- Case Report
- Open Access
A diagnostic dilemma: a case report
© Comer and Edgar; licensee BioMed Central Ltd. 2009
- Received: 27 December 2008
- Accepted: 29 January 2009
- Published: 29 January 2009
A seventy nine year old lady presented with acute bilateral foot drop and paraesthesia of her lower limbs as a presenting feature of Wegener's Granulomatosis (WG).
There was no evidence of pulmonary involvement and her renal function was normal. WG can masquerade as very diverse pathology. It is recognised that neuropathy can occur early and often in the absence of more classical pulmonary and renal findings, often resulting in a delay in diagnosis.
Anti-neutrophil cytoplasmic antibody (ANCA) testing was particularly useful in this case permitting early diagnosis.
- Antineutrophil Cytoplasmic Antibody
- Joint Position Sense
- ANCA Testing
A seventy nine year caucasian lady presented with bilateral foot-drop and lower limb dysaesthesia. This was of sudden onset. Left leg weakness and initial dysaesthesia of the left foot, progressed over 48 hours to involve her right leg. Apart from thoracic shingles nine months earlier and pulmonary tuberculosis in her youth, she had no significant past medical history. There were no upper or lower respiratory symptoms and she denied any joint pain, myalgia, sweats or haematuria. She was on no regular medication, was a non smoker, and consumed only minimal alcohol. Family history was unremarkable and she had no children.
On examination, there was a non-blanching erythematous reticular rash on the anterior aspect of both calves. She had bilateral foot-drop, with grade 0/5 power in all foot movements. Knee jerks were brisk, but ankle jerks were absent. She had bilaterally flexor plantar responses. There was loss of pin-prick sensation to mid calf bilaterally. Joint position sense and vibration sense were absent to below the knees. The remainder of the clinical examination was normal and she had a normal body mass index.
A myelogram and cerebrospinal fluid analysis was normal. Neurophysiology demonstrated normal responses in the arms but absent sensory and motor responses in both legs, in keeping with severe bilateral lumbosacral plexopathy or length dependent neuropathy. An MRI scan of her spine (to exclude a compressive lumbosacral polyradiculopathy) showed only mild age related cerebral atrophy and scattered degenerative changes. There was no evidence of spinal cord or nerve root compromise. Chest x-ray demonstrated evidence of old acid fast disease.
12 months after the initiation of treatment she is clinically well, with almost complete resolution of bilateral foot-drop and no overt complications of treatment.
WG, a triad of granulomatous lesions involving the upper and lower airways, a systemic vasculitis and necrotising crescentic vasculitis involving the kidney, was first described in 1932 by Klinger et al . Patients with WG usually present with symptoms and signs of upper airway or of lower airway disease. Less commonly patients present solely with symptoms of renal disease. The diagnosis of WG rests on the recognition of typical clinical features, supported wherever possible by confirmatory tissue histology. The advent of anti-neutrophil cytoplasmic antibody (ANCA) testing in the last 20 years has provided a valuable additional element in what can in certain cases be a very difficult diagnosis. Despite advances in our understanding of granuloma formation and improvements in treatment the pathogenesis of WG remains poorly understood. Treatment is based on combination immunosuppressive regimes to induce remission followed by lower dose maintenance therapy. Without treatment, the prognosis is poor, with a median survival time of four months . With treatment, the chance of remission and long term survival is high with 7-year survival figures of 58% for those patients over the age of 60 and a corresponding value of 29% for those patients aged less than 60 .
This case was a diagnostic dilemma because an elderly female patient presented with peripheral neuropathy of uncertain origin. A common cause was not identified, but steroid therapy was commenced on an empirical basis. There was no obvious clinical responses in terms of weakness or sensation, however there was a dramatic response in terms of the detectable acute phase response. Of itself this suggested a steroid responsive inflammatory cause, however it was the detection of high titre C-ANCA, confirmed by positive PR3-ANCA that indicated the underlying diagnosis of WG. This provided justification for recommencement of immunosuppressive therapy, which continues.
Elderly people with WG present disproportionably with CNS involvement (4.5 fold more commonly) and less often with the classical symptoms . Previous studies have shown that this cohort of patients characteristically present with symptoms and signs of pulmonary infiltrates and renal impairment rather than features of upper airway disease. This atypical presentation does not however imply a more indolent course and elderly patients require long term immunosuppressive treatment in the same way as their younger counterparts. Accurate confirmation or exclusion of the diagnosis of WG has enormous implications. An accurate and prompt diagnosis is potentially life saving, but the inappropriate use of immunosuppressive medication can have severe detrimental effects.
Indications for ANCA testing 
Glomerulonephritis, especially rapidly progressive glomerulonephritis
Pulmonary haemhorrhage, especially pulmonary renal syndrome
Cutaneous vasculitis with systemic features
Multiple lung nodules
Chronic destructive disease of the upper airways
Long standing sinusitis or otitis
Subglottic tracheal stenosis
Mononeuritis multiplex or other peripheral neuropathy
In this case, ANCA testing was used appropriately, in line with these international consensus guidelines and proved useful in establishing a diagnosis. It is important to emphasise that ANCA testing should only be requested in these defined clinical situations and not be used as a screening test for vasculitis in patients with non-specific presentations .
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.
- Klinger H: Grenzformen der periarteritis nodosa. Z Pathol. 1931, 42: 455-80.Google Scholar
- Langford CA, Hoffman GS: Rare diseases. 3: Wegener's granulomatosis. Thorax. 1999, 54 (7): 629-37.PubMed CentralView ArticlePubMedGoogle Scholar
- Weiner SR, Paulus HE, Weisbart RH: Wegener's Granulomatosis in the elderly. Arthritis and Rheumatism. 1986, 29 (9): 1157-1159. 10.1002/art.1780290915.View ArticlePubMedGoogle Scholar
- Krafcik SS, Covin RB, Lynch JP, Sitrin RG: Wegener's granulomatosis in the elderly. Chest. 1996, 109 (2): 430-7. 10.1378/chest.109.2.430.View ArticlePubMedGoogle Scholar
- Boucelma M, Hakem D, Ibrir M, Kadri N, Youcef-Ouali D, Ouadahi N, Berrah A: Wegener's Granulomatosis and necrotizing ulceration of the breast. Revue de Medecine Interne. 2005, 26 (2): 155-7. 10.1016/j.revmed.2004.09.020.View ArticlePubMedGoogle Scholar
- Blundell AG, Roe S: Wegener's Granulomatosis presenting as a pleural effusion. BMJ. 2003, 327: 95-96. 10.1136/bmj.327.7406.95.PubMed CentralView ArticlePubMedGoogle Scholar
- Vittaz L, Ramanoelina J, Mahr A, Cohen R, Cohen P, Reach G, Guillevin L: Pituitary involvement in Wegener's granulomatosis. Two cases. [French]. Presse Medicale. 2004, 33 (22): 1585-90. 10.1016/S0755-4982(04)98998-1.View ArticleGoogle Scholar
- Weijtens O, Mooy N, Paridaens D: Horner's syndrome as manifestation of Wegener's granulomatosis. Eye. 2004, 18 (8): 846-8. 10.1038/sj.eye.6701324.View ArticlePubMedGoogle Scholar
- Edgar JD, McMillan SA, Bruce IN, Conlan SK: An audit of ANCA in routine clinical practice. Postgraduate Medical Journal. 1995, 71 (840): 605-12. 10.1136/pgmj.71.840.605.PubMed CentralView ArticlePubMedGoogle Scholar
- Edgar JD: The clinical utility of ANCA positivity. Annals of the Rheumatic Diseases. 1996, 55 (8): 494-6. 10.1136/ard.55.8.494.PubMed CentralView ArticlePubMedGoogle Scholar
- Rao JK, Weinberger M, Oddone EZ, Allen NB, Landsman P, Feussner JR: The role of antineutrophil cytoplasmic antibody (c-ANCA) testing in the diagnosis of Wegener's Granulomatosis. Ann Int Med. 1995, 123: 925-932.View ArticlePubMedGoogle Scholar
- Savige J, Dimech W, Fritzler M, Goeken J, Hagen EC, Jennette JC, McEvoy R, Pusey C, Pollock W, Trevisin M, Wiik A, Wong R, International Group for Consensus Statement on Testing and Reporting of Antineutrophil Cytoplasmic Antibodies (ANCA): Addendum to the International Consensus Statement on testing and reporting of antineutrophil cytoplasmic antibodies. Quality control guidelines, comments, and recommendations for testing in other autoimmune diseases. Am J Clin Pathol. 1999, 111 (4): 507-513.PubMedGoogle Scholar
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.