Relevant bibliographies by topics / Hyperkeratotic form of lichen planus

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Academic literature on the topic 'Hyperkeratotic form of lichen planus'

Author: Grafiati
Published: 5 June 2025
Last updated: 16 July 2025

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Journal articles on the topic "Hyperkeratotic form of lichen planus"

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Proschenko, A. M., N. A. Zelinskaya, N. S. Proschenko, L. L. Reshetnyk, N. V. Chervonna, and O. V. Bida. "Peculiarities of the format of genetic blood systems in patients with oral lichen planus." Medicni perspektivi 29, no. 3 (2024): 128–37. http://dx.doi.org/10.26641/2307-0404.2024.3.313595.

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The number of patients with oral lichen planus (OLP) has increased due to the raise of aggressive forms of the disease (erosive, ulcerative and hyperkeratotic forms) with a possible risk of malignancy. There are isolated researches which indicate a genetic determinism to OLP, but more often these conclusions are based on insufficiently adequate and out of date methods, which make it impossible to correctly interpret the obtained data. The aim was to identify a genetical predisposition with a programmed risk to the oral lichen planus. The main group – 278 patients with the OLP (aged 26-65 years
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Proschenko, A.M., N.S. Proschenko, N.A. Zelinskaya, L.L. Reshetnyk, N.V. Chervonna, and O.V. Bida. "Peculiarities of the format of genetic blood systems in patients with oral lichen planus." Medicni perspektivi 29, no. 3 (2024): 128–37. https://doi.org/10.26641/2307-0404.2024.3.313595.

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The number of patients with oral lichen planus (OLP) has increased due to the raise of aggressive forms of the disease (erosive, ulcerative and hyperkeratotic forms) with a possible risk of malignancy. There are isolated researches which indicate a genetic determinism to OLP, but more often these conclusions are based on insufficiently adequate and out of date methods, which make it impossible to correctly interpret the obtained data. The aim was to identify a genetical predisposition with a programmed risk to the oral lichen planus. The main group – 278 patients with the OLP (aged 26-65
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Reshetnyk, L., and T. Shuminskaya. "Configuration of integration features of genetic determinism systems of erythrocyte antigens in patients with oral lichen planus." SUCHASNA STOMATOLOHIYA 121, no. 4 (2024): 17. http://dx.doi.org/10.33295/1992-576x-2024-4-17.

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Relevance. Over the past few years, the number of patients with oral lichen planus (OLP) has almost doubled due to the increase in aggressive forms of OLP with a possible risk of malignancy. Only a few isolated studies indicate a genetic determinism for OLP, but more often these data were obtained based on insufficiently adequate and modern research methods, which complicate the correct interpretation of the obtained results. Purpose: to study the presence of genetic determinism of erythrocyte blood antigens to oral lichen planus. Materials and methods. The patients were divided into 2 groups
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Zainullin, T. A., E. V. Ivanova, D. A. Moiseev, et al. "Features of differential diagnosis of lichen planus and lichenoid reaction of the oral cavity: histopathological analysis." Clinical Dentistry (Russia) 28, no. 1 (2025): 18–24. https://doi.org/10.37988/1811-153x_2025_1_18.

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Lichen planus is a chronic autoimmune skin-mucosal disease that often affects the oral cavity and can affect the esophagus, the mucous membrane of the genitals, the skin and its appendages. Lichenoid reactions are considered as lesions clinically similar to lichen planus erythematosus, but differing in pathogenesis, etiology and, consequently, treatment approaches. The main provoking factors of lichenoid reactions are medicines and dental materials. The aim of the study was to identify histopathological differences between lichen planus erythematosus and lichenoid reactions of the oral cavity
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5

Mammadova, S., N. Kerimova, and G. Huseynova. "MODERN ASPECTS OF THE TREATMENT OF LICHEN PLANUS OF THE ORAL MUCOSA." Danish scientific journal, no. 67 (December 26, 2022): 47–48. https://doi.org/10.5281/zenodo.7495315.

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<strong>Abstract</strong> Lichen planus (LP) is a nodular chronic disease that occurs on the skin and visible mucous membranes. With this disease, the mucous membrane of the oral cavity and the red border of the lips are often affected. The disease is more common in women aged 40 to 65 years. The causes of lichen planus have not been fully elucidated. There are neurogenic, viral, bacterial, autoimmune theories of this disease. Recently, there has been a &quot;rejuvenation&quot; of those suffering from this disease. This is due to increased contact with a viral infection, a significant change i
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Barannik, N. G., R. Y. Tsymbaliuk, O. M. Manukhina, A. V. Sydoryako, and K. P. Volchykhina. "The content of the total protein, protein fractions and blood serum proteins in patients with different forms of lichen ruber planus." Modern medical technology, no. 2(49) (July 20, 2021): 31–36. http://dx.doi.org/10.34287/mmt.2(49).2021.5.

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Purpose of the study. Establishing the role of processes of proteolysis of mixed saliva in the development and course of lichen planus of the oral mucosa.&#x0D; Materials and methods. A comprehensive examination of 102 patients with lichen planus aged 21 to 70 years and 20 people in the control group, whose age and sex composition corresponded to that in the study group. BioRad (USA) reagent kits were used to determine the total protein content of mixed saliva. The content of protein fractions of mixed saliva was determined by polyacrylamide gel electrophoresis in the presence of sodium dodecy
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Molochkov, V. A., Yulia V. Molochkova, and M. A. Bobrov. "Differential diagnosis between acrokeratosis verruciformis of Hopf and hypertrophic lichen planus." Russian Journal of Skin and Venereal Diseases 19, no. 4 (2016): 238–41. http://dx.doi.org/10.18821/1560-9588-2016-19-4-238-241.

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The article is devoted to the differential diagnosis of hypertrophic form of lichen planus (CPL) with acrokeratosis verruciformis of Hopf (AVH). It is very rare hyperkeratotic genodermatosis usually inherited in an autosomal dominant manner. Due to the marked clinical similarity of these two dermatoses crucial for the correct diagnosis is histological study of the lesion with the identification of histological feature unique for AVH - papillomatosis as a “church steeples”. Two clinical cases diagnosed last year in the department of dermatology and dermatooncology in Moscow regional research an
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Emechebe, D., R. P. Mendoza, and E. Heilman. "A rare case of genital porokeratosis clinically misdiagnosed as lichen planus." American Journal of Clinical Pathology 156, Supplement_1 (2021): S47—S48. http://dx.doi.org/10.1093/ajcp/aqab191.096.

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Abstract Introduction/Objective Porokeratosis is a clonal disorder of keratinization characterized by atrophic patches surrounded by a histologically distinctive hyperkeratotic ridge-like border called the cornoid lamella. Porokeratosis occurring on the genital area is considered a rare entity and much more unusual when in isolated form Methods/Case Report This is a case of a 54-year old man who presented with a penile lesion that has been present for 10 years, unchanged, non-bleeding and non-pruritic. There was no history of genital ulcer or inguinal swelling, neither any history of sexual pr
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Shchava, Svetlana N., Irina N. Ivanova, and Elena A. Serdyukova. "Combination of actinic, hypertrophic and typical forms of lichen planus in one patient." Russian Journal of Skin and Venereal Diseases 25, no. 1 (2022): 41–47. http://dx.doi.org/10.17816/dv105743.

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Lichen planus is a chronically occurring dermatosis of a multifactorial nature, which is characterized by the appearance of flat polygonal itchy papules on the skin and mucous membranes. Dermatosis is often associated with diabetes mellitus and diseases of the gastrointestinal tract, extremely rarely with oncological diseases. Antimalarial drugs with photoprotective, anti-inflammatory, weak immunosuppressive effect are recommended for treatment.&#x0D; Actinic and hypertrophic forms of lichen planus are atypical forms of the disease. Actinic or tropical lichen planus is rare in the Russian Fede
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Kolenko, Yu, N. Zelinskaya, O. Tkach, and A. Griban. "Configuration of integration features of genetic determination of erythrocyte antigen systems in patients with lichen planus of the oral mucosa." SUCHASNA STOMATOLOHIYA 116, no. 5 (2023): 4. https://doi.org/10.33295/1992-576x-2023-5-4.

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Aim: to study the genetic determination of erythrocyte blood antigens to the oral mucosa. Materials and methods. The subjects of the study were 248 LP patients aged 26–65 years. Determination of genetic markers in blood and saliva (oral fluid) was carried out using a hemagglutination reaction. Rabbit liquid absorbed sera anti-M, anti-N, goat liquid absorbed sera anti-P, goat liquid absorbed sera anti- Lea and anti-Leb, hemagglutinating iso-sera á, b and isoimmune anti-Rhesus sera anti-D group Oáb (I) were used Ab (II), Bá (III) and AB (IV) of the Kiev city blood transfusion station. Results. I
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Book chapters on the topic "Hyperkeratotic form of lichen planus"

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Ly, Fatimata. "Pigmentary Disorders in Black Skin from Pathophysiology to Treatment." In Pigmentation Disorders - Etiology and Recent Advances in Treatments. IntechOpen, 2023. http://dx.doi.org/10.5772/intechopen.109773.

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Pigmentary disorders are frequent and more visible in patients with darker phototypes (Fitzpatrick’s IV–VI). They also have an important psychological impact and are the cause of inappropriate cosmetic practices. Pigmentary disorders comprise a wide range of pathologies, and the pathophysiological mechanisms have evolved considerably in recent years. Pigment disorders vary in their clinical presentation from achromia to hyperpigmentation to hypopigmentation. Inflammatory dermatoses, such as acne, are often complicated by postinflammatory hyperpigmentation; psoriasis and lichen planus are accompanied by dyschromia. Some skin diseases, such as mycosis fungoides, have atypical presentations in the form of hypopigmented plaques. All these dyschromias have an important impact on the quality of life and are responsible for practices such as voluntary cosmetic depigmentation with products like dermocorticoids, hydroquinone and mercury salts, and various depigmenting products. This practice is at the origin of pigmentary disorders, such as exogenous ochronosis, lichen-like and lupus-like dermatoses, and periorbital hyperpigmentation. Therapeutic management is difficult and relies on chemical (peeling), physical (laser), and medicinal means (tranexamic acid); hence, the interest is in prevention through early diagnosis and the avoidance of favorable factors.
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Bobrova Margarita, Taranik Maksim, and Kopanitsa Georgy. "Using Neural Networks for Diagnosing in Dermatology." In Studies in Health Technology and Informatics. IOS Press, 2019. https://doi.org/10.3233/978-1-61499-975-1-211.

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The paper deals with neural networks for decision support in diagnosing in dermatology. There were several iterations during development. We classified six diseases using ANN: (1) Psoriasis, (2) Seborrheic dermatitis, (3) Lichen planus, (4) Pityriasis rosea, (5) Cronic dermatitis, (6) Pityriasis rubra pilaris. At first, we used all 35 attributes to conclude skin disease diagnosis with the accuracy of 96.9%. Then, we reduced the set of analyzed attributes by Pearson correlation approach to eight attributes and increased the accuracy to 98.64%. Data collection time was reduced. Thereby, the speed of the diagnosing process was increased and, as a result, it was possible to form a treatment plan more effectively. The tools used for neural network development were the Python language, Keras library and PyCharm platform.
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Conference papers on the topic "Hyperkeratotic form of lichen planus"

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Gorbatova, Ekaterina Aleksandrovna, and Marina Vladlenovna Kozlova. "THE IMPORTANCE OF BIOLOGICAL MARKERS IN THE PROGNOSIS OF ORAL LICHEN PLANUS." In Themed collection of papers from Foreign intemational scientific conference «Joint innovation - joint development». Medical sciences . Part 2. Ьу НNRI «National development» in cooperation with PS of UA. June 2023. Crossref, 2023. http://dx.doi.org/10.37539/230629.2023.28.79.010.

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The dynamics of the levels of biological markers in the oral fluid is closely related to the degree of severity of inflammatory phenomena of the oral mucosa. The concentration of squamous cell carcinoma antigen &gt;500 mcg/ml (527 mcg/ml) is characteristic of erosive-ulcerative form, &gt;1000 mcg/ml (985 mcg/ml) should be considered as a predictor of exacerbation or recurrence of lichen planus after 90 days of follow-up.
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Gorbatova, Ekaterina Alexsandrovna, and MarinaVladlenovna Kozlova. "DYNAMICS OF SQUAMOUS CELL CARCINOMA ANTIGEN CONCENTRATION IN PATIENTS WITH LICHEN PLANUS OF THE ORAL MUCOSA." In Themed collection of papers from Foreign international scientific conference «Joint innovation - joint development». by HNRI «National development» in cooperation with PS of UA. February 2025. - Harbin (China). Crossref, 2025. https://doi.org/10.37539/250227.2025.91.57.006.

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In modern views on the etiopathogenesis of lichen planus (LP), the leading role is given to disturbances in the immune status. The level of cytokines in the oral fluid correlates with the concentration of the squamous cell carcinoma (SCC) antigen. In 80% of patients with the erosive-ulcerative form of LP, with an increase in the SCC level in mixed saliva after treatment, clinical manifestation of the disease was diagnosed after 90 days.
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