Dermatomyositis

27,942views

Dermatomyositis

MRCP revision

MRCP revision

Acute intermittent porphyria
Autoimmune hemolytic anemia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Sickle cell disease (NORD)
Alpha-thalassemia
Beta-thalassemia
Anemia of chronic disease
Iron deficiency anemia
Sideroblastic anemia
Aplastic anemia
Immune thrombocytopenia
Polycythemia vera (NORD)
Antiphospholipid syndrome
Antithrombin III deficiency
Factor V Leiden
Protein C deficiency
Protein S deficiency
Hemophilia
Vitamin K deficiency
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Von Willebrand disease
Hemolytic-uremic syndrome
Thrombotic thrombocytopenic purpura
Paroxysmal nocturnal hemoglobinuria
Myelodysplastic syndromes
Myelofibrosis (NORD)
Acute leukemia
Chronic leukemia
Hodgkin lymphoma
Non-Hodgkin lymphoma
Neuroblastoma
5-alpha-reductase deficiency
Androgen insensitivity syndrome
Congenital adrenal hyperplasia
Kallmann syndrome
Thyroglossal duct cyst
Pancreatic neuroendocrine neoplasms
Zollinger-Ellison syndrome
Multiple endocrine neoplasia
Carcinoid syndrome
Hyperparathyroidism
Hypoparathyroidism
Hyperprolactinemia
Pituitary adenoma
Prolactinoma
Delayed puberty
Premature ovarian failure
Constitutional growth delay
Growth hormone deficiency
Hypopituitarism
Hypoprolactinemia
Pituitary apoplexy
Sheehan syndrome
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Thyroid eye disease (NORD)
Thyroid storm
Toxic multinodular goiter
Euthyroid sick syndrome
Postpartum thyroiditis
Riedel thyroiditis
Subacute granulomatous thyroiditis
Thyroid cancer
Bacillus cereus (Food poisoning)
Campylobacter jejuni
Clostridium difficile (Pseudomembranous colitis)
Escherichia coli
Helicobacter pylori
Listeria monocytogenes
Salmonella (non-typhoidal)
Salmonella typhi (typhoid fever)
Shigella
Staphylococcus aureus
Vibrio cholerae (Cholera)
Yersinia enterocolitica
Coxsackievirus
Cytomegalovirus
Herpes simplex virus
Mumps virus
Ascending cholangitis
Gallstone ileus
Alcohol-associated liver disease
Alpha 1-antitrypsin deficiency
Budd-Chiari syndrome
Cholestatic liver disease
Cirrhosis
Gilbert's syndrome
Hemochromatosis
Hepatic encephalopathy
Viral hepatitis
Jaundice
Non-alcoholic fatty liver disease
Portal hypertension
Primary biliary cholangitis
Primary sclerosing cholangitis
Reye syndrome
Wilson disease
Acute pancreatitis
Chronic pancreatitis
Pancreatic pseudocyst
Hirschsprung disease
Intussusception
Ischemic colitis
Microscopic colitis
Necrotizing enterocolitis
Protein losing enteropathy
Short bowel syndrome (NORD)
Small bowel bacterial overgrowth syndrome
Small bowel ischemia and infarction
Tropical sprue
Volvulus
Whipple's disease
Autoimmune hepatitis
Celiac disease
Eosinophilic esophagitis (NORD)
Benign liver tumors
Hepatocellular adenoma
Hepatocellular carcinoma
Familial adenomatous polyposis
Juvenile polyposis syndrome
Peutz-Jeghers syndrome
Gastric cancer
Abdominal hernias
Achondroplasia
Developmental dysplasia of the hip
Muscular dystrophy
Osteomalacia and rickets
Osteoporosis
Paget disease of bone
Gout
Osteoarthritis
Compartment syndrome
Ankylosing spondylitis
Dermatomyositis
Juvenile idiopathic arthritis
Limited systemic sclerosis (CREST syndrome)
Mixed connective tissue disease
Polymyositis
Psoriatic arthritis
Raynaud phenomenon
Reactive arthritis
Rheumatoid arthritis
Sjogren syndrome
Systemic lupus erythematosus
Septic arthritis
Spondylitis
Baker cyst
Bursitis
Polymyalgia rheumatica
Temporomandibular joint dysfunction
Transient synovitis
Bone tumors
Fibromyalgia
Sciatica
Carpal tunnel syndrome
Rotator cuff tear
Prions (Spongiform encephalopathy)
Adenovirus
Eastern and Western equine encephalitis virus
Epstein-Barr virus (Infectious mononucleosis)
HIV (AIDS)
JC virus (Progressive multifocal leukoencephalopathy)
Lymphocytic choriomeningitis virus
Measles virus
Poliovirus
Rabies virus
Varicella zoster virus
West Nile virus
Cerebral palsy
Neurofibromatosis
Tuberous sclerosis
Erb-Duchenne palsy
Creutzfeldt-Jakob disease
Neurogenic bladder
Treponema pallidum (Syphilis)
Vitamin B12 deficiency
Acoustic neuroma (schwannoma)
Glaucoma
Amyloidosis
Focal segmental glomerulosclerosis (NORD)
Membranous nephropathy
Minimal change disease
Renal tubular acidosis
Nephroblastoma (Wilms tumor)
Non-urothelial bladder cancers
Transitional cell carcinoma
Renal cell carcinoma
Urinary incontinence
Renal cortical necrosis
Nephrotic syndromes: Pathology review
Renal tubular defects: Pathology review
Renal tubular acidosis: Pathology review
Cardiac preload
Bacillus anthracis (Anthrax)
Bacteroides fragilis
Bordetella pertussis (Whooping cough)
Corynebacterium diphtheriae (Diphtheria)
Coxiella burnetii (Q fever)
Francisella tularensis (Tularemia)
Moraxella catarrhalis
Bacterial epiglottitis
Laryngomalacia
Bronchodilators: Beta 2-agonists and muscarinic antagonists
Bronchodilators: Leukotriene antagonists and methylxanthines
Cytomegalovirus infection after transplant (NORD)
Graft-versus-host disease
Post-transplant lymphoproliferative disorders (NORD)
Transplant rejection
Anaphylaxis
Food allergy
Type I hypersensitivity
Hemolytic disease of the newborn
Pemphigus vulgaris
Type II hypersensitivity
Serum sickness
Type III hypersensitivity
Contact dermatitis
Type IV hypersensitivity
Atopic dermatitis
Lichen planus
Psoriasis
Erythema multiforme
Stevens-Johnson syndrome
Bullous pemphigoid
Acne vulgaris
Skin cancer

Transcript

Watch video only

In dermatomyositis, “-itis” refers to inflammation, “myos-“ to the muscles and “dermato-“ to the skin, so dermatomyositis is an inflammatory disorder which involves both the skin and the muscles.

Dermatomyositis is considered to be an autoimmune disease, meaning that the immune system has gone rogue and started attacking its own muscles and skin.

Okay, normally, the cells of the immune system are always hanging around, ready and excited to spot and fight against anything foreign that could cause harm inside the body.

B- lymphocytes produce antibodies against a specific part of these foreign pathogens, called antigen.

The tips of these antibodies strongly binds to this antigen, while the base of the antibody, called the constant region, gets recognized by complement proteins.

These complement proteins are a group of small proteins made by the liver that work together.

One complement protein cuts or cleaves the next one, activating it and creating an enzymatic cascade.

This process gets started with C1, the first of the complement proteins, which binds to the Fc, or the constant region of two antibody attached to the pathogen.

C1 then cleaves C2 and C4.

Portions of the C2 and C4 binds to the antigen and form an enzymatic complex that cleaves C3 into two portions, C3a and C3b.

C3b joins the enzymatic complex and then the complex is able to cleave C5 into two portions, C5a and C5b portion.

C5a and C3a float off into the blood where they attract other cells of the immune system to the affected area.

Meanwhile, C5b, C6, C7, C8 and multiple C9 proteins, come together on the surface of the pathogen to form the membrane attack complex or MAC.

The MAC attacks pathogenic cells, such as bacteria, by creating a channel in the cell membrane.

Because cells have more solutes in them than the outside environment, water flows into the cell by the process of osmosis, and that causes the cell to swell up and burst, which is called cell lysis.

In dermatomyositis, immune cells confuse normal muscle and skin proteins with foreign antigens.

This process is called molecular mimicry because from the perspective of the immune cells, a host protein is mimicking a foreign or tumor protein.

When normal proteins in our body trigger an immune response, that protein is called an autoantigen.

These autoantigens get picked up by B- lymphocytes, which begin producing antibodies against them.

In dermatomyositis, the autoantigens are usually found in various spots, like the endothelial cells lining the capillaries in muscle and skin cells, as well as soluble antigens coming from the nucleus or cytoplasm of destroyed muscle cells and skin cells.

So, in the first case, autoantibodies attach to the endothelial cells lining the capillaries near the perimysium, which is a sheath of connective tissue around bundles of muscle fibers.

Upon binding, these antibodies activate the complement cascade, leading to formation of the membrane attack complex which causes the endothelial cells to lyse.

The complement proteins also attract more inflammatory cells, like macrophages, to the area.

Key Takeaways

Dermatomyositis (DM) is a rare autoimmune disease that leads to inflammation and damage of the muscles and skin. It is associated with complement system activation, and autoantibodies like ANA, anti-Mi-2 and, anti-Jo-1 which result in proximal muscle weakness and photosensitive skin rashes. DM presents with muscle weakness, which often becomes worse over time, as well as a distinctive skin rash.

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. "Clinical Immunology" Elsevier (2018)
  6. "Dermatomyositis" Clinics in Dermatology (2006)
  7. "Treatment of clinically amyopathic dermatomyositis in adults: a systematic review" British Journal of Dermatology (2016)
  8. "Treatment of clinically amyopathic dermatomyositis in adults: a systematic review" British Journal of Dermatology (2016)