Fever, renal failure, and diffuse alveolar hemorrhage: Unraveling the ANCA vasculitis connection.

Background: Microscopic polyangiitis (MPA), a small-vessel antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis, may present insidiously with prolonged fever, renal dysfunction, and pulmonary infiltrates--often mimicking infections, especially in tropical settings. Case presentation: A 6...

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Publicado en:Critical Care & Shock Vol. 28; no. 6; pp. 279 - 287
Autores principales: Gandikota, Prathyusha, Narayanasamy, Senthil, Chenguttuvan, Avinash, Pandurangan, Viswanathan
Formato: case study diagnostic images tables/charts Journal Article
Publicado: Critical Care & Shock Journal 2025
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Critical Care & Shock Journal
      place: Houston, Texas
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        atl: Fever, renal failure, and diffuse alveolar hemorrhage: Unraveling the ANCA vasculitis connection.
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        au:
          Gandikota, Prathyusha
          Narayanasamy, Senthil
          Chenguttuvan, Avinash
          Pandurangan, Viswanathan
        affil: Department of General Medicine, Sri Ramachandra Institute of Higher Education and Research, Chennai, Tamil Nadu, India
      sug:
        subj:
          Microscopic Polyangiitis Radiography
          Microscopic Polyangiitis Therapy
          Fever Etiology
          Renal Insufficiency Etiology
          Hemorrhage Etiology
          Antibodies, Antineutrophil Cytoplasmic Analysis
          Vasculitis Chemically Induced
          Male
          Middle Age
          Comorbidity
          Dyspnea Etiology
          Fatigue Etiology
          Edema Etiology
          Autoimmune Diseases
          Critical Care
          Immunosuppressive Agents Therapeutic Use
          Vasculitis Immunology
          Biopsy Methods
          Tomography, X-Ray Computed
          Bronchoscopy
          Steroids Administration and Dosage
          Administration, Oral
          Hemodialysis
          Middle Aged: 45-64 years
          Male
      ab: Background: Microscopic polyangiitis (MPA), a small-vessel antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis, may present insidiously with prolonged fever, renal dysfunction, and pulmonary infiltrates--often mimicking infections, especially in tropical settings. Case presentation: A 61-year-old man with longstanding type 2 diabetes, hypertension, and a previous cerebrovascular accident presented with a 3-month history of low-grade fever, exertional dyspnea, fatigue, and pedal edema. He initially received meropenem for pan-resistant Klebsiella urinary infection; later received Helicobacter pylori therapy for gastritis. However, he remained febrile with rising creatinine. On admission, he was tachypneic, hypoxemic, and oliguric, with bilateral lung infiltrates, microscopic hematuria, and anemia (hemoglobin 5.5 g/dl). Infectious workup--including tropical fevers and tuberculosis--were negative. Perinuclear ANCA (P-ANCA) titre >200 U/ml, computerized tomography (CT) lung findings consistent with diffuse alveolar hemorrhage (DAH), and bronchoalveolar lavage positive for hemosiderin- laden macrophages established the diagnosis of MPA. Due to poor renal reserve, the biopsy was deferred. Treatment included intravenous pulse methylprednisolone (1 g/day x 3), three cycles of plasma exchange, and supportive low-efficiency dialysis. He improved clinically, was weaned off oxygen, and transitioned to oral steroids. Conclusion: This case illustrates the diagnostic challenge of MPA presenting as prolonged pyrexia of unknown origin (PUO) with pulmonaryrenal syndrome in a tropical context. After excluding infectious causes, early consideration of ANCA-associated vasculitis and prompt immunosuppressive therapy can be lifesaving.
      pubtype: Academic Journal
      doctype:
        case study
        diagnostic images
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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