Kawasaki disease

Last updated: February 04, 2023

Kawasaki disease

V

V

Familial hypercholesterolemia
Multiple endocrine neoplasia
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Albinism
Cystic fibrosis
Gaucher disease (NORD)
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Hemochromatosis
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Krabbe disease
Leukodystrophy
Niemann-Pick disease types A and B (NORD)
Fabry disease (NORD)
Tay-Sachs disease (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Phenylketonuria (NORD)
Cystinuria (NORD)
Aromatic L-amino acid decarboxylase deficiency (NORD)
Sickle cell disease (NORD)
Spinocerebellar ataxia (NORD)
IgA nephropathy (NORD)
Focal segmental glomerulosclerosis (NORD)
Muscular dystrophies and mitochondrial myopathies: Pathology review
Wiskott-Aldrich syndrome
Muscular dystrophy
Hemophilia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Alport syndrome
Alpha-thalassemia
Beta-thalassemia
Congenital adrenal hyperplasia
Primary adrenal insufficiency
Waterhouse-Friderichsen syndrome
Hyperaldosteronism
Cushing syndrome
Conn syndrome
Thyroglossal duct cyst
Hyperthyroidism
Graves disease
Thyroid eye disease (NORD)
Toxic multinodular goiter
Thyroid storm
Hypothyroidism
Hashimoto thyroiditis
Riedel thyroiditis
Thyroid cancer
Hypocalcemia
Hypercalcemia
Hyperparathyroidism
Hypoparathyroidism
Diabetes mellitus
Diabetic retinopathy
Diabetic nephropathy
Hyperpituitarism
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Gigantism
Acromegaly
Hypopituitarism
Pituitary apoplexy
Sheehan syndrome
Hypoprolactinemia
Constitutional growth delay
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Precocious puberty
Delayed puberty
Premature ovarian failure
Polycystic ovary syndrome
Androgen insensitivity syndrome
Kallmann syndrome
5-alpha-reductase deficiency
Multiple endocrine neoplasia
Pancreatic neuroendocrine neoplasms
Zollinger-Ellison syndrome
Carcinoid syndrome
Pheochromocytoma
Neuroblastoma
Myelodysplastic syndromes
Nephrotic syndromes: Pathology review
Reye syndrome
Tourette syndrome
Fragile X syndrome
Valvular heart disease: Pathology review
Sleep apnea
HIV (AIDS)
Heart blocks: Pathology review
Malabsorption syndromes: Pathology review
Tuberculosis: Pathology review
Hypothyroidism: Pathology review
Inflammatory bowel disease: Pathology review
Osteoporosis medications
Osteoarthritis
Acute pancreatitis
Major depressive disorder
Bipolar and related disorders
Generalized anxiety disorder
Panic disorder
Obsessive-compulsive disorder
Body dysmorphic disorder
Post-traumatic stress disorder
Physical and sexual abuse
Schizoaffective disorder
Schizophreniform disorder
Delusional disorder
Schizophrenia
Delirium
Amnesia
Dissociative disorders
Anorexia nervosa
Bulimia nervosa
Factitious disorder
Somatic symptom disorder
Attention deficit hyperactivity disorder
Tourette syndrome
Autism spectrum disorder
Rett syndrome
Neuroleptic malignant syndrome
Skin cancer: Clinical
Spina bifida
Amenorrhea: Clinical
Cervical cancer: Clinical
Seizures: Clinical
Leukemia: Clinical
Headaches: Clinical
Portal hypertension
Cirrhosis
Cirrhosis: Pathology review
Kawasaki disease
Lymphedema
Persistent truncus arteriosus
Transposition of the great vessels
Total anomalous pulmonary venous return
Hypoplastic left heart syndrome
Patent ductus arteriosus
Ventricular septal defect
Coarctation of the aorta
Atrial septal defect
Tricuspid valve disease
Pulmonary valve disease
Mitral valve disease
Aortic valve disease
Dilated cardiomyopathy
Restrictive cardiomyopathy
Hypertrophic cardiomyopathy
Cor pulmonale
Acyanotic congenital heart defects: Pathology review
Cyanotic congenital heart defects: Pathology review
Valvular heart disease: Pathology review
Prinzmetal angina
Aneurysms
Acute leukemia
Acute pyelonephritis
Acute kidney injury: Clinical
Poliovirus
Renal tubular acidosis

Transcript

Watch video only

Kawasaki disease isn’t at all related to the motorcycle and engine company, other than the fact that they were both founded or first described in Japan. Kawasaki disease is a vasculitis or an inflammation of the blood vessels, that mostly affects the coronary arteries but can also affect any large- or medium-sized arteries as well. With Kawasaki disease, the immune system attacks the arteries. Ultimately, it’s not quite known why this happens though, some theories suggest it has some infectious cause, though autoimmune reactions and genetic predisposition probably play a part as well.

Whatever the case, when the endothelial cells in the blood vessels are attacked, they become damaged which exposes the underlying collagen and tissue factor found in the middle layer of the blood vessel, or the tunica media.

And this leads to a few serious problems: First, these exposed materials increase the chance of blood coagulation. When blood coagulates it forms clots that can block blood flow in the coronary arteries, leading to ischemia of the heart muscle.

Secondly, damaged endothelial cells in coronary arteries mean weak artery walls, which can lead to coronary aneurysms. These aneurysms form because fibrin is deposited into the blood vessel wall as part of the healing process. Fibrin makes the vessel stiffer, less elastic, and unable to gently stretch with high arterial pressures; instead, the arteries develop permanent bulges that we call aneurysms. Aneurysms 8mm or larger are at the most risk of rupturing, which reduces blood flow to the heart, causing ischemia and potentially myocardial infarction, or heart attack.

And third, in some cases, the fibrosis doesn’t lead to aneurysms, but instead, the fibrosis of the blood vessel walls make the vessel walls thicker, which reduces the lumen diameter and restricts blood flow. If blood flow’s restricted or reduced, the heart again might become ischemic, leading to a heart attack.

Kawasaki disease is most commonly seen in infants and children under five years old and is more likely to affect boys. This disease is self-limited which means that the inflammation will resolve after 6 to 8 weeks but if we left it untreated, there is a 20-25% risk of the heart complications we went over.

Alright, so let’s look at the symptoms of Kawasaki disease. We rarely see any cardiac symptoms in the first few weeks unless the patient has an underlying heart condition already, and so cardiac symptoms typically evolve later.

Now the classic symptoms of Kawasaki disease are as follows: conjunctivitis with limbus sparing (which is red eyes with a margin right around the iris that is still white), a rash that might extend across other parts of the body, and starts polymorphous but later desquamates, or flakes off, adenopathy, or enlarged lymph nodes, especially the cervical lymph nodes. A strawberry tongue which is when the top layer of cells on their tongue slough off giving the tongue a very red, “strawberry” like appearance, also their mouth and throat may look really red too and their lips might become dry and cracked. Their hands and feet might get swollen and develop a rash as well. And finally, they might have 5 or more days of high fever that typically doesn’t resolve with antipyretics.

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. "Kawasaki disease: etiopathogenesis and novel treatment strategies" Expert Review of Clinical Immunology (2016)
  5. "Diagnosis of Kawasaki disease" International Journal of Rheumatic Diseases (2017)
  6. "Diagnosis and management of kawasaki disease" Am Fam Physician (2015)