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A case of myeloperoxidase–antineutrophil cytoplasmic antibody positive-polyarteritis nodosa complicated by interstitial pneumonia and rapidly progressive renal failure

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Abstract

A 73-year-old woman was admitted to our hospital because of persistent high fever and cough, generalized myalgia, and renal dysfunction. Laboratory examination revealed severe inflammatory signs, pulmonary fibrosis, progression of renal impairment with active nephritic urinary sediments, and a high titer of myeloperoxidase–antineutrophil cytoplasmic antibody, indicating that she might have microscopic polyangiitis with interstitial pneumonia and rapidly progressive glomerulonephritis. Her renal biopsy, however, showed tubulointerstitial changes with mild glomerular abnormalities, and renal angiography revealed that she had vascular lesions of medium-sized arteries, which were compatible with classical polyarteritis nodosa. Tissue biopsy of the clinically affected organ should be considered in anyone suspected to have vasculitis.

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References

  1. Jennette C, Falk RJ (1997) Small-vessel vasculitis. N Engl J Med 337:1512–1523

    Article  PubMed  CAS  Google Scholar 

  2. Weyand CM, Goronzy JJ (2003) Medium- and large-vessel vasculitis. N Engl J Med 349:160–169

    Article  PubMed  CAS  Google Scholar 

  3. Savage COS, Harper L, Cockwell P, Adu D, Howie A (2000) ABC of arterial and vascular disease: vasculitis. BMJ 320:1325–1328

    Article  PubMed  CAS  Google Scholar 

  4. Gutierrez E (2004) Microscopic polyangiitis. In: Latinis KM, Dao K, Gutierrez E, Shepherd R, Velazquez CR (eds) Rheumatology subspecialty consult. Lippincott Williams & Wilkins, Philadelphia, pp 150–152

    Google Scholar 

  5. Henderson J, Cohen J, Jackson J, Wiselka M (2002) Polyarteritis nodosa presenting as a pyrexia of unknown origin. Postgrad Med J 78:685–686

    Article  PubMed  CAS  Google Scholar 

  6. Matsumoto T, Homma S, Okada M, Kuwabara N, Kira S, Hoshi T, Uekusa T, Saiki S (1993) The lung in polyarteritis nodosa: a pathologic study of 10 cases. Hum Pathol 7:717–724

    Article  Google Scholar 

  7. Guillevin L, Visser H, Noel LH, Pourrat J, Vernier I, Gayraud M, Oksman F, Lesavre P (1994) Antineutrophil cytoplasm antibodies in systemic polyarteritis nodosa with and without hepatitis B virus infection and Churg–Strauss syndrome—62 patients. J Rheumatol 21:1173–1174

    PubMed  Google Scholar 

  8. Sano K, Sakaguchi N, Ito M, Koyama M, Kobayashi, Hotchi M (2001) Histological diversity of vasculitic lesions in MPO-ANCA-positive autopsy cases. Pathol Int 51:460–466

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Toshiro Sugimoto.

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Sugimoto, T., Kanasaki, K., Koyama, T. et al. A case of myeloperoxidase–antineutrophil cytoplasmic antibody positive-polyarteritis nodosa complicated by interstitial pneumonia and rapidly progressive renal failure. Clin Rheumatol 26, 429–432 (2007). https://doi.org/10.1007/s10067-005-0142-9

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  • DOI: https://doi.org/10.1007/s10067-005-0142-9

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