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New-onset of eosinophilic granulomatosis with polyangiitis without eosinophilia and eosinophilic infiltration under benralizumab treatment: A case report.

• Authors : Yonezawa H; Department of Rheumatology, Seirei Hamamatsu General Hospital, Hamamatsu, Shizuoka, Japan.; Ohmura SI

Subjects: Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/complications ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/diagnosis ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/drug therapy

• Source: Modern rheumatology case reports [Mod Rheumatol Case Rep] 2023 Dec 29; Vol. 8 (1), pp. 145-149.Publisher: Oxford University Press Country of Publication: England NLM ID: 101761026 Publication Model: Print Cited Medium: Internet ISSN:

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[Eosinophilic Lung Diseases: Time Pressure in the Maze of Differential Diagnoses].

• Authors : Hahn S; Klinik für Pneumologie, Universitätsspital Zürich.; Heizmann E

Subjects: Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/diagnosis ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/drug therapy ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/pathology

• Source: Praxis [Praxis (Bern 1994)] 2025 Jan; Vol. 114 (1), pp. 34-37.Publisher: Aerzteverlag medinfo AG Country of Publication: Switzerland NLM ID: 101468093 Publication Model: Print Cited Medium: Print ISSN:

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Refractory PR3-positive ANCA-associated vasculitis with eosinophilia requiring anti-IL-5 therapy: A case report.

• Authors : Anderson E; Department of Medicine, Oregon Health & Science University, Portland, OR, USA.; Friedman MA

Subjects: Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/complications ; Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/diagnosis ; Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/drug therapy

• Source: Modern rheumatology case reports [Mod Rheumatol Case Rep] 2023 Jun 19; Vol. 7 (2), pp. 431-434.Publisher: Oxford University Press Country of Publication: England NLM ID: 101761026 Publication Model: Print Cited Medium: Internet ISSN:

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A case of atypical IgG4-related disease presenting hypereosinophilia, polyneuropathy, and liver dysfunction.

• Authors : Mukoyama H; Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.; Murakami K

Subjects: Immunoglobulin G4-Related Disease*/Immunoglobulin G4-Related Disease*/Immunoglobulin G4-Related Disease*/complications ; Immunoglobulin G4-Related Disease*/Immunoglobulin G4-Related Disease*/Immunoglobulin G4-Related Disease*/diagnosis ; Immunoglobulin G4-Related Disease*/Immunoglobulin G4-Related Disease*/Immunoglobulin G4-Related Disease*/pathology

• Source: Modern rheumatology case reports [Mod Rheumatol Case Rep] 2023 Dec 29; Vol. 8 (1), pp. 172-177.Publisher: Oxford University Press Country of Publication: England NLM ID: 101761026 Publication Model: Print Cited Medium: Internet ISSN:

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Acute Cholecystitis Associated with Eosinophilic Granulomatosis with Polyangiitis That Responded to Glucocorticoid Therapy.

• Authors : Ozaka S; Department of Gastroenterology, Faculty of Medicine, Oita University, Japan.; Department of Infectious Disease Control, Faculty of Medicine, Oita University, Japan.

Subjects: Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/complications ; Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/drug therapy ; Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/diagnosis

• Source: Internal medicine (Tokyo, Japan) [Intern Med] 2023 May 15; Vol. 62 (10), pp. 1501-1506. Date of Electronic Publication: 2022 Sep 28.Publisher: Japanese Society of Internal Medicine Country of Publication: Japan NLM ID: 9204241 Publication Model: Print-Electronic Cited Medium:

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Clinical Characteristics of EGPA Patients in Comparison to GPA Subgroup with Increased Blood Eosinophilia from POLVAS Registry.

• Authors : Drynda, Anna¹ (AUTHOR); Padjas, Agnieszka² (AUTHOR); Wójcik, Krzysztof² (AUTHOR)

• Source: Journal of Immunology Research. 4/25/2024, Vol. 2024, p1-13. 13p.

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Systemic eosinophilic disease presenting as dacryoadenitis.

• Authors : Danesh K; University of California Los Angeles, Los Angeles, California, USA.; Cohen LM

Subjects: Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/complications ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/diagnosis ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/pathology

• Source: Orbit (Amsterdam, Netherlands) [Orbit] 2023 Feb; Vol. 42 (1), pp. 107-111. Date of Electronic Publication: 2021 Sep 12.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8301221 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Fatal cerebral venous sinus thrombosis with preceding thrombocytopenia in a patient with new-onset eosinophilic granulomatosis with polyangiitis.

• Authors : Tanomogi N; Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan.; Ota T

Subjects: Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/diagnosis ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/diagnosis ; Thrombocytopenia*

• Source: Modern rheumatology case reports [Mod Rheumatol Case Rep] 2023 Jun 19; Vol. 7 (2), pp. 410-415.Publisher: Oxford University Press Country of Publication: England NLM ID: 101761026 Publication Model: Print Cited Medium: Internet ISSN:

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A diagnostic score for eosinophilic granulomatosis with polyangiitis among eosinophilic disorders.

• Authors : Takahashi H; Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.; Komai T

Subjects: Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/diagnosis ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/diagnosis ; Eosinophilia*/Eosinophilia*/Eosinophilia*/diagnosis

• Source: Allergology international : official journal of the Japanese Society of Allergology [Allergol Int] 2023 Apr; Vol. 72 (2), pp. 316-323. Date of Electronic Publication: 2022 Sep 29.Publisher: Elsevier Country of Publication: England NLM ID: 9616296 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1440-1592

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Mepolizumab is highly effective in a rare case of Wells syndrome: Eosinophilic granulomatosis with polyangiitis overlap.

• Authors : Trica OC; Department of Dermatology, 'Dr Boit and Dr Schuh' Dermatological Practice, Tuttlingen, Germany.; Mocan LP

Subjects: Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/diagnosis ; Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/Churg-Strauss Syndrome*/drug therapy ; Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/Granulomatosis with Polyangiitis*/diagnosis Wells syndrome

• Source: Dermatologic therapy [Dermatol Ther] 2022 Nov; Vol. 35 (11), pp. e15799. Date of Electronic Publication: 2022 Sep 09.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 9700070 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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