Results 91 to 100 of about 19,540 (227)

WHO classification of skin tumours: key updates in the fifth edition

Histopathology, Volume 88, Issue 3, Page 555-568, February 2026.
This review article summarizes the key updates in the 5th edition of the WHO Classification of Skin Tumours. It provides an overview of the major changes and new entities specific to the skin section, covering areas such as epidermal, melanocytic, mesenchymal and other tumours. The 5th edition of the World Health Organization Classification of Tumours (
Gabrielle Goldman‐Lévy, Raymond Barnhill, Boris C. Bastian, Werner Kempf, David Elder, Pedram Gerami, Wayne Grayson, Dmitry Kazakov, Daniela Massi, Jane Messina, Arnaud de la Fouchardière, Alexander J. Lazar, Thomas Brenn, Brian Rous, Andrew Field, Anthony Gill, Jennelle C. Hodge, Joseph D Khoury, Katia Leite, Shahin Sayed, Puay Hoon Tan, Rosalie Elenitsas, Eduardo Calonje, Lyn M. Duncan, Liang Zhiyong, Holger Moch, Rajendra Singh, Harshima Wijesinghe, Ian Cree, Dilani Lokuhetty   +29 more
wiley   +1 more source

Noninvasive Urinary Monitoring of Progression in IgA Nephropathy. [PDF]

, 2019
Standard methods for detecting and monitoring of IgA nephropathy (IgAN) have conventionally required kidney biopsies or suffer from poor sensitivity and specificity.
Fervenza, Fernando C, Lafayette, Richard A, Sarwal, Minnie M, Sarwal, Reuben D, Yang, Joshua YC   +4 more
core   +1 more source

When Autoimmunity Meets Malignancy: A Rare Case of Concomitant Systemic Lupus and Multiple Myeloma

Clinical Case Reports
The association between systemic lupus erythematosus (SLE) and multiple myeloma (MM) is rare, with fewer than 20 cases reported in the literature, raising questions about the link between chronic immune dysregulation and oncogenesis.
Solohery Jean Noël Ratsimbazafy, Havantsoa Nomena Fandresena Andrianarisambatra, Rajo Païdia Radinasoa, Hitsy Andraina Razafindrazaka, Tahianasoa Randriamampianina, Rija Mikhaël Miandrisoa, Fidiarivony Ralison, Hanta Marie Danielle Vololontiana   +7 more
doaj   +1 more source

Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency [PDF]

, 2017
In this study, we describe four patients from two unrelated families of different ethnicities with a primary immunodeficiency, predominantly manifesting as susceptibility to Epstein-Barr virus (EBV)–related diseases.
Abolhassani, Agematsu, Agematsu, Agematsu, Aguilar, Alkhairy, Alkhairy, Allam, Annika C. Karlsson, Asghar Aghamohammadi, Aydan Ikinciogullari, Bertrand Boisson, Borst, Bryceson, Callan, Casanova, Casanova, Chaigne-Delalande, Chan, Cinque, Cohen, David A. Price, De Colvenaer, de Miranda, Emily S.J. Edwards, Emma Gostick, Faitelson, Figen Dogu, Goodwin, Han, Hassan Abolhassani, Helen C. Su, Helen F. Matthews, Hendriks, Hendriks, Hintzen, Hislop, Hislop, Huie Jing, Itan, Itan, Jacobs, Jacquot, Jean-Laurent Casanova, Joshua J. McElwee, Juliet Frederiksen, Jung, Kircher, Kwon, Lennart Hammarström, Lens, Likun Du, Mami Matsuda-Lennikov, Marcus Buggert, Michael J. Lenardo, Mingyan Fang, Munitic, Nima Rezaei, Nolte, Nurdan Tacyildiz, Palendira, Palendira, Picard, Price, Qiang Pan-Hammarström, Roederer, Rosa Romano, Rozina Caridha, Salzer, Sangeeta Bade, Scholtysik, Scott, Sevgi Kostel Bal, Silva, Stephan Borte, Stuart G. Tangye, Sule Haskologlu, Tangye, Tangye, Taylor, Tesselaar, Tesselaar, Umaimainthan Palendira, van Montfrans, Vossen, Waggoner, Yu Zhang   +86 more
core   +2 more sources

Idiopathic noncirrhotic portal hypertension: current perspectives [PDF]

, 2016
The term idiopathic noncirrhotic portal hypertension (INCPH) has been recently proposed to replace terms, such as hepatoportal sclerosis, idiopathic portal hypertension, incomplete septal cirrhosis, and nodular regenerative hyperplasia, used to describe ...
D'AMATI, Giulia, Gioia, Stefania, Nicoletti, Valeria, PENTASSUGLIO, ILARIA, RIGGIO, Oliviero, VALENTE, MICHELE   +5 more
core   +1 more source

Prolonged Impairment of Immunological Memory After Anti-CD20 Treatment in Pediatric Idiopathic Nephrotic Syndrome

Frontiers in Immunology, 2019
Anti-CD20 therapy is effective in idiopathic nephrotic syndrome (INS). However, transient or sustained hypogammaglobulinemia predisposing to an increased risk of infectious diseases can follow treatment in some patients. We analyzed the long-term effects
Manuela Colucci, Rita Carsetti, Jessica Serafinelli, Salvatore Rocca, Laura Massella, Antonio Gargiulo, Anna Lo Russo, Claudia Capponi, Nicola Cotugno, Ottavia Porzio, Andrea Onetti Muda, Paolo Palma, Francesco Emma, Francesco Emma, Marina Vivarelli, Marina Vivarelli   +15 more
doaj   +1 more source

Impact of rare diseases in oral health [PDF]

, 2016
Rare diseases (RD) are those that present a lower prevalence than 5 cases per 10.000 population. The main objective of this review was to study the effect on oral health in rare diseases, while the secondary objective of the study is theme upgrade ...
Castellanos Cosano, Lizett, Machuca Portillo, Guillermo, Molina García, Ana, Posada de la Paz, Manuel   +3 more
core   +2 more sources

A Late-Diagnosed Case of Common Variable Immunodeficiency

Ahi Evran Medical Journal
Common Variable Immunodeficiency (CVID) is the most common form of primary immunodeficiency (PID). CVID is characterized by decreased serum immunoglobulin levels, decreased or absent antibody production, and normal or low B-lymphocyte counts.
Coşkun Doğan, Nurhan Kasap, Cihan Örçen   +2 more
doaj   +1 more source

Late-Onset Antibody Deficiency Due to Monoallelic Alterations in NFKB1

Frontiers in Immunology, 2019
Adult-onset primary immunodeficiency is characterized by recurrent infections, hypogammaglobulinemia, and poor antibody response to vaccines. In this study, we have analyzed targeted gene panel sequencing results of 270 patients diagnosed with antibody ...
Claudia Schröder, Claudia Schröder, Georgios Sogkas, Manfred Fliegauf, Manfred Fliegauf, Thilo Dörk, Di Liu, Leif G. Hanitsch, Sophie Steiner, Carmen Scheibenbogen, Roland Jacobs, Bodo Grimbacher, Bodo Grimbacher, Bodo Grimbacher, Bodo Grimbacher, Reinhold E. Schmidt, Reinhold E. Schmidt, Reinhold E. Schmidt, Reinhold E. Schmidt, Faranaz Atschekzei, Faranaz Atschekzei   +20 more
doaj   +1 more source

Comparison of diagnostic criteria for Common Variable Immunodeficiency Disorder

Frontiers in Immunology, 2014
Common Variable Immunodeficiency disorders (CVID) are the most frequent symptomatic primary immune deficiency condition in adults. The genetic basis for the condition is not known and no single clinical feature or laboratory test can establish the ...
Rohan eAmeratuga, Maia eBrewerton, Charlotte eSlade, Anthony eJordan, David eGillis, Richard eSteele, Wikke eKoopmans, See-Tarn eWoon   +7 more
doaj   +1 more source