Rhinoscleroma: a French national retrospective study of epidemiological and clinical features

Loïc de Pontual1, Philippe Ovetchkine, Diana Rodriguez

  • 1Assistance Publique-Hôpitaux de Paris, Service de Pédiatrie, Université Paris 13, Hôpital Jean Verdier, Bondy, France.

Abstract

Insights

Rhinoscleroma (RS) is a rare upper respiratory tract disease. Familial cases suggest host genetics influence disease development, impacting pathogenesis in endemic areas.

Area of Science:

  • Infectious Diseases
  • Genetics
  • Otolaryngology

Background:

  • Rhinoscleroma (RS) is a rare, chronic granulomatous upper respiratory tract disease.
  • It is caused by Klebsiella rhinoscleromatis infection.
  • Risk factors and pathogenesis of RS remain unclear, despite geographic prevalence.

Purpose of the Study:

  • To investigate risk factors and pathogenesis of Rhinoscleroma (RS).
  • To identify potential genetic influences on host response to Klebsiella rhinoscleromatis.

Main Methods:

  • Retrospective review of 11 Rhinoscleroma (RS) cases diagnosed between 1990-2005 in French University Hospitals.
  • Standardized questionnaire sent to pathologists and otolaryngology specialists.
  • Analysis of patient history, clinical presentation, diagnostic findings, treatment, and follow-up.

Main Results:

  • Eleven RS cases identified, median age 35.7 years.
  • Three patients with familial history presented with early-onset disease; two consanguineous families identified.
  • Most patients were immigrants from RS-endemic areas; HIV infection noted in two sporadic cases.
  • Klebsiella rhinoscleromatis confirmed in 5/11 biopsies; granulomas with Mikulicz cells observed in all.
  • Eight patients showed no relapse after prolonged antibiotic treatment.

Conclusions:

  • Early-onset RS in familial/consanguineous cases suggests host genetic control.
  • Genetic factors may play a role in Rhinoscleroma pathogenesis in endemic regions.
  • Further research into host-pathogen interactions is warranted.

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