Patient with mesenteric ischemia and granulomatosis with polyangiitis, a rare association: Case report

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Juan Sebastián Suárez Niño
Juan Sebastián Montealegre Díaz
Jaime Arturo Hernández Ruiz
Gabriela Urdinola Hernández

Abstract

Granulomatosis with polyangiitis (GPA) is a small vessel vasculitis, it is associated with antineutrophil cytoplasmic antibodies (ANCA), it mainly involves the upper respiratory tract and gastrointestinal involvement is present in 4-20%. However, mesenteric ischemia is one of the more unusual associations. A case is reported of a 64-year-old man with chronic rhino-sinus symptoms, who consulted for abdominal pain associated with palpable purpuric lesions; later, with symptoms of acute abdomen that required emergency exploratory laparotomy where mesenteric ischemia was evident. The differential of systemic thromboembolic causes was performed, common causes were ruled out and during the diagnostic exercise, a positive ANCA proteinase 3 (PR3) GPA was documented, through clinical, paraclinical and histopathological criteria. Treatment with cyclophosphamide and corticosteroids was initiated, there was significant improvement of the initial clinical manifestations.

Keywords:
Granulomatosis with polyangiitis, Mesenteric ischemia, Case report

Article Details

References

Geetha D, Jefferson JA. ANCA-Associated Vasculitis: Core Curriculum 2020. Am J Kidney Dis [Internet]. 2020 Jan;75(1):124–37. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0272638619308261

Salvador F. ANCA associated vasculitis. Eur J Intern Med. 2020;74:18–28.

Acosta S. Mesenteric ischemia. Curr Opin Crit Care. 2021;21(2):171–8.

Beaulieu RJ, Arnaoutakis KD, Abularrage CJ, Efron DT, Schneider E, Black JH. Comparison of open and endovascular treatment of acute mesenteric ischemia. J Vasc Surg. 2014;59(1):159–64.

Mohammad AJ. An update on the epidemiology of ANCA-associated vasculitis. Rheumatology (Oxford); 2020;59:42–50.

Hunter RW, Welsh N, Farrah TE, Gallacher PJ, Dhaun N. ANCA associated vasculitis. BMJ [Internet]. 2020;369:m1070.

Bossuyt X, Cohen Tervaert JW, Arimura Y, Blockmans D, Flores-Suáez LF, Guillevin L, et al. Revised 2017 international consensus on testing of ANCAs in granulomatosis with polyangiitis and microscopic polyangiitis. Nat Rev Rheumatol. 2017;13(11):683–92.

Houben E, Bax WA, Van Dam B, Slieker WAT, Verhave G, Frerichs FCP, et al. Diagnosing ANCAassociated vasculitis in ANCA positive patients A retrospective analysis on the role of clinical symptoms and the ANCA titre. Medicine. 2016;95(40):e5096.

Pereira Beceiro J, Rodríguez Alonso A, Bonelli Martín C, Pérez Valcárcel J, Mosquera Seoane T, Cuerpo Pérez MÁ. Prostatitis y retención aguda de orina como comienzo de granulomatosis de Wegener. Reumatol Clin. 2014;10(6):409–12.

Halawani HM, Khalife M. Gastrointestinal complication of granulomatosis with polyangiitis. N Engl J Med. 2016;374(22):2159–2159.

Storesund B, Gran JT, Koldingsnes W. Severe intestinal involvement in Wegener’s granulomatosis: Report of two cases and review of the literature. Br J Rheumatol. 1998;37(4):387–90.

Veinot JP, Logan CA, Jane Thomas M. Wegener’s granulomatosis arteritis causing small bowel infarction. Pathology. 2003;35(3):268–9.

Sato H, Shima K, Sakata H, Ohtoh T. Granulomatosis with polyangiitis with intestinal involvement successfully treated with rituximab and surgery. BMJ Case Rep. 2019;12(8):e230355.

Ha HK, Lee SH, Rha SE, Kim JH, Byun JY, Lim HK, et al. Radiologic features of vasculitis involving the gastrointestinal tract. Radiographics. 2000;20(3):779–94.

Ladrón de Guevara D, Cerda F, Ángela Carreño M, Piottante A, Bitar P. Actualización en el estudio de Granulomatosis con poliangeitis (Granulomatosis de Wegener). Rev Chil Radiol. 2019;25(1):26–34.

Guillevin L, Durand-Gasselin B, Cevallos R, Gayraud M, Lhote F, Callard P, et al. Microscopic polyangiitis: Clinical and laboratory findings in eighty-five patients. Arthritis Rheum. 1999;42(3):421–30.

Hoffman GS, Specks U. Antineutrophil cytoplasmic antibodies. Arthritis Rheum. 1998;41(9):1521–37.

Oshita H, Matsumoto H, Hoshino T, Omori K, Okamoto N, Awaya Y. Wegener’s granulomatosis in which rheumatoid factor was useful for evaluating the disease status: a case report. Cases J. 2009;2(1):6323.

Kisacik B, Onder ME, Sayarlioglu M, Onat AM. Symmetric polyarthritis as an initial symptom in granulomatosis with polyangiitis: A report of six cases and review of the literature. Eur J Rheumatol. 2018;5(3):191–3.

Noritake DT, Weiner SR, Bassett LW, Paulus HE, Weisbart R. Rheumatic manifestations of Wegener’s granulomatosis. J Rheumatol. 1987;14(5):949–51.

Sablé-Fourtassou R, Cohen P, Mahr A, Pagnoux C, Mouthon L, Jayne D, et al. Antineutrophil cytoplasmic antibodies and the Churg-Strauss syndrome. Ann Intern Med. 2005;143(9):632–8.