Results 131 to 140 of about 51,001 (340)

Unusual dermoscopic features of multiple pilomatricomas, including a rare bullous variant

Dermatology Reports
Dear Editor, Pilomatricoma, or Malherbe’s calcifying epithelioma, is a benign neoplasm derived from hair follicle matrix cells. It usually presents as a solitary, firm, slow-growing subcutaneous nodule.
Caterina Mariarosaria Giorgio, Mario Diplomatico, Gaetano Licata, Luca Damiani, Francesco Esposito, Eugenia Veronica Di Brizzi, Filomena Barbato   +6 more
doaj   +1 more source

Tocilizumab for severe and refractory mucous membrane pemphigoid

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Elevated IL‐6 levels identified in mucous membrane pemphigoid support IL‐6 blockade, with tocilizumab demonstrating clinical benefit in nine patients with severe and refractory mucous membrane pemphigoid. Abstract Background Mucous membrane pemphigoid (MMP) is a rare autoimmune blistering disease involving mucous membranes with a potentially ...
Billal Tedbirt, Maud Maho‐Vaillant, Julie Gueudry, Marie‐Laure Golinski, Marion Marcaillou, Blanche Bergeret, Guillaume Chambon, Pierre Bouchetemble, Soumeya Bekri, Abdellah Tebani, Hervé Maillard, Cécile Morice, Anais Vautier, Edgar‐Pierre Libert, Christelle Le Roux‐Villet, Marion Carrette, Olivier Boyer, Vivien Hébert, Sébastien Calbo, André Gillibert, Pascal Joly   +20 more
wiley   +1 more source

Desmoglein ELISA in the Diagnosis of Pemphigus and Its Correlation with the Severity of Pemphigus Vulgaris

Iranian Journal of Allergy, Asthma and Immunology, 2009
Anti-desmoglein 3 and 1 autoantibodies are involved in the pathogenesis of pemphigus diseases. Our objective was to assess the value of ELISA in the diagnosis of pemphigus and its correlation with the severity of pemphigus vulgaris.
Mortazavi Hossein, Shahdi Majid , Amirzargar Ali Akbar , S.Naraghi Zahra, Valikhani Mahin , Daneshpazhooh Maryam, Vasheghani-Farahani Amir, Sedaghat Mojtaba, Chams-Davatchi Cheyda   +8 more
doaj  

Bullous mastocytosis: a Case Report

Journal of the Egyptian Women’s Dermatologic Society
Mastocytosis is a disorder characterized by abnormal mast cell proliferation. The skin is the most common site of involvement. Extracutaneous involvement occurs in systemic mastocytosis with infiltrations in the gastrointestinal tract, lymph nodes, bone ...
Galal El Enany, Noha Nagui, Hanan Nada, Mona R.E. Abdel-Halim, Iman Sany, Ahmad Nada, Omar El Ghanam, Mona M. Korany   +7 more
doaj   +1 more source

[Bullous amyloidosis].

[Rinsho ketsueki] The Japanese journal of clinical hematology, 1993
Although bullous amyloid lesions are very rare, the cutaneous lesions of this type can be a crucial manifestation of plasma cell dyscrasia. [Case Report] A 66-year-old man with a six-year history of multiple myeloma (IgG-lambda, lambda-type Bence Jones proteins) was admitted to the hospital because of hemorrhagic bullous lesions of the skin, chronic ...
openaire   +2 more sources

Incidence of pemphigoid diseases in Northern Germany in 2016 – first data from the Schleswig‐Holstein Registry of Autoimmune Bullous Diseases

, 2021
Nina van Beek, Anna-Karina Weidinger, S Schneider, Andreas Kleinheinz, Regine Gläser, Maike M. Holtsche, Anabelle von Georg, Christoph M. Hammers, Franziska Hübner, Ana Luiza Lima, Damian Gola, Christian D. Sadik, Detlef Zillikens, Alexander Katalinic, Enno Schmidt, Inke R. König   +15 more
openalex   +1 more source

Targeting type 2 inflammation in bullous pemphigoid: current and emerging therapeutic approaches [PDF]

, 2023
Wu Han Toh, Hua-En Lee, Chun‐Bing Chen
openalex   +1 more source

Epidermal necrolysis sequelae: A cohort study on prevalence and risk factors

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Long‐term sequelae after epidermal necrolysis are frequent, multiple and often severe. Cutaneous, ocular and psychological complications are more frequent, with significant socioeconomic impact. Cluster analysis identifies distinct patient profiles, highlighting the need for personalized multidisciplinary follow‐up.
Thanh Vy Nguyen, Thomas Bettuzzi, Karim Zaghbib, Julie Gueudry, Audrey Colin, Kmar Bel Hareth, Narimane Terkmane, Emilie Sbidian, Nicolas de Prost, Saskia Ingen‐Housz‐Oro   +9 more
wiley   +1 more source

Prurigo Pigmentosa: Review of the Literature, Impact of Ketogenic Diets and Proposal of a Hypothesis

Indian Journal of Dermatology
Prurigo pigmentosa (PP) is characterized by an initially pruritic inflammatory rash on the torso and nape of the neck, which fades subsequently to leave a reticular macular hyperpigmentation.
Deniz Demircioğlu, Emel Öztürk Durmaz, Cüyan Demirkesen, Sedef Şahin   +3 more
doaj   +1 more source

Development of Multidisciplinary Consensus‐Informed Guidance for the Management of Paediatric Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis Among Clinicians From Australasian Tertiary Referral Hospitals

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Background Paediatric Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) is a rare, severe mucocutaneous reaction requiring coordinated multidisciplinary care. Existing guidelines provide evidence‐based recommendations, but implementation across tertiary paediatric hospitals requires practical consensus on local resources.
Patrick David Mahar, Thomas Lee, David Orchard, Amy Gray, Laura Scardamaglia, Susan Robertson, Monique Bertinetti, Warwick Teague, Danielle Nizzero, Claire Grills, Ryan Toholka, Danni Bao, Julian Kelly, Joanne Grindlay, Thomas Rozen, Mark Oliver, Nicole Alexander, Ashan Fernando, Anu Matthew, Kiri Chan, Sonia R. Grover, Emma McDonald, Li‐Chuen Wong, Marius Rademaker, Diana Purvis, Katherine Dear, Stephanie Weston, Vanessa Morgan, Anne Halbert, Orli Wargon, Gayle Fischer, Erin Mewton, Emma King   +32 more
wiley   +1 more source