Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.jaad.2009.10.030 | DOI Listing |
Publication Analysis
Top Keywords
adult perniosis
4
perniosis cryoglobulinemia
4
cryoglobulinemia retrospective
4
retrospective study
4
study review
4
review literature
4
adult
1
cryoglobulinemia
1
retrospective
1
study
1
Similar Publications
Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System Inflammation.
J Clin Immunol
August 2024
Laboratory of Neurogenetics and Neuroinflammation, Imagine Institute, INSERM UMR1163, Paris, France.
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.
A case of Rowell syndrome after a herpes simplex infection and prolonged sun exposure.
Skin Health Dis
August 2024
MVZ Dermatologisches Zentrum Bonn Bonn Germany.
Article Synopsis
- Rowell Syndrome is a rare condition that combines features of erythema exudativum multiforme (EEM) and lupus erythematosus (LE).
- The new diagnostic criteria include three major criteria (different types of LE, EEM-like skin lesions, and a specific antibody pattern) and several minor criteria (chilblains and certain positive antibody tests).
- Treatment options are similar to those for EEM and LE, often showing positive results with medications like oral cortisone and azathioprine, and the presented case showed good improvement with topical treatments following a herpes infection and sun exposure.
Chilblain Lupus Erythematosus.
N Engl J Med
July 2024
Kaohsiung Medical University, Kaohsiung, Taiwan.
Chilblains as a non-specific skin eruption in a patient with myelodysplastic neoplasm.
Eur J Dermatol
June 2024
Department of Dermatology, Ehime University Graduate School of Medicine, Toon, Ehime, Japan.
Diagnosis and management of COVID toes in outpatients: a case report.
J Med Case Rep
June 2024
University Center for Primary Care and Public Health, Unisanté, Lausanne, Switzerland.
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.
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!