Granulomatosis with Polyangiitis
"Granulomatosis with Polyangiitis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN.
Descriptor ID |
D014890
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MeSH Number(s) |
C08.381.483.950 C14.907.940.897.249.750 C20.111.193.875
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Concept/Terms |
Granulomatosis with Polyangiitis- Granulomatosis with Polyangiitis
- Granulomatosis with Polyangiitides
- Polyangiitides, Granulomatosis with
- Polyangiitis, Granulomatosis with
- with Polyangiitides, Granulomatosis
- with Polyangiitis, Granulomatosis
- Wegener Granulomatosis
- Granulomatosis, Wegener
- Wegener's Granulomatosis
- Granulomatosis, Wegener's
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Below are MeSH descriptors whose meaning is more general than "Granulomatosis with Polyangiitis".
Below are MeSH descriptors whose meaning is more specific than "Granulomatosis with Polyangiitis".
This graph shows the total number of publications written about "Granulomatosis with Polyangiitis" by people in this website by year, and whether "Granulomatosis with Polyangiitis" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1984 | 0 | 1 | 1 | 2009 | 2 | 0 | 2 | 2014 | 1 | 1 | 2 | 2015 | 1 | 0 | 1 | 2020 | 1 | 0 | 1 | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Granulomatosis with Polyangiitis" by people in Profiles.
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Rivera M, Villafranca A, Khamooshi P, Reyes V, Sanchez J, Manadan A. Reasons for hospitalization and in-hospital mortality for anti-neutrophil cytoplasmic antibody vasculitides: analysis of the National Inpatient Sample. Clin Rheumatol. 2022 Jan; 41(1):159-166.
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Yin K, March RJ, Hoopes CW, Balk RA, Raman J, Lateef OB, Tiwari A, Bak E, Karlson KJ, Edwards NM, Dobrilovic N. Extracorporeal membrane oxygenation in the management of granulomatosis with polyangiitis. J Card Surg. 2021 Feb; 36(2):743-747.
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Amber KT, Bunyan A, Lee JJ, Duvvuri A. Granulomatosis with polyangiitis (GPA) initially presenting as sigmoiditis with the later development of spontaneous subcapsular hematoma. Int J Colorectal Dis. 2016 Jul; 31(7):1365-6.
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Sreih AG, Mandhadi R, Aldaghlawi F, Khan A, Irshad V, Finn K, Block JA. ANCA-associated vasculitis in Hispanic Americans: an unrecognized severity. Clin Rheumatol. 2015 May; 34(5):943-8.
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Al-Fakhouri A, Manadan A, Gan J, Sreih AG. Central diabetes insipidus as the presenting symptom of granulomatosis with polyangiitis. J Clin Rheumatol. 2014 Apr; 20(3):151-4.
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Grindler D, Cannady S, Batra PS. Computed tomography findings in sinonasal Wegener's granulomatosis. Am J Rhinol Allergy. 2009 Sep-Oct; 23(5):497-501.
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Cannady SB, Batra PS, Koening C, Lorenz RR, Citardi MJ, Langford C, Hoffman GS. Sinonasal Wegener granulomatosis: a single-institution experience with 120 cases. Laryngoscope. 2009 Apr; 119(4):757-61.
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Keshavarzian A, Saverymuttu SH, Chadwick VS, Lavender JP, Hodgson HJ. Noninvasive investigation of the gastrointestinal tract in collagen-vascular disease. Am J Gastroenterol. 1984 Nov; 79(11):873-7.
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