Literature DB >> 15980955

ANCA-negative pauci-immune crescentic glomerulonephritis complicated with recurrent massive gastrointestinal hemorrhage.

Tamaki Harada1, Takashi Uzu, Tomoko Namba, Ryohei Yamamoto, Ken Takahara, Atsushi Yamauchi.   

Abstract

On April 25, 2003, a 62-year-old Japanese man had been admitted to a hospital because of heavy proteinuria and elevated serum creatinine level, and purpura on the lower extremities. On May 15, 2003, he was referred to our hospital for evaluation and treatment. Serum immunoglobulin and complements were within normal ranges. Immune serology was negative for antinuclear antibody, antiglomerular basement membrane antibody, and antineutrophil cytoplasmic antibodies. Histological examination of a percutaneous renal biopsy specimen revealed that all of the glomeruli had severe crescent formation without deposits of immunoreactants. A diagnosis of antineutrophil cytoplasmic antibody-negative pauci-immune crescentic glomerulonephritis was made. The patient was treated with one cycle of steroid pulse therapy (1000 mg methylprednisolone daily, given on 3 consecutive days), and subsequently with prednisolone (60 mg/day). Despite this treatment, renal failure progressed rapidly and hemodialysis was started 1 month after the acute presentation. On May 30, 2003, he suddenly developed massive hematochezia. A technetium-targeted red-blood-cell scan suggested bleeding in the small intestine. On June 11, he presented with massive melena. A bleeding ulcer was found in the third part of the duodenum, and was treated successfully with endoscopy, using a heater probe. On June 19, he presented with massive hematochezia again. Mesenteric angiography revealed active bleeding from the iliac branch of the superior mesenteric artery. He was treated with continuous intraarterial vasopressin infusion by a catheter seated in the branch artery. The majority of patients with pauci-immune crescentic glomerulonephritis, one of the most common causes of rapidly progressive glomerulonephritis, have glomerular disease as part of a systemic vasculitis. Massive gastrointestinal bleeding, although rare, should be considered one of the serious complications in these patients.

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Year:  2005        PMID: 15980955     DOI: 10.1007/s10157-005-0344-0

Source DB:  PubMed          Journal:  Clin Exp Nephrol        ISSN: 1342-1751            Impact factor:   2.801


  10 in total

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Journal:  J Gastroenterol       Date:  2001-04       Impact factor: 7.527

2.  Rapid recurrence of ANCA-negative pauci-immune vasculitis after cadaveric renal transplantation.

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Journal:  Am J Kidney Dis       Date:  2001-07       Impact factor: 8.860

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Journal:  J Am Soc Nephrol       Date:  1997-02       Impact factor: 10.121

4.  Classical polyarteritis nodosa and microscopic polyarteritis with medium vessel involvement--a comparison of the clinical and laboratory features.

Authors:  G S Kirkland; J Savige; D Wilson; W Heale; R A Sinclair; R N Hope
Journal:  Clin Nephrol       Date:  1997-03       Impact factor: 0.975

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Journal:  Semin Gastrointest Dis       Date:  1995-10

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Review 7.  The pathology of vasculitis involving the kidney.

Authors:  J C Jennette; R J Falk
Journal:  Am J Kidney Dis       Date:  1994-07       Impact factor: 8.860

Review 8.  Rapidly progressive glomerulonephritis.

Authors:  W K Bolton
Journal:  Semin Nephrol       Date:  1996-11       Impact factor: 5.299

Review 9.  Microscopic polyangiitis: clinical aspects and treatment.

Authors:  F Lhote; P Cohen; T Généreau; M Gayraud; L Guillevin
Journal:  Ann Med Interne (Paris)       Date:  1996

Review 10.  Antineutrophil cytoplasmic autoantibodies and associated diseases: a review.

Authors:  J C Jennette; R J Falk
Journal:  Am J Kidney Dis       Date:  1990-06       Impact factor: 8.860

  10 in total
  5 in total

Review 1.  ANCA-negative pauci-immune crescentic glomerulonephritis.

Authors:  Min Chen; Cees G M Kallenberg; Ming-Hui Zhao
Journal:  Nat Rev Nephrol       Date:  2009-04-28       Impact factor: 28.314

2.  Pauci-immune crescentic glomerulonephritis associated with use of trimethoprim-sulfamethoxazole.

Authors:  Shruti S Hegde; Vanesa Bijol; Bertrand L Jaber
Journal:  CEN Case Rep       Date:  2016-06-07

3.  AP-VAS 2012 case report: a case of ANCA-negative pauci-immune crescentic glomerulonephritis associated with IL-6-producing adenosquamous cell carcinoma of the lung.

Authors:  Takashi Morikawa; Atsuhiro Yoshida; Shinya Kobayashi; Mikiko Shibata; Masahiro Hamada; Masatsugu Kishida; Chizuko Kitabayashi; Haruko Daga; Yoshio Konishi; Koji Takeda; Masahito Imanishi
Journal:  CEN Case Rep       Date:  2013-03-14

Review 4.  Diagnostic approach to patients with suspected vasculitis.

Authors:  E Suresh
Journal:  Postgrad Med J       Date:  2006-08       Impact factor: 2.401

5.  A case of a 6-year-old girl with anti-neutrophil cytoplasmic autoantibody-negative pauci-immune crescentic glomerulonephritis.

Authors:  Maki Shimizu; Takanori Sekiguchi; Natsuko Kishi; Aya Goji; Tomoko Takahashi; Hiroko Kozan; Zenichi Sakaguchi; Yukiko Kinoshita; Sato Matsuura; Kenichi Suga; Maki Urushihara; Shuji Kondo; Shoji Kagami; Katsuaki Ohara
Journal:  Clin Exp Nephrol       Date:  2011-03-01       Impact factor: 2.617

  5 in total

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