Mucous Membrane Disorders




Abstract


Examination of the oral cavity can provide important diagnostic information for dermatologic diagnosis and therefore should be included in every skin examination. A variety of skin disorders can be accompanied by mucous membrane involvement. For example, erythema multiforme and systemic lupus erythematosus can cause erosions in the mouth, nose, or eyes. However, this chapter focuses on disorders either exclusively or predominantly confined to mucous membranes, usually of the oral cavity.


Mucous membrane disorders are divided into two broad categories: (1) erosions and ulcerations and (2) white lesions ( Table 22.1 ). Erosions are lesions in which the mucosal epithelium is partly denuded. Ulcerations extend through the epidermis into the underlying tissue, which in mucous membranes is called lamina propria rather than dermis. Erosive and ulcerative diseases range in frequency from common (aphthous stomatitis) to rare (pemphigus), and their causes are idiopathic, immunologic, infectious, and malignant.








Categorization of mucous membrand disorders:



  • 1.

    Erosions and ulcerations


  • 2.

    White lesions




Table 22.1

Mucous Membrane Disorders


























































































Etiology History Physical Examination Differential Diagnosis Laboratory Test
Ulcers
Aphthous stomatitis (common cause) Unknown Recurrent disease Sharply demarcated, round, yellowish erosions surrounded by erythema Herpes simplex
Behçeťs syndrome
Inflammatory bowel disease
Pemphigus and pemphigoid (uncommon causes) Autoimmune May have associated skin lesions Ragged erosions and ulcerations; intact blisters rarely present Aphthous stomatitis
Erythema multiforme
Biopsy with immunofluorescence
Viral infections Primary herpes simplex
Coxsackievirus
Fever, malaise Gingivitis; blisters also on lips Aphthous stomatitis
Erythema multiforme
Tzanck smear or culture
Fever Vesicles in posterior oral cavity Aphthous stomatitis
Syphilis Treponema pallidum Sexual contact Indurated , painless ulcer Malignancy Serologic test for syphilis
Deep fungal infection Histoplasmosis Immunosuppressed Systemically ill; indurated ulcer Malignancy Biopsy with culture
Malignancy Nonhealing ulcer Indurated ulcer Major aphthous ulcer Biopsy
White lesions
Thrush Candida albicans Found in newborns and immunosuppressed patients “Curd-like” papules, easily scraped off Lichen planus
Geographic tongue
KOH preparation
Lichen planus Unknown Chronic disease; may have associated skin lesions Reticulated white lines; sometimes erosions are present Candidiasis
Leukoplakia
Secondary syphilis
Biopsy
Leukoplakia Chronic irritation Smoking
Denture trauma
White patches and plaques Lichen planus
Secondary syphilis
White sponge nevus
Leukokeratosis
Biopsy
Squamous cell carcinoma Smoking
Alcohol
Prior leukoplakia
Indurated or ulcerated plaque Leukoplakia
Major aphthous ulcer
Erosive lichen planus
Chancre
Deep fungal infection
Biopsy

KOH, Potassium hydroxide.


White spots are hyperkeratotic lesions of the oral mucosa. Thickened stratum corneum of mucous membranes appears white because of maceration from continuous wetness. Malignancy must be ruled out as a cause.




White lesions represent hyperkeratosis.





Aphthous Stomatitis




Key Points




  • 1.

    Most common cause of recurrent oral ulcers


  • 2.

    Ulcers have a yellow base and peripheral erythema


  • 3.

    Multiple therapies indicate lack of effective treatment




Definition


Aphthous stomatitis is a common, recurrent, idiopathic disorder of the mouth most often manifest by multiple small, “punched-out” ulcers ( Fig. 22.1 ).




Figure 22.1


Aphthous stomatitis – round, punched-out ulcer with a white-yellow necrotic surface.


Incidence


Recurrent aphthous stomatitis is a common disease, occurring in 20% to 60% of the general population. It is most common in young adults; the 60% prevalence was found in a survey of students attending professional schools.


History


A history of previous episodes is invariable. Recurrences are sometimes precipitated by trauma from biting or misguided toothbrushes. Some patients correlate outbreaks with emotional stress. Lesions are usually preceded by a 1-day prodrome of discomfort in the area of involvement. The ulcers are painful and sometimes interfere with eating.


Physical Examination


Lesions in aphthous stomatitis appear as 2- to 5-mm, round, punched-out ulcers with a yellowish necrotic surface and surrounding erythema. Lesions may be single but more often are multiple. The buccal and labial mucosae are the most common locations.




Aphthous stomatitis is the most common cause of oral ulceration.



Differential Diagnosis


Recurrent aphthous stomatitis is most often confused with herpes simplex infection . Recurrent herpes simplex rarely occurs inside the mouth. When it does, it appears as grouped small vesicles or erosions on an erythematous base. A Tzanck preparation or culture proves the diagnosis of herpes infection.




Herpes simplex rarely recurs inside the mouth.



The oral ulcerations in Behçeťs syndrome are indistinguishable from those of aphthous stomatitis. However, Behçeťs syndrome is distinguished by its extraoral manifestations. The classic triad consists of oral ulcerations, genital ulcerations, and ocular inflammation (iridocyclitis) ( Fig. 22.2 ). Erythema nodosum, thrombophlebitis, arthritis, and neurologic and intestinal involvement may also occur. Patients with inflammatory bowel disease, particularly ulcerative colitis , occasionally have oral ulcerations that resemble aphthous stomatitis.




Oral ulcerations in Behçeťs syndrome look like aphthous stomatitis.



Differential Diagnosis for Aphthous Stomatitis





  • Herpes simplex infection



  • Behçeťs syndrome



  • Oral ulcers from inflammatory bowel disease







Figure 22.2 A.


Behçeťs syndrome. A . Oral ulcers on hard palate. B . Erosions on the penis.


Laboratory and Biopsy


Usually, a biopsy is not required. If a biopsy is performed, the findings will not be diagnostic and will show only ulceration and nonspecific inflammation, composed primarily of lymphocytes. The only other laboratory test to consider is a complete blood count, to screen for the questionable association of iron or folate deficiency anemia in some patients with aphthous stomatitis.


Therapy


The variety of therapies that have been recommended for this disease indicates that a highly successful treatment is lacking. If an underlying iron or folate deficiency is detected, it should be corrected. The ulcerations are usually treated topically. Tetracycline suspension (250 mg/5 mL) “swished and swallowed” four times daily helps in some patients. Patients in whom tetracycline therapy fails are treated with topical steroids in a gel (e.g., fluocinonide, Lidex gel) or a special adherent base (e.g., triamcinolone, Kenalog in Orabase) applied three times daily or with a spray preparation (e.g., beclomethasone, Vanceril) applied three to four times daily. Intralesional steroids (triamcinolone, Kenalog-10) are useful in patients with large aphthous ulcerations. Oral prednisone is effective in aphthous stomatitis but should be used for only a short course in patients with severe, incapacitating disease. Colchicine and pentoxifylline (Trental) have also been reported to be helpful in preventing recurrent disease, but the clinical trials were not controlled.


Pain relief can be obtained with topical anesthetics such as dyclonine hydrochloride (Dyclone liquid) or topical lidocaine (viscous Xylocaine) used 20 minutes before meals. These preparations numb the entire mouth, including the taste buds, for 1 to 2 hours and allow for pain-free, albeit taste-free, dining.



Therapy for Aphthous Stomatitis


Initial





  • Topical steroids




    • Fluocinonide gel 0.05%



    • Triamcinolone in Orabase




  • Tetracycline “swish and swallow”



  • Dyclonine hydrochloride 1% solution



  • Lidocaine jelly 2%



Alternative





  • Intralesional triamcinolone



  • Systemic treatment (colchicine/pentoxifylline)




Course and Complications


For minor aphthous stomatitis, spontaneous healing occurs within 4 to 14 days. Large aphthous ulcers (major aphthous ulcers) take as long as 6 weeks to heal. Individual ulcers lasting much longer than that should be examined by biopsy to rule out malignancy. Recurrences are common and range in frequency from occasional to almost continuous. In most patients, the disease eventually remits, but the time course is highly variable – from 5 to 15 years or longer.


Pathogenesis


Factors implicated in the pathogenesis include emotional and physical stress, hormones, infection, and autoimmunity. An immune mechanism is the most favored cause. Circulating T lymphocytes cytotoxic against oral mucosa have been identified and appear to play a role.




Leukoplakia




Key Points




  • 1.

    White plaques can signify cancer


  • 2.

    Indurated white plaques require biopsy


  • 3.

    Smoking is most frequent cause




Definition


Leukoplakia literally means “white plaque” ( Fig. 22.3 ). Some clinicians simply use that as the definition of the disease, defining leukoplakia as “a white patch or plaque that cannot be characterized clinically or pathologically as any other disease.” Others use the term leukokeratosis to describe a white patch that is histologically benign, and reserve the term leukoplakia for a white patch or plaque in which epithelial dysplasia is present pathologically. The authors prefer the second definition. Either way, the important point to remember is that, for white plaques on mucous membranes, a dysplastic change should be considered a possible cause.


Mar 20, 2019 | Posted by in Dermatology | Comments Off on Mucous Membrane Disorders

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