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Littérature scientifique sur le sujet « Autoimmune oral lesion »

Auteur : Grafiati

Publié le 9 mars 2023

Mis à jour le 31 juillet 2025

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Articles de revues sur le sujet "Autoimmune oral lesion"

L., Vijayalakshmi, Bharathi S., and Manipriya S. "A Clinico Epidemiological Study of Oral Manifestations in Auto Immune Skin Diseases." International Journal of Pharmaceutical and Clinical Research 15, no. 12 (2023): 1396–400. https://doi.org/10.5281/zenodo.11202636.

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<strong>Introduction:</strong>  Autoimmune diseases are characterized by presence of auto antibodies that are directed against structures of the self-resulting in tissue damage and degeneration. Auto immune disorder often involves oral mucosa. Oral involvement is the first and most important or often it may be the only sign of such disease process. Oral mucosal lesions are erythema, erosions, ulcers rarely vesicle which are clinically similar and often non-specific. Timely recognition and therapy of oral lesion is critical as it may prevent skin involvement in pemphigus vulgaris. Based on

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Tarakji, Bassel. "Pemphigus Vulgaris in Old Patient." Case Reports in Dentistry 2021 (August 23, 2021): 1–3. http://dx.doi.org/10.1155/2021/3946161.

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Pemphigus vulgaris (PV) is a chronic, autoimmune, intraepidermal blistering disease of the skin and mucous membranes. The first clinical manifestation is often the development of intraoral lesions, and later, the lesions involve the other mucous membranes and skin. The etiological factors of this disease still remain unknown, although the presence of autoantibodies is consistent with an autoimmune disease. A 73-year-old man had bullous lesions on gingiva, oral mucosa first, then scalp, trunk, and face. An oral medicine specialist suspects the lesion in differential diagnosis in the first prese

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Pinheiro, Juliana Barchelli, Camila Tirapelli, Claudia Helena Lovato da Silva, et al. "Oral Nodular Lesions in Patients with Sjögren’s Syndrome: Unusual Oral Implications of a Systemic Disorder." Brazilian Dental Journal 28, no. 3 (2017): 405–12. http://dx.doi.org/10.1590/0103-6440201601013.

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Abstract Sjögren’s syndrome (SS) is a systemic chronic autoimmune disorder affecting the lacrimal and salivary glands. SS may manifest as primary SS (pSS) or secondary SS (sSS), the latter occurring in the context of another autoimmune disorder. In both cases, the dry eyes and mouth affect the patient’s quality of life. Late complications may include blindness, dental tissue destruction, oral candidiasis and lymphoma. This paper reports two cases of SS, each of them presenting unusual oral nodular lesion diagnosed as relapsed MALT lymphoma and mucocele. The importance of the diagnosis, treatme

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Anitua, Eduardo, Mohammad H. Alkhraisat, Asier Eguia, and Laura Piñas. "Oral Pemphigoid Recalcitrant Lesion Treated with PRGF Infiltration. Case Report." Dentistry Journal 9, no. 11 (2021): 137. http://dx.doi.org/10.3390/dj9110137.

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Mucous membrane pemphigoid (MMP) is a heterogeneous group of chronic autoimmune subepithelial blistering diseases. Oral involvement is present in almost all patients, may represent the onset of the disease, and causes different degrees of pain, dysphagia, soreness, and bleeding. Treatment is based on systemic and/or oral corticoids, or other immunosuppressants. Occasionally, oral lesions can show a poor response to standard treatments. We present the case of a 61-year-old female patient with a painful extensive MMP oral ulcerative lesion recalcitrant to previous systemic azathioprine and local

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Bhateja, Sumit, Aksilat Saciideva, Geetika Arora, Vaibhav Malhotra, and Taniya Malhotra. "Ocular manifestations of oral mucosal lesions." Indian Journal of Clinical and Experimental Ophthalmology 10, no. 4 (2024): 627–33. https://doi.org/10.18231/j.ijceo.2024.110.

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Autoimmune blistering diseases refer to a diverse group of conditions that primarily target the skin and mucosa. However, in some cases, other organ systems can be involved, depending on the specific pathophysiology of the disease. Owing to the increased possibility of blindness associated with delayed diagnosis and treatment, it is essential to be aware of and detect ocular manifestations of these diseases at an early stage. The present article discusses the various oral mucosal lesions encountered in daily practice with emphasis on the ocular manifestations of each lesion.

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Kitakawa, Dárcio, Gabriela Máximo, Maria Clara Ferreira Coelho, Felipe da Silva Peralta, Dárcio Kitakawa, and Luis Felipe das Chagas e Silva de Carvalh. "Erythema multiforme: A case report with oral manifestations." International Journal of Case Reports and Images 13, no. 2 (2023): 61–65. http://dx.doi.org/10.5348/101328z01gm2022cr.

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Introduction: Erythema multiforme (EM) is an acute, immune-mediated mucocutaneous disease, which may be related to herpes simplex virus, use of certain medications, autoimmune disease, radiation, immunization, pregnancy, period, and food additives or chemicals. It is a condition that occurs predominantly in young adults, with a slight female preponderance and no predilection. Clinically, EM presents erosive and erythematous plaques, affecting mainly the lips and oral mucosa, called target lesions, which may progress to vesiculobullous lesions. The aim of this study is to report a case shown as

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Cai, Q., and T. Yoo. "Oral Administration Decreases Autoimmune Hearing Loss Lesion in the Mice." Journal of Allergy and Clinical Immunology 117, no. 2 (2006): S18. http://dx.doi.org/10.1016/j.jaci.2005.12.073.

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Serpico, R., G. Pannone, A. Santoro, et al. "Report of a Case of Discoid Lupus Erythematosus Localised to the Oral Cavity: Immunofluorescence Findings." International Journal of Immunopathology and Pharmacology 20, no. 3 (2007): 651–53. http://dx.doi.org/10.1177/039463200702000325.

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Discoid Lupus Erythematosus (DLE) is a chronic disease with a typical cutaneous involvement. This pathology rarely involves mucosa: oral cavity is interested in 20% of DLE patients. We describe a case of oral DLE in a 50-year-old woman with an anamnesis for autoimmune disorders. This study shows the helpful role of immunofluorescence in the diagnosis of autoimmune diseases. The first diagnostic step was the clinical observation of the oral mucosa: the lesion area was erythematous, athrophic and hyperkeratotic. The patient then underwent laboratory examination. We utilized human epithelial cell

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Ohki, Masafumi, and Shigeru Kikuchi. "Nasal, Oral, and Pharyngolaryngeal Manifestations of Pemphigus Vulgaris: Endoscopic Ororhinolaryngologic Examination." Ear, Nose & Throat Journal 96, no. 3 (2017): 120–27. http://dx.doi.org/10.1177/014556131709600311.

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Pemphigus vulgaris is an autoimmune blistering disorder that involves the skin and mucous membranes. Few reports have described nasal and oropharyngolaryngeal lesions in pemphigus vulgaris using an endoscopic ororhinolaryngologic examination. We retrospectively reviewed the clinical records of 11 patients with pemphigus vulgaris between 2001 and 2013 with respect to their symptoms, lesion sites, lesion features, and treatments received. All patients had undergone an endoscopic ororhinolaryngologic examination. Their mucosa-related symptoms were sore throat, oral pain, odynophagia, gingival ble

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Sadat, SM Anwar, and Akhter Imam. "Pemphigus Vulgaris as Oral Mucosal Ulcer Progressive to Skin Lesion:." Update Dental College Journal 3, no. 2 (2014): 43–47. http://dx.doi.org/10.3329/updcj.v3i2.17999.

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Among all the life threatening diseases, autoimmune diseases are among most notorious and complicated diseases. As these diseases have no specific cause or responsible organism, it is therefore very difficult to distinguish and diagnose and thus stands as a major threat for public health. It is assumed that the reason for these diseases may be from genetic to environmental factors, from stress to idiopathic origin. Pemphigus Vulgaris(PV) is such an autoimmune blistering disease that frequently affects the mucous membrane and skin. Very often it starts from oral cavity and Dentists therefore th

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Thèses sur le sujet "Autoimmune oral lesion"

FRANCESCHINI, FABIO GIULIO. "Correlazioni esistenti tra parodontologia e medicina orale. Lesioni delle mucose orali versus malattia parodontale. Aspetti diagnostici e terapeutici." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2011. http://hdl.handle.net/10281/19339.

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Our study describes the relationship between periodontal disease and oral mucosal lesions. At first we analysed classification criteria of oral lesions in order to provide a point of reference for an adequate description. In a second time we started to describe periodontal disease, that is a common pathology all over the world with high costs for therapy and rehabilitations. Also classification of periodontal disease is important, because there are different types of disease, with various clinical aspects. We used the AAP (American Academy of Periodontology) classification of 1999, that report

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Figueiredo, João Manuel Prata de. "Líquen plano : estudo de casos clínicos." Master's thesis, 2012. http://hdl.handle.net/10400.14/13665.

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O Líquen Plano é uma doença muco cutânea auto-imune que afecta a mucosa oral (Líquen Plano Oral) podendo também afectar pele, mucosa genital, escalpe e unhas. A etiologia exacta do Líquen Plano permanece desconhecida. Esta patologia afecta mais comummente mulheres de meia-idade e raramente afecta crianças. Clinicamente, as lesões de Líquen Plano Oral apresentam-se sob a forma de estrias brancas (estrias Wickham), pápulas brancas, placas brancas, lesões eritematosas, erosivas ou bulhosas. Estas lesões usualmente são simétricas e bilaterais. O diagnóstico do Líquen Plano Oral é efectuado através

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Livres sur le sujet "Autoimmune oral lesion"

Yurdakul, Sebahattin, Emire Seyahi, and Hasan Yazici. Behçet’s syndrome. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0135.

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Behçet's syndrome is a systemic inflammatory panvasculitis (affecting all sizes of vessels) of unknown aetiology. It is in vogue to include it among the systemic autoinflammatory conditions. Behçet's syndrome is more frequent along the ancient 'Silk Route' across Asia than it is in Western countries. The usual onset is the second or third decade, equally affecting either gender. However, young patients and male patients have more severe disease. Almost all patients have recurrent oral ulceration. Scar-forming genital ulcers, a variety of skin lesions including acneiform, erythema nodosum-like

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Chapitres de livres sur le sujet "Autoimmune oral lesion"

Murgia, Martina Salvatorina, Germano Orrù, and Cinzia Casu. "Labial Immunological Diseases." In Common Lip Diseases: A Clinical Guide. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815238631124010004.

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Autoimmune diseases are caused by autoantibodies targeting structural proteins present in the skin and mucosa. The oral mucosa is frequently affected in these diseases, in particular by lichen planus, recurrent aphthous stomatitis, erythema multiforme, Stevens-Johnson syndrome and pemphigus. Clinical symptoms are heterogeneous and may present clinically with erythema, erosions and ulcers localized on the oral mucosa, causing a plethora of local and systemic symptoms, including pain, dysphagia, difficulty in eating and speaking and general malaise. The multiplicity and similarity of the clinica

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SU Kucuk, Ozlem, and Nazan Taslidere. "Pemphigus Vulgaris." In Wound Healing - Recent Advances and Future Opportunities [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.104814.

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Pemphigus vulgaris is a life-threatening bullous disease characterized by acantholysis resulting in the formation of intraepithelial blebs in the mucous membranes and skin. It is a chronic autoimmune bullous dermatosis caused by the production of autoantibodies against desmoglein 1 and 3. It often begins with blisters and erosions on the oral mucosa, followed by lesions on other mucous membranes and drooping blisters that may spread to the skin. If there is clinical suspicion, the diagnosis can be confirmed by cytological examination, histopathological examination, direct and indirect immunofl

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Yurdakul, Sebahattin, Emire Seyahi, and Hasan Yazici. "Behçet’s syndrome." In Oxford Textbook of Rheumatology. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0135_update_003.

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Behçet’s syndrome is a systemic inflammatory panvasculitis (affecting all sizes of vessels) of unknown aetiology. It is in vogue to include it among the systemic autoinflammatory conditions. Behçet’s syndrome is more frequent along the ancient ’Silk Route’ across Asia than it is in Western countries. The usual onset is the second or third decade, equally affecting either gender. However, young patients and male patients have more severe disease. Almost all patients have recurrent oral ulceration. Scar-forming genital ulcers, a variety of skin lesions including acneiform, erythema nodosum-like

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Actes de conférences sur le sujet "Autoimmune oral lesion"

Moraes, Lucas Grobério Moulim de, Caroline Colnago Demuner, Paula Zago Melo Dias, Giselle Alves de Oliveira, and Marcelo Ramos Muniz. "Atypical course of schistosomal myelitis: a diagnostic challenge." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.531.

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Acute myelitis is a severe neurological complication of schistosomiasis which clinical features present as lower limb weakness, sensory disturbance and intestinal or bladder dysfunction. A 60-year-old male farmer presented with low back pain and progressive paresis of right lower limb that worsened to plegia over ten months. MRI demonstrated hypersignal lesions in the T2/FLAIR (T2- weighted-Fluid-Attenuated Inversion Recovery) sequence in the ninth dorsal segment level. A Kato-Katz examination was negative for Schistosoma mansoni and a rectal biopsy confirmed an active infection. The patient r

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