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ANCA negative pulmonary vasculitis: a challenging diagnosis.
Zhang, Yimeng; Mayor, Kara; Mahdi, Amar.
Afiliação
  • Zhang Y; Renal Medicine, University Hospitals of North Midlands NHS Trust, Stoke-on-Trent, UK yimeng.zhang@nhs.net.
  • Mayor K; University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Mahdi A; University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
BMJ Case Rep ; 17(6)2024 Jun 19.
Article em En | MEDLINE | ID: mdl-38901853
ABSTRACT
A man in his 40s with end-stage kidney disease due to IgA nephropathy and receiving peritoneal dialysis presented with a 1-week history of breathlessness, cough and nosebleeds. CT scan of the chest revealed ground glass changes while blood tests indicated elevated inflammatory markers and a negative vasculitis screen. This included negative ANCA and anti-GBM antibodies. Initial treatment for suspected atypical pneumonia with antibiotics yielded no clinical improvement.Over the course of the admission, his symptoms progressively worsened, leading to oxygen dependency with a FiO2 of 40% and episodes of haemoptysis. Suspicions of pulmonary vasculitis arose due to clinical deterioration, prompting consultation with a tertiary vasculitis centre. It was subsequently concluded that the clinical and radiological findings correlated with ANCA-negative pulmonary vasculitis or a rare case of IgA-associated pulmonary capillaritis. Treatment with methylprednisolone and rituximab led to significant improvement, allowing rapid oxygen withdrawal. The patient was discharged with a tapering prednisolone regimen.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Anticitoplasma de Neutrófilos Limite: Adult / Humans / Male Idioma: En Revista: BMJ Case Rep Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Anticitoplasma de Neutrófilos Limite: Adult / Humans / Male Idioma: En Revista: BMJ Case Rep Ano de publicação: 2024 Tipo de documento: Article País de publicação: Reino Unido