Literature DB >> 20201181

Wegener's granulomatosis: a diagnostic challenge.

Ali Bin Sarwar Zubairi1, Hammad Bin Liaquat, Shahid Javed Husain, Kulsoom Fatima.   

Abstract

Wegener's Granulomatosis (WG) is a necrotizing granulomatous vasculitis that primarily involves small vessels in the body. Patient usually presents in the fourth to fifth decade. The clinical presentation is variable; however, majority of patients (90%) seek medical attention for nasal and sinus symptoms with or without lower respiratory symptoms of cough, dyspnoea and haemoptysis. The typical form of WG tends to involve the triad of upper and lower respiratory tract and the kidneys; while involvement of other organs like ocular, cutaneous, rheumatological, neural, gastrointestinal and lower genito-urinary tract is occasionally seen. A "limited" form with clinical findings isolated to the upper respiratory tract or lungs, occur in approximately one-fourth of cases. We present a case of Wegener's Gmnulomatosis in an eighty five year old lady who presented with an acute pneumonia-like illness. She underwent an extensive work-up to reach a definitive diagnosis.

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Year:  2009        PMID: 20201181

Source DB:  PubMed          Journal:  J Pak Med Assoc        ISSN: 0030-9982            Impact factor:   0.781


  2 in total

1.  Pulmonary renal syndrome in a patient with vasculitis: Case report and review of literature.

Authors:  Aijaz Zeeshan Khan Chachar; Omer Sabir; Irfan Haider; Imrana Tanvir; Kashif Rafique; Nauman Tarif
Journal:  Pak J Med Sci       Date:  2015 Nov-Dec       Impact factor: 1.088

2.  Granulomatosis with Polyangiitis Presenting as Pyrexia of Unknown Origin, Leukocytosis, and Microangiopathic Haemolytic Anemia.

Authors:  Sima Terebelo; Iona Chen
Journal:  Case Rep Rheumatol       Date:  2017-07-24
  2 in total

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