Names |
- Microscopic polyarteritis
Abbreviations: MPA Category: Vascular system |
Prevalence |
Published: No data on US prevalence.
ARI Data: An estimated 11,952 cases in the U.S. Female/Male ratio: 3.1x. |
Age of Onset |
No data. |
Description |
Microscopic polyangiitis (MPA) is a disorder that causes inflammation in the blood vessels. The inflammation can affect many of the body's organ systems including the kidneys, nervous system, skin, lungs, etc. Microscopic polyangiitis is believed to be autoimmune because the development of the disease is thought to come from an overreaction in the immune system that causes inflammation in the body's tissues and blood vessels. The disease can be confused with others such as polyarteritis nodosa (PAN), granulomatosis with polyangiitis (GPA), and cutaneous leukocytoclastic angiitis (CLA). However, in 1994, The Chapel Hill Consensus Conference defined MPA as a separate disorder.
Evidence of autoimmunity: Antibody No ICD-10 Code.   SNOMED Code: 1144805008
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Patient Groups |
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Symptoms |
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Resources |
Link to Clinical Trials Link to PubMed |
References |
Link to Cleveland Clinic
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Profile by: Lauren DunnProfile updated September 2024Charts generated Feb 19, 2025 at 06:51 PM ET |
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Microscopic polyangiitis sex breakdown
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Microscopic polyangiitis age breakdown
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