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      An Institution Based Cross-Sectional Observational Aetiological Study Correlating the Clinico-Pathological Findings in Patients Presenting with Acquired Palmoplantar Keratoderma

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          Abstract

          Background:

          Palmoplantar keratoderma (PPK) is a heterogeneous group of hereditary or acquired disorders characterised by excessive epidermal thickening of the palms and soles. Proper knowledge about the aetiology of the disease and clinico-demographic profile helps in planning management and predicting outcomes.

          Aims and Objective:

          To determine the prevalence of different dermatoses and describe their clinico-histological correlation in acquired palmoplantar keratoderma.

          Materials and Methods:

          An institution-based cross-sectional study conducted after obtaining Ethics-Committee permission and consent from participants. Patients of any age or gender presenting with acquired PPK were recruited. The calculated sample size was 67 by using the prevalence rate (p) of 22.2%, allowable error (L) of 10%, the confidence level of 95% ( z = 1.96), and an infinite population size of 20,000. Patients were evaluated by taking demographic and clinical data in a pre-designed case record form, necessary laboratory investigations and histopathological examination that wereevaluated by three blinded experts. The pooled data were analysed with statistical software.

          Results:

          Among the 67 participants, Psoriasis was diagnosed clinically in 39 (58.2%) and histologically in 7 (10.4%), Lichen planus (LP) clinically in 16 (23.9%) and histologically in 9 (13.4%), Pityriasis rubra pilaris (PRP) in 8 (11.9%) patients clinically and 7 (10.4%) histologically and Hyperkeratotic eczema (HKE) in 4 (6%) clinically and 43 (64.2%) histopathologically. There was very poor inter-rater agreement (Kappa = 0.148, SE 0.0047, 95% CI 0.057 to 0.24). The clinico-pathological correlation was found to be agreeable in 17.9% Psoriasis, 56.2% LP and 87.5% PRP. HKE was commonly misdiagnosed as Psoriasis in 65.1% of patients.

          Conclusion:

          Hyperkeratotic lesions of the palm and sole often present with overlapping clinical features and a skin biopsy has to be done to aid in diagnosis.

          Limitation:

          Stratification of the clinical expertise of clinicians was done during the analysis.

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          Most cited references20

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          Palmoplantar psoriasis is associated with greater impairment of health-related quality of life compared with moderate to severe plaque psoriasis

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            Management of refractory pityriasis rubra pilaris: challenges and solutions

            Pityriasis rubra pilaris (PRP) is a rare chronic inflammatory papulosquamous skin disease. Its clinical presentation and evolution is very variable. The most frequent clinical features are follicular papules, progressing to yellow-orange erythroderma with round small areas of normal skin and the well-demarcated palmoplantar keratoderma. Actually, six different types of PRP have been described based on clinical characteristics, age of onset, and prognosis. The pathogenesis is still unknown, and treatment can be challenging. Available treatments are mainly based on case reports or case series of clinical experience because no controlled randomized trials have never been performed because of the rarity of the condition. Traditional systemic treatment consists in retinoids, which are actually considered as first-line therapy, but refractory cases that do not respond or relapse after drug interruption do exist. In recent years, numerous reports have demonstrated the efficacy of new agents such as biological drugs. This article is an overview on available therapeutic options, in particular for refractory forms of PRP.
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              Inherited Disorders of Cornification

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                Author and article information

                Journal
                Indian J Dermatol
                Indian J Dermatol
                IJD
                Indian J Dermatol
                Indian Journal of Dermatology
                Wolters Kluwer - Medknow (India )
                0019-5154
                1998-3611
                Nov-Dec 2023
                09 January 2024
                : 68
                : 6
                : 603-610
                Affiliations
                [1] From the Department of Dermatology, Bankura Sammilani Medical College, Bankura, India
                [1 ] Department of Dermatology, Deben Mahata Government Medical College and Hospital, Purulia, India
                [2 ] Department of Dermatology, College of Medicine and Sagore Datta Hospital, Kolkata, West Bengal, India
                Author notes
                Address for correspondence: Dr. Indrayudh Sen, Bidhannagar, Junbedia Bypass Road, Panchbaga, Bankura - 722 101, West Bengal, India. E-mail: indrayudh91@ 123456gmail.com
                Article
                IJD-68-603
                10.4103/ijd.ijd_572_23
                10868998
                38371533
                b03469c9-c04c-424b-81a0-c6b5830c71a5
                Copyright: © 2023 Indian Journal of Dermatology

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : June 2023
                : September 2023
                Categories
                Original Article

                Dermatology
                acquired palmoplantar keratoderma,hyperkeratotic eczema,lichen planus,pityriasis rubra pilaris,psoriasis

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