1,086 results match your criteria: "Pityriasis Rubra Pilaris"

Background: Erythroderma is a dermatologic condition characterized by widespread red and scaly skin. The causes include, but are not limited to, psoriasis, eczema, drug eruptions, pityriasis rubra pilaris (PRP), and cutaneous T-cell lymphoma. Most of these are typified by Type 2 (e.

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Background: While IL-23 inhibitors, which include guselkumab, tildrakizumab, and risankizumab, are currently FDA-approved solely for the treatment of psoriasis, several other inflammatory skin conditions have been associated with elevated IL-23 levels. The purpose of this review is to summarize and interpret the literature surrounding the off-label uses of IL-23 inhibitors in dermatologic practice.

Methods: We conducted searches on PubMed and for clinical trials, observational studies, case series, and case reports assessing use of the three IL-23 inhibitors for non-psoriatic dermatologic conditions.

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Pityriasis rubra pilaris (PRP) presents a diagnostic challenge due to its varied clinical manifestations and the scarce literature on scalp involvement. This article presents a case report of a 59-year-old female with PRP solely affecting the scalp, detailing its clinical, trichoscopic, and histopathological features. Trichoscopy revealed a novel finding of white-silvery scales forming hair casts with a triangular shape, distinct from the existing literature.

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Erythroderma in the elderly.

J Dermatol

November 2024

Department of Dermatology, Fukushima Medical University, Fukushima, Japan.

Erythroderma is the end-stage condition caused by various inflammatory diseases, presenting with widespread generalized coalesced erythema on the trunk and extremities. Erythroderma is not a disease itself, but rather is a symptom expressing erythrodermic condition, which is frequently associated with inguinal lymphadenopathy, chills, and mild fever. The clinical characteristics include sparing the folds of the trunk and extremities (deck-chair sign), and cobblestone-like disseminated grouping prurigo; however, the deck-chair sign is not specific to papulo-erythroderma (Ofuji disease).

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Pityriasis rubra pilaris.

J Am Acad Dermatol

November 2024

Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina, Charleston, South Carolina.

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Long-Standing Remission After Tildrakizumab Treatment in a Case of Refractory Type I Pityriasis Rubra Pilaris in a Breast Cancer Patient.

Clin Cosmet Investig Dermatol

October 2024

Dermatology Unit, Azienda Unità Sanitaria Locale- IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Pityriasis rubra pilaris (PRP) is a rare chronic inflammatory skin disease characterised by follicular keratotic papules and perifollicular erythema coalescing into orange-red scaly plaques, and palmoplantar keratoderma. Characteristic islands of sparing are usually observed. A standardised therapeutic approach is lacking owing to the infrequent occurrence of this disease.

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A young female with rapid progression of erythroderma and palmoplantar keratoderma.

Int J Rheum Dis

October 2024

Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan.

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Revisiting risankizumab: a newer biologic drug in dermatology.

Ital J Dermatol Venerol

October 2024

Department of Dermatology, Katihar Medical College, Al-Karim University, Katihar, India.

Article Synopsis
  • - Risankizumab is an FDA-approved medication for treating moderate to severe plaque psoriasis and shows promise for various other skin conditions.
  • - A thorough review of literature was conducted using databases like PubMed and Google Scholar to explore risankizumab's effectiveness in dermatology.
  • - Besides psoriasis, risankizumab has been successfully used for conditions such as hidradenitis suppurativa and pyoderma gangrenosum, and it is considered to have a good safety record.
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Article Synopsis
  • Cutaneous reactions to mRNA COVID-19 vaccines can include various skin issues, especially in patients with existing dermatologic diseases.
  • A case report details a 73-year-old man with atopic dermatitis who developed severe erythroderma after each Pfizer-BioNTech vaccine dose, which covered 95% of his body.
  • Quick identification and treatment of erythroderma are crucial to prevent serious complications, highlighting the need for awareness of this reaction in susceptible individuals.
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A 59-year-old man presented with a five-month history of widespread, salmon-colored, scaly plaques. Skin examination revealed salmon-colored plaques with "islands of sparing" on the trunk and waxy keratoderma on the palms and soles. Histopathology of the lesion showed alternating orthokeratosis and parakeratosis in vertical and horizontal directions, consistent with a diagnosis of pityriasis rubra pilaris (PRP).

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Introduction And Importance: Pityriasis rubra pilaris is a rare inflammatory papulosquamous disorder which manifests in six clinical subtypes affecting both pediatric and adult populations.

Presentation Of Case: A 14-year-old female presented with multiple itchy scaly lesions on her hands and legs which began as vesicles 9 days after birth. Histopathological examination confirmed the diagnosis of pityriasis rubra pilaris.

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Article Synopsis
  • - Wong-type dermatomyositis (WTDM) is a rare variant of dermatomyositis first identified in 1969, combining features of classic dermatomyositis and pityriasis rubra pilaris, but has limited documentation due to its rarity and possible clinical oversight.
  • - A review of existing literature suggests that WTDM behaves more like a subtype of classic dermatomyositis rather than just a combination of symptoms from both conditions, indicating a better treatment response with traditional DM therapies.
  • - Clinicians are advised to conduct thorough evaluations for WTDM patients, including detailed medical histories, exams, and lab tests, and to monitor for systemic issues or cancer, while further research is needed to explore its underlying mechanisms and long
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Article Synopsis
  • Abrocitinib is a JAK1 inhibitor mainly approved for treating moderate-to-severe atopic dermatitis in those 12 and older, but this review explores its off-label uses.
  • Researchers found 37 studies using Abrocitinib for conditions beyond atopic dermatitis, with common cases including vitiligo, prurigo nodularis, and hand eczema, each having 12 reported instances.
  • All but one of the 103 patients studied experienced favorable outcomes with Abrocitinib, highlighting its potential for treating multiple skin conditions.
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Successful Treatment of Refractory Extensive Pityriasis Rubra Pilaris With Risankizumab and Acitretin.

Cutis

August 2024

Drs. Khalil and Hamburger are from Larkin Community Hospital Palm Springs Campus, Hialeah, Florida. Dr. Hirt is from Larkin Community Hospital South Miami Campus, Florida. Dr. Kerdel is from Florida Academic Dermatology Center, Coral Gables.

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Comment on "Erythrodermic Pityriasis Rubra Pilaris Following COVID-19 Vaccination".

Cutis

August 2024

Dr. Daungsupawong is from Private Academic Consultant, Phonhong, Lao People's Democratic Republic. Dr. Wiwanitkit is from the Department of Research Analytics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, India.

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Article Synopsis
  • - Pityriasis rubra pilaris (PRP) is a rare skin condition characterized by chronic inflammation and scaly patches, affecting mostly the extremities while sparing the trunk.
  • - A 43-year-old woman with a history of atopic dermatitis presented with itchy skin lesions, and after thorough examination and biopsy, she was diagnosed with atypical adult PRP (type II).
  • - The patient was treated with narrowband UVB phototherapy, leading to complete clearance of skin lesions within two months, and she has remained lesion-free for two years during follow-up.
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Tofacitinib for Pityriasis Rubra Pilaris: A Case Report.

Clin Cosmet Investig Dermatol

August 2024

Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, 400011, People's Republic of China.

Article Synopsis
  • * A case study demonstrated that tofacitinib, a JAK inhibitor, effectively treated pityriasis rubra pilaris without significant side effects.
  • * The success of tofacitinib may be linked to its ability to block the JAK/STAT signaling pathway, which reduces the expression of various pro-inflammatory cytokines.
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Article Synopsis
  • Pityriasis rubra pilaris (PRP) is a rare skin disease that causes red and scaly patches, making it hard to treat.
  • Because PRP is uncommon and can sometimes get better on its own, studying how to treat it is tricky.
  • New medicines that target specific parts of the immune system, like IL-17 and IL-23, have shown some promise for treating PRP, but more research is needed to understand how well they work.
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Guselkumab - In Psoriasis and Beyond.

Dermatol Pract Concept

July 2024

Department of Dermatology, Katihar Medical College, Karim Bagh, Katihar, Bihar, India.

Introduction: Guselkumab is an interleukin 23p19 inhibitor, and the first in this group, to be approved by the US Food and Drug Administration for the management of moderate to severe psoriasis. Apart from its utility in psoriasis, there are a number of other dermatologic conditions where guselkumab has demonstrated value.

Objectives: The aim of this narrative review is to describe the utility of guselkumab in psoriasis as well as its implication in off-label dermatologic disorders.

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Article Synopsis
  • Pityriasis rubra pilaris (PRP) is a rare skin disease that looks a lot like psoriasis and affects the skin on the palms and soles.
  • Some recent treatments using special medicines called monoclonal antibodies have shown good results for people with PRP.
  • One case of an adult diagnosed with an unusual type of PRP showed major improvement after receiving a specific treatment and emphasized the importance of genetic testing in figuring out tricky skin diseases.
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