Results 111 to 120 of about 1,581,690 (305)

Falsely low IgG4 in routine analysis - How not to miss IgG4 disease [PDF]

, 2016
Background IgG4 disease can have apparently “normal” levels of IgG4 due to antigen excess conditions. IgG4 measurement therefore appears falsely low.
Carruthers, Chari, Deshpande, Ghazale, Hamano, Heidelberger, Jacobs, Jefferis, Kamisawa, Kamisawa, Khosroshahi, Khosroshahi, Lock, Mahajan, Matasubayashi, Morselli-Labate, Neild, Oxelius, Oxelius, Parker, Pieringer, Sadler, Shimosegawa, Umehara, Umehara   +24 more
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Interfollicular Plasmacytosis and Hyperplastic Germinal Centers in Idiopathic Multicentric Castleman Disease, Idiopathic Plasmacytic Lymphadenopathy Subtype

American Journal of Hematology, EarlyView.
Stephanie Quon, Clarissa Skorupski, Christophe Langlois, Lee Mozessohn, Carlo Hojilla, Luke Y. C. Chen   +5 more
wiley   +1 more source

Renal Manifestations of IgG4-Related Disease: A Concise Review

International Journal of Nephrology
IgG4-related disease (IgG4-RD) is an immune-mediated disorder marked by fibro-inflammatory masses that can infiltrate multiple organ systems. Due to its relatively recent discovery and limited understanding of its pathophysiology, IgG4-related disease ...
Shahrukh T. Towheed, Wayel Zanjir, Kevin Yi Mi Ren, Jocelyn Garland, Marie Clements-Baker   +4 more
doaj   +1 more source

The great pretender : Autoimmune Pancreatitis [PDF]

, 2014
Autoimmune pancreatitis is a benign disorder which frequently presents with symptoms and imaging suggestive of pancreatic malignancy. Up to 21% of pancreatoduodenectomies performed for suspected pancreatic cancer are found to have benign disease ...
Azzopardi, Neville
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Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients

PLoS ONE, 2017
Objectives To assess efficacy and safety of rituximab (RTX) as induction therapy, maintenance of remission and treatment of relapses in a cohort of IgG4-related disease (IgG4-RD) patients.
M. Ebbo, A. Grados, M. Samson, M. Groh, A. Loundou, A. Rigolet, B. Terrier, C. Guillaud, C. Carra-Dallière, F. Renou, A. Pozdzik, P. Labauge, S. Palat, J. Berthelot, J. Pennaforte, A. Wynckel, C. Lebas, N. Le Gouellec, T. Quéméneur, K. Dahan, F. Carbonnel, G. Leroux, A. Perlat, A. Mathian, P. Cacoub, E. Hachulla, N. Costedoat-Chalumeau, J. Harlé, N. Schleinitz   +28 more
semanticscholar   +1 more source

IgG4-related disease: Changing epidemiology and new thoughts on a multisystem disease

Journal of Translational Autoimmunity, 2020
IgG4-related disease (IgG4-RD) represents an immune-mediated fibroinflammatory condition with peculiar histopathologic changes that can affect various organs. In 2012 its unified nomenclature was published, which allows to abandon other synonymous names.
A. Floreani, K. Okazaki, K. Uchida, M. Gershwin   +3 more
semanticscholar   +1 more source

Immunotherapy‐Related Cutaneous Toxicities in Melanoma: A Dermoscopic Perspective

JEADV Clinical Practice, EarlyView.
Dermoscopy serves as a valuable tool in the everyday dermatological and oncological practice for melanoma patients, allowing for the prompt identification of immune‐related cutaneous toxicities and guiding clinicians toward appropriate therapeutic decisions.
Grażyna Kamińska‐Winciorek, Iris Zalaudek, Karolina Zarańska, Bożena Cybulska‐Stopa   +3 more
wiley   +1 more source

Evaluation of IgG4+ Plasma Cell Infiltration in Patients with Systemic Plasmacytosis and Other Plasma Cell-infiltrating Skin Diseases

Acta Dermato-Venereologica, 2018
Systemic plasmacytosis is a rare skin disorder characterized by marked infiltration of plasma cells in the dermis. IgG4-related disease is pathologically characterized by lymphoplasmacytic infiltration rich in IgG4+ plasma cells, storiform fibrosis, and ...
Shintaro Takeoka, Masahiro Kamata, Carren Sy Hau, Mihoko Tateishi, Saki Fukaya, Kotaro Hayashi, Atsuko Fukuyasu, Takamitsu Tanaka, Takeko Ishikawa, Takamitsu Ohnishi, Yuko Sasajima, Shinichi Watanabe, Yayoi Tada   +12 more
doaj   +1 more source

Refractory Eczema as a Presenting Feature of Common Variable Immunodeficiency

JEADV Clinical Practice, EarlyView.
ABSTRACT Common variable immunodeficiency (CVID) is the most prevalent symptomatic inborn error of immunity (IEI) in adults. It presents with recurrent infections and non‐infectious complications, including autoimmunity, lymphoproliferation and dermatitis.
Mercedes Sanchez‐Diaz, Lars Matthies, Andrea Vanegas Ramirez   +2 more
wiley   +1 more source

A case of primary Hodgkin's lymphoma of the parotid gland. Case report and differentian diagnosis from Kuttner's Syndrom [PDF]

, 2018
We report a rare case of primary Hodgkin’s lymphoma (HL) of the submandibular gland, with initially diagnosis of Kuttner’s Syndrom. A 48 years old man was referred to our hospital foe evaluation of a submandibular mass.
Di Cello, P., Gabriele, R., Izzo, L., Izzo, P., Izzo, S., Millarelli, F., Pugliese, F., Razionale, F., Scarano Catanzaro, V.   +8 more
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