| Literature DB >> 29650301 |
J Reverso-Meinietti1, F Vandenbos2, K Risso3, J Coyne1, S Leroy4, B Padovani5, F Burel-Vandenbos6.
Abstract
INTRODUCTION: Pulmonary intravascular talcosis is a rare condition occurring in intravenous drug users injecting oral medications. Talc results in a foreign-body granulomatous reaction giving a radiological haematogenic miliary appearance mimicking miliary tuberculosis. Drug users represent a population at risk for both these conditions and their distinction may be challenging. CASE REPORT: We reported the case of a man, 33 year-old, intravenous drug addict, detected by the health services because he was the partner of a person who died of contagious and multi-resistant tuberculosis. Chest X-ray and CT scan showed a typical miliary appearance. Despite negative microbiology, clinical diagnosis of miliary tuberculosis was retained. Due to the lack of radiological improvement despite appropriate antibiotic treatment, re-evaluation and trans-bronchial biopsy were undertaken. The presence of granulomas centered by birefringent foreign bodies in polarized light led to a diagnosis of pulmonary intravascular talcosis.Entities:
Keywords: Drug abuse; Granulomatose pulmonaire; Intravascular talcosis; Miliaire pulmonaire; Pulmonary granulomatosis; Pulmonary miliary; Talcose intravasculaire; Toxicomanie; Tuberculose; Tuberculosis
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Year: 2018 PMID: 29650301 DOI: 10.1016/j.revmed.2018.03.017
Source DB: PubMed Journal: Rev Med Interne ISSN: 0248-8663 Impact factor: 0.728