RSS-Feed abonnieren
DOI: 10.1055/a-0977-2777
Gastrointestinal involvement in patients with vasculitis: IgA vasculitis and eosinophilic granulomatosis with polyangiitis
Publikationsverlauf
submitted 26. Februar 2019
accepted after revision 29. Mai 2019
Publikationsdatum:
22. Oktober 2019 (online)
Abstract
Background and study aims Among vasculitides, IgA vasculitis (IgAV) and eosinophilic granulomatosis with polyangiitis (EGPA) frequently damage the gastrointestinal tract. However, only a few studies have investigated the entire gastrointestinal tract in patients with IgAV or EGPA by endoscopy. The aim of this study was to clarify endoscopic characteristics of patients with IgAV and those with EGPA.
Patients and methods Clinicopathological and endoscopic findings were retrospectively compared between 33 patients with IgAV and 19 patients with EGPA.
Results Gastrointestinal involvement was observed in 33 patients with IgAV (100 %) and in 8 patients with EPGA (42 %; P = 0.0001). Duodenal involvement was more frequent in patients with IgAV (75.8 %) than in those with EGPA (21.1 %, P = 0.0002). Jejunoileal involvement was frequent in both groups (IgAV 94.4 %; EGPA 77.8 %). Gastric mucosal erythema was more frequent in patients with IgAV (18.2 %) than in those with EGPA (0 %, P = 0.0481). Duodenal mucosal erythema (IgAV 54.6 %; EGPA 21.1 %, P = 0.0227), ulcer (IgAV 33.3 %; EGPA 0 %, P = 0.0041), and hematoma-like protrusion (IgAV 21.1 %; EGPA 0 %, P = 0.039) were more frequently observed in patients with IgAV than in those with EGPA.
Conclusions Frequent duodenal involvement, gastric mucosal erythema, and duodenal lesions including erythema, ulcer, and hematoma-like protrusion are characteristic of patients with IgAV. Because jejunoileal involvement was frequent in both groups of patients, small-bowel endoscopies should be performed for diagnosis of small-bowel lesions in patients with IgAV and EGPA.
-
References
- 1 Jennette JC, Falk RJ, Andrassy K. et al. Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis Rheum 1994; 37: 187-192
- 2 Jennette JC, Falk RJ, Bacon PA. et al. 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum 2013; 65: 1-11
- 3 Louie CY, DiMaio MA, Charville GW. et al. Gastrointestinal tract vasculopathy: clinicopathology and description of a possible “new entity” with protean features. Am J Surg Pathol 2018; 42: 866-876
- 4 Mills JA, Michel BA, Bloch DA. et al. The American College of Rheumatology 1990 criteria for the classification of Henoch-Schönlein purpura. Arthritis Rheum 1990; 33: 1114-1121
- 5 Martinez-Frontanilla LA, Haase GM, Ernster JA. et al. Surgical complications in Henoch-Schönlein Purpura. J Pediatr Surg 1984; 19: 434-436
- 6 Chumbley LC, Harrison Jr EG, DeRemee RA. Allergic granulomatosis and angiitis (Churg-Strauss syndrome). Report and analysis of 30 cases. Mayo Clin Proc 1977; 52: 477-484
- 7 Zhang Y, Huang X. Gastrointestinal involvement in Henoch-Schönlein purpura. Scand J Gastroenterol 2008; 43: 1038-1043
- 8 Nishiyama R, Nakajima N, Ogihara A. et al. Endoscope images of Schönlein-Henoch purpura. Digestion 2008; 77: 236-241
- 9 Esaki M, Matsumoto T, Nakamura S. et al. gastrointestinal involvement in Henoch-Schönlein purpura. Gastrointest Endosc 2002; 56: 920-923
- 10 Tsurikisawa N, Oshikata C, Tsuburai T. et al. Th17 cells reflect colon submucosal pathologic changes in active eosinophilic granulomatosis with polyangiitis. BMC Immunol 2015; 16: 75
- 11 Gioffredi A, Maritati F, Oliva E. et al. Eosinophilic granulomatosis with polyangiitis: an overview. Front Immunol 2014; 5: 549
- 12 Fries JF, Hunder GG, Bloch DA. et al. The American College of Rheumatology 1990 criteria for the classification of vasculitis. Summary. Arthritis Rheum 1990; 33: 1135-1136
- 13 Masi AT, Hunder GG, Lie JT. et al. The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis). Arthritis Rheum 1990; 33: 1094-1100
- 14 Szer IS. Henoch-Schönlein purpura: when and how to treat. J Rheumatol 1996; 23: 1661-1665
- 15 Pagnoux C, Mahr A, Cohen P. et al. Presentation and outcome of gastrointestinal involvement in systemic necrotizing vasculitides: analysis of 62 patients with polyarteritis nodosa, microscopic polyangiitis, Wegener granulomatosis, Churg-Strauss syndrome, or rheumatoid arthritis-associated vasculitis. Medicine (Baltimore) 2005; 84: 115-128
- 16 Akdamar K, Agrawal NM, Varela PY. The endoscopic appearance of anaphylactoid purpura. Gastrointest Endosc 1973; 20: 68-69
- 17 Kishikawa H, Nishida J, Takarabe S. et al. “Circular reddish lesions”: a possibly characteristic endoscopic finding in Henoch-Schönlein purpura. Endoscopy 2013; 45: E33-E34
- 18 Skogestad E. Capsule endoscopy in Henoch-Schonlein purpura. Endoscopy 2005; 37: 189
- 19 Stancanelli B, Vita A, Vinci M. et al. Bleeding of small bowel in Henoch-Schönlein syndrome: the successful diagnostic role of video capsule endoscopy. Am J Med 2006; 119: 82-84
- 20 PreudʼHomme DL, Michail S, Hodges C. et al. Use of wireless capsule endoscopy in the management of severe Henoch-Schonlein purpura. Pediatrics 2006; 118: 904-906
- 21 Ichikawa R, Hosoe N, Imaeda H. et al. Evaluation of small-intestinal abnormalities in adult patients with Henoch-Schönlein purpura using video capsule. Endoscopy 2011; 43: 162-163
- 22 Assmann G, Molinger M, Pfreundschuh M. et al. Gastrointestinal perforation due to vasculitis at primary diagnosis of eosinophilic granulomatosis with polyangiitis (EGPA) despite a high dose glucocorticosteroids treatment. Springerplus 2014; 3: 404
- 23 Ohnuki Y, Moriya Y, Yutani S. et al. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss Syndrome) complicated by perforation of the small intestine and cholecystitis. Intern Med 2018; 57: 737-740
- 24 Franco DL, Ruff K, Mertz L. et al. Eosinophilic granulomatosis with polyangiitis and diffuse gastrointestinal involvement. Case Rep Gastroenterol 2014; 8: 329-336
- 25 Sánchez R, Aparicio JR, Baeza T. et al. Capsule endoscopy diagnosis of intestinal involvement in a patient with Churg-Strauss syndrome. Gastrointest Endosc 2006; 6: 1082-1084
- 26 Beye B, Lesur G, Claude P. et al. Small bowel involvement documented by capsule endoscopy in Churg-Strauss syndrome. Pan Afr Med J 2015; 22: 41
- 27 Suzuki T, Matsushima M, Arase Y. et al. Double-balloon endoscopy-diagnosed multiple small intestinal ulcers in a Churg-Strauss syndrome patient. World J Gastrointest Endosc 2012; 4: 194-196
- 28 Kawasaki K, Eizuka M, Murata O. et al. Eosinophilic granulomatosis with polyangiitis involving the small intestine: radiographic and endoscopic findings. Endoscopy 2015; 47: 492-494
- 29 Yoshioka T, Kusaka T, Seno H. Colonic findings in Churg-Strauss syndrome. Endoscopy 2013; 45: 185-186
- 30 Gong EJ, Kim do H, Chun JH. et al. Endoscopic findings of upper gastrointestinal involvement in primary vasculitis. Gut Liver 2016; 10: 542-548
- 31 Audemard-Verger A, Terrier B, Dechartres A. et al. Characteristics and Management of IgA vasculitis (Henoch-Schönlein) in adults: data from 260 patients included in a French multicenter retrospective survey. Arthritis Rheumatol 2017; 69: 1862-1870
- 32 Durel CA, Berthiller J, Caboni S. et al. Long-term followup of a multicenter cohort of 101 patients with eosinophilic granulomatosis with polyangiitis (Churg-Strauss). Arthritis Care Res (Hoboken) 2016; 68: 374-387