Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.ad.2015.10.021 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
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.
View Article and Find Full Text PDFA Clinico-Epidemiological Study on Porokeratosis.
Indian J Dermatol
August 2024
Department of Dermatology, Mysore Medical College and Research Institute, Mysore, Karnataka, India.
Article Synopsis
- Porokeratosis (PK) is a chronic skin condition that presents as elevated, hyperkeratotic papules or plaques with a distinct raised border, linked to mutations in the mevalonate kinase enzyme.
- The study involved 11 patients, mostly females, with Mibelli's type being the most common form observed; diagnostic techniques included clinical evaluation, dermoscopy indicating a double-marginated border, and histopathological examination showing the cornoid lamella.
- Regular monitoring is essential for early detection of potential malignant changes in PK variants, emphasizing the importance of using dermoscopy for non-invasive diagnosis.
Intradermal Syringocystadenoma Papilliferum on the Popliteal Fossa: A Rare Dermal Variant in an Atypical Location.
R I Med J (2013)
July 2024
Department of Dermatology, Warren Alpert Medical School of Brown University, Providence, Rhode Island.
Article Synopsis
- Syringocystadenoma papilliferum (SCAP) is a harmless lump usually found on the scalp and face, often starting in childhood.
- A 55-year-old man had a rare SCAP lump on the back of his knee that didn't hurt and was small in size.
- The doctors took a sample of the lump and decided to remove it, as this type of SCAP is very uncommon in that area of the body.
A case of filgrastim-induced neutrophilic dermatosis of the dorsal hands in a patient with Felty Syndrome.
Dermatol Online J
December 2023
Department of Dermatology, Baylor College of Medicine, Houston, Texas, USA.
Article Synopsis
- * Felty syndrome, which can occur in long-term rheumatoid arthritis patients, involves symptoms like neuropathy and low white blood cell counts, and treatments for it might trigger Sweet syndrome.
- * A 64-year-old man with Felty syndrome and a complicated medical history developed painful skin lesions on his hands, leading to a diagnosis of NDDH based on a skin biopsy and other lab results.
Life-threatening hypereosinophilic syndrome in a patient with rheumatoid arthritis: a case report.
ARP Rheumatol
January 2024
Rheumatology Department, Centro Hospitalar Lisboa Ocidental - EPE, Hospital de Egas Moniz, Lisboa, Portugal.
Article Synopsis
- Hypereosinophilia is rare in rheumatoid arthritis (RA) but can occur in severe, long-term cases, particularly where there are extra-articular symptoms and high rheumatoid factor levels.
- A 46-year-old woman with untreated severe RA experienced critical symptoms leading to cardiac arrest, prompting emergency medical intervention that revealed hypereosinophilia and inflammatory conditions.
- After ruling out other causes, she was diagnosed with hypereosinophilic syndrome associated with RA and successfully treated with glucocorticoids and methotrexate, achieving clinical remission within 12 weeks.
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!