2010
DOI: 10.1093/rheumatology/keq093
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Localized vasculitis of the gastrointestinal tract: a case series

Abstract: LVGT is an uncommon form of vasculitis that can be associated with significant morbidity and mortality.

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Cited by 61 publications
(67 citation statements)
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“…9,10,12,37,46,54 GB-SOV was found in 20 (33%) patients and GB-SV in 41 (67%). Forms of SV that affected the GB were PAN (n ¼ 10), 4,12,22,32,38,45,46,51,54 HBV-associated vasculitis (n ¼ 8), 10,11,17,38,46,56,60 cryoglobulinemic (essential or HCVassociated) vasculitis (n ¼ 6), 9,14,19,36,50 MPA (n ¼ 4), 5,31,38,40 EGPA (Churg-Strauss) (n ¼ 4), 20,43,48,61 IgA vasculitis (Henoch-Schönlein) (n ¼ 2), 23,28 giant cell arteritis (n ¼ 1), 47 and vasculitis associated with autoimmune diseases (n ¼ 6) 11,16,18,42,58 (see Table 4). Systemic diseases with associated vasculitis included RA (n ¼ 3), 11,16,18 SLE (n ¼ 2), 42,58 and systemic sclerosis (n ¼ 1).…”
Section: Overall Resultsmentioning
confidence: 96%
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“…9,10,12,37,46,54 GB-SOV was found in 20 (33%) patients and GB-SV in 41 (67%). Forms of SV that affected the GB were PAN (n ¼ 10), 4,12,22,32,38,45,46,51,54 HBV-associated vasculitis (n ¼ 8), 10,11,17,38,46,56,60 cryoglobulinemic (essential or HCVassociated) vasculitis (n ¼ 6), 9,14,19,36,50 MPA (n ¼ 4), 5,31,38,40 EGPA (Churg-Strauss) (n ¼ 4), 20,43,48,61 IgA vasculitis (Henoch-Schönlein) (n ¼ 2), 23,28 giant cell arteritis (n ¼ 1), 47 and vasculitis associated with autoimmune diseases (n ¼ 6) 11,16,18,42,58 (see Table 4). Systemic diseases with associated vasculitis included RA (n ¼ 3), 11,16,18 SLE (n ¼ 2), 42,58 and systemic sclerosis (n ¼ 1).…”
Section: Overall Resultsmentioning
confidence: 96%
“…Six patients were identified by the Cleveland Clinic database search and 55 patients from the PubMed search. Originally, 83 cases were identified as GV in the literature; however, 28 patients were excluded: 15 patients from a single study, 6 1 patient with IgA vasculitis (Henoch-Schönlein), 35 and 4 with Kawasaki disease 13 did not have sufficient data and 8 cases classified as GB-SOV in whom inadequate follow-up 3,29,38,44,54 or an initial treatment with glucocorticoids and/or cytotoxic agents 33,42 could not guarantee the extent of GV. In addition, 3 patients previously diagnosed with autoimmune diseases (1 each with systemic lupus erythematosus [SLE], 42 rheumatoid arthritis [RA], 42 and mixed connective tissue disease 33 ) did not have involvement of other tissues at the time of GV diagnosis.…”
Section: Overall Resultsmentioning
confidence: 99%
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