A5030508084- Autoimmune Bullous Skin Diseases
- Coagulation, Bradykinin, Polyphosphates, and Angioedema
- Urticaria and Related Conditions
- Autoimmune and Inflammatory Disorders
- Oral Health Pathology and Treatment
- Drug-Induced Adverse Reactions
- Skin and Cellular Biology Research
- Dermatological diseases and infestations
- Oral and gingival health research
- Cancer and Skin Lesions
- Skin Diseases and Diabetes
- Dermatological and Skeletal Disorders
- Eosinophilic Disorders and Syndromes
- Genetic and rare skin diseases.
- Nail Diseases and Treatments
- Education and Teacher Training
- Monoclonal and Polyclonal Antibodies Research
- Food Allergy and Anaphylaxis Research
- Higher Education Teaching and Evaluation
- Dermatology and Skin Diseases
- Educational theories and practices
- Systemic Lupus Erythematosus Research
- Platelet Disorders and Treatments
- Chemotherapy-related skin toxicity
- Dermatological and COVID-19 studies
Hospital Clínic de Barcelona
2014-2025
Universitat de Barcelona
2012-2022
Consorci d’Atenció Primària de Salut Barcelona Esquerra
2021
Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
2004-2013
Universidad Rovira i Virgili
2009-2013
Universidad de Granada
2000
Epidermolysis bullosa acquisita (EBA) is a complex autoimmune bullous disease with variable clinical presentations and multiple possible diagnostic tests, making an international consensus on the diagnosis of EBA essential. To obtain criteria for EBA. The International Bullous Diseases Group (IBDG) met three times to discuss For final voting exercise, 22 experts from 14 different countries voted 50 items. When > 30% disagreed proposal, discussion was held re‐voting carried out. In total, 48...
Data on the clinical patterns and histopathology of SARS-CoV-2 related skin lesions, as well their relationship with severity COVID-19 are limited.Retrospective analysis a prospectively collected cohort patients infection in teaching hospital Barcelona, Spain, from 1 April to May 2020. Clinical, microbiological therapeutic characteristics, clinicopathological direct immunofluorescence immunohistochemical findings biopsies were analyzed.Fifty-eight out 2761 (2.1%) either consulting emergency...
Facial discoid dermatosis (FDD) is a condition characterized by papules-plaques primarily affecting the face. FDD has been associated with psoriasis, seborrheic dermatitis, and pityriasis rubra pilaris. We conducted retrospective multicenter study 13 patients diagnosed in Spain (2014-2022). Patient demographics, clinical presentations, histopathological findings, treatment outcomes were collected. shows as erythematous-orange, nummular papules and/or plaques dry scales that affect facial...
Abstract Background Prognosis of patients with bullous pemphigoid (BP) is controversial, a 1‐year mortality rate ranging from 6% to 48%. Objective To determine the large cohort BP and identify prognostic factors associated early mortality. Methods Patients diagnosed between January 1, 1990 December 31, 2010 in referral unit for blistering skin diseases at university hospital Spain were studied retrospectively. Outcome measures during first year after diagnosis, standardized poor factors....
Abstract Background Confusion exists regarding interstitial granulomatous dermatitis (IGD) and palisaded neutrophilic (PNGD). Objective To determine whether IGD PNGD are two different entities, or they must be considered as subtypes of the same reactive pattern, thus unification nomenclature is necessary. Methods Observational retrospective multicentre study patients with evaluated between 1999 2019 review their clinical histological features. Results We identified 52 (38 women 14 men)....
Abstract Background Cyclophosphamide has been commonly used for the treatment of pemphigus vulgaris and mucous membrane pemphigoid with satisfactory results. Published data this therapeutic approach bullous are scant showed significant morbidity mortality. Objective To assess clinical efficacy safety low‐dose oral cyclophosphamide (CFM) (50–100 mg/day) in patients refractory pemphigoid. Methods We conducted a retrospective study including treated CFM department Dermatology Hospital Clínic...
We report 4 patients with relatively asymptomatic, annular brownish plaques arising in the skin creases. The lesions had remained stable for months despite many topical treatments. Histological examination revealed an atrophic epidermis a dermal lichenoid inflammatory infiltrate showing marked pigmentary incontinence. These clinical and pathological features were consistent lichen planus pigmentosus-inversus, rare, recently described variant of planus, only 10 cases reported to date. It has...
BACKGROUND Gorlin-Goltz syndrome (GGS) is an autosomal dominant disorder mainly characterized by the presence of multiple basal cell carcinomas (BCC), odontogenic keratocysts jaw, and volar pits. This associated with a wide spectrum developmental anomalies neoplasms. OBJECTIVE To describe dermoscopic characteristics cutaneous GGS lesions performing histopathologic correlation. MATERIALS AND METHODS Cutaneous tumors from five patients affected were included. Clinical dermoscopy images...
Abstract Pancreatic panniculitis is a rare type that only occurs in 2–3% of all patients with pancreatic diseases. It usually described association benign disease and less commonly carcinoma. We describe case as the first manifestation underlying ampullary adenocarcinoma new pancreatitis, polyarthritis ( PPP ‐Syndrome). may be cutaneous allograft rejection after simultaneous pancreas‐kidney transplantation.
Background Scabies is a neglected tropical disease of the skin, causing severe itching, stigmatizing skin lesions and systemic complications. Since 2015, DerMalawi project provide an integrated diseases clinics Tele-dermatology care in Malawi. Clinic based data suggested progressive increase scabies cases observed. To better identify treat individuals with region, we shifted from clinic-based model to community outreach programme. Methodology/Principal findings From May Tele-dermatological...
We report the case of a woman who developed subacute cutaneous lupus erythematosus (SCLE) after exposure to sun while taking cinnarizine and thiethylperazine. The patient recalled that 10 years previously, similar eruption had appeared sunbathing, she was only cinnarizine. SCLE development in this probably drug related there is some evidence played an important pathogenic role.
Granuloma faciale (GF) is a rare, benign inflammatory dermatosis of unknown cause. Some reports have suggested that it could be part the spectrum IgG4-related sclerosing diseases. characterized by single or multiple red-brown nodules, most frequently occurring on face, and can produce severe disfigurement. Treatment difficult, poor outcomes are often seen. Rituximab monoclonal antibody against CD-20 approved US Food Drug Administration for treatment some autoimmune tumoral diseases.To...