Warning: simplexml_load_file(): SSL operation failed with code 1. OpenSSL Error messages: error:14095126:SSL routines:ssl3_read_n:unexpected eof while reading in /home/manuscriptpro/public_html/pdf/index.php on line 429

Warning: simplexml_load_file(): SSL: Success in /home/manuscriptpro/public_html/pdf/index.php on line 429



Full Text Journal Articles about
Churg Strauss Disease

Advertisement

Find full text journal articles






Cutaneous manifestations of childhood Eosinophilic Granulomatosis with Polyangiitis (cEGPA): A case-based review.

Catherine Bridges, Mary Elizabeth Reed Shenk, Kari Martin, Alison Launhardt,

BACKGROUND/OBJECTIVES:This study seeks to better define the clinical presentation and histopathology of cutaneous manifestations in childhood eosinophilic granulomatosis with polyangiitis (cEGPA). METHODS:Case reports were collected from Ovid Medline Database and PubMed using keyword identifiers from 1946 to 2017. Adult patients ≥ 18 years and cases not diagnosed with EGPA by the author were ... Read more >>

Pediatr Dermatol (Pediatric dermatology)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Cardiovascular and Lung Involvement in Patients with Autoimmune Pancreatitis.

Sara Nikolic, Katharina Brehmer, Nikola Panic, Roberto Valente, J-Matthias Löhr, Miroslav Vujasinovic,

INTRODUCTION:Immunoglobulin G4-related disease (IgG4-RD) is a systemic immune-mediated disease characterised pathologically by the infiltration of IgG4-bearing plasma cells into the involved organs. Autoimmune pancreatitis (AIP) is a form of chronic pancreatitis with a heavy lymphocytic infiltration and two distinct histopathological subtypes, namely: lymphoplasmacytic sclerosing pancreatitis (AIP type 1) and idiopathic ... Read more >>

J Clin Med (Journal of clinical medicine)
[2020, 9(2):]

Cited: 0 times

View full text PDF listing >>



Advertisement

The continuous rediscovery and the benefit-risk ratio of thioguanine, a comprehensive review.

Ahmed B Bayoumy, Melek Simsek, Margien L Seinen, Chris J J Mulder, Azhar Ansari, Godefridus J Peters, Nanne K De Boer,

Introduction: In the 1950s, thioguanine (TG), a thiopurine-derivative together with azathioprine (AZA) and mercaptopurine (MP), were developed for the treatment of childhood leukemia. Over the years, the use of TG was also explored for other, mainly immune-mediated and inflammatory, diseases such as in the field of dermatology and rheumatology (e.g. ... Read more >>

Expert Opin Drug Metab Toxicol (Expert opinion on drug metabolism & toxicology)
[2020, :1-13]

Cited: 0 times

View full text PDF listing >>



Multiple ulcerations and perforation in the small intestine after steroid treatment in eosinophilic granulomatosis with polyangiitis: a case report and literature review.

Yukinobu Ito, Makoto Yoshida, Tatsuo Sugiyama, Hirotake Masuda, Mitsuo Mori, Noriyuki Kimura, Michinobu Umakoshi, Ken Miyabe, Yukitsugu Kudo-Asabe, Akiteru Goto,

Eosinophilic granulomatosis with polyangiitis (EGPA), formerly called Churg-Strauss syndrome, is an uncommon disease with pathological features consisting of systemic necrotizing vasculitis, eosinophilic infiltration, and granulomatous or nongranulomatous extravascular eosinophilic inflammation. EGPA preferentially affects certain organ systems, including the airways, peripheral nerves, heart, kidney, and gastrointestinal tract. Although gastrointestinal involvement, such ... Read more >>

Cardiovasc. Pathol. (Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology)
[2019, 47:107193]

Cited: 0 times

View full text PDF listing >>



[SYSTEMIC REVIEW OF EOSINOPHILIC DERMATOSES PATIENTS TREATED WITH TNF-Α INHIBITORS AND USTEKINUMAB].

Mati Rozenblat, Michael Ziv,

AIMS:This study aims to critically review the pros and cons of biological drugs as treatments and triggers of eosinophilic dermatoses. BACKGROUND:Eosinophilic dermatoses syndromes are rare diseases with a prominent eosinophilic infiltration mechanism. These syndromes have several known treatments with limited success. Several physicians worldwide suggested possible advantages of using specific ... Read more >>

Harefuah (Harefuah)
[2020, 159(1):34-37]

Cited: 0 times

View full text PDF listing >>



CD71- Alveolar Macrophages in Idiopathic Pulmonary Fibrosis: A Look beyond the Borders of the Disease.

Ermanno Puxeddu, Daniela Fraboni, Giuseppe Cillis, Francesco Cavalli, Francesco Buccisano, Paola Rogliani,

Am. J. Respir. Crit. Care Med. (American journal of respiratory and critical care medicine)
[2019, 200(11):1444-1446]

Cited: 0 times

View full text PDF listing >>



A Case of Cutaneous Arteritis Presenting as Infiltrated Erythema in Eosinophilic Granulomatosis With Polyangiitis: Features of the Unique Morphological Evolution of Arteritis as a Diagnostic Clue.

Rie Shiiyama, Ko-Ron Chen, Masafumi Ishibashi,

Eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome) is a rare systemic vasculitis affecting small- and medium-sized vasculature, associated with asthma and eosinophilia. Different levels of vasculitis in cutaneous lesions have been observed, including dermal small vessel vasculitis and subcutaneous muscular vessel vasculitis. Although the EGPA-associated small vessel vasculitis described ... Read more >>

Am J Dermatopathol (The American Journal of dermatopathology)
[2019, 41(11):832-834]

Cited: 0 times

View full text PDF listing >>



Updates in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis for the ENT surgeon.

Matthew L Coates, Marcos Martinez Del Pero,

ENT involvement is common in ANCA-associated vasculitis (AAV), particularly in GPA and EGPA. Early recognition and treatment is important for good outcomes, yet evidence suggests that UK ENT surgeons may not consistently recognise the early features of AAV, despite a similar incidence to vestibular schwannoma. AAV is a rapidly advancing ... Read more >>

Clin Otolaryngol (Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Symmetric polyneuropathy after viral symptomatology - not always Guillain-Barré Syndrome.

Michiel Keyzer, Anne Hoorens, Jo Van Dorpe, Anne-Marie Bogaert,

Introduction: Guillain-Barré Syndrome usually presents with ascending symmetric polyneuropathy, typically preceded by a viral infection. Despite the low incidence, physicians will often include Guillain-Barré Syndrome in their differential diagnosis. However, another underlying cause of polyneuropathy known as ANCA-associated vasculitis (AAV) is even more rare than Guillain-Barré Syndrome and therefore is ... Read more >>

Acta Clin Belg (Acta clinica Belgica)
[2020, :1-8]

Cited: 0 times

View full text PDF listing >>



Idiopathic Hypereosinophilia and Venous Thromboembolism: Is There a Pathophysiological or Clinical Link? Description of an Intriguing Clinical Case.

Pierpaolo Di Micco, Olga Scudiero, Barbara Lombardo, Corrado Lodigiani,

Thrombosis events usually occur after prolonged bedrest, pregnancy, hormonal therapy, recent surgery and in the presence of inherited or acquired thrombophilia. However, several other diseases are often associated with thrombosis although their frequency is not easily estimated. Eosinophilia is one of these conditions. From a clinical viewpoint it is very difficult ... Read more >>

J Blood Med (Journal of blood medicine)
[2020, 11:73-76]

Cited: 0 times

View full text PDF listing >>



Idiopathic Orbital Pseudotumor Preceding Systemic Inflammatory Disease in Children.

Mai Tsukikawa, Sara E Lally, Carol L Shields, Ralph C Eagle, Forrest J Ellis, Barry N Wasserman,

PURPOSE:To describe four pediatric cases in which isolated orbital pseudotumor preceded the development of a systemic inflammatory disease by months to years. METHODS:The medical records of all patients with the clinical diagnosis of orbital pseudotumor seen at the Ocular Oncology Service of Wills Eye Hospital and Northern Virginia Ophthalmology Associates ... Read more >>

J Pediatr Ophthalmol Strabismus (Journal of pediatric ophthalmology and strabismus)
[2019, 56(6):373-377]

Cited: 0 times

View full text PDF listing >>



ANCA associated vasculitis.

Fernando Salvador,

Vasculitis is characterized by inflammation of the vascular wall. It reaches vessels of different sizes and locations, conditioning multisystem and complex manifestations that require a holistic approach. Antineutrophil cytoplasmic antibody-associated vasculitis has an annual incidence rate of 20 per million inhabitants. It is the result of the interaction of infectious, ... Read more >>

Eur. J. Intern. Med. (European journal of internal medicine)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Allergic bronchopulmonary aspergillosis.

Gayatri Patel, Paul A Greenberger,

Allergic bronchopulmonary aspergillosis (ABPA) occurs in patients with asthma or cystic fibrosis, and results in pulmonary infiltrates, tenacious mucus plugs that harbor hyphae of Aspergillus fumigatus, elevations of total serum immunoglobulin E concentration and peripheral blood and sputum eosinophilia. Bronchiectasis is an irreversible complication of ABPA. The key to early ... Read more >>

Allergy Asthma Proc (Allergy and asthma proceedings)
[2019, 40(6):421-424]

Cited: 0 times

View full text PDF listing >>



A case of repetitive myocardial infarction with unobstructed coronaries due to Churg-Strauss syndrome.

Ying X Gue, Sanjay Prasad, David Isenberg, Diana A Gorog,

BACKGROUND:Myocardial infarction is most commonly caused by thrombosis occurring on a background of coronary atherosclerosis, resulting in reduced coronary flow. Less often, myocardial infarction can occur in the absence of coronary disease. The pathomechanism of myocardial infarction in such patients is heterogeneous and more challenging to diagnose and treat. European ... Read more >>

Eur Heart J Case Rep (European heart journal. Case reports)
[2019, 3(2):]

Cited: 0 times

View full text PDF listing >>



Acute Respiratory Distress Syndrome Requiring Extracorporeal Membrane Oxygenation as the Initial Presentation of Anti-neutrophillic Cytoplasmic Auto-antibody Positive Vasculitis.

Suhali Kundu, Shaurya Sharma, Ramandeep Minhas, Joshua Scheers-Masters, Paul C Saunders,

Acute respiratory distress syndrome (ARDS) is a life-threatening inflammatory state of lung injury that can require acute interventions including mechanical ventilation as well as emergent veno-venous extracorporeal membrane oxygenation (VV-ECMO) for management. Etiologies of ARDS are not clearly discernible in certain cases and can vary from sepsis, pneumonia, trauma and intoxication. Anti-nuclear cytoplasmic auto-antibody (ANCA)-associated vasculitis (AAV) is a group ... Read more >>

Cureus (Cureus)
[2019, 11(11):e6135]

Cited: 0 times

View full text PDF listing >>



[Unexpected death due to eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)].

I Landín, E Barbería, C Dasi, J Arimany-Manso,

Eosinophilic granulomatosis with polyangiitis (EGPA), or Churg-Strauss syndrome, is a rare disease characterized by disseminated necrotizing vasculitis with extravascular granulomas occurring among patients with asthma and tissue eosinophilia. Clinically, it presents in various ways and progresses in three phases: prodromic (asthma and rhino-sinusitis), eosinophilic (peripheral eosinophilia and organ involvement), and ... Read more >>

An Sist Sanit Navar (Anales del sistema sanitario de Navarra)
[2019, 42(1):83-87]

Cited: 0 times

View full text PDF listing >>



Hypereosinophilia as a Cause of Recurrent Stroke.

Srikant Venkatakrishnan, Anupam Gupta, Meeka Khanna, Madhu Nagappa, Cecil Ross,

Ann Indian Acad Neurol (Annals of Indian Academy of Neurology)
[2020, 23(1):118-119]

Cited: 0 times

View full text PDF listing >>



Eosinophilic granulomatosis with polyangiitis: the multifaceted spectrum of clinical manifestations at different stages of the disease.

Alvise Berti, Sara Boukhlal, Matthieu Groh, Divi Cornec,

Introduction: Eosinophilic granulomatosis with polyangiitis (EGPA) usually occurs in patients with late-onset asthma and sustained peripheral blood eosinophilia and classically presents with a clinical multifaceted spectrum of manifestations, which may vary at the different stages of the natural history of the disease.Areas covered: We reviewed EGPA clinical presentation, focusing on ... Read more >>

Expert Rev Clin Immunol (Expert review of clinical immunology)
[2020, 16(1):51-61]

Cited: 0 times

View full text PDF listing >>



[Current treatment of eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome)].

F Moosig, J Holle,

For the treatment of eosinophilic granulomatosis with polyangiitis (EGPA) much less data are available when compared to the other anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV). At the same time EGPA also differs in many aspects from AAVs. Treatment is guided by the German and international guidelines. An adapted induction therapy ... Read more >>

Z Rheumatol (Zeitschrift fur Rheumatologie)
[2019, 78(4):333-338]

Cited: 0 times

View full text PDF listing >>



Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.

Lynn D Condreay, Laura R Parham, Xiaoyan A Qu, Jonathan Steinfeld, Michael E Wechsler, Benjamin A Raby, Steven W Yancey, Soumitra Ghosh,

Treatment of patients with the rare disease eosinophilic granulomatosis with polyangiitis (EGPA) with mepolizumab, a monoclonal antibody to interleukin-5 (IL-5) that reduces blood eosinophil counts, as an add-on therapy to glucocorticoid treatment, results in more accrued weeks in remission, reductions in glucocorticoid use and reductions in relapse rate. However, treatment ... Read more >>

Rheumatol. Int. (Rheumatology international)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Cutaneous Vasculitis as Early Presentation of Eosinophilic Granulomatosis with Polyangiitis without Systemic Symptoms.

Wahinuddin Sulaiman, Aris Chandran Abdullah, Sin Fah Chung, Norain Karim, Jyi Jong Tang,

Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome) is a rare vasculitis in children. It commonly presents with respiratory symptoms, especially asthma, allergic rhinitis, and peripheral eosinophilia. Involvement of other systems, such as renal and cardiac, may carry a poor prognosis. Anti-neutrophil cytoplasmic antibodies have been found less frequently ... Read more >>

Oman Med J (Oman medical journal)
[2019, 34(4):345-349]

Cited: 0 times

View full text PDF listing >>



Eosinophilic Granulomatosis With Polyangiitis: Clinical Predictors of Long-term Asthma Severity.

Alvise Berti, Divi Cornec, Marta Casal Moura, Robert J Smyth, Lorenzo Dagna, Ulrich Specks, Karina A Keogh,

BACKGROUND:The long-term clinical course of asthma in patients with eosinophilic granulomatosis with polyangiitis (EGPA) remains unclear. We aimed to characterize long-term asthma in EGPA and to identify baseline predictors of long-term asthma severity. METHODS:This retrospective cohort study included patients who fulfilled standardized criteria for EGPA who were followed up in ... Read more >>

Chest (Chest)
[2020, :]

Cited: 0 times

View full text PDF listing >>



Recent advances in eosinophil-related diseases.

Hiroshi Nakajima,

Allergol Int (Allergology international : official journal of the Japanese Society of Allergology)
[2019, 68(4):401-402]

Cited: 0 times

View full text PDF listing >>



Eosinophilic granulomatosis with polyangiitis in a Nigerian woman.

Ngozi Lina Ekeigwe, Olufemi Adelowo, Ehiaghe Lonia Anaba, Hakeem Olaosebikan,

Eosinophilic granulomatosis with polyangiitis (EGPA), previously called Churg-Strauss Syndrome, is a systemic autoimmune disease that is usually associated with asthma and eosinophilia. It is a rare condition associated with antineutrophil cytoplasmic antibodies (ANCA). We report a case of a 52-year-old Nigerian woman who presented with bilateral leg swelling with multiple ... Read more >>

BMJ Case Rep (BMJ case reports)
[2019, 12(6):]

Cited: 0 times

View full text PDF listing >>



Necrotizing Sarcoid Granulomatosis with Pneumothorax.

Mihan Pourabdollah, Seyed Reza Saghebi, Mitra Abdolahi, Mitra Sadat Rezaei,

Necrotizing sarcoid granulomatosis (NSG) is a rare granulomatous pneumonitis which is composed of a background of sarcoidosis-like granulomas, granulomatous vasculitis, and variable amount of necrosis. We reported a case of a 38-year-old nonsmoking woman presented with left-sided chest pain and dyspnea for three days. Chest CT scan exhibited collapse consolidation ... Read more >>

Case Rep Med (Case Reports in Medicine)
[2019, 2019:4648720]

Cited: 0 times

View full text PDF listing >>



Advertisement

Disclaimer
2.3156 s