Two cases of perniosis in a free flap and a graft site of the hands.

Clin Exp Dermatol

Dermatopathology Department, St. John's Institute of Dermatology, St Thomas' Hospital, Westminster Bridge Road, London, SE1 7EH, UK.

Published: October 2019

Download full-text PDF

Source
http://dx.doi.org/10.1111/ced.13879DOI Listing

Publication Analysis

Top Keywords

cases perniosis
4
perniosis free
4
free flap
4
flap graft
4
graft site
4
site hands
4
cases
1
free
1
flap
1
graft
1

Similar Publications

[Translated article] Use of Anifrolumab in Systemic Lupus Erythematosus, Cutaneous Lupus Erythematosus, and Other Autoimmune Dermatoses.

Actas Dermosifiliogr

January 2025

Servicio de Dermatología, Hospital de Figueres, Fundació Salut Empordà, Girona, Spain; Servicio de Dermatología, Hospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain. Electronic address:

Article Synopsis
  • Anifrolumab is a drug that blocks a specific receptor (IFNAR1) and is approved for treating moderate-to-severe systemic lupus erythematosus (SLE).
  • * In clinical trials, it has shown effectiveness for skin-related lupus issues, even though it's not specifically approved for cutaneous lupus erythematosus (CLE).
  • * Ongoing studies aim to assess its effectiveness for different types of lupus and related conditions, while its common side effects include respiratory infections and herpes zoster.
View Article and Find Full Text PDF

Systemic complications of Aicardi Goutières syndrome using real-world data.

Mol Genet Metab

October 2024

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address:

Article Synopsis
  • Aicardi Goutières Syndrome (AGS) is a rare genetic disorder characterized by a range of systemic health issues and delayed diagnosis, prompting researchers to analyze longitudinal data from medical records to better understand its burden.* -
  • The study included 167 individuals with genetically confirmed AGS, compiling information on demographics, age of onset, and neurological complications; the most frequent genetic mutations associated with AGS were identified.* -
  • Results revealed that gastrointestinal issues were the earliest systemic complications, while neurological symptoms such as tone abnormalities and irritability were prevalent, usually manifesting in infancy.*
View Article and Find Full Text PDF
Article Synopsis
  • - Two cases of chilblain lupus erythematosus (CLE) were reported that may have been triggered by ultraviolet (UV) nail lamps.
  • - The cases, alongside existing literature, indicate a potential connection between the use of UV nail lamps and the development or reactivation of CLE.
  • - More research is necessary to verify this link, but healthcare providers should be cautious about the risks associated with UV nail lamps, particularly for patients with conditions sensitive to light.
View Article and Find Full Text PDF
Article Synopsis
  • Hereditary C1q deficiency (C1QDef) is a rare genetic disorder that disrupts the complement system and can cause symptoms similar to systemic lupus erythematosus (SLE).
  • A study of 12 genetically confirmed C1QDef patients showed elevated expression of interferon-stimulated genes and high levels of interferon alpha in their blood and cerebrospinal fluid, indicating significant immune dysfunction.
  • Treatment with Janus-kinase inhibitors had mixed results, with one patient improving while others continued to struggle with their condition, highlighting the complexity of managing C1QDef.
View Article and Find Full Text PDF
Article Synopsis
  • The most common skin condition linked to COVID-19 is pseudochilblains, commonly referred to as "COVID toes," which are hard to diagnose without a specific test.
  • Two women, aged 30 and 22, were treated for these lesions during the pandemic; neither showed respiratory symptoms, but one had positive serology and both had distinct clinical difficulties post-cold exposure.
  • Their cases highlight the variability of COVID-19 symptoms, suggesting that skin lesions may indicate an interferon response and should be considered in diagnoses during primary care visits.
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!