Open Access

An unusual complication of polyarteritis nodosa with massive retroperitoneal hemorrhage: a case report

International Archives of Medicine20103:31

DOI: 10.1186/1755-7682-3-31

Received: 6 February 2010

Accepted: 11 November 2010

Published: 11 November 2010

Abstract

Background and Case report

Polyarteritis Nodosa (PAN) is a systemic necrotizing vasculitis that affects medium-sized and occasionally involves small arteries leading to the disruption of the internal and external elastic lamina and contribute to the development of aneurysms. Aneurysms develop at bifurcation of major blood vessels; they are prone to thrombosis, rupture and haemorrhage. Retroperitoneal haemorrhage around kidneys was previously reported in patients with PAN. We report a case of massive retroperitoneal bleeding from inferior pancreaticoduodenal artery aneurysm rupture in a 70-year-old female with PAN.

Conclusion

Prognosis of untreated PAN is very poor with 20% 5 year survival rate, therefore early recognition of the disease will prevent catastrophic complications and improves survival.

Case presentation

A 78-year-old woman presented with fever, anorexia and significant (34 pound) weight loss of three months duration. Three weeks prior to the presentation, she noticed pain and bluish discoloration of her finger tips, which later turned to black with worsening pain. Her past history was significant for hypertension and 35 pack years of smoking. She was febrile with temperature of 100.4°F and other vital signs were stable.

Physical examination demonstrated blackish discoloration of her finger tips involving right index, right and left middle finger [Figure 1]. She also had black lesion on her hard palate [Figure 2]. All peripheral pulses were felt symmetrically. Rest of the examination was unremarkable. Her white cell count was elevated at 13,000/mm3 and erythrocyte sedimentation rate was also elevated at 66 mm/hour. Three sets of blood cultures were drawn and empirical antibiotic therapy was begun with piperacillin tazobactum and vancomycin for possible septic embolism.
Figure 1

White arrow pointing the gangrenous index finger.

Figure 2

White arrow pointing black colored lesion in the hard palate.

Workup for endocarditis with transesophageal echocardiogram showed no vegetations. Serologic evaluation for vasculitis with Anti nuclear antibody (ANA), C and P-Anti neutrophil cytoplasmic antibody (ANCA), Anticardiolipin antibody, Rheumatoid factor, and Hepatitis panel did not reveal any abnormality. All three sets of blood cultures showed no growth.

On 3rd day of hospitalization, she developed severe pain and distension of the left side of the abdomen; in association with hypotension and tachycardia. Emergent computer tomography (CT) scan of abdomen showed large retroperitoneal hemorrhage. Further evaluation with mesenteric angiogram revealed multiple visceral artery aneurysms and bleeding from inferior pancreatic duodenal artery aneurysm that was successfully embolized [Figure 3]. She received three units packed red blood cells (PRBC) transfusion and was stabilized hemodynamically.
Figure 3

Mesenteric angiogram showing multiple visceral artery aneurysms (arrow heads) and Inferior pancreaticoduodenal artery along with the retro peritoneal hemorrhage.

She was diagnosed with Polyarteritis Nodosa (PAN) after her mesenteric artery aneurysms in accordance with American College of Rheumatology (ACR) 1990 criteria and was treated with cyclophosphamide and prednisone with resolution of fever and symptomatic improvement. She subsequently underwent amputation of her gangrenous fingertips and discharged.

Discussion

Polyarteritis Nodosa (PAN) is a rare form of vasculitis, a multisystem disease, most commonly affects kidney and skin. Prevalence varies from 3-30/100000 [1]. Incidence increases with age; most commonly affects the people in sixth decade as with our patient [2]. The prognosis of untreated PAN is almost always fatal and most patients would die in 2 years.

As with most other patients of PAN our patient had constitutional symptoms like low grade fever, anorexia and weight loss. Hypertension, mild renal insufficiency is commonly seen; however renal insufficiency was not seen in our patient until she developed hemorrhagic shock, which later improved with resuscitation.

In general cutaneous manifestations account for 25-60% which includes livedoreticularis, tender subcutaneous nodules, nonhealing ulcers and gangrene, as seen in our patient [3]. Involvement of abdomen is seen in 50% of people with PAN; symptoms are related to the mesenteric vasculitis causing postprandial abdominal pain, gastrointestinal bleeding, acalculous cholecystitis and pancreatitis. Our patient did not have these symptoms [4].

Aneurysms develop at bifurcation of major blood vessels; they are prone to thrombosis, rupture and hemorrhage, and aneurysms correlates with the severity of the illness [5]. Visceral artery aneurysms rupture results in bleeding into major organs like liver, kidney have been described in the literature [6]. Our patient developed abdominal pain and distension as a result of retroperitoneal hemorrhage from the inferior pancreatic duodenal artery aneurysm rupture, which is unique and has not been reported in the literature to the best of our knowledge. She underwent mesenteric-angiogram which revealed multiple aneurysms involving the superior and inferior pancreatico duodenal arteries and other mesenteric vessels.

Diagnosis of PAN should be confirmed with biopsy whenever possible; however in the absence of biopsy diagnosis can be made with angiogram in with other clinical features in accordance with ACR 1990 criteria to diagnose PAN, which has sensitivity and specificity of 82% and 85% respectively [7]. Workup for secondary causes of vasculitis was negative. Combination of steroids and cyclophosphamide has shown better outcome compared to steroids alone. Most of the studies recommend treatment for one year [8].

Conclusion

As PAN peaks around the age where atherosclerotic disease is also common, vasculitis should always be considered in the differential diagnosis of the patient presenting with ischemic gangrene and unexplained retroperitoneal bleeding.

Consent

Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Declarations

Acknowledgements

We sincerely acknowledge Dr Sahibzada U. Latif for his valuable contribution in the manuscript preparation.

Authors’ Affiliations

(1)
Department of Internal Medicine, Michigan State University
(2)
Department of Internal Medicine, Kalamazoo Center for Medical studies, Michigan State University
(3)
Department of Critical Care Medicine, Sparrow Hospital

References

  1. Mahr A, Guillevin L, Poissonnet M, Ayme S: Prevalences of polyarteritis nodosa, microscopic polyangiitis, Wegener's granulomatosis, and Churg-Strauss syndrome in a French urban multiethnic population in 2000: a capture-recapture estimate. Arthritis Rheum 2004, 51:92–99.View ArticlePubMedGoogle Scholar
  2. Watts RA, Lane SE, Bentham G, Scott DG: Epidemiology of systemic vasculitis: a ten-year study in the United Kingdom. Arthritis Rheum 2000, 43:414–419.View ArticlePubMedGoogle Scholar
  3. Ebert EC, Hagspiel KD, Nagar M, Schlesinger N: Gastrointestinal involvement in polyarteritis nodosa. Clin Gastroenterol Hepatol 2008, 6:960–966.View ArticlePubMedGoogle Scholar
  4. Painter RW: Sequential gastrointestinal complications of polyarteritis nodosa. Am J Gastroenterol 1971, 55:383–386.PubMedGoogle Scholar
  5. Ewald EA, Griffin D, McCune WJ: Correlation of angiographic abnormalities with disease manifestations and disease severity in polyarteritis nodosa. J Rheumatol 1987, 14:952–956.PubMedGoogle Scholar
  6. Cornfield JZ, Johnson ML, Dolehide J, Fowler JE Jr: Massive renal hemorrhage owing to polyarteritis nodosa. J Urol 1988, 140:808–809.PubMedGoogle Scholar
  7. Lightfoot RW Jr, Michel BA, Bloch DA, Hunder GG, Zvaifler NJ, McShane DJ, Arend WP, Calabrese LH, Leavitt RY, Lie JT, Masi AT, Mills JA, Stevens MB, Wallace SL: The American College of Rheumatology 1990 criteria for the classification of polyarteritis nodosa. Arthritis Rheum 1990, 33:1088–1093.View ArticlePubMedGoogle Scholar
  8. Leib ES, Restivo C, Paulus HE: Immunosuppressive and corticosteroid therapy of polyarteritis nodosa. Am J Med 1979, 67:941–947.View ArticlePubMedGoogle Scholar

Copyright

© Peddi et al. 2010

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Advertisement