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1.
Med Oral Patol Oral Cir Bucal ; 26(3): e357-e360, 2021 May 01.
Article in English | MEDLINE | ID: mdl-33340078

ABSTRACT

BACKGROUND: Exfoliative and erosive cheilitis, may be a source of speech and chewing discomfort, but may also be an aesthetic issue for the patients affected. Such a clinical presentation may implicate a variety of inflammatory conditions, including atopic (eczematous) cheilitis. Topical and systemic agents, e.g. corticosteroids, have been used to treat inflammatory lip conditions. Topical tacrolimus has also been used in some inflammatory lip conditions. MATERIAL AND METHODS: We performed a retrospective clinical analysis of atopic cheilitis patients. RESULTS: Between 2015 and 2020, we addressed 7 (seven) patients with atopic dermatitis affecting only lips and were diagnosed as atopic-eczematous cheilitis. They were treated with 0.03 per cent topical tacrolimus ointment and responded completely. CONCLUSIONS: These cases represent an underreported atopy / eczema event;-few cases of atopic cheilitis without concomitant dermal lesions appear in the literature. We are also showing and discussing yet another application of tacrolimus in a local atopic form of inflammation affecting the lips.


Subject(s)
Cheilitis , Tacrolimus , Administration, Topical , Cheilitis/drug therapy , Esthetics, Dental , Humans , Immunosuppressive Agents , Lip , Retrospective Studies , Tacrolimus/therapeutic use , Treatment Outcome
3.
Dermatology ; 228(2): 158-65, 2014.
Article in English | MEDLINE | ID: mdl-24557145

ABSTRACT

AIMS: To assess the efficacy and safety of rituximab in refractory pemphigus and the possible benefit of an additional prophylactic infusion at 6 months. METHODS: Seventeen patients with pemphigus vulgaris, 1 with pemphigus foliaceus and 1 with pemphigus vegetans were treated with 4 weekly infusions of rituximab (375 mg/m(2)). Nine patients received an additional prophylactic infusion after 6 months while the rest received no maintenance therapy. In case of recurrence, an additional single infusion was administered. RESULTS: Control of the disease was obtained after 3-8 weeks. End of the consolidation phase for all patients was observed after 16 weeks. Patients remained in full remission for 7-42 months. All immunosuppressive agents, including prednisone, were discontinued after 2-12 months. The disease relapsed in 5 out of 9 patients who received the additional prophylactic infusion, and in 3 out of 10 patients among those skipping the prophylactic additional infusion. CONCLUSION: One course of rituximab and treatment of relapses is highly effective and well tolerated in the treatment of refractory pemphigus. In this pilot study of 19 patients, the prophylactic infusion does not appear to have provided any additional benefit to the patients receiving it.


Subject(s)
Antibodies, Monoclonal, Murine-Derived/therapeutic use , Immunologic Factors/therapeutic use , Pemphigus/drug therapy , Adult , Aged , Antibodies, Monoclonal, Murine-Derived/administration & dosage , Dermatology , Female , Hospitals, University , Humans , Immunologic Factors/administration & dosage , Infusion Pumps , Male , Middle Aged , Pemphigus/diagnosis , Pilot Projects , Prospective Studies , Recurrence , Rituximab , Treatment Failure , Treatment Outcome
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