Results 41 to 50 of about 3,759 (229)

Adult-onset Still's disease with atypical cutaneous manifestations [PDF]

, 2018
The diagnosis of adult-onset Still's disease (AOSD) can be very difficult. There are no specific tests available, and diagnosis is usually based on a symptom complex and the well-described typical evanescent rash seen in the majority of patients. However,
Juarez, Pablo, Jucglà, Anna, López de Recalde, Mercè, Morales-Ivorra, Isabel, Narváez García, Francisco Javier, Nolla Solé, Joan Miquel, Pascual, María   +6 more
core   +1 more source

Congenital cutaneous mastocytosis mistaken for non‐accidental injury

, 2023
Pediatric Investigation, Volume 7, Issue 3, Page 218-219, September 2023.
Emma Porter, Cynthia Heffron, Lesley Ann Murphy, Cathal O'Connor   +3 more
wiley   +1 more source

Aggressive systemic mastocytosis with skin involvement, the type of generaled urticaria pigmentosa (clinical case)

Vestnik Dermatologii i Venerologii, 2017
The authors describe the clinical observation of a case of the aggressive systemic mastocytosis with skin involvement, the type of generalized urticaria pigmentosa.
E. V. Sokolovskiy, V. V. Iastrebov, A. V. Shcherbatykh, E. R. Machulaitene   +3 more
doaj   +1 more source

Clinical efficacy of omalizumab in chronic spontaneous urticaria is associated with a reduction of FcεRI-positive cells in the skin [PDF]

, 2017
Background. Treatment with omalizumab, a humanized recombinant monoclonal anti-IgE antibody, results in clinical efficacy in patients with Chronic Spontaneous Urticaria (CSU). The mechanism of action of omalizumab in CSU has not been elucidated in detail.
Ashton-Chess, Joanna, Bauer, Andrea, Brehler, Randolf, Canvin, Janice, Erpenbeck, Veit J., Georgiou, Panayiotis, Gericke, Janine, Hillenbrand, Rainer, Jarvis, Philip, Kangas, Michael, Maurer, Marcus, Metz, Martin, Staubach, Petra   +12 more
core   +1 more source

Prostaglandin D2-supplemented “functional eicosanoid testing and typing” assay with peripheral blood leukocytes as a new tool in the diagnosis of systemic mast cell activation disease: an explorative diagnostic study [PDF]

, 2014
Background: Systemic mast cell activation disease (MCAD) is characterized by an enhanced release of mast cell-derived mediators, including eicosanoids, which induce a broad spectrum of clinical symptoms.
A Böhm, C Akin, Christina Ziemann, D Schäfer, D Schäfer, D Schäfer, D Schäfer, D Schäfer, Dirk Schäfer, E Brzezińska-Błaszczyk, E Torrey, EA Mellor, FW Velten, G Krishnaswamy, G Riccioni, G Woszczek, Gerhard J Molderings, GJ Molderings, GJ Molderings, GJ Molderings, GJ Molderings, GS Katsanos, HJ Cooke, HP Horny, HPM van der Kleij, HW Baenkler, HW Baenkler, I Alvarez-Twose, I Kaneko, J Tolar, JA Awad, JA Boyce, JC Cardet, JD Morrow, JH Butterfield, JH Butterfield, JH Butterfield, JH Butterfield, K Alfter, K Brune, K Karimi, K Karimi, K Nordlind, K Tanaka, K Tatemoto, Katrin Jensen, L Maintz, LJ Roberts, M Frieri, M Kulka, M Raithel, M Reinke, M Schmid, MJ Hamilton, N Sismanopoulos, Norbert-Folke Rath, P Valent, P Valent, Peter Dreßen, PJ Turner, R Ramires, RA Lewis, RC Benyon, S Georgin-Lavialle, S O’Sullivan, SA Krumins, SE Dahlén, SJ Galli, SL Lundström, Stefan Brettner, T Luna-Gomes, T Ugajin, U Abel, U Förster, UW Kolck   +74 more
core   +2 more sources

A Perspective on the Use of NB-UVB Phototherapy vs. PUVA Photochemotherapy [PDF]

, 2018
Narrowband UVB (NB-UVB) phototherapy and psoralen-UVA (PUVA) photochemotherapy are widely used phototherapeutic modalities for a range of skin diseases.
Ahmad, Archier, Archier, Aslam, Atzmony, Aydogan, Behrens-Williams, Berroeta, Bhatnagar, Bhatnagar, Bilsland, Bilsland, Bishnoi, Boswell, Brazzelli, Bruynzeel, Calzavara-Pinton, Calzavara-Pinton, Cameron, Cameron, Carter, Chalmers, Chauhan, Chen, Clayton, Collins, Cunningham, Dawe, Dawe, Dawe, Dawe, De, Decock, Der-Petrossian, Diederen, El-Mofty, Engin, Farnaghi, Fernandez-Guarino, Foerster, Garritsen, George, Godt, Gordon, Grandi, Green, Grundmann-Kollmann, Halpern, Harrop, Healy, Hearn, Hindson, Hindson, Hofer, Holme, Hoot, Hudson-Peacock, Ibbotson, Ibbotson, Iraji, Karvonen, Kerscher, Khafagy, Knobler, Kolde, Larko, Lever, Lindelof, Ling, Man, Man, Man, Man, Markham, Mastalier, Mckenna, Menage, Messenger, Millington, Mobacken, Mohamed, Morgado-Carrasco, Murray, Norris, Olsen, Parrish, Pavlovsky, Radakovic, Robinson, Roelandts, Roelandts, Ros, Rosen, Rosen, Rosen, Salem, Sapam, Sevrain, Sezer, Sivaramakrishnan, Snellman, Solak, Stern, Stern, Stern, Stern, Stern, Stern, Tanew, Tanew, Taylor, Tegner, Tzaneva, Van, Van, Wackernagel, Warren, Westerhof, Yones, Yones   +119 more
core   +3 more sources

Mastocitose sistêmica na infância: relato de 3 casos Systemic mastocytosis in childhood: report of 3 cases

Jornal de Pediatria, 2002
Objetivo: mastocitose é o termo usado para um grupo de moléstias caracterizadas pelo acúmulo de mastócitos na pele, com ou sem comprometimento de outros órgãos.
Evódie I. Fernandes, Beatriz C. de Faria, André Cartell, Boaventura A. dos Santos, Tania F. Cestari   +4 more
doaj   +1 more source

Diagnosis and treatment of urticaria in primary care

İstanbul Kuzey Klinikleri, 2019
Urticaria, also known as hives among people, is a very common disease characterized by erythematous, edematous, itchy, and transient plaques that involve skin and mucous membranes.
Melek Aslan Kayiran, Necmettin Akdeniz
doaj   +1 more source

Diagnosis, management and the burden of symptoms of mastocytosis from the physician's perspective: A nationwide study

British Journal of Haematology, EarlyView.
Summary Mastocytosis is categorized into cutaneous mastocytosis (CM), mast cell sarcoma and systemic mastocytosis (SM). Within SM, indolent SM (ISM) is the more frequent subtype. Adult patients with CM but without an extracutaneous biopsy are classified as having mastocytosis in the skin (MIS), a provisional diagnosis.
Julien Rossignol, Laurence Bouillet, Cristina Bulai‐Livideanu, Stéphane Barete, Julie Bruneau, Clément Gourguechon, Laura Polivka, Angèle Soria, Olivier Lortholary, Trevor Stanbury, Benoit Bouquillon, Cedric Sauvage, Rose Marie Javier, Olivier Hermine, Michel Arock, the CEREMAST Network   +15 more
wiley   +1 more source

Chronic Mastocytosis. Case Report and Literature Review

Revista Finlay, 2023
Chronic cutaneous mastocytosis is a genodermatosis of unknown etiology and that is within the group of rare or infrequent diseases. They are characterized by the growth and accumulation of mast cells in the skin and other organs of unknown cause and ...
Iraima Mayón Moya, Danibys Garcell Peña, José Manuel Peraza Ramos   +2 more
doaj