Wegener Granulomatosis with Oral Involvement as Primary Manifestation: A Case Study

Authors

  • Abbas Javadzadeh 1.Oral & Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran 2.Associate Professor of Oral Medicine, Oral and Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Mahdokht Rashed 1.Oral & Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran 2.Assistant Professor of Oral and maxillofacial medicine, Oral and Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Mehrdad Radvar Professor of Periodontitis, Oral and Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Nooshin Mohtasham 1.Oral & Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran 2.Professor of Oral and Maxillofacial Pathology, Oral and Maxillofacial Diseases Research Center, Department of Oral and Maxillofacial Pathology, Mashhad University of Medical Sciences, Mashhad, Iran
  • Pegah Mosannen Mozaffari 1. Oral & Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran 2.Associate Professor of Oral Medicine, Oral and Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  • Sedigheh Modarres Mousavy Post Graduate Student of Oral and Maxillofacial Medicine, Oral and Maxillofacial Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Abstract:

Introduction: Wegener Granulomatosis is a rare multisystemic disease with an unknown cause, characterized by necrotic granulomatous lesions in respiratory tract, systemic vasculitis in small arteries and veins and necrotizing glomerulonephritis. Wegener can affect any organ including kidneys, eyes or other organs but classically affects upper and lower respiratory tract. One of the rare but important signs of this disease is oral involvement, generally occurring in 6-13% of patients, however, oral involvement as the primary manifestation of disease, occurs in only 5-6% of cases. The most common oral manifestation is strawberry gingivitis. Patients: Our patient was a 35 year-old man with gingival bleeding during brushing which began approximately 45 days before referring to the department of oral and maxillofacial diseases, Mashhad Dental School. In intraoral examination, his gingiva had a papillomatous appearance and was purple in color (strawberry appearance). Due to the presence of strawberry appearance in absence of plaque, primary diagnosis of Wegener granulomatosis was established and the patient was referred for histopathological evaluation. In laboratory tests, C-ANCA was positive and P-ANCA was negative. Finally, diagnosis of Wegener granulomatosis was confirmed and his treatment was started. Rheumatologic condition of patient's lungs was evaluated by chest X-ray and CT-scan and blood tests, biochemistry tests and urine analysis were performed for the patient. He did not have pulmonary or renal involvement. In our study, the patient was followed up after 1, 2 and 11 months from the first visit. Discussion: Up to now, few reports have been published on Wegener disease with oral involvement and in most of these articles, Wegener was diagnosed after respiratory symptoms and kidney or other organs involvement. Only in few studies was Wegener diagnosis confirmed on the basis of oral symptoms and gingival involvement. Immediate and aggressive administration of immunotherapy treatments are required due to the fatal nature of the disease as the survival rate of patients with untreated WG is low and 90% of these patients die within 1 year after respiratory or kidney involvement .

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

wegener granulomatosis with oral involvement as primary manifestation: a case study

introduction: wegener granulomatosis is a rare multisystemic disease with an unknown cause, characterized by necrotic granulomatous lesions in respiratory tract, systemic vasculitis in small arteries and veins and necrotizing glomerulonephritis. wegener can affect any organ including kidneys, eyes or other organs but classically affects upper and lower respiratory tract. one of the rare but imp...

full text

Wegener Granulomatosis: Otologic Manifestation as First Symptom

Introduction Wegener granulomatosis is a systemic vasculitis affecting small and medium-sized vessels of the upper and lower respiratory tract and kidneys. Objective To describe a case of Wegener disease with atypical manifestation. Resumed Report We describe the case of a 50-year-old woman with chronic otitis media and sensorineural hearing loss as the primary symptoms, without other manifesta...

full text

[Wegener's granulomatosis with oral mucosal involvement as first manifestation].

Wegener’s granulomatosis (WG) is an autoimmune disease, which particularly affects the upper respiratory pathways, lungs and kidney. Oral mucosal involvement presents in around 5%--10% of cases and may be the first disease symptom. Predominant manifestation is granulomatous gingivitis erythematous papules; mucosal necrosis and non-specific ulcers with or without impact on adjacent structures. C...

full text

Wegener granulomatosis with meningeal involvement.

The clinical, radiographic, and neuropathologic features of the case of a 41-year-old man with Wegener granulomatosis presenting with neurologic symptoms are correlated. CT and MR scans of the head demonstrated extensive meningeal thickening and enhancement. The importance of considering this diagnosis, confirmed by antineutrophil cytoplasmic autoantibodies, is emphasized.

full text

Wegener s granulomatosis with granulomatous liver involvement.

We report on a patient with biopsy proven systemic Wegener's granulomatosis (WG) with a granulomatous necrotising manifestation of WG in the liver, lung, parotid gland and skin with subsequent death of liver failure. Liver involvement in WG is an exceedingly rare, though potentially fatal, organ manifestation of WG.

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 6  issue 2

pages  89- 95

publication date 2017-06-01

By following a journal you will be notified via email when a new issue of this journal is published.

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023