info] The list below shows further conditions that may have similar clinical features: Diabetic amyotrophy. Guillain-Barré syndrome. Post-polio syndrome.[patient.info]

  • Benign Adult Familial Myoclonic Epilepsy

    The diagnosis is made by biopsy (skin, muscle, liver, brain) showing periodic acid-Schiff positive glycogen-like intracellular inclusion bodies (Lafora bodies).[neuroweb.us] Brain MRI shows often cerebellar atrophy.[neuroweb.us]

  • Celiac Disease

    Muscle biopsy showed inflammatory changes in five. One patient had evidence of inclusion body myositis.[dx.doi.org]

  • Myositis

    Muscle biopsy reveals inclusion bodies i.e. rimmed vacuoles formed due to the collection of abnormal proteins.[kenhub.com] Possible inclusion body myositis If the muscle shows only inflammation (invasion of nonnecrotic muscle fibers by mononuclear cells)—without other pathologic features of inclusion[ncbi.nlm.nih.gov] In inclusion body myositis, findings on muscle biopsy may show the presence of vacuolated muscle fibers with basophilic granular deposits, the presence of varying degrees[rheumatologyadvisor.com]

  • Amyotrophic Lateral Sclerosis Type 1

    Electromyography (EMG) and occasionally muscle biopsy are needed to confirm the diagnosis. Inclusion body myositis has a more benign prognosis than MND.[patient.info] The list below shows further conditions that may have similar clinical features: Diabetic amyotrophy. Guillain-Barré syndrome. Post-polio syndrome.[patient.info]

  • Progressive Bulbar Palsy

    Electromyography (EMG) and occasionally muscle biopsy are needed to confirm the diagnosis. Inclusion body myositis has a more benign prognosis than MND.[patient.info] The list below shows further conditions that may have similar clinical features: Diabetic amyotrophy. Guillain-Barré syndrome. Post-polio syndrome.[patient.info]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Electromyography (EMG) and occasionally muscle biopsy are needed to confirm the diagnosis. Inclusion body myositis has a more benign prognosis than MND.[patient.info] The list below shows further conditions that may have similar clinical features: Diabetic amyotrophy. Guillain-Barré syndrome . Post-polio syndrome .[patient.info]

  • Upper Motor Neuron Disease

    Electromyography (EMG) and occasionally muscle biopsy are needed to confirm the diagnosis. Inclusion body myositis has a more benign prognosis than MND.[patient.info] The list below shows further conditions that may have similar clinical features: Diabetic amyotrophy. Guillain-Barré syndrome. Post-polio syndrome.[patient.info]

  • Motor Neuron Disease

    Electromyography (EMG) and occasionally muscle biopsy are needed to confirm the diagnosis. Inclusion body myositis has a more benign prognosis than MND.[patient.info] The list below shows further conditions that may have similar clinical features: Diabetic amyotrophy. Guillain-Barré syndrome. Post-polio syndrome.[patient.info]

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