13 research outputs found
Naevus Lentiginosus Linearis: A Distinct Skin Disorder
Comment in Acta Derm Venereol. 2011 Mar;91(2):209; author reply 209.Congenital naevi of the melanocytic system include numerous types, which differ in their clinical appearance, pattern of distribution, and histopathological features (1). Examples are large congenital melanocytic naevus, macular naevus spilus, papular naevus spilus, café-au-lait macules of neurofibromatosis 1, café-au-lait macules arranged in broad bands as noted in McCune-Albright syndrome, partial unilateral lentiginosis, naevus achromicus (naevus depigmentosus), phylloid hypermelanosis, and phylloid hypomelanosis (1–3).
We describe here two patients with a systematized pigmentary naevus that differed from all naevi reported so far.Ye
Incontinencia pigmenti. Estudio descriptivo de la experiencia en dos centros hospitalarios.
Incontinentia pigmenti is a rare genodermatosis of inheritance linked to the Xchromosome that affects tissues derived from ectoderm. The aim of the study is to review, as completely as possible, the cases diagnosed in paediatric patients in two hospitals. A retrospective cross-sectional study was carried out, using the clinical, analytical, radiological, and genetic data of paediatric patients diagnosed with incontinentia pigmenti from 2004 to 2018. The data collected were analysed and evaluated at a multidisciplinary level. A total of thirteen patients diagnosed with incontinentia pigmenti were included in the study. All of them were female. A genetic study was performed on 11 patients, which confirmed findings compatible with incontinentia pigmenti in 10 of them. Extracutaneous involvement associated with the disease was observed at neurological level (radiological findings in 6 cases, and clinical expression in 3 of them), ophthalmological level (4 cases), dental level (7 cases), and haematological level (4 cases). A presentation is given of the most complete study published so far of incontinentia pigmenti in Spain. In this study, the results of the disease manifestations were similar to the largest case series published internationally, which reinforces the importance of a multidisciplinary study and follow-up
Nueva mutación SLC27A4 asociada a síndrome ictiosis prematuridad y síndrome compartimental.
Colagenosis perforante reactiva adquirida como síndrome paraneoplásico de adenocarcinoma de pulmón
Comunicación - HU549 - 202102
Descripción: Comunicación es un curso de formación general, sin prerrequisito, de carácter práctico y dirigido a
los estudiantes de los primeros ciclos de las carreras de la Facultad de Ciencias de la Salud (Medicina,
Odontología, Terapia Física, Nutrición y Dietética, Psicología y Medicina Veterinaria). En el curso, se asume el
proceso de redacción, más allá de sus aspectos técnicos, como una práctica interactiva, participativa y de
orientación sociocrítica.
Propósito: Esta asignatura busca desarrollar la competencia general de comunicación escrita, del modelo
educativo UPC, en el nivel 1. Esto implica desarrollar las habilidades explicativas y argumentativas básicas del
estudiante en la variedad académica del español. De este modo, estará en la capacidad de producir textos
académicos y profesionales de manera coherente, informada y adecuada a las necesidades discursivas y
temáticas generales de las carreras de Ciencias de la Salud. Asimismo, por su enfoque de intervención en la
realidad social de la salud en nuestro país, el curso busca convertirse en un punto de partida hacia la
investigación y la consecución de la misión de la universidad
Consenso español sobre el hemangioma infantil.
Infantile haemangiomas are benign tumours produced by the proliferation of endothelial cells of blood vessels, with a high incidence in children under the age of one year (4-10%). It is estimated that 12% of them require treatment. This treatment must be administered according to clinical practice guidelines, expert experience, patient characteristics and parent preferences. The consensus process was performed by using scientific evidence on the diagnosis and treatment of infantile haemangiomas, culled from a systematic review of the literature, together with specialist expert opinions. The recommendations issued were validated by the specialists, who also provided their level of agreement. This document contains recommendations on the classification, associations, complications, diagnosis, treatment, and follow-up of patients with infantile haemangioma. It also includes action algorithms, and addresses multidisciplinary management and referral criteria between the different specialities involved in the clinical management of this type of patient. The recommendations and the diagnostic and therapeutic algorithms of infantile haemangiomas contained in this document are a useful tool for the proper management of these patients