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An unexpected asymptomatic epiglottal site of Kimura disease.
Dezoteux, F; Dubois, R; Lefèvre, G; Lecoutre, J P; Staumont-Sallé, D; Carpentier, O.
Affiliation
  • Dezoteux F; Dermatology Department, University of Lille, CHU Lille, 2, avenue Oscar Lambret, 59000 Lille, France. Electronic address: fdezoteux@gmail.com.
  • Dubois R; Institute of Pathology, University of Lille, CHU Lille, 2, avenue Oscar Lambret, 59000 Lille, France.
  • Lefèvre G; Laboratory of Immunology and Clinical Immunology Unit, University of Lille, CHU Lille, 2, avenue Oscar Lambret, 59000 Lille, France.
  • Lecoutre JP; Otolaryngology Department, Victor Provo Hospital, 11, boulevard Lacordaire, 59100 Roubaix, France.
  • Staumont-Sallé D; Dermatology Department, University of Lille, CHU Lille, 2, avenue Oscar Lambret, 59000 Lille, France.
  • Carpentier O; Internal Medicine Department, Victor Provo Hospital, 11, boulevard Lacordaire, 59100 Roubaix, France.
Eur Ann Otorhinolaryngol Head Neck Dis ; 136(1): 47-49, 2019 Feb.
Article in En | MEDLINE | ID: mdl-30712651
ABSTRACT

INTRODUCTION:

Kimura disease (KD) is a chronic lymphoproliferative disorder of unknown etiology that affects the skin and lymph nodes, mostly observed in males of Asian descent. The natural history of asymptomatic epiglottal KD remains unknown. This rare site of KD is often only diagnosed when tumor growth starts to obstruct the upper airways. OBSERVATION A 34-year-old North African male presented with fatigue and multiple, slowly progressive, fluctuating skin nodules in the right mandibular and retroauricular regions. Computed tomography of the head and neck revealed a large soft tissue tumor close to the right mandibular body and unexpected thickening of the epiglottis. Transnasal laryngoscopy confirmed the CT findings and showed thickening of the epiglottis. The diagnosis of KD was based on histological examination of biopsy specimens taken from the right mandibular tumor, a cervical lymph node, and the epiglottis.

DISCUSSION:

Most cases of KD with epiglottal involvement present with dysphonia and dysphagia. No consensus guidelines are available concerning the complementary investigations that should be performed. This case report raises the question of whether patients with suspected KD should be systematically screened for lesions in unusual and potentially dangerous anatomic sites.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Laryngeal Diseases / Epiglottis / Angiolymphoid Hyperplasia with Eosinophilia Type of study: Guideline / Qualitative_research Limits: Adult / Humans / Male Language: En Journal: Eur Ann Otorhinolaryngol Head Neck Dis Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Laryngeal Diseases / Epiglottis / Angiolymphoid Hyperplasia with Eosinophilia Type of study: Guideline / Qualitative_research Limits: Adult / Humans / Male Language: En Journal: Eur Ann Otorhinolaryngol Head Neck Dis Year: 2019 Document type: Article