A5087439688- Cutaneous lymphoproliferative disorders research
- Nail Diseases and Treatments
- Fungal Infections and Studies
- Autoimmune and Inflammatory Disorders
- Lymphoma Diagnosis and Treatment
- Autoimmune Bullous Skin Diseases
- Cutaneous Melanoma Detection and Management
- Dermatological and Skeletal Disorders
- Genetic and rare skin diseases.
- Chemotherapy-related skin toxicity
- Hematological disorders and diagnostics
- Orthopedic Surgery and Rehabilitation
- Dermatological and COVID-19 studies
- Genital Health and Disease
- Oral Health Pathology and Treatment
- Dermatologic Treatments and Research
- Nonmelanoma Skin Cancer Studies
- Melanoma and MAPK Pathways
- melanin and skin pigmentation
- Inflammatory Myopathies and Dermatomyositis
- Cancer and Skin Lesions
- Hedgehog Signaling Pathway Studies
- Skin Diseases and Diabetes
- Parvovirus B19 Infection Studies
- Infectious Diseases and Mycology
Oxfam
2020
John Wiley & Sons (United States)
2020
John Wiley & Sons (United Kingdom)
2020
Hudson Institute
2020
Hospital Universitario 12 De Octubre
2013-2019
Research Institute Hospital 12 de Octubre
2014-2018
Comunidad de Madrid
2016
Universidad Complutense de Madrid
2016
Data regarding response to treatment in lymphomatoid papulosis (LyP) are scarce.To assess the daily clinical practice approach LyP and first-line treatments.This was a retrospective study enrolling 252 patients with LyP.Topical steroids, methotrexate phototherapy were most common treatments, prescribed for 35%, 20% 14% of patients, respectively. Complete (CR) achieved 48% treated patients. Eczematous lesions significantly increased relative risk (RR) not achieving CR (RR = 1.76; 95% CI...
Abstract Background Reliable prognostic factors for patients with primary cutaneous anaplastic large cell lymphoma ( PCALCL ) are lacking. Objective To identify specific survival in . Methods Using the convenience sampling method, diagnosed from May 1986 to August 2017 16 University Departments were retrospectively reviewed. Results One hundred eight included (57 males). Median age at diagnosis was 58 years. All of them showed T1‐3N0M0 stages. Seventy per cent cases presented a solitary...
Abstract: The presence of a granulomatous reaction in cutaneous lymphomas has been described the past, especially mycosis fungoides (MF), where “granulomatous” variant disease is well known. We describe patient with MF (GMF) who followed for 13 years presenting erythematosquamous plaques on his fingers and toes, ankles, heels, abdomen, which microscopic examination showed lichenoid admixed neoplastic proliferation small-sized, atypical CD4 + lymphocytes. GMF characterized by intermingled...
Abstract Onychoheterotopia is a rare condition characterized by ectopic nail tissue growth. It digital mass that commonly misdiagnosed. We describe 6‐year‐old girl who presented with onychoheterotopia after trauma to the digit. Her was incorrectly diagnosed as common wart. important include in differential diagnosis of masses, especially setting previous traumatic injury.
Acta Derm Venereol 95 © 2014 The Authors. doi: 10.2340/00015555-2001 Journal Compilation 2015 Dermato-Venereologica. ISSN 0001-5555 A 53-year-old woman presented with an isolated and nontender necrotic nodule on her left eyelid, which had begun as a small rapid-growing inflammatory papule 3 weeks earlier. Physical examination revealed 15 mm, erythematous, firm but mobile crusted core (Fig. 1A). No other cutaneous or mucosal lesions were identified. There was neither regional lymphadenopathy...
Neurocristic cutaneous hamartomas (NCHs) are rarely reported tumors with divergent differentiation derived from persistently active pluripotent cells the neural crest. They result aberrant development of neuromesenchyme, and they can express fibrogenic, melanocytic, and/or neurosustentacular differentiation. Thus, congenital melanocytic nevus also represents a neurocristic dysplasia skin in which melanogenic arrested located reticular dermis, nodular proliferative hamartoma may arise within...
Abstract: Congenital melanocytic nevi (CMN) are benign proliferations that usually present at birth. A somatic mosaicism for an NRAS point mutation is responsible the several phenotypic abnormalities may be associated with congenital nevi. We report case of a 7-year-old boy proliferative nodule (PN) arising in Giant CMN completely excised and visceral intraspinal melanoma metastases no evidence primary cutaneous melanoma. The careful analysis clinical, morphologic, molecular features allowed...
Classically known as the "Great Imitator", diagnosis of syphilis continues to be an enormous challenge. We describe a case isolated oral lesions sole presentation secondary and only clinical clue previously undiagnosed human immunodeficiency virus infection. The current increase in new cases is leading reemergence forgotten old scenarios, which physicians should bear mind within differential their daily practice.