#Granulomatosis with polyangiitis

[disabledsysboxes]

Autoimmune - 6

[zalien333]

Finally got my appointment for a transnasal endoscopy and tracheoscopy for the 2nd Sept, luckily having local anesthetic but I'm almost certain I've had this before and ended up needing to be put to sleep 😅 but hopefully it goes OK, been waiting since March

[munaeem]

Who is affected by granulomatosis with polyangiitis?

Understanding Granulomatosis with Polyangiitis (GPA): A Comprehensive Guide Granulomatosis with polyangiitis (GPA) is a rare autoimmune disease that primarily affects the blood vessels in various organs. This condition, also known as Wegener’s granulomatosis, can have a profound impact on those who are affected by it. In this blog post, we will explore the symptoms, diagnosis, and therapy…

[futuremarketshubham]

The Global Eosinophilic Granulomatosis with Polyangiitis Treatment Market Is Expected to Register Growth at 5.2% CAGR through 2033- FMI Study

The global eosinophilic granulomatosis with polyangiitis treatmentmarket is currently valued at US$ 173.8 Million in 2023 and is anticipated to expand at a CAGR of  5.2%. Owing to the technological advances in healthcare the market is likely to propel to US$ 288.5 Million by 2033.

The growing occurrences of churg strauss syndrome and other allergic reactions and asthma, rising geriatric population, and growing incidences of churg Strauss syndrome in children are expected to drive the growth of the market during the assessment period.

The increasing awareness among patients regarding this condition and the availability of effective therapeutics are projected to bolster the eosinophilic granulomatosis with polyangiitis treatment market in developed economies. Furthermore, with the rising support from government organizations and the development of the healthcare facilities and infrastructure are projected to supplement the development of the overall market in the forecast period.

The development of modern therapeutics and the increasing number of players with a strong drug pipeline are considered as the key factors that are likely to contribute substantially towards the development of the global eosinophilic granulomatosis with polyangiitis treatment market in the next few years.

The manufacturers are involved in the production of eosinophilic granulomatosis with polyangiitis treatment market in a larger capacity. Research and innovation are also conducted to launch innovative products for eosinophilic granulomatosis with polyangiitis therapeutics.

North America dominates the eosinophilic granulomatosis with polyangiitis treatment market due to the presence of key market players' presence, along with recent product launches and established healthcare infrastructure, which will accelerate the market's growth in the region. The significant R&D investments in Europe abode well for market growth.

Download Sample Report to learn about recent in the EosinophilicGranulomatosis with Polyangiitis Treatment Marketby FMI @ https://www.futuremarketinsights.com/reports/sample/rep-gb-16455

Key Takeaways from the Market Study

As of 2023, the eosinophilic granulomatosis with polyangiitis treatment market was valued at US$ 173.8Million

From 2023 to 2033, the eosinophilic granulomatosis with polyangiitis treatment industry is poised to grow at 5.2% CAGR

By 2033, the eosinophilic granulomatosis with polyangiitis treatment market is slated to reach a valuation of US$ 288.5 Million

Based on the distribution channel, hospital pharmacy segment accounts for   market share of 35.7% during the forecast period. 

China is poised to yield a CAGR of 4.8% with respect eosinophilic granulomatosis with polyangiitis treatment in 2033.

“Growing healthcare spending and growing the incidence of asthma across the world and rapid rise in the geriatric population are expected to radically transform the market in the coming years,” comments an analyst at FMI.

Competitive Landscape

Some of the key players present in the global eosinophilic granulomatosis with polyangiitis treatment markets are Genentech Inc., F. Hoffmann-La Roche AG, Cephalon Inc., Teva Pharmaceutical Industries Ltd., Amgen Inc., Sanofi S.A., Koninklijke DSM N.V, AstraZeneca, Novartis International AG, GlaxoSmithKline LLC, Baxter Healthcare Corporation and others.

The research report presents a comprehensive assessment of the market and contains thoughtful insights, facts, historical data, and statistically supported and industry-validated market data. It also contains projections using a suitable set of assumptions and methodologies. The research report provides analysis and information according to market segments such as geographies, application, and industries.

In April 2021 -- Genentech, a member of the Roche Group announced that the U.S. Food and Drug Administration (FDA) has approved the company’s supplemental Biologics License Application for Xolair® (omalizumab) prefilled syringe for self-injection across all approved U.S. indications. Xolair is the only FDA-approved biologic designed to target and block immunoglobulin E (IgE) for the treatment of moderate to severe persistent allergic asthma, chronic idiopathic urticaria (CIU) and nasal polyps.

In December 2020 - Amgen announced that the U.S. Food and Drug Administration (FDA) has approved RIABNI™ (rituximab-arrx), a biosimilar to Rituxan® (rituximab), for the treatment of adult patients with Non-Hodgkin's Lymphoma (NHL), Chronic Lymphocytic Leukemia (CLL), Granulomatosis with Polyangiitis (GPA) (Wegener's Granulomatosis), and Microscopic Polyangiitis (MPA).

More Valuable Insights Available

FMI, in its new offering, presents an unbiased analysis of the market, presenting historical demand data (2018 to 2022) and forecast statistics for the period of 2023 to 2033.

The study divulges essential insight into eosinophilic granulomatosis with polyangiitis treatment market by drug class (Steroids, Immunosuppressant, Biologics, Immune Globulins) by Route of Administration (Oral, Intravenous, Intramuscular) by Distribution Channel (Hospital Pharmacies, Drug stores, Retail Pharmacies, Online Pharmacies) by Region - Global Forecast 2023 to 2033

About the Healthcare Division at Future Market Insights

The healthcare team at Future Market Insights offers expert analysis, time efficient research, and strategic recommendations with an objective to provide authentic insights and accurate results to help clients worldwide. With a repertoire of over 100+ reports and 1 million+ data points, the team has been analyzing the industry lucidly in 50+ countries for over a decade. The team provides a brief analysis on key trends including competitive landscape, profit margin, and research development efforts.

About Future Market Insights (FMI)

Future Market Insights (FMI) is a leading provider of market intelligence and consulting services, serving clients in over 150 countries. FMI is headquartered in Dubai, and has delivery centers in the UK, U.S. and India. FMI's latest market research reports and industry analysis help businesses navigate challenges and make critical decisions with confidence and clarity amidst breakneck competition. Our customized and syndicated market research reports deliver actionable insights that drive sustainable growth. A team of expert-led analysts at FMI continuously tracks emerging trends and events in a broad range of industries to ensure that our clients prepare for the evolving needs of their consumers.

Key Companies Profiled

Genentech Inc

F. Hoffmann-La Roche AG

Cephalon Inc.

Teva Pharmaceutical Industries Ltd.

Amgen Inc.

Sanofi S.A.

Koninklijke DSM N.V

AstraZeneca

Novartis International AG

GlaxoSmithKline LLC

Baxter Healthcare Corporation

Key Segments Covered in Eosinophilic Granulomatosis with Polyangiitis Treatment Market Industry Survey:

Steroids

Immunosuppressant

Biologics

Immune Globulins

Eosinophilic Granulomatosis with Polyangiitis Treatment Market by Route of Administration:

Oral

Intravenous

Intramuscular

Eosinophilic Granulomatosis with Polyangiitis Treatment Market by Distribution Channel:

Hospital Pharmacies

Drug stores

Retail Pharmacies

Online Pharmacies

Eosinophilic Granulomatosis with Polyangiitis Treatment Market by Region:

North America

Latin America

Europe

South Asia

East Asia

Oceania

Middle East & Africa (MEA)

[drpedi07]

Granulomatosis with Polyangiitis (Wegener) Calculator

Granulomatosis with polyangiitis (GPA), formerly known as Wegener granulomatosis, is a rare multisystem autoimmune disease of unknown etiology. Its hallmark features include necrotizing granulomatous inflammation and pauci-immune vasculitis in small- and medium-sized blood vessels

[fletchingbrilliant]

🌙some wildly cheap commissions!🌙

🙃 for some even wilder reasons 🙃

hey y'all. long post thingie but it's got cute pictures so please check it out

TRANSCRIPT OF POST

hey frens got something kinda somber to talk about. most of you are very aware of the existence of my beautiful fiance and co-creator of basically everything i do. zae and i are getting handfasted (marriage for pagans) in october, and have been living together for about 10 years. in 2021, zae got really fucking sick, and after a few false starts, was diagnosed with a rare for of vasculitis called granulomatosis with polyangiitis, GPA for short. it’s an autoimmune disease that causes inflammation in blood vessels and other tissues, ultimately stopping blood from getting to the parts of the body that need it, affecting many areas, but primarily the respiratory system. while the cause isn’t known, it usually presents in people in their 50’s or 60’s, but complications from a third bout of covid-19 appears to have made it emerge way earlier for our boy. at least, that’s what we think. his case is extremely aggressive, advancing faster than anyone could have expected. in zae’s case, it actually attacked his kidneys first, and then went after his lungs, causing both to threaten shutting down for good. he was extremely anemic and needed a ton of transfusions, narrowly avoiding dialysis, and we spent weeks in the hospital keeping him alive. he was placed on two different kinds of chemotherapy to combat the disorder. he lost his hair, went through even more fatigue and pain on top of what the disease had already put him through, and had to accept a plethora of changes to his life that will last forever. a lot of you out there have harrowing experiences of your own when it comes to chronic and potentially terminal conditions, too, I’m certain. “it’s not fun” is an understatement. though there were a couple of really fucking close calls, zae’s GPA went into remission. his hair grew back fuller and more luscious than it had ever been before. (i later learned these are affectionately referred to as “chemo curls.”) remission for gpa is usually expected to last at least 5 years, potentially up to 20, before any symptoms resurface. but zae’s case was particularly aggressive, so of course he’s not so lucky. he’s relapsing now. his symptoms have been slowly returning, and it’s been decided that he’s going back on chemo. it’s no surprise that this shit is expensive, even with insurance. we’re still paying off the care he received last time because ‘murca. being disabled myself, work has been… let’s call it inconsistent, yeah? yeah, that’s a nice and comfortable thing to call it. no one’s doing well financially these days, so we of course have to get creative. long story short(er), i’m doing a commission special! for the next MONTH, i am offering fast commissions at crazy-low prices to try and help us create a cushion to keep us afloat and relatively comfortable while we begin the chemo process again. there’s several options for a variety of budgets, because i really hate the idea of seeking something for nothing, and i absolutely abhor having to reach out in this way. it makes me feel vulnerable and icky and… i’m sure you all understand that, too. i can’t thank you all enough just for following me, and engaging with mine and zae’s work. it may sound trite, but that really makes a difference to us, especially when we’re dealing with something so painful. so if you can’t or don’t want to partake of the sale, please know that you are still a huge help to us, and we seriously appreciate each and every one of you. like, so fucking much. thanks y’all love, fletch

END TRANSCRIPT

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please DM me if you're interested in something, and thank you again

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[unhonestlymirror]

It makes me sick to see "arguments" in defence of russia as "but their culture..." - did you know that a Wegeners granulomatosis was renamed because it was discovered(?) by the nazi doctor, Wegener? And they renamed it to granulomatosis with polyangiitis, and nothing bad happened. Did you know that a nazi Germany actually had a bunch of good doctors/artists/singers/etc who supported and even participated in the fucking genocide? We don't forgive nazis, then why should we forgive ruzzia?

Why do people still glorify russia? Why do people STILL draw Ukraine and Belarus as russia's sisters? Why do people use russian names for Ukrainian and Belaruthian cities and history? Why do people completely ignore what russia does to Ukraine? Why do people ignore the total linguicide of Belarus? Why do people erase us and glorify our rapist?

Sometimes, I feel like most of us never studied WW2 at school. Everyone is just ready to glorify the new hitler. Seems like most people are able to understand what Eastern Europeans feel only when a russian rocket hits their house. Otherwise, they just don't understand why rusliet or drawing Belarus with prorussian flag or drawing MY COUNTRY AS RUSSIA'S SISTER is fucking disgusting and very offensive.

I wish every such content maker to find out how it feels to live under russian occupation. Seems like the experience of real people is not enough for them.

[does-truth-matter]

The CDC has quietly changed who should AVOID the MMR vaccine.

https://www.cdc.gov/vaccines/vpd/mmr/public/index.html

They now state that ANYONE that “Has a parent, brother or sister with a history of immune system problems” should AVOID THE MMR VACCINE!

What exactly is an 'immune system problem?" Every autoimmune disorder.

* Achalasia

* Addison’s disease

* Adult Still's disease

* Agammaglobulinemia

* Alopecia areata

* Amyloidosis

* Amyotrophic lateral sclerosis (Lou Gehrigs)

* Ankylosing spondylitis

* Anti-GBM/Anti-TBM nephritis

* Antiphospholipid syndrome

* Autoimmune angioedema

* Autoimmune dysautonomia

* Autoimmune encephalomyelitis

* Autoimmune hepatitis

* Autoimmune inner ear disease (AIED)

* Autoimmune myocarditis

* Autoimmune oophoritis

* Autoimmune orchitis

* Autoimmune pancreatitis

* Autoimmune retinopathy

* Autoimmune urticaria

* Axonal & neuronal neuropathy (AMAN)

* Baló disease

* Behcet’s disease

* Benign mucosal pemphigoid

* Bullous pemphigoid

* Castleman disease (CD)

* Celiac disease

* Chagas disease

* Chronic inflammatory demyelinating polyneuropathy (CIDP)

* Chronic recurrent multifocal osteomyelitis (CRMO)

* Churg-Strauss Syndrome (CSS) or Eosinophilic Granulomatosis (EGPA)

* Cicatricial pemphigoid

* Cogan’s syndrome

* Cold agglutinin disease

* Congenital heart block

* Coxsackie myocarditis

* CREST syndrome

* Crohn’s disease

* Dermatitis herpetiformis

* Dermatomyositis

* Devic’s disease (neuromyelitis optica)

* Discoid lupus

* Dressler’s syndrome

* Endometriosis

* Eosinophilic esophagitis (EoE)

* Eosinophilic fasciitis

* Erythema nodosum

* Essential mixed cryoglobulinemia

* Evans syndrome

* Fibromyalgia

* Fibrosing alveolitis

* Giant cell arteritis (temporal arteritis)

* Giant cell myocarditis

* Glomerulonephritis

* Goodpasture’s syndrome

* Granulomatosis with Polyangiitis

* Graves’ disease

* Guillain-Barre syndrome

* Hashimoto’s thyroiditis

* Hemolytic anemia

* Henoch-Schonlein purpura (HSP)

* Herpes gestationis or pemphigoid gestationis (PG)

* Hidradenitis Suppurativa (HS) (Acne Inversa)

* Hypogammalglobulinemia

* IgA Nephropathy

* IgG4-related sclerosing disease

* Immune thrombocytopenic purpura (ITP)

* Inclusion body myositis (IBM)

* Interstitial cystitis (IC)

* Juvenile arthritis

* Juvenile diabetes (Type 1 diabetes)

* Juvenile myositis (JM)

* Kawasaki disease

* Lambert-Eaton syndrome

* Leukocytoclastic vasculitis

* Lichen planus

* Lichen sclerosus

* Ligneous conjunctivitis

* Linear IgA disease (LAD)

* Lupus

* Lyme disease chronic

* Meniere’s disease

* Microscopic polyangiitis (MPA)

* Mixed connective tissue disease (MCTD)

* Mooren’s ulcer

* Mucha-Habermann disease

* Multifocal Motor Neuropathy (MMN) or MMNCB

* Multiple sclerosis

* Myasthenia gravis

* Myositis

* Narcolepsy

* Neonatal Lupus

* Neuromyelitis optica

* Neutropenia

* Ocular cicatricial pemphigoid

* Optic neuritis

* Palindromic rheumatism (PR)

* PANDAS

* Parkinson's disease

* Paraneoplastic cerebellar degeneration (PCD)

* Paroxysmal nocturnal hemoglobinuria (PNH)

* Parry Romberg syndrome

* Pars planitis (peripheral uveitis)

* Parsonage-Turner syndrome

* Pemphigus

* Peripheral neuropathy

* Perivenous encephalomyelitis

* Pernicious anemia (PA)

* POEMS syndrome

* Polyarteritis nodosa

* Polyglandular syndromes type I, II, III

* Polymyalgia rheumatica

* Polymyositis

* Postmyocardial infarction syndrome

* Postpericardiotomy syndrome

* Primary biliary cirrhosis

* Primary sclerosing cholangitis

* Progesterone dermatitis

* Psoriasis

* Psoriatic arthritis

* Pure red cell aplasia (PRCA)

* Pyoderma gangrenosum

* Raynaud’s phenomenon

* Reactive Arthritis

* Reflex sympathetic dystrophy

* Relapsing polychondritis

* Restless legs syndrome (RLS)

* Retroperitoneal fibrosis

* Rheumatic fever

* Rheumatoid arthritis

* Sarcoidosis

* Schmidt syndrome

* Scleritis

* Scleroderma

* Sjögren’s syndrome

* Sperm & testicular autoimmunity

* Stiff person syndrome (SPS)

* Subacute bacterial endocarditis (SBE)

* Susac’s syndrome

* Sympathetic ophthalmia (SO)

* Takayasu’s arteritis

* Temporal arteritis/Giant cell arteritis

* Thrombocytopenic purpura (TTP)

* Tolosa-Hunt syndrome (THS)

* Transverse myelitis

* Type 1 diabetes

* Ulcerative colitis (UC)

* Undifferentiated connective tissue disease (UCTD)

* Uveitis

* Vasculitis

* Vitiligo

* Vogt-Koyanagi-Harada Disease

Wonder how many doctors are paying attention?

~shared from Jodi Wilson

[septalperforation]

Septal Perforation Repair: Improve Breathing and Comfort

Introduction

The nasal septum is a wall attached to the cartilage and bone standing between the two nostrils, which helps regulate airflow and keep the structure of the nose. When this fine structure in the nose gets a hole or tear, the result is septal perforation. It might lead to difficulty in breathing, regular nosebleeds, and massive amounts of discomfort, thereby affecting the lifestyle of a person.

What is a Septal Perforation?

Septal perforation is a hole in the nasal septum, which is the thin structure made of bone and cartilage that divides the nasal cavity. The variation in size is usually from small to large, with the effect being from mild discomfort to quite serious health issues. A small perforation might not even be symptomatic at all, while larger ones are functionally symptomatic and include chronic infections, trouble breathing, and cosmetic changes.

Causes of Septal Perforation

A septal perforation may result from several factors, which include:

Trauma: Of the more common etiologies, it could occur due to accidents, sports trauma, and even nasal procedures that are overly aggressive like cauterization or surgical interventions.

Surgery Complications: After septal surgery, commonly referred as septoplasty or rhinoplasty perforations may take place as a surprise particularly when the vascularity of the septum has been compromised.

Chronic Inflammations: Chronic sinusitis or infections affect the nasal tissue adversely and contribute to perforation of the septum.

Autoimmune Disorders: Specific autoimmune disorders, such as granulomatosis with polyangiitis or lupus, are other causes of septal perforation that result from the autoimmune system's attack on the body's healthy tissues.

Infection: Bacterial or fungal infections, especially those that linger for some time, may break down nasal tissue and cause perforation.

Tumors: Tumors, least of all cancerous growths, in the nasal cavity are very rare causes of septal perforation.

Symptoms of Septal Perforation 

The symptoms of septal perforation are of varying nature and mainly depend on the size and location of the perforation. The commonest symptoms are:

Nosebleeds: Irritation of the blood vessels around the perforation is not uncommon from frequent, unexplained nosebleeds.

Whistle: Many patients develop a prominent whistling sound while breathing, particularly if the perforation is of small size.

Nasal Congestion: Sometimes, people feel like their nose cavities are somehow congested or blocked all the time, which becomes really burdensome for them to 

breathe consecutively.

Crusting and Scabbing: In the case of denuded cartilage or bone within the perforation, the overlying tissue of the lung mucosa may desiccate, which leads to crusting and scabbing of the nose.

Septal perforation diagnosis

If you suspect that you have an injury which might cause a septal perforation you should make an appointment with your family ENT (otolaryngologist) who will refer you to have the medical evaluation. Diagnosis is a process that involves :

History: The doctor will ask you regarding your symptoms, past history of nasal trauma, any surgery, or substances of abuse.

Physical Examination: Your doctor will use a nasal speculum and bright light to examine your nasal cavity for any views of perforation.

Endoscopy: For further localization and visualization, nasal endoscopy may sometimes be required to examine the nasal cavities and the septum more closely. A very narrow tube, attached to a micro-camera, is inserted into the nose to present the images in detail.

Conclusion The condition is very serious, grossly debilitating, and may have effects on daily life. Symptoms can range from mild discomfort to possible life-threatening conditions, which are due to trauma, surgical intervention, or even underlying medical conditions. Fortunately, the advancement of these medical and surgical treatments led to the establishment of diverse ways in the management and repair of septal perforations. When one thinks they might be experiencing a septal perforation repair, you should see a specialist for discussion of symptoms, diagnosis, or treatment options suitable to each individual.

[kaushalkumar1711]

All You Should Know About Dacryocystitis 

Dacryocystitis: Meaning 

Dacryocystitis (dak-ree-oh-sis-ty-tus) is when your tear sac, which is part of your tear system, becomes inflamed and infected. The tear sac connects to your tear duct, which helps drain tears from your eyes to your nose. 

This condition occurs when something blocks the normal flow of tears, causing the fluid to get trapped and possibly become infected. The blockage can happen in the tear sac, the ducts, or the tear duct itself. 

Difference between acute and chronic dacryocystitis  

There are two types of dacryocystitis: acute and chronic. The main difference is time. Acute dacryocystitis appears suddenly and usually clears up within three months, while chronic dacryocystitis lasts longer. 

Chronic dacryocystitis is often connected to whole-body or autoimmune conditions like granulomatosis with polyangiitis, sarcoidosis, and lupus. People with chronic dacryocystitis may also have long-lasting conjunctivitis (pink eye). 

The types of germs that cause and affect acute and chronic dacryocystitis treatment may also differ. 

Symptoms of Dacryocystitis 

Signs can include: 

Eye pain. 

Swelling around your eye. 

Red or darkened skin. 

A sore with pus in the inner corner of your eyelids. 

Fever. 

When concerning chronic dacryocystitis treatment, the symptoms might be milder, like watery eyes and no fever. 

Causes of Dacryocystitis 

Dacryocystitis occurs when your tear duct gets blocked, stopping tears from flowing from your eyes to your nasal cavity.  

In newborns, a membrane blocking the duct is usually the cause. For children and adults, various factors can lead to blockages, such as:  

Aging, particularly in people over 40. 

Trauma from injuries or surgeries involving the nose. 

Medical conditions that affect the immune system or cause inflammation, like sinusitis. 

Unusual nasal structure. 

Tumors. 

Certain medications, including some blood pressure and glaucoma drugs, antiviral treatments, and cancer therapies. 

Retained punctal plugs used in eye treatments. 

Diagnosis and Tests for Dacryocystitis Surgery  

Your healthcare provider may suspect your condition based on how your eyes look, whether your nose is affected, and your medical history. 

Dacryocystitis treatment tests may include:  

An eye exam. 

Pressing on the swollen area to see if discharge comes out through the small hole at the corner of your eye. 

Taking a sample of discharge for lab testing to identify the infection-causing germ. 

A blood test to check white blood cell levels, which can indicate infection, and to find the underlying cause of the eye condition. 

Using a yellow dye in your eye to check for blockages based on how the dye moves through your tear system. 

Imaging tests to uncover causes of dacryocystitis. 

Extra dacryocystitis surgery tests if you’ve had blood in your tears or vision problems. 

Management and Treatment of Dacryocystitis Surgery  

How to Prevent Dacryocystitis  

You can't prevent most types of dacryocystitis, but you can lower your risk of infections by washing your hands often and not touching your eyes. Also, try to stay away from crowds or people who are sick. 

What can I expect if I have dacryocystitis? 

Sometimes dacryocystitis will go away on its own, but you should always talk to your doctor if you have symptoms. If not treated, dacryocystitis can lead to an open sore and might cause vision problems. 

Dacryocystitis is a condition that affects the tear sac, leading to inflammation and possible infection. Whether acute or chronic, it's important to recognize the symptoms and seek medical advice for proper treatment. While some cases may resolve on their own, timely intervention can prevent complications and ensure better eye health. Practicing good hygiene and avoiding infections can help reduce the risk of developing dacryocystitis. If you suspect you or your child may have this condition, consult with Shri Venkatesh Eye Institute & Surgical Center to address any concerns and get the right care for chronic dacryocystitis treatment.  

[rickypowell23]

Vasculitis: Causes, Symptoms, Types & Treatment - Anna Arthritis Care

Vasculitis is a group of rare diseases that cause inflammation of blood vessels. There are many types of vasculitis, such as giant cell arteritis (GCA), microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss), Behçet’s, as well as others. https://www.annaarthritiscare.com.au/services/vasculitis/

[scottrichmonder]

Vasculitis: Causes, Symptoms, Types & Treatment - Anna Arthritis Care

Vasculitis is a group of rare diseases that cause inflammation of blood vessels. There are many types of vasculitis, such as giant cell arteritis (GCA), microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss), Behçet’s, as well as others. https://www.annaarthritiscare.com.au/services/vasculitis/

[stphns3311]

Vasculitis: Causes, Symptoms, Types & Treatment - Anna Arthritis Care

Vasculitis is a group of rare diseases that cause inflammation of blood vessels. There are many types of vasculitis, such as giant cell arteritis (GCA), microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss), Behçet’s, as well as others. https://www.annaarthritiscare.com.au/services/vasculitis/

[paulkattupalli]

Granulomatosis with Polyangiitis (formerly Wegener Granulomatosis) 

Granulomatosis with Polyangiitis (formerly Wegener Granulomatosis)  Key Points  Granulomatosis with polyangiitis is a systemic necrotizing, mostly small vessel vasculitis of unknown etiology that manifests as granulomatous lesions of the upper respiratory tract, lungs and kidneys.  -Formerly known as Wegener Granulomatosis, it was renamed because of the eponymous individual’s association with…

[robingentile01]

Vasculitis: Causes, Symptoms, Types & Treatment - Anna Arthritis Care

Vasculitis is a group of rare diseases that cause inflammation of blood vessels. There are many types of vasculitis, such as giant cell arteritis (GCA), microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss), Behçet’s, as well as others. https://www.annaarthritiscare.com.au/services/vasculitis/

[bizznessupdates]

Vasculitis: Causes, Symptoms, Types & Treatment - Anna Arthritis Care

Vasculitis is a group of rare diseases that cause inflammation of blood vessels. There are many types of vasculitis, such as giant cell arteritis (GCA), microscopic polyangiitis (MPA), granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA or Churg-Strauss), Behçet’s, as well as others. https://www.annaarthritiscare.com.au/services/vasculitis/