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Open AccessJournal ArticleDOI

Cheilitis Granulomatosa: A Review

William A. Critchlow, +1 more
- 01 Jun 2014 - 
- Vol. 8, Iss: 2, pp 209-213
TLDR
Cheilitis granulomatosa is a cosmetically disturbing and persistent idiopathic lip swelling that can occur by itself or as part of the Melkersson–Rosenthal syndrome, which includes facial palsy and a plicated tongue.
Abstract
Cheilitis granulomatosa (CG) is a cosmetically disturbing and persistent idiopathic lip swelling. It is one manifestation of orofacial granulomatosis (OFG), which is a clinical entity describing facial and oral swelling in the setting of non-caseating granulomatous inflammation and in the absence of systemic disease such as Crohn’s disease and sarcoidosis. CG can occur by itself or as part of the Melkersson–Rosenthal syndrome, which includes facial palsy and a plicated tongue. Other proposed causes of OFG include dietary allergens such as cinnamon and benzoates. Similar orofacial swelling may be an early manifestation of Crohn’s disease or sarcoidosis, and so clinical history is important in diagnosis. The cause of CG has not been wholly elucidated, but a current hypothesis holds that a random influx of inflammatory cells is responsible. Other granulomatous and edematous causes of lip swelling must be investigated prior to diagnosis. Options for treatment include dietary modifications, antibiotics, systemic or intralesional corticosteroids, and surgery, although treatment is not always necessary. CG should be considered in the differential of persistent lip swelling.

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Citations
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Journal ArticleDOI

Differential Diagnosis of Cheilitis - How to Classify Cheilitis?

TL;DR: Classification based on primary differences in the duration and etiology of individual groups of cheilitis is suggested, as follows: mainly reversible (simplex, angular/infective, contact/eczematous, exfoliative, drug-related); mainly irreversible (actinic, granulomatous), glandular, plasma cell.
Journal ArticleDOI

Melkersson⁻Rosenthal Syndrome in Childhood: Report of Three Paediatric Cases and a Review of the Literature.

TL;DR: Close multidisciplinary follow-up of these children with a team composed of paediatricians, neurologists, neuro-ophthalmologists, dermatologists, and otolaryngologists is crucial to guarantee exhaustive management and treatment success, while minimising relapses.
Journal ArticleDOI

Lip leishmaniasis: a case series with molecular identification and literature review.

TL;DR: Seven rare cases of lip leishmaniasis in Iran are reported, the importance of clinical and diagnostic features of lesions are emphasized, the phylogenetic kinship of isolated parasites are characterized, and the literature on lip leishingmaniasis is reviewed.
Journal ArticleDOI

Melkersson-Rosenthal syndrome: a case report of a rare disease with overlapping features.

TL;DR: A 71-year old, non-allergic female patient with no familial and personal history of angioedema presented, a few days after a possible herpes simplex or varicella-zoster virus infection, with monolateral facial paraesthesia and lower lip edema, and treatment failure with both drugs finally suggested a Melkersson–Rosenthal syndrome, which was confirmed by histologic findings of non caseating granulomas on lip biopsy.
Journal ArticleDOI

Dermatoscopy of Cutaneous Granulomatous Disorders.

TL;DR: In this paper, the authors discuss dermatoscopic findings of various granulomatous disorders and their pattern may also prove useful in distinguishing between various disorders, but detailed accurate assessment of various findings and their patterns may be useful in differentiating among them.
References
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Journal ArticleDOI

Orofacial granulomatosis--a 20-year review.

TL;DR: The aim of this review was to analyse the developments in the understanding of the aetiology, pathogenesis and treatment protocols, with particular emphasis on management and outcomes of OFG since this entity was first described in 1985.
Journal ArticleDOI

Cheilitis granulomatosa: overview of 13 patients with long-term follow-up--results of management

TL;DR: Although a relationship has been proposed between Melkersson–Rosenthal syndrome (and the monosymptomatic form, cheilitis granulomatosa) and Crohn’s disease on the basis of the orofacial swelling and similar histology, several studies of Melkerson– Rosenthal syndrome have not found an association with Crohn's disease.
Journal ArticleDOI

Improvement in orofacial granulomatosis on a cinnamon‐ and benzoate‐free diet

TL;DR: The impact of dietary manipulation in patients with OFG can be significant, particularly with regard to oral inflammation, and a CB‐free diet can be recommended as primary treatment.
Journal ArticleDOI

Distinguishing orofacial granulomatosis from crohn's disease: two separate disease entities?

TL;DR: Initial presentation of OFG does not necessarily predict development of CD, although this is more likely in childhood, and abnormalities in inflammatory markers, hematology and oral features of ulceration, and buccal‐sulcal involvement are factors more commonly associated with CD.
Journal ArticleDOI

Review article: cinnamon‐ and benzoate‐free diet as a primary treatment for orofacial granulomatosis

TL;DR: Improvements have been reported with cinnamon‐ and benzoate‐free diets and the aetiology remains unclear but may involve an allergic component.
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