Abstracts
Melkersson-Rosenthal syndrome (MRS) consists of persistent or recurrent orofacial edema, relapsing facial palsy and fissured tongue. The complete triad of symptoms is uncommon, varying from 8 to 25%. The presentation of only one symptom is more common. The most frequent complaint is facial edema and enlargement of the lips. We describe a case of a 17-year-old Brazilian girl with limited edema of the lower lip and fissured tongue due to MRS. Her complaints had started two years before. She referred previous clinical treatments without success. We proposed intralesional injection of triamcinolone at 20 mg every 15 days associated with oral clofazimine at 50 mg/day for three months. The lip became normal after four triamcinolone injections. Recent studies have considered MRS a granulomatous disease, and possibly the initial presentation of Crohn’s disease in orofacial area of some patients. MRS patients, therefore, should be screened and monitored for gastrointestinal symptoms. Corticosteroid treatment seems to be effective in reducing lip enlargement. We discus the clinical features of this disease, the treatment, and the importance of corticosteroid therapy in cases of MRS-related facial palsy.
crohn’s disease; cheilitis; melkersson-rosenthal syndrome; treatment
A síndrome de Melkerson-Rosenthal (SMR) caracteriza-se por edema orofacial, paralisia facial recorrente e língua plicada. A tríade completa é incomum, com freqüência variando de 8 a 25%, sendo que a apresentação mais comum é a presença de somente um sintoma. A queixa mais freqüente é o edema facial e/ou no lábio. No presente relato, descreve-se o caso de uma jovem, 17 anos, com edema no lábio persistente e língua plicada devido à SMR. A paciente informou que o edema e as alterações na língua haviam se iniciado há 2 anos. Tratamentos prévios haviam sido realizados, porém sem sucesso. Propôs-se a injeção intralesional de 20mg de triancinolona a cada 15 dias, associada a 5mg ao dia de clofazimine por três meses. O lábio voltou ao seu aspecto normal após quatro infiltrações da medicação. Estudos recentes têm considerado a SMR como uma doença granulomatosa, sendo a fase inicial da apresentação orofacial da Doença de Crohn em alguns pacientes. Assim, pacientes com SMR deveriam ser avaliados e seguidos quanto à presença de sintomas gastroenterológicos. O tratamento com corticosteróides tem se mostrado efetivo em reduzir a tumefação do lábio associada a essa doença. Discute-se características clínicas, tratamento e importância da terapia com corticosteróides na paralisia facial associada à SMR.
doença de crohn; queilite; síndrome de melkersson-rosenthal; tratamento
CASE REPORT
Cheilitis granulomatosa associated with melkersson-rosenthal syndrome
Denise Utsch GonçalvesI; Mariana Moreira de CastroII; Cláudia Pena GalvãoII; Alexandre Zoni Rodrigues BrandãoIII; Míriam Cabral Moreira de CastroIV; José Roberto LambertucciV
IMedical doctor, ENT specialist, Adjunct Professor of the Ophthalmology, Otorhinolaryngology and Speech Therapy Department of the UFMG Medical School
IIMedical ENT resident, at the UFMG Clinical Hospital
III Medical ENT resident, at the UFMG Clinical Hospital G
IVMasters degree, medical doctor, ENT specialist. Teacher of the residency program on Otorhinolaryngology at the UFMG Clinical Hospital and the Santa Casa de Misericordia Hospital
VPost Doctor, internal medicine specialist, Adjunct Professor of the Internal Medicine Department of the UFMG Medical School
SUMMARY
Melkersson-Rosenthal syndrome (MRS) consists of persistent or recurrent orofacial edema, relapsing facial palsy and fissured tongue. The complete triad of symptoms is uncommon, varying from 8 to 25%. The presentation of only one symptom is more common. The most frequent complaint is facial edema and enlargement of the lips. We describe a case of a 17-year-old Brazilian girl with limited edema of the lower lip and fissured tongue due to MRS. Her complaints had started two years before. She referred previous clinical treatments without success. We proposed intralesional injection of triamcinolone at 20 mg every 15 days associated with oral clofazimine at 50 mg/day for three months. The lip became normal after four triamcinolone injections. Recent studies have considered MRS a granulomatous disease, and possibly the initial presentation of Crohns disease in orofacial area of some patients. MRS patients, therefore, should be screened and monitored for gastrointestinal symptoms. Corticosteroid treatment seems to be effective in reducing lip enlargement. We discus the clinical features of this disease, the treatment, and the importance of corticosteroid therapy in cases of MRS-related facial palsy.
Keywords: crohns disease, cheilitis, melkersson-rosenthal syndrome, treatment.
INTRODUCTION
Swelling of the lips, plicated tongue (lingua plicata), and recurring facial paralysis characterize the Melkersson-Rosenthal syndrome (MRS). The classical triad occurs in 8% to 25% of cases.1 Most of these cases present with few symptoms; the usual finding is granulomatous cheilitis (Mieshers cheilitis) which is the most common form.1
Mieshers cheilitis is characterized by recurring and painless localized lip swelling, and is part of the orofacial granulomatosis group (OFG).1 The chronic and recurring nature of the inflammation leads to fibrosis and permanent lip swelling, which makes treatment difficult, and relapses frequent. Histologically it is characterized by non-caseating granulomatous inflammation.2,3
Recent studies have suggested an association between the OFG and Crohns disease (CD), based on the histological similarity between both conditions and the occurrence of MRS manifestations as the initial presentation of CD.3,4 Conceivably these findings could be different presentations of the same entity.5
The aim of this study is to present the case report of a patient with granulomatous cheilitis and plicated tongue that had an excellent response to treatment with intralesional triamcinolone. We report the clinical progression, treatment options and the possible association between MRS and CD.
CASE REPORT
A female Caucasian patient aged 17 years presented progressive and persistent swelling of the lips during the last two years.
The physical examination showed localized swelling in the lower lip (Figure 1) and plicated tongue. Histology of the affected lip revealed inflammation consisting of non-caseating granulomas. An assessment of the digestive tract was within normal limits.
Treatment involved intralesional injection of a corticosteroid (triamcinolone 20mg/ml, 1ml each 15 days during 60 days) and clofazimine (50mg/day) during 90 days. The lip swelling reduced markedly after the first month of treatment. Full resolution occurred after 4 sessions of corticosteroid use.
DISCUSSION
Orofacial granulomatosis may precede or follow the diagnosis of CD by years. It could be seen as an oral mucosal manifestation of inflammation presenting in the digestive tract.5 Patients with MRS should be warned about the possible development of CD, and should undergo an assessment of the digestive tract.4,5
The accepted treatment of orofacial granulomatosis with lip swelling is the intralesional injection of corticosteroids, combined or not with oral clofazimine.3.6 Follow-up shows that local treatment alone is less effective than combined treatment with local corticosteroids and systemic anti-inflammatory drugs.6
CONCLUSION
The Melkerson-Rosenthal syndrome has been described as a granulomatous disease, which has implications for its treatment. Follow-up of granulomatous cheilitis has shown that intralesional triamcinolone combined with oral clofazimine is an effective treatment.
REFERENCES
Paper submitted to the ABORL-CCF SGP (Management Publications System) on August 15th, 2005 and accepted for publication on May 29th, 2006. cod. 654.
Minas Gerais Federal University (UFMG) - Medical School.
Ophthalmology, Otorhinolaryngology and Speech Therapy Department of the UFMG Medical School - Av. Prof. Alfredo Balena, 190, sala 3005, Bairro Santa Efigênia Belo Horizonte, MG, CEP 30130-100. FAPEMIG.
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1Sciubba JJ, Said-Al-Naief N. Orofacial granulomatosis: presentation, pathology and management of 13 cases. J Oral Pathol Med 2003;32:576-85.
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2Bogerieder T, Rogler G, Vogt T, Landthaler M, Stolz W. Orofacial granulomatosis as the initial presentation of Crohn disease in a adolescent. Dermatology 2003;206:273-8.
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3El Hakim M, Chauvin P. Orofacial granulomatosis presenting as a persistent lip swelling: review of 6 new cases. J Oral Maxillofac Surg 2004;62:1114-7.
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4Van de Scheur MR, Van der Waal RIF, Volker-Dieben HJ, Klinkeberg-Knol EC, Starink TM. Orofacial granulomatosis in a patient with Crohns disease. J Am Acad Dermatol 2003;49:952-4.
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5Lloyd DA, Payton KB, Guenther L, Frydman W. Melkersson Rosenthal syndrome on Crohns disease: one disease or two? Report of a case and discussion of the literature. J Clin Gastroenterol 1994;18:213-7.
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6Mignogna MD, Fedele S, Lo Russo L, Adamo D, Satriano RA. Effectiveness of small-volume, intralesional delayed-release triamcinolone injections in orofacial granulomatosis: a pilot study. J Am Acad Dermatol 2004;51:265-8.
Publication Dates
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Publication in this collection
16 May 2007 -
Date of issue
Feb 2007
History
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Received
15 Aug 2005 -
Accepted
29 May 2006