Tag: Vasculitis

Affecting individuals of all ages, vasculitis occurs when the body's immune system mistakenly attacks its own blood vessels. Understanding the diagnosis, symptoms, and treatment options is essential when dealing with a condition where the medical term for inflammation of a vessel is so critical to define.

Systemic diseases affect the entire body, rather than a single organ or body part. A prime example of what disease attacks the whole body is systemic lupus erythematosus (SLE), an autoimmune disorder that can damage the skin, joints, kidneys, and nervous system.

While the visible purple skin spots known as purpura signal bleeding under the skin, their relationship with blood clots is complex and dependent on the underlying cause. The answer to "does purpura cause blood clots?" is not a simple yes or no, as some types are a direct result of dangerous clotting, while others are linked to low platelet counts and a higher risk of bleeding.

According to the Centers for Disease Control (CDC), at least 1.7 million adults in the U.S. develop sepsis each year, a condition that can lead to multiple organ dysfunction syndrome (MODS), one of the most critical answers to what disease attacks all your organs. While no single illness universally harms every organ at once, several systemic conditions can cause widespread damage throughout the body via inflammation, infection, or abnormal protein buildup.

Behcet's disease, a rare chronic inflammatory disorder, typically emerges in a person's 20s or 30s, though it can affect individuals at any age. The specific ICD 10 code for Behcet's disease is M35.2 and is vital for accurate medical coding, insurance processing, and health record maintenance.

Affecting fewer than 1 in 100,000 people in the United States and Northern Europe, Behçet's disease is often confused with other conditions. While many people search for **what is Bassetts disease?**, the term is a common misspelling for the actual condition, Behçet's disease—a rare, inflammatory autoimmune disorder.

Affecting only about 3 in 100,000 people, what is the Wegener disease, formally known as Granulomatosis with Polyangiitis (GPA), is a rare autoimmune disorder that causes inflammation of the blood vessels. It can impact nearly any organ system in the body, but primarily affects the respiratory tract and kidneys.

Vasculitis can affect blood vessels in virtually any part of the body, meaning a single, specific diagnosis is not always possible. A team-based approach, often led by a rheumatologist, is therefore essential to manage this rare and complex condition, and find the right doctor who handles vasculitis and its varying symptoms.

While Steroid-Responsive Meningitis-Arteritis (SRMA) is a well-documented immune-mediated disease in dogs, the query, 'What is SRMA in humans?,' arises because it is not a recognized human diagnosis. Instead, human recurrent meningitis has diverse origins, including infections, anatomical defects, or autoimmune conditions.

The autoimmune disorder granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis, is a rare type of vasculitis affecting the respiratory tract and kidneys. This condition's name was officially updated to reflect its underlying pathology more accurately while moving away from an association with its descriptor, who had a complex past.