10 research outputs found

    Isolated lip dermatitis (atopic cheilitis), successfully treated with topical tacrolimus 0.03%

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    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. We performed a retrospective clinical analysis of atopic cheilitis patients. 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. 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

    Study of Langerhans cells in oral squamous cell carcinoma: immunohistochemical identification with S-100 protein

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    IN THE PRESENT STUDY AN EFFORT WAS MADE TO INVESTIGATE ORAL SQUAMUS CELL CARCINOMA FOR THE PRESENCE OF LANGERHANS CELLS (L.C) IN FORMALIN-FIXED, PARAFIN-EMBEDED MATERIAL, BY USING S-100 PROTEIN IN THE INDIRECT IMMUNOPEROXIDASE METHOD. ITWAS FOUND THAT: 1) S-100 PROTEIN IS A GOOD MARKER FOR THE IMMUNOHISTOCHEMICAL IDENTIFICATION OF L.C IN ORAL SQUAMUS CELL CARCINOMA, IN PARAFIN SECTIONS. 2) THE INDIRECT IMMUNOPEROXIDASE METHOD AS WE USED IT IN COMBINATION WITH TRYPSIN, GIVES SATISFACTORY RESULTS FOR THE DEFINITION OF S-100 POSITIVE L.C. 3) A GREATER NUMBER OF L.C IN THE NEOPLASTIC EPITHELIUM OF ORAL SQUAMUS CELL CARCINOMA INCOMPARISON WITH THAT OF THE CONNECTIVE TISSUE ADJACENT TO THE NEOPLASTIC EPITHELIUM AND IN THE NON- NEOPLASTIC EPITHELIUM IS A STATISTICALLY SIGNIFICANT DIFFERENCE. 4) THE NUMBER OF L.C IN THE CONNECTIVE TISSUE, ADJACENT TO THE NEOPLASTIC EPITHELIUM WAS GREATER THAN THAT OF THE LAMINA PROPRIA OF THE NON-NEOPLASTICEPITHELIUM IN A STATISTICALLY SIGNIFICANT DIFFERENCE AS WELL. 5) THERE WAS A POSITIVE RELATIONSHIP BETWEEN THE NUMBER OF L.C AND THE NUMBER OF LYMPHOCYTES INTHE CONNECTIVE TISSUE ADJACENT TO THE NEOPLASTIC EPITHELIUM. THE FINDINGS ARE INDICATIONS OF A LOCAL IMMUNOLOGIC REACTIONS OF THE HOST TOWARDS THE DEVELOPINGTUMOR, WHICH THROUGH THE IMMUNOLOGIC FUNCTIONS OF L.C AND THE LYMPHOCYTES OF ORAL MUCOSA AND PARTICULARLY THROUGH OF L.C FOR PRESENTING ANTIGENS TO T-LYMPHOCYTES.ΟΙ ΑΝΟΣΟΒΙΟΛΟΓΙΚΕΣ ΔΙΕΡΓΑΣΙΕΣ ΣΤΟ ΒΛΕΝΝΟΓΟΝΟ ΤΟΥ ΣΤΟΜΑΤΟΣ ΠΙΣΤΕΥΕΤΑΙ ΟΤΙ ΠΡΑΓΜΑΤΟΠΟΙΟΥΝΤΑΙ ΚΥΡΙΩΣ ΜΕ ΤΑ LANGERHANS ΚΥΤΤΑΡΑ. ΓΙ'ΑΥΤΟ ΣΚΟΠΟΣ ΤΗΣ ΕΡΓΑΣΙΑΣ ΑΥΤΗΣ ΕΙΝΑΙ Η ΔΙΕΡΕΥΝΗΣΗ ΤΟΥ ΑΚΑΝΘΟΚΥΤΤΑΡΙΚΟΥ ΚΑΡΚΙΝΩΜΑΤΟΣ ΤΟΥ ΣΤΟΜΑΤΟΣ ΓΙΑ ΝΑ ΕΞΑΚΡΙΒΩΘΕΙ Η ΤΥΧΟΝ ΠΑΡΟΥΣΙΑ ΚΑΙ Η ΕΝΔΕΧΟΜΕΝΗ ΑΥΞΗΣΗ 'Η ΜΕΙΩΣΗ ΤΩΝ LANGERHANS ΚΥΤΤΑΡΩΝ Σ'ΑΥΤΟ. ΩΣ ΜΕΘΟΔΟΣ ΑΝΙΧΝΕΥΣΗΣ ΤΩΝ ΚΥΤΤΑΡΩΝ ΑΥΤΩΝ ΧΡΗΣΙΜΟΠΟΙΗΘΗΚΕ Η ΑΝΟΣΟΙΣΤΟΧΗΜΙΚΗ (ΕΜΜΕΣΟΣ ΑΠΕΡΟΞΕΙΔΑΣΗ) ΚΑΙ ΩΣ ΔΕΙΚΤΗΣ (MARKER) Η S-100 ΠΡΩΤΕΙΝΗ. ΤΑ LANGERHANS ΚΥΤΤΑΡΑ (L.C) ΜΕΤΡΗΘΗΚΑΝ ΣΤΙΣ ΕΞΗΣ ΠΕΡΙΟΧΕΣ: ΝΕΟΠΛΑΣΜΑΤΙΚΟ ΕΠΙΘΗΛΙΟ, ΣΤΡΩΜΑ ΤΟΥ ΟΓΚΟΥ, ΦΥΣΙΟΛΟΓΙΚΟ ΕΠΙΘΗΛΙΟ, ΧΟΡΙΟ ΦΥΣΙΟΛΟΓΙΚΟΥ ΕΠΙΘΗΛΙΟΥ. ΒΡΕΘΗΚΕ ΟΤΙ: 1) Η S-100 ΠΡΩΤΕΙΝΗ ΕΙΝΑΙ ΑΡΙΣΤΟΣ ΔΕΙΚΤΗΣ ΓΙΑ ΤΗΝ ΑΝΙΧΝΕΥΣΗ ΤΩΝ ΚΥΤΤΑΡΩΝ L.C ΣΤΟ ΑΚΑΝΘΟΚΥΤΤΑΡΙΚΟ ΚΑΡΚΙΝΩΜΑ ΤΟΥ ΣΤΟΜΑΤΟΣ. 2) Η ΤΕΧΝΙΚΗ ΤΗΣ ΕΜΜΕΣΟΥ ΑΝΟΣΟΥΠΕΡΟΞΕΙΔΑΣΗΣ ΣΕ ΣΥΝΔΥΑΣΜΟ ΜΕ ΤΗ ΧΡΗΣΗ ΘΡΥΨΙΝΗΣ ΕΙΝΑΙ ΙΚΑΝΟΠΟΙΗΤΙΚΗ ΜΕΘΟΔΟΣ ΓΙΑ ΤΗΝ ΜΕΛΕΤΗ ΤΩΝ ΚΥΤΤΑΡΩΝ ΑΥΤΩΝ. 3) ΤΑ L.C ΗΤΑΝ ΠΕΡΙΣΣΟΤΕΡΑ ΣΤΟ ΝΕΟΠΛΑΣΜΑΤΙΚΟ ΕΠΙΘΗΛΙΟ ΠΑΡΑ ΣΤΟ ΦΥΣΙΟΛΟΓΙΚΟ ΕΠΙΘΗΛΙΟ ΚΑΙ ΣΤΟ ΣΤΡΩΜΑ ΤΟΥ ΟΓΚΟΥ ΣΕ ΒΑΘΜΟ ΣΤΑΤΙΣΤΙΚΗΣ ΣΗΜΑΝΤΙΚΟ. 4) ΤΑ L.C ΗΤΑΝ ΠΕΡΙΣΣΟΤΕΡΑ ΣΤΟ ΣΤΡΩΜΑ ΤΟΥ ΟΓΚΟΥ ΠΑΡΑ ΣΤΟ ΧΟΡΙΟ ΤΟΥ ΦΥΣΙΟΛΟΓΙΚΟΥ ΕΠΙΘΗΛΙΟΥ. 5) ΥΠΗΡΧΕ ΘΕΤΙΚΗ ΣΥΣΧΕΤΙΣΗ ΜΕΤΑΞΥ ΤΟΥ ΑΡΙΘΜΟΥ ΤΩΝ L.C ΚΑΙ ΤΟΥ ΑΡΙΘΜΟΥ ΤΩΝ Τ-ΛΕΜΦΟΚΥΤΤΑΡΩΝ ΣΤΟ ΣΤΡΩΜΑ ΤΟΥ ΟΓΚΟΥ. ΤΑ ΕΥΡΗΜΑΤΑ ΑΥΤΑ ΥΠΟΔΗΛΩΝΟΥΝ ΟΤΙ ΣΤΟ ΑΚΑΝΘΟΚΥΤΤΑΡΙΚΟ ΚΑΡΚΙΝΩΜΑ ΤΟΥ ΣΤΟΜΑΤΟΣ ΑΝΑΠΤΥΣΣΕΤΑΙ ΜΙΑ ΤΟΠΙΚΗ ΑΝΟΣΟΛΟΓΙΚΗ ΑΝΤΙΔΡΑΣΗ, ΠΟΥ ΕΚΦΡΑΖΕΤΑΙ ΜΕΣΩ ΤΩΝ L.C ΚΑΙ ΤΩΝ ΛΕΜΦΟΚΥΤΤΑΡΩΝ. Ο ΡΟΛΟΣ ΤΩΝ L.C ΦΑΙΝΕΤΑΙ ΟΤΙ ΕΙΝΑΙ ΠΡΩΤΑΡΧΙΚΗΣ ΣΗΜΑΣΙΑΣ ΚΑΙ ΣΤΗΡΙΖΕΤΑΙ ΚΥΡΙΩΣ ΣΤΗΝ ΙΔΙΟΤΗΤΑ, ΠΟΥ ΕΧΟΥΝ ΝΑ ΠΑΡΟΥΣΙΑΖΟΥΝ ΑΝΤΙΓΟΝΑ, ΣΤΑ Τ- ΛΕΜΦΟΚΥΤΤΑΡΑ

    Biologic agents and oral diseases; therapeutic prospects and restrictions

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    Abstract: Biologic agents (BAs) are synthesized by the products of living organisms and are widely used in the treatment of inflammatory and neoplastic conditions with favorable results. The purpose of this review is to provide an update of the biologic agents reported to have been used in treatment of diseases that affect the oral mucosa, as off-label indications. Identification of cases studies referring to the use of biologic agents in patients with Sjögren syndrome (including patients with MALT-lymphomas), pemphigus (vulgaris, foliaceous, paraneoplastic), mucous membrane pemphigoid, oral lichen planus, Behcet’s disease, orofacial granulomatosis, and recurrent aphthous ulceration (RAU), was achieved using Pubmed –Medline database , performing both electronic search (with key words infliximab, etanercept, adalimumab, rituximab, efalizumab, epratuzumab and alefacept , oral diseases, oral manifestations, dermatologic diseases, immune mediated diseases, biologic agents , anti-TNF agents, monoclonal antibodies, anti-B cell agents, anti T-cell agents ) and hand search to identify articles that referred specifically to patients with oral involvement..  According to the literature so far the use of BAs in patients that suffered from refractory forms of the immune-related diseases of the oral mucosa seems in general a clinically encouraging therapeutic option, but not without side effects including secondary infections, and also with a questionable economic cost-effect. Indeed, more studies in larger groups and longer period of time are required in order to confirm their efficacy and safety.  </p

    Real world evidence: Patients with refractory pemphigus treated with Rituximab.

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    BACKGROUND: Pemphigus is a group of autoimmune blistering diseases, potentially life-threatening. Rituximab received FDA approval in June 2018 for the treatment of moderate to severe pemphigus vulgaris. OBJECTIVES: To evaluate the efficacy and safety of rituximab in patients with pemphigus, resistant to previous therapies or unable to receive classic immunosuppressive treatment due to serious adverse events or comorbidities. MATERIALS AND METHODS: Twenty-five patients (9 men, 16 women), mean age 49.4 ± 15.9 years (range 21-74 years), mean disease duration 4 ± 2.7 years (range 0.25-10 years) were included in the study: 19 patients with pemphigus vulgaris and 6 with pemphigus foliaceous. The efficacy of rituximab was evaluated according to the control of disease, retention of remission, disease severity, previous treatments and adverse reactions. During COVID-19 pandemic patients are monitored closely through tele-dermatology. RESULTS: Twenty-three out of 25 patients had great improvement, 2 out of 25 ceased therapy due to adverse events (arthralgias and dyspnea). Sixteen out of 23 received additional course after 8 months (range 5-60 months). More aged patients presented more frequently adverse events and underwent additional courses (p = 0.002). Rituximab was found superior to classic immunosuppressive treatment in terms of efficacy and safety, with larger periods of remission and lower doses of corticosteroids and immunosuppressants. No major adverse events were noticed. CONCLUSIONS: Rituximab is a very effective treatment of pemphigus and, remarkably, superior to classic immunosuppressive treatment
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