|Year : 2019 | Volume
| Issue : 6 | Page : 499-506
Bullous lichen planus: Case report and review
Abhilesh Babu1, Sreeja Chellaswamy2, Sathish Muthukumar2, Bhavna Pandey2, Merlin Jayaraj2, Serena Francis2
1 Department of Oral and Maxillofacial Pathology, Chettinad Dental College and Research Institute, Kelambakkam, Tamil Nadu, India. Current address: Chettinad Dental Collge and Research Institute, Kelambakkam, Tamil Nadu, India
2 Department of Oral and Maxillofacial Pathology, Chettinad Dental College and Research Institute, Kelambakkam, Tamil Nadu, India
|Date of Web Publication||28-May-2019|
Dr. Abhilesh Babu
Chettinad Dental College and Research Institute, Kelambakkam, Tamil Nadu
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Lichen planus is a chronic inflammatory mucocutaneous disorder that is seen in skin and oral mucosa. Definitive etiology for oral lichen planus remains unknown. It may or may not be associated with skin lesions. Different clinical patterns such as reticular, plaque, erosive, bullous, and atrophic are seen in oral mucosa of which bullous lichen planus is a rare entity. We present a unique case of bullous lichen planus in a 20-year-old male without skin manifestations along with the review of literature comprising various case reports of bullous lichen planus.
Keywords: Biopsy, bullous lichen planus, histopathology, review
|How to cite this article:|
Babu A, Chellaswamy S, Muthukumar S, Pandey B, Jayaraj M, Francis S. Bullous lichen planus: Case report and review. J Pharm Bioall Sci 2019;11, Suppl S2:499-506
|How to cite this URL:|
Babu A, Chellaswamy S, Muthukumar S, Pandey B, Jayaraj M, Francis S. Bullous lichen planus: Case report and review. J Pharm Bioall Sci [serial online] 2019 [cited 2019 Jun 18];11, Suppl S2:499-506. Available from: http://www.jpbsonline.org/text.asp?2019/11/6/499/258884
| Introduction|| |
Oral lichen planus is a chronic inflammatory mucocutaneous disorder that is T-cell mediated. Prevalence of oral lichen planus in Indian population is 2.6%. Women have higher predisposition to oral lichen planus and the condition is seen at the peak age of 30–60 years. Commonly seen variant of oral lichen planus is reticular type whereas erosive type of lichen planus is the second most common type.
Bullous lichen planus (BLP) is relatively a rare variant of lichen planus. Most patients with BLP are associated with multifocal involvement and skin lesions. BLP is commonly associated with burning sensation and pain. Presence of bullae is seen in association with the white striae. Clinically, at times BLP can be presented as erosive lichen planus as the fragile bullae formed can easily get ruptured, which makes it difficult to diagnose. If the erosive component is severe, epithelial separation from the underlying mucosa may occur, which leads to bullae formation. An unambiguous aspect of the etiology and pathogenesis of BLP is not well established, owing to a relatively low number of cases reported.
| Case Report|| |
A 21-year-old male patient reported to the Dental outpatient department of Chettinad Dental College and Research Institute with a chief complaint of reddish white patches on his right inner cheek region and palate for past 2 months with associated burning sensation. Patient gave a clinical history of a small swelling that was seen in the palate initially. He felt fluid-filled swelling that ruptured subsequently. The reddish-white lesion in the palate enlarged to the present size. A similar lesion was noted around the same period in the right buccal mucosa. The patient was previously under topical antifungal therapy that temporarily reduced the burning sensation.
Patient had no relevant medical, dental, or familial history and maintained good oral hygiene. He had no chewing or smoking habit and consumes spicy foods.
On inspection of right buccal mucosa [Figure 1], a single erythematous lesion with radiating white striae was seen of size 4×2 cm at the level of occlusal plane extending anteriorly from 45 to distal aspect of 47 posteriorly. It was soft in consistency with elevated white irregular margins. Over the palate [Figure 2], a single elevated erythematous lesion interspersed with white striae was seen measuring 4×4cm; extending anteriorly 1cm behind the incisive papilla; posteriorly up to fovea palatina; laterally 5mm below the free gingival margins of 16, 17, 26, and 27; and posteriorly extending to 1cm above the soft palate. The lesion did not affect the palatal rugae and incisive papilla but had covered the mid-palatine raphae. The lesion contained multiple minute round erythematous projections of varying sizes surrounded by white striae. The surface was rough and non-tender on palpation. The patient presented with no other skin abnormalities.,
Correlating with the clinical history and presentation, the lesion was provisionally diagnosed as “bullous lichen planus,” along with lichen planus pemphigoides, pemphigus, pemphigoid, allergic stomatitis, erythroleukoplakia, and erythematous candidiasis.
Patient’s basic hematological parameters were evaluated and found to be within normal limits. Patient was referred for incisional biopsy of the lesion.
Macroscopic findings: Two bits of soft tissue specimen were placed in 10% formalin. Specimens were taken from right buccal mucosa and palate. Both the tissues processed for histopathological evaluation.
Microscopic findings: Orthokeratinized stratified squamous epithelium of varying thickness with flat to elongated rete pegs. Areas of basal cell degeneration were evident. Juxta-epithelial connective tissue shows dense infiltration of chronic inflammatory cells of lymphocytes interspersed with increased capillaries. Presence of intraepithelial cleft [Figure 3] and [Figure 4].
|Figure 3: Acanthosis, juxta epithelial connective tissue shows dense infiltration of inflammatory cells interspersed with increased capillaries|
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|Figure 4: The rate process are flat to elongated areas of basal cell degeneration; presence of intra-epithelial cleft is evident|
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On the basis of the histopathological features, the lesion in right buccal mucosa and palate was diagnosed as BLP.
Patient was advised for medical and stress management. He was advised to take prednisolone 20mg and was tapered over period of 6 weeks. Topical application of Kenacort was also prescribed to the patient. Regression of lesion was seen completely over the end of 6 weeks.
| Discussion|| |
Lichen planus is a chronic inflammatory autoimmune disease in which autoantibodies are generated against the basal keratinocytes, leading to its degeneration. The etiology of the lesion is not well defined although stress is a commonly associated factor in these patients. Cell-mediated immunity is mostly responsible for the pathogenesis of oral lichen planus (OLP). It could be either triggered by endogenous or exogenous factors. Exogenous factors include drugs, restoration, infections, and food allergies. Endogenous factors include genetic factors and autoimmunity.
The characteristics of lichen planus are flattened, polygonal, pruritic, and violaceous papules with grayish-white scaly surfaces. The sites affected usually include flexor surfaces of wrists, forearms, dorsal surfaces of hands, shins, and genital areas.
Andreasen has classified oral lichen planus into reticular, papular, plaque, atrophic, erosive, and bullous. The commonly presented variant is reticular, which presents the characteristic clinical feature called Wickham’s striae that is seen as interlacing white lines. Most frequently affected site is buccal mucosa. Other commonly affected sites are tongue, gingiva, and lower lip.
Other rare variants of lichen planus that are seen are annular lichen planus, lichen planus pigmentosus, and lichen planus planopilaris. Erosive lichen planus in which the genital areas and gingiva are affected together is referred as vulvovaginal-gingival syndrome (female equivalent)/penogingival syndrome (male equivalent) and collectively called as “genito-gingival syndrome.” Lichen planus lesions replacing hair follicles with scarring tissue have also been reported. This type is called lichen planus planopilaris, which is more seen in women. This type has also been reported under BLP cases. There are three types: classic lichen planus planopilaris, with frontal fibrosing alopecia, which mostly affects postmenopausal women and Graham Little syndrome in which scarring alopecia is seen in scalp only, involving loss of hair in pubis or axilla or other areas.
Bullous lichen planus
There are two variants of BLP: familial and nonfamilial. The familial variant is more common than the nonfamilial variant. Familial BLP occurs at an earlier age with longer duration of disease and more extensive eruptions, and increased tendency to involve nails is seen in familial BLP when compared to nonfamilial variants. Pathogenesis of familial variants maybe attributable to genetic factors.
In BLP, blisters develop adjacent to or on preexisting lichen plants lesions in oral mucosa as well as lower extremities. It might be associated with alopecia. BLP that affects nails appear as hemorrhagic crusty lesions resulting in exposure of nail bed and finally nail atrophy.
Oral BLP is associated with cutaneous lesions. The lesion can be seen with an intact bullae or eroded surface superimposed or juxtaposed with white striae.
Demographic data and history
On the review of the aforementioned articles [Table 1], oral BLP shows no clear gender predilection with peak of incidence occurring at third to sixth decade of life. The medical and dental history does not reveal a clear establishment between systemic conditions and oral BLP. However, a special condition of oral BLP occurs due to the usage of a drug—labetalol. It shows the importance of ruling out the drug history in diagnosing oral BLP. Two case reports show patients with dermal disease developing oral BLP. No habitual or familial history is seen in these patients. The patients mostly have a complaint of burning sensation or pain or both in their oral cavity. Most commonly associated factor in these case reports is the consumption of spicy food. The presented case of 21-year-old male patient has spicy dietary habits and was subjected to a stressful lifestyle.
On the review of the aforementioned articles [Table 2], oral BLP shows skin manifestations in almost all cases except one. Oral BLP shows an earlier onset of lesions over the extremities especially the lower and later spreads to the body. Pruritic violaceous papular appearance is seen in most cases, which is accompanied by bullae formation later associated with pigmentations. The bullae contain clear fluid. Most commonly affected intraoral site is buccal mucosa, seldom arising in tongue, palate, and labial mucosa. Oral BLP shows bilateral occurrence in almost all cases. The lesion appears to be seen as an erythematous area/intact bullae in the center surrounded by white striae at the periphery. The patient presented with only oral manifestations without the involvement of any skin lesions. The unilateral buccal lesion in this case shows erythematous center surrounded by interspersed white striae and light pigmentation. It was soft in consistency. The palatal lesion was elevated with multiple minute round erythematous projections of varying sizes interspersed with white striae.
Diagnosis of oral lichen planus can be clinically verified with the presence of pathognomic appearance of Wickham’s striae in reticular lichen planus bilaterally. The definitive diagnosis for oral lichen planus can be rendered only with histological evaluation of the lesion.
The differential diagnosis of oral BLP can be lichen planus pemphigoides, pemphigus, pemphigoid, allergic stomatitis, erythroleukoplakia, and erythematous candidiasis.
BLP is commonly misdiagnosed as lichen planus pemphigoid. In lichen planus lichenoids (LPP), the lesions that developed were mostly de novo are on previously existing lichen planus (LP) lesions. Rarely in LPP, bullae would develop only in lesion without affecting the surrounding skin. Hence this makes the differentiation even more difficult. LPP has the presence of circulating autoantibodies in the blood that are absent in BLP. Possibility of drug/restorative material induced lichenoid reactions should also be ruled out.
Commonly performed investigations in BLP are hemogram, renal and liver function tests, anti-hepatitis B and C tests, and urine analysis [Table 3]. Blood picture is commonly taken to rule out any nutritional deficiencies such as iron deficiency or immunodeficiency, which could be the underlying cause for lichen planus. There have been several surveys conducted, which established a strong relationship between hepatitis B/hepatitis C infected patients to occurrence of oral lichen planus in them. Liver function tests are performed to rule out chronic liver disease, which shows strong relation to OLP. The most common ones are chronic active hepatitis and primary biliary cirrhosis. LP patients are prone to urolithiasis. Renal function tests/urine analysis can also be performed in precaution to see the presence of any renal problem. Immunofluorescence is carried out to rule out lichen planus pemphigoides. Cytosmear is taken to rule out any candida super-infection. Biopsy is the confirmatory test to diagnose BLP. The set criteria of histopathological features can only confirm the presence of BLP. In the case presented, blood picture and biopsy were performed to confirm the diagnosis of BLP.
In most cases, the lesions depict hyperkeratosis with hypergranulosis or acanthosis or both [Table 4]. Moderate-to-dense lymphocytic band is seen mostly in papillary dermis. Basal cell degeneration is seen in most of the cases reported. Presence of saw-tooth rete ridges is seen rarely. Clear epithelial or subepithelial clefts are present in most of the cases with the presence of civatte or colloid bodies. The histopathology of our patient was also similar to that of BLP in the literature with absence of civatte or colloidal bodies.
Systemic drugs such as prednisolone or topical application such as triamcinolone when used separately or together give good prognosis [Table 3]. Phototherapy such as broadband ultraviolet-B therapy has proven to help in the eradication of BLP. Usage of retinoids such as tretinoin can also help in controlling the lesions. Usage of immunomodulators such as tacrolimus/pimecrolimus has helped in the control of autoimmune activity, which helps in the regression of BLP. Oral minipulse therapy in which betamethasone 5mg is given once daily over two consecutive days in a week. This has proven to be very effective in eradicating the lesion. Clobetasol has poor prognosis as the lesion persisted even after using it. Adjuvant drugs such as benzydamine oral rinse and topical clotrimazole can also be given. The patient was under the medication of prednisolone 20mg and topical application of triamcinolone 0.1% for 6 weeks. The dosage of prednisolone was tapered over 6 weeks. He was also advised for stress management. The lesion regressed completely after 6 weeks.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3], [Table 4]