AI Article Synopsis

  • - Granulomatosis with polyangiitis (GPA) is a rare inflammatory disease that primarily affects the respiratory system and involves inflammation of small to medium blood vessels.
  • - Diagnosis can be challenging due to vague symptoms and varying clinical presentations, often leading to misdiagnosis, especially in older patients.
  • - The report highlights two elderly cases where GPA was only identified 4 to 6 years after the initial symptoms, despite multiple diagnostic procedures being performed.

Article Abstract

Granulomatosis with polyangiitis (GPA) is defined as a necrotizing granulomatous inflammation usually involving the upper and lower respiratory tract with necrotizing vasculitis affecting predominantly small to medium vessels. Because of non-specific symptoms, its radiological presentation, and the diversity of its clinical expression, it is not uncommon to for it to be misdiagnosed, especially in the elderly. Although biopsy and histological examination seem to be essential for GPA diagnosis, their results are sometimes ambiguous and not helpful in making a decision. In this report, we present difficulties in the recognition of GPA in two elderly patients in whom, despite twice performing a diagnostic thoracotomy, GPA was recognized almost 4 and 6 years after the first symptoms.

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Source
http://dx.doi.org/10.5603/ARM.2019.0064DOI Listing

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