| Literature DB >> 31469613 |
Ryota Yoshimoto1, Kitaru Tanaka1, Tomoki Kawahata1, Sayaka Takatori1, Kyohei Takatori1, Kohei Eguchi1, Daisuke Fujishiro1, Satoru Kodama1, Atsushi Kobayashi1, Kensaku Okamoto1, Sayaka Yuzawa2, Tsuguhito Ota1, Yuichi Makino1.
Abstract
Giant cell arteritis (GCA) is a type of large vessel vasculitis, and it involves the aorta, large vessels and terminal branches of the external carotid artery, especially the temporal artery. Temporal artery biopsy is a simple tool for the diagnosis of vasculitis, however, the histopathological findings do not always differentiate between the small-vessel vasculitis and GCA. We report the case of 72-year-old male who initially had a clinical diagnosis of GCA, then in the course of treatment, diagnostic histopathological approach revealed the necrotizing vasculitis with bronchocentric granulomatosis in the inflammatory nodule of the lung. The manifestations of patients with systemic vasculitis represent the disorders of multiple organ systems thus are diverse and may vary through the course of the disease. Presentation of unexpected features such as insufficient response to antibiotics, sinusitis, runny nose, discomfort of frontal region or pachymeningitis which anticipates re-evaluation of systemic vasculitis that may lead us to an appropriate diagnosis and the treatment.Entities:
Keywords: GCA; GPA; Giant cell arteritis; granulomatosis with polyangiitis; polyangiitis overlap syndrome
Mesh:
Year: 2019 PMID: 31469613 DOI: 10.1080/25785826.2019.1657377
Source DB: PubMed Journal: Immunol Med ISSN: 2578-5826