Adult-onset Still disease (AOSD), a systemic inflammatory disorder, is characterized by high fever, evanescent rash, arthritis, and hyperferritinaemia. AOSD is also reported to be associated with other skin lesions, including persistent pruritic papules and plaques. This study aimed to assess the significance of dyskeratotic skin lesions in Japanese AOSD patients.We retrospectively assessed the histology of persistent pruritic skin lesions and evanescent rashes and the relationship between dyskeratotic cells, serum markers, and outcomes in 20 Japanese AOSD patients, comparing AOSD histology with that of dermatomyositis (DM), drug eruptions, and graft-versus-host disease (GVHD).As the results, Persistent pruritic lesions were characterized by scattered single keratinocytes with an apoptotic appearance confined to the upper layer of the epidermis and horny layer without inflammatory infiltrate. In contrast to AOSD, the histology of DM, drug eruption, and GVHD demonstrated dyskeratotic cells in all layers of the epidermis with inflammatory infiltrate. AOSD with evanescent rash showed no dyskeratotic cells. The dyskeratotic cells in pruritic AOSD lesions stained positive for ssDNA and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling, indicating apoptosis. Serum IL-18 was significantly higher in AOSD patients with dyskeratotic cells than those without, and generally required higher doses of glucocorticoids, immunosuppressants, and biologic agents. Two of ten AOSD patients with dyskeratotic cells died from hemophagocytic lymphohistiocytosis.In conclusion, Persistent pruritic AOSD skin lesions are characterized by dyskeratotic cells with apoptotic features, involving the upper layers of the epidermis. There may be a link to elevated IL-18. This dyskeratosis may be a negative prognostic indicator.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015626PMC
http://dx.doi.org/10.1097/MD.0000000000019051DOI Listing

Publication Analysis

Top Keywords

dyskeratotic cells
32
persistent pruritic
20
skin lesions
20
aosd patients
12
aosd
11
dyskeratotic
9
pruritic skin
8
adult-onset disease
8
evanescent rash
8
japanese aosd
8

Similar Publications

Acantholytic Dyskeratotic Acanthoma of the Nail Revealed by a Longitudinal Erythronychia.

Skin Appendage Disord

December 2024

Dermatology Department, Habib Thameur Hospital, "Genodermatoses and Cancers LR12SP03", Tunis, Tunisia.

Introduction: Focal acantholytic dyskeratosis is a distinctive histological pattern first described by Ackerman in 1972, consisting of focal suprabasal clefts in the epidermis and dyskeratotic cells at all levels of the epidermis with hyperkeratosis and parakeratosis. The first case of subungual acantholytic dyskeratosis acanthoma (ADA) was reported in 1990. This subungual variant is a very rare entity.

View Article and Find Full Text PDF

Cervical cancer is one of the biggest challenges in global health, thus it forms a critical need for early detection technologies that could improve patient prognosis and inform treatment decisions. This development in the form of an early detection mechanism increases the chances of successful treatment and survival, as early diagnosis promptly offers interventions that can dramatically reduce the rate of deaths attributed to this disease. Here, a customized Convolutional Neural Network (CNN) model is proposed for cervical cancerous cell detection.

View Article and Find Full Text PDF

Introduction: Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a potentially life-threatening, drug-induced adverse reaction characterized by skin eruptions, lymphadenopathy, fever, and a broad range of other bodily manifestations. The spectrum of histopathologic and clinical presentations is wide; therefore, DRESS syndrome can mimic other diseases.

Case Presentation: We present a case of a 4-year-old male patient who started chemotherapy with vincristine, cytarabine, and etoposide.

View Article and Find Full Text PDF
Article Synopsis
  • Transient acantholytic dermatosis, or Grover's disease, is a skin condition that causes red, itchy bumps mainly on the trunk, mostly seen in men over 50, and can be triggered by heat, sweat, sun exposure, and some medications.
  • A case study highlighted a 65-year-old man with a severe rash and a confirmed SARS-CoV-2 infection, who developed COVID-19 pneumonia, showing the link between Grover's disease and COVID-19.
  • The patient’s skin lesions improved with corticosteroids, suggesting that awareness of Grover's disease in COVID-19 patients is important for diagnosis and treatment.
View Article and Find Full Text PDF
Article Synopsis
  • - Hailey-Hailey disease is a rare skin disorder that typically appears in adults, caused by a mutation in the ATP2C1 gene, leading to weak connections between skin cells, resulting in painful blistering and lesions primarily in flexible areas of the body.
  • - The disease has no specific gender or racial preference, with its prevalence being approximately 1 in 50,000 people, and is characterized by an unpredictable course that includes periods of flare-ups and remissions often triggered by environmental factors like heat and friction.
  • - Diagnosis relies on clinical examination and specific histopathological findings, with treatment focusing on alleviating symptoms through a variety of topical and systemic medications, although there is currently no cure and no well-established treatment protocols
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!