Literature DB >> 31980882

Mucous membrane pemphigoid-otorhinolaryngological manifestations: a retrospective cohort study.

Ory Madgar1,2, Avital Baniel3,4, Noam Yarom5,4,6, Eran Glikson7,4, Tal Zeeli3, Eli Sprecher3,4, Eran E Alon7,4.   

Abstract

INTRODUCTION: Mucous membrane pemphigoid (MMP) refers to a heterogeneous group of rare, chronic, inflammatory, mucous membrane-dominated, sub-epithelial blistering diseases that manifest with a varying constellation of oral, ocular, cutaneous, genital, nasopharyngeal, esophageal, and laryngeal lesions. MMP can progress to scarring in affected areas, which may lead to devastating complications including ocular involvement leading to blindness as well as laryngeal involvement leading to airway obstruction.
MATERIALS AND METHODS: A retrospective chart review was conducted for patients that were followed in two tertiary academic centers between 2009 through 2017 for upper aerodigestive tract manifestations of MMP. Patients with significant underlying skin involvement suggestive of bullous pemphigoid as well as MMP with isolated ocular involvement were excluded.
RESULTS: Twenty-seven patients were diagnosed with MMP and followed in two tertiary referral medical centers. The most common site of initial presentation was the oral cavity, and all patients had oral cavity involvement at some point. Two-thirds of our patients had complete remission or remission with intermittent relapses disease. Patients with mild to moderate disease showed excellent response to topical steroid treatment. For more severe disease, high-dose prednisone was insufficient, as in most cases relapse occurred at some point of time during tapering down.
CONCLUSIONS: MMP is a rare autoimmune disorder that may present with a wide spectrum of head and neck manifestations and, potentially, catastrophic sequelae. This work highlights the experience of two tertiary centers with MMP in an attempt to draw attention to this unusual disorder.

Entities:  

Keywords:  Bullous disease; MMP; Mucous membrane pemphigoid; Pemphigoid

Mesh:

Year:  2020        PMID: 31980882     DOI: 10.1007/s00405-020-05812-3

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  3 in total

Review 1.  Blistering mucocutaneous diseases of the oral mucosa--a review: part 2. Pemphigus vulgaris.

Authors:  Mark R Darling; Tom Daley
Journal:  J Can Dent Assoc       Date:  2006-02       Impact factor: 1.316

Review 2.  Blistering mucocutaneous diseases of the oral mucosa--a review: part 1. Mucous membrane pemphigoid.

Authors:  Mark R Darling; Tom Daley
Journal:  J Can Dent Assoc       Date:  2005-12       Impact factor: 1.316

3.  Describing the gingival involvement in a sample of 182 Italian predominantly oral mucous membrane pemphigoid patients: A retrospective series.

Authors:  P-G Arduino; R Broccoletti; M Carbone; D Conrotto; E Pettigiani; S Giacometti; A Gambino; A Elia; M Carrozzo
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2017-03-01
  3 in total

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