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Melioidosis: Missed opportunities and opportunistic pathogens
Institution:1. Junior Consultant (Infectious Diseases), PD Hinduja National Hospital & Medical Research Centre, Mumbai, India;2. Consultant Rheumatologist, PD Hinduja National Hospital & Medical Research Centre, Mumbai, India;3. Consultant Nephrologist, PD Hinduja National Hospital and Medical Research Centre, Mumbai, India;4. Consultant (Infectious Diseases), PD Hinduja National Hospital & Medical Research Centre, Mumbai, India;1. Classified Specialist (Dermatology), Command Hospital (SC), Pune 40, India;2. Clinical Tutor, Department of Dermatology, Armed Forces Medical College, Pune & Command Hospital (SC), Pune 40, India;3. Classified Specialist (Pathology), Military Hospital, Barackpore, West Bengal, India;4. Classified Specialist (Dermatology), Military Hospital, Barackpore, West Bengal, India;1. Senior Advisor (Surgery) & GI Surgeon, 5 Air Force Hospital, Jorhat, India;2. Senior Advisor (Surgery) & GI Surgeon, Army Hospital (R&R), New Delhi, India;1. Classified Specialist (Pathology), Base Hospital, Delhi Cantt., India;2. Senior Advisor (Surgery) & GI Surgery, Base Hospital, Delhi Cantt., India;3. Senior Advisor (Pathology) & Nephropathologist, Army Hospital (Research & Referral), Delhi Cantt., India;4. Dean & Dy Commandant, Armed Forces Medical College, Pune 411040, India;5. Director & Commandant, Armed Forces Medical College, Pune 411040, India
Abstract:A 31-year Indian homemaker, known to have Systemic Lupus Erythematosus (SLE) and lupus nephritis, was admitted previously in another medical care unit with fever, hemoptysis, arthralgia, and joint swelling. She had been treated with antibiotics and corticosteroids for probable diffuse alveolar hemorrhage (DAH) with clinical and radiological resolution. She was readmitted one month later for similar complaints. Her autoimmune workup revealed evidence of active lupus. Her chest imaging showed the presence of well-circumscribed macronodular lesions with halo sign, but Bronchoalveolar Lavage (BAL) cultures and serum galactomannan were negative. BAL tested positive for hemosiderin-laden macrophages. She was treated with corticosteroids, plasmapheresis, and empiric antibiotics with partial clinical response. One week later, her fever recurred, and she developed new-onset myositis. Bactec blood cultures grew Burkholderia pseudomallei. She received treatment for 3 months with good clinical and radiological resolution. In hindsight, a CT-guided biopsy of the lung lesion may have provided an earlier diagnosis of melioidosis.
Keywords:Melioidosis  Invasive aspergillosis  Mimicker  Immunocompromised
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