Top Tweets for #polyangiitis
Red Flags Raising Suspicion of #Eosinophilic #Granulomatosis with #Polyangiitis: An EGPAware European #Consensus #Infographic.
https://t.co/8escqGpvCE
#Infographic: 25 Red Flags Raising Suspicion of #Eosinophilic #Granulomatosis with #Polyangiitis (#EGPA). https://t.co/8escqGpvCE
Post hoc ADVOCATE analysis: Avacopan improved kidney recovery, reduced relapse, and lowered glucocorticoid toxicity in people with GPA or MPA and kidney involvement. #nephrology #nephtwitter #granulomatosis #polyangiitis https://t.co/VrCohbnQVm
Baseline #eosinophil counts may be useful predictors for both the presence and motor involvement of peripheral #neuropathy in patients with eosinophilic #granulomatosis with #polyangiitis (EGPA), as demonstrated by a recent study of the KEIO-#vasculitis cohort.
In EGPA, baseline blood eosinophil count strongly predicted both the presence and the severity of peripheral neuropathy:
◦ No neuropathy: median 2,340/μL
◦ Sensory neuropathy: 4,276/μL
◦ Sensorimotor neuropathy: 11,859/μL
(stepwise increase, P = 0.004)
Clinically useful eosinophil cutoff values in EGPA found were:
◦ ≥2,468/μL → predicts any peripheral neuropathy (sensitivity 90 %, specificity 75 %)
◦ ≥6,724/μL → predicts sensorimotor (more severe) neuropathy (sensitivity 80 %, specificity 71 %)
*Imai Y, Ishigaki S, Akiyama M, Kaneko Y. Distinct predictors of peripheral neuropathy in antineutrophil cytoplasmic antibody-associated vasculitis: KEIO-vasculitis cohort. Semin Arthritis Rheum, 2025.
🔗https://t.co/QfFLnV8omC
Flow charts showing EULAR-recommended induction therapies for patients with active new-onset or relapsing #granulomatosis with #polyangiitis (GPA)/microscopic polyangiitis (MPA) with and without organ- or life-threatening disease in panel A, and mainenance therapies for patients achieving remission in panel B (diagrams adapted from Hellmich et al).
*From: Hellmich B. Mapping a path forward: Addressing disease burden, pathways and solutions in #ANCA-associated vasculitis. Rheumatology (Oxford), 2025.
🔗https://t.co/CQQ0naOh3Q
#Myeloperoxidase-Antibody Positivity and Progression to Microscopic #Polyangiitis in Interstitial Lung Disease: A Case Series
https://t.co/3DRTV4MkeB
#ILD
Unusual Mouth and Nose Symptoms Reveal Rare and Serious Autoimmune Disorder Linked to COVID-19
https://t.co/LLRhe2Kpzd
#COVID19 #Autoimmune #SARSCoV2 #granulomatosis #polyangiitis #Health #News
A Rare Case of Autoimmune #PulmonaryAlveolarProteinosis Developing During the Course of #Eosinophilic #Granulomatosis With #Polyangiitis
https://t.co/DPCq1Pne7R
Insights from comparison of serum #IgG4 between #T2-#eosinophilic #asthma and #eosinophilic #granulomatosis with #polyangiitis/#idiopathic #hypereosinophilic #syndrome. Open Access. https://t.co/GTFzFTEz7Z
The most frequent cutaneous manifestations in #granulomatosis with #polyangiitis (GPA), formerly called #Wegener's granulomatosis, is palpable purpura (30%–50% of patients). However, skin lesions may be polymorphic and include papule, nodule, vesicle (blisters of 0.5 cm or less), bullae (blisters larger than 0.5 cm), and ulcer with livedo reticularis. Vascular injury, primarily in the superficial dermis with increased permeability, may cause blisters instead of purpura or ulcers, whereas severe organ damage suggests deeper vascular involvement. Early glucocorticoid tapering or sparing therapy with rituximab or avacopan may be effective in treating GPA-associated blisters.
#Fasenra Approved in Europe as an add-on treatment in adults with relapsing or #refractory #eosinophilic #granulomatosis with #polyangiitis (EGPA). Its original indication is as an add-on maintenance treatment in adults with severe #eosinophilic #asthma. https://t.co/ceyhgwdk8L
Microscopic #polyangiitis clinical presentation of may differ depending on the age of onset of the disease. In a Canadian cohort (n = 31 cases) younger patients presented with more aggressive and classic #vasculitis-like presentations, with multi-system organ involvement and statistically significant higher incidence of renal, pulmonary, and cutaneous manifestations. In contrast, elderly patients had a predominant of constitutional and non-specific symptoms with often delayed diagnosis.
🔗https://t.co/vQ4iz5uyYA
🔹#RespirologyCaseReports
Endobronchial ultrasound-guided #cryobiopsy for diagnosing a case of #granulomatosis with #polyangiitis
https://t.co/OYAiYqCOV1
#EBUS
Intravenous #methylprednisolone (IVMP) 1.0 g/day pulse improves all-cause #mortality in patients with severe microscopic #polyangiitis and #granulomatosis with polyangiitis.
🔗https://t.co/sfHguEtMbo
Real-life data about the PEXIVAS reduced-dose glucocorticoid regimen in #granulomatosis with polyangiitis and microscopic #polyangiitis (Abstract 0725 https://t.co/7x34Hr0OMP)
@TerrierBen
#ACR23
#ACRambassador
🖱️Welcome to share this wonderful review about Anti-neutrophil #cytoplasmic antibody, #vasculitis, #granulomatosis with #polyangiitis:
https://t.co/bnwh9mf6Mb
@DanielVargasMD @COchestrads @NASCISociety @CURadiology @RanishKhawaja @OSUMedPedsRes @WuMarkusY @Camiurzua @EBRheum
📑Share a review that summarizes ##Cutaneous #manifestations of anti-neutrophil #cytoplasmicantibody associated vasculitis
⭕️Key word: #aneurism #dissection #endoleak #sealing
🧐Welcome to share and read: https://t.co/bnwh9mf6Mb
50 years old lady with #hemoptysis and impaired #Kidney function.
#Inflammatory markers are raised.
#C_ANAC and #P_ antibodies ANCA are positive
What is the most likely diagnosis or differential diagnosis ?
In #Granulomatosis with #Polyangiitis #GPA - dont be fooled - 15 to 40% have specific skin lesions, and can have Pyoderma gangrenosum-like presentation
#ccfhm23
Open Life Sciences | Vol. 18
Granulomatous polyangiitis involving the fourth ventricle: Report of a rare case and a literature review
▶️https://t.co/cyRpXN3SV7
#polyangiitis #granulomatosis #vasculitis
Review: #Hypereosinophilic syndrome ( #HES ) and #eosinophilic #granulomatosis with #polyangiitis ( #EGPA ): two sides of the same coin. Open Access. https://t.co/vv6nGUhkgs
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