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Correspondence |
We read with interest the article "Reversed halo sign in lymphomatoid granulomatosis" by Benamore et al [1] in the August issue of the BJR, in which the authors describe a case of lymphomatoid granulomatosis associated with reverse halo sign. The other causes of reversed halo sign described in the literature include pulmonary tuberculosis [2], pulmonary zygomycosis [3] and pulmonary small vessel vasculitis [4]. Herein, we wish to report a further cause of reversed halo sign on CT — Wegener's granulomatosis.
A 28-year-old male presented to the Chest Clinic with history of fever, cough and chest pain of 1 months' duration. The patient also complained of anorexia, weight loss and epistaxis. There were no arthralgias, oliguria, or neurological or skin involvement. A chest radiograph showed bilateral extensive areas of patchy consolidation. Biochemical investigations revealed normal liver function tests but serum creatinine was 3.8 mg dL–1. Complete blood count showed evidence of mild anaemia with thrombocytosis. Urine microscopy revealed 50–60 red blood cells per high power field, and 24-h urinary protein was 1.2 g. A provisional diagnosis of systemic vasculitis was considered. A high-resolution CT scan showed widespread nodular opacities, with some of the nodules demonstrating the reversed halo sign (Figure 1
); areas of consolidation were also seen. Renal biopsy was performed, which was suggestive of necrotizing vasculitis with crescentic glomerulonephritis; immunofluorescence microscopy revealed pauci-immune IgG deposits. Anti-neutrophil cytoplasmic antibodies, detected by indirect immunofluorescence, displayed a diffuse granular cytoplasmic pattern. A diagnosis of Wegener's granulomatosis was made and the patient was started on bolus intravenous methylprednisolone (1 g day–1) for three consecutive days followed by oral prednisolone (60 mg day–1). Simultaneously oral cyclophosphamide at a dose of 150 mg day–1 was also started. The patient showed significant response and at 3 months the chest radiograph and urine analysis was completely normal. Oral cyclophosphamide was stopped after 3 months and the patient was started on oral azathioprine (150 mg day–1). Prednisolone was tapered, and at 6 months the dose was maintained at 7.5 mg day–1. The patient has continued to be on low-dose prednisolone and oral azathioprine for the past 2 years.
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Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research Chandigarh, India. E-mail: ritesh{at}indiachest.org; riteshpgi{at}gmail.com
Received for publication September 5, 2007. Revision received September 10, 2007. Accepted for publication September 17, 2007.
References
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