Issue |
J Oral Med Oral Surg
Volume 24, Number 1, January 2018
|
|
---|---|---|
Page(s) | 22 - 23 | |
Section | Cas clinique / Short case report | |
DOI | https://doi.org/10.1051/mbcb/2017035 | |
Published online | 25 May 2018 |
Short Case Report
Sjögren syndrome hidden by previous parotidectomy and cervicofacial radiotherapy
1
Center Léon Bérard, Surgical Department,
28 rue Laennec,
69008
Lyon, France
2
Faculty of Dentistry,
11 rue Guillaume Paradin,
69008
Lyon, France
* Correspondence: anne-gaelle.bodard@lyon.unicancer.fr
Received:
1
September
2017
Accepted:
3
October
2017
Introduction: Sjögren’s syndrome (SS) is a chronic inflammatory auto-immune disease of the exocrine glands which incidence increases with age. Sex ratio is 9.9 female for 1 male. Observation: A 67-year-old female patient presented for xerostomia leading to major functional impairment. The medical history of the patient was pulmonary sarcoidosis, with join and adenoid involvement, considered as cured; left partial parotidectomy, with a diagnosis of acinous carcinoma, followed 7 years later by a total parotidectomy due to tumor recurrence, and followed by external radiotherapy (70 Gy). Arterial hypertension, hypothyroïditis and diabetes mellitus were also noticed. She reported xerostomia and xerophtalmia. Seric anti-SSA antibodies were positive and histologic findings were compatible with SS. Commentaries: Despite other co-morbidities, the diagnosis was hidden by previous parotidectomy and cervical radiotherapy. Thus, SS should not be underdiagnosed in patients with complex medical history.
Key words: syndrome / Sjögren / xerostomy
© The authors, 2018
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