A5044012555- Autoimmune Bullous Skin Diseases
- Fungal Infections and Studies
- Neonatal skin health care
- Autoimmune and Inflammatory Disorders
- Cancer and Skin Lesions
- Chemotherapy-related skin toxicity
- Histiocytic Disorders and Treatments
- Teratomas and Epidermoid Cysts
- Vascular anomalies and interventions
- Urticaria and Related Conditions
- Hidradenitis Suppurativa and Treatments
- Vascular Malformations and Hemangiomas
- Mast cells and histamine
- Nail Diseases and Treatments
- Antifungal resistance and susceptibility
- Infectious Diseases and Mycology
- Sympathectomy and Hyperhidrosis Treatments
- Dermatology and Skin Diseases
- Eosinophilic Disorders and Syndromes
- Genetic and rare skin diseases.
- Skin and Cellular Biology Research
- Colorectal and Anal Carcinomas
- Cell Adhesion Molecules Research
- Food Allergy and Anaphylaxis Research
- Dermatological and Skeletal Disorders
University Hospital Limerick
2023
Children's Health Ireland at Crumlin
2022-2023
Our Lady of Lourdes Hospital
2023
Mayo Clinic in Arizona
2019
Coccidioidomycosis is a fungal infection that endemic to the semiarid regions of southwestern United States, particularly Arizona and California.1,2 It primarily pulmonary infection, acquired via inhalation spores. Cutaneous manifestations coccidioidomycosis are common can occur 3 pathogenic mechanisms: reactive eruptions, primary cutaneous secondary dissemination skin.2
Abstract A 50-year-old man with a background of prostate cancer was admitted fever, weight loss, polyarthritis, symptomatic anaemia and raised inflammatory markers. Multiple tender indurated violaceous plaques on the trunk limbs were suggestive Sweet syndrome. Skin biopsies revealed neutrophilic dermal infiltrate pandermal vasculitis affecting small vessels. Laboratory screening (including rheumatoid factor, anticyclic citrullinated peptide, antinuclear antibody, antineutrophil cytoplasm...
Kaposiform lymphangiomatosis is a rare lymphatic anomaly that occurs in children and associated with life-threatening complications. The somatic mutation NRAS Q61R (c.182A>G) has been identified lesional tissue samples of patients kaposiform lymphangiomatosis, can be used to differentiate this condition from other complex anomalies guide treatment. Tissue sampling inherently risky due its involvement thoracic abdominal organs coagulopathy. Analysis cell-free DNA isolated blood plasma...
Abstract An 8-year-old boy with epidermolytic ichthyosis (EI) due to a heterozygous KRT1 mutation presented striking bullous skin eruption. Microbiological swabs were sent, and oral antibiotics prescribed for suspected impetigo. He deteriorated clinically, developing fever more extensive pustular rash reminiscent of generalized psoriasis (GPP). Skin biopsies from two distinct cutaneous sites revealed histology strongly supportive psoriasis. Oral ciclosporin was commenced in addition...
Dermatofibrosarcoma protruberans (DFSP) is an uncommon, locally aggressive tumour arising.it accounts for 0.1% of all malignancies.Although it can present any time from the neonatal period onwards, paediatric cases are rare, and account 6% DFSP.The cause dermatofibrosarcoma protuberans not known but, injury to skin in affected location could be a risk factor.It occur within pre-existing scars tattoos.Clinical presentation typically as solitary plaque or nodule most often on trunk...
This is the case of an infant with a persistent dermatitis affecting perioral, acral and napkin areas, in whom simple oral therapy provided rapid treatment response.