Inclusion body myopathy

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Inclusion body myopathy

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Skin anatomy and physiology
Skin histology
Pigmentation skin disorders: Pathology review
Acneiform skin disorders: Pathology review
Papulosquamous and inflammatory skin disorders: Pathology review
Vesiculobullous and desquamating skin disorders: Pathology review
Viral exanthems of childhood: Pathology review
Skin cancer: Pathology review
Anatomy of the muscles and nerves of the posterior abdominal wall
Anatomy of the brachial plexus
Anatomy of the pectoral and scapular regions
Vessels and nerves of the gluteal region and posterior thigh
Anatomy of the hip joint
Anatomy of the knee joint
Anatomy clinical correlates: Bones, joints and muscles of the back
Anatomy clinical correlates: Clavicle and shoulder
Anatomy clinical correlates: Axilla
Anatomy clinical correlates: Arm, elbow and forearm
Anatomy clinical correlates: Wrist and hand
Anatomy clinical correlates: Median, ulnar and radial nerves
Development of the axial skeleton
Development of the muscular system
Skeletal muscle histology
Bone remodeling and repair
Neuromuscular junction and motor unit
Sliding filament model of muscle contraction
Slow twitch and fast twitch muscle fibers
Muscle contraction
Muscle spindles and golgi tendon organs
Back pain: Pathology review
Rheumatoid arthritis and osteoarthritis: Pathology review
Seronegative and septic arthritis: Pathology review
Gout and pseudogout: Pathology review
Systemic lupus erythematosus (SLE): Pathology review
Scleroderma: Pathology review
Sjogren syndrome: Pathology review
Bone disorders: Pathology review
Bone tumors: Pathology review
Myalgias and myositis: Pathology review
Neuromuscular junction disorders: Pathology review
Acetaminophen (Paracetamol)
Non-steroidal anti-inflammatory drugs
Glucocorticoids
Opioid agonists, mixed agonist-antagonists and partial agonists
Antigout medications
Osteoporosis medications
Coxsackievirus
Human papillomavirus
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Human herpesvirus 6 (Roseola)
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Parvovirus B19
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Lichen planus
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Albinism
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Human herpesvirus 8 (Kaposi sarcoma)
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Acne vulgaris
Bullous pemphigoid
Pemphigus vulgaris
Bone histology
Lambert-Eaton myasthenic syndrome
Myasthenia gravis
Antiphospholipid syndrome
Raynaud phenomenon
Scleroderma
Sjogren syndrome
Systemic lupus erythematosus
Compartment syndrome
Muscular dystrophy
Dermatomyositis
Inclusion body myopathy
Muscular dystrophies and mitochondrial myopathies: Pathology review
Neurofibromatosis
Osteoarthritis
Ankylosing spondylitis
Gout
Psoriatic arthritis
Reactive arthritis
Rheumatoid arthritis
Septic arthritis
Achondroplasia
Cleidocranial dysplasia
Osteomyelitis
Bone tumors
Osteomalacia and rickets
Osteoporosis
Paget disease of bone
Carpal tunnel syndrome
Erb-Duchenne palsy
Klumpke paralysis
Rotator cuff tear
Fibromyalgia
Polymyalgia rheumatica

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Inclusion body myopathy

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In inclusion body myopathy, “myopathy” refers to muscle disease and “inclusion body” refers to the presence of inclusions, or vacuoles, formed by clumps of protein that collect within the muscle fibers.

There’s a sporadic form, sporadic meaning that it strikes at random, which is the most common and is also called inclusion body myositis - because it causes muscle inflammation.

There’s also a rare hereditary form, that causes no muscle inflammation.

Normally, the cells of the immune system are ready to spot and destroy anything foreign that could cause the body harm.

To help with this, most cells in the body have a set of proteins that come together to form a major histocompatibility complex, or MHC, class I proteins which sits on the surface of their cell membrane.

These surface proteins act kind of like a serving platter, presenting molecules from within the cell for the immune system, so that it can have a way of performing ongoing surveillance.

Normally the MHC class I proteins serves up a normal harmless molecule from the cell - a self-antigen, and there’s no response.

But if a cell is invaded by a pathogen like a virus, then viral proteins are served upon on the MHC class I proteins.

When these viral antigens are displayed on the cell surface, it sparks an immune response.

Specifically, a type of T-lymphocyte, called a CD8+ T-cell or a cytotoxic T-cell, will bind to the antigen presented by the MHC class I proteins.

If the cytotoxic T-cell binds strongly, than the antigen is recognized as foreign, and the cytotoxic T-cell secretes inflammatory molecules and enzymes - like perforin and granzymes.

Perforin is able to form holes in the infected cell and that allows the granzymes to enter the cell.

Once inside, the granzymes induce apoptosis, or programmed cell death - which destroys the cell.

And as if that weren’t enough, the cytotoxic T-cells have a protein called Fas ligand on their surface.

Fas ligand binds to a protein called Fas on the surface of the infected cell.

And when these two combine, it triggers a cascade of signaling events inside the target cell that also leads to apoptosis.

So either way - the infected cell is doomed.

Okay, now, in sporadic inclusion body myositis there are features of inflammation and degeneration.

The exact mechanism is unclear, but one thought is that the trigger may be a virus that infects and damages myocytes.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "GNE myopathy: from clinics and genetics to pathology and research strategies" Orphanet Journal of Rare Diseases (2018)
  6. "Hereditary inclusion-body myopathies" Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2015)
  7. "GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges" Neurotherapeutics (2018)