Page 321 - The Vasculitides, Volume 1: General Considerations and Systemic Vasculitis

Systemic Vasculitis of the Gastrointestinal Tract 295

[76] Huber AM King J, McLaine P, et al. A randomized, placebo-controlled trial of
prednisolone in early Henoch-Schonlein purpura. BMC Med. 2004; Apr 2; 2:7.

[77] Schwab J, Benya E, Lin R, et al. Contrast enema in children with Henoch-Schonlein
purpura. J. Pediatr. Surg. 2005; 40:1221-1223.

[78] Chanouzas D, Morgan MD. Advances in therapies for antineutrophil cytoplasmic
antibody-associated vasculitides. Int. J. Adv. Rheumatol. 2011; 9:85-94.

[79] Guillevin L, Cohen P, Gayraud M, et al. Churg-Strauss syndrome. Clinical study and
long-term follow-up of 96 patients. Medicine 1999; 78:26-37.

[80] Akbulut S. Multiple ileal perforations in a patient with Wegener’s granulomatosis: a
case report and literature review. J. Gastrointest. Surg. 2012; 16:857-862.

[81] Bligny D, Mahr A, Toumelin P, et al. Predicting mortality in systemic Wegener’s
granulomatosis: a survival analysis based on 93 patients. Arthritis. Rheum. 2004; 51:83-
91.

[82] Hoffman G, Kerr G, Leavitt R, et al. Wegener’s granulomatosis: an analysis of 158
patients. Ann. Intern. Med. 1992; 116:488-498.

[83] Aasarod K, Iversen BM, Hammerstrom J, et al. Wegener’s granulomatosis: clinical
course in 108 patients with renal involvement. Nephrol. Dial. Transplant. 2000;
15:611-618.

[84] Koldingsnes W, Nossent H. Predictors of organ damage and survival in Wegener’s
granulomatosis. Rheumatology 2002; 41:572-581.

[85] Samim M, Pronk A, Verheijen PM. Intestinal perforation as an early complication in
Wegener’s granulomatosis. World J. Gastrointest. Surg. 2010; 2:169-171.

[86] Yildrim AC, Kocak E, Yildiz P, et al. Multiple intestinal perforation in a patient with
Wegener’s granulomatosis: a case report and review of the literature. Gastroenterol.
Clin. Biol. 2010; 34:712-715.

[87] Strivens RL, Bateman A, Arden NK, et al. Intestinal perforation and jejunal
haemorrhage due to Wegener’s granulomatosis. Clin. Exp. Rheumatol. 2005; Jan-Feb;
23:124.

[88] Ueda S, Matsumoto M, Ahn T, et al. Microscopic polyangiitis complicated with
massive intestinal bleeding. J. Gastroenterol. 2001; 36:264-270.

[89] Tsai CN, Chang CM, Chuang CH, et al. Extended colonic ulcerations in a patient with
microscopic polyangiitis. Ann. Rheum. Dis. 2004; 63:1521-1522.

[90] Passam FH, Diamantis ID, Perisinaki G, et al. Intestinal ischaemia as the first
manifestation of vasculitis. Semin. Arthritis. Rheum. 2004; 34:431-441.

[91] Guillevin L, Lhote F, Gayraud M, et al. Prognostic factors in polyarteritis nodosa and
Churg-Strauss syndrome: a prospective study in 342 patients. Medicine 1996; 75:17-28.

[92] Guillevin L, Pagnoux C, Seror R, et al. The Five-Factor Score revisited: assessment of
prognoses of systemic necrotising vasculitides based on the French Vasculitis Study
Group (FVSG) cohort. Medicine 2011; 90:19-27.

[93] Ebert EC, Hagspiel KD. Gastrointestinal and hepatic manifestations of systemic lupus
erythematosus. J. Clin. Gastroenterol. 2011; 45:436-441.

[94] Kasahara Y, Tanaka B, Nishino M, et al. Intestinal involvement in Behcet’s disease:
review of 136 surgical cases in the Japanese literature. Dis. Colon. Rectum. 1981;
24:103-106.

[95] Lee JY, Park J, Kim EH, et al. Simultaneous involvement of nervous and
gastrointestinal systems in Behcet’s disease. Ann. Dermatol. 2012; 24:225-227.

Complimentary Contributor Copy