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IgG4-related sclerosing disease
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TLDR
AIP as discussed by the authors : AIP is a clinicopathological organization that provides a platform for the development and management of medical care.http://www.aip.org.cn/Citations
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Journal ArticleDOI
Recommendations for the nomenclature of IgG4-related disease and its individual organ system manifestations
John H. Stone,Arezou Khosroshahi,Vikram Deshpande,John K.C. Chan,J. Godfrey Heathcote,Rob C. Aalberse,Atsushi Azumi,Daniel Bloch,William R. Brugge,Mollie N. Carruthers,Wah Cheuk,Lynn D. Cornell,Carlos Fernandez-del Castillo,Judith A. Ferry,David G. Forcione,Günter Klöppel,Daniel L. Hamilos,Terumi Kamisawa,Satomi Kasashima,Shigeyuki Kawa,Mitsuhiro Kawano,Yasufumi Masaki,Kenji Notohara,Kazuichi Okazaki,Ji Kon Ryu,Takako Saeki,Dushyant V. Sahani,Yasuharu Sato,Thomas C. Smyrk,James R. Stone,Masayuki Takahira,Hisanori Umehara,George Webster,Motohisa Yamamoto,Eunhee S. Yi,Tadashi Yoshino,Giuseppe Zamboni,Yoh Zen,Suresh T. Chari +38 more
TL;DR: John H. Stone, Arezou Khosroshahi, Vikram Deshpande, John K.Stone, Masayuki Takahira, Hisanori Umehara, George Webster, Motohisa Yamamoto, Eunhee Yi, Tadashi Yoshino, Giuseppe Zamboni, Yoh Zen, and Suresh Chari.
Journal ArticleDOI
Rituximab therapy leads to rapid decline of serum IgG4 levels and prompt clinical improvement in IgG4-related systemic disease.
TL;DR: Treatment with rituximab led to prompt clinical and serologic improvement in these patients with refractory IgG4-RSD, and is a viable treatment option for this condition, suggesting that ritUXimab achieves its effects in IgG 4- RSD by depleting the pool of B lymphocytes that replenish short-lived IgG3-secreting plasma cells.
Journal ArticleDOI
Endoscopic retrograde pancreatography criteria to diagnose autoimmune pancreatitis: an international multicentre study
Aravind Sugumar,Michael J. Levy,Terumi Kamisawa,George Webster,Myung-Hwan Kim,Felicity Enders,Zahir Amin,Todd H. Baron,Michael H. Chapman,Nicholas I. Church,Jonathan E. Clain,Naoto Egawa,Gavin Johnson,Kazuichi Okazaki,Randall K. Pearson,Stephen P. Pereira,Bret T. Petersen,Samantha Read,Raghuwansh P. Sah,Neomal S. Sandanayake,Naoki Takahashi,Mark Topazian,Kazushige Uchida,Santhi Swaroop Vege,Suresh T. Chari +24 more
TL;DR: The ability to diagnose AIP based on ERP features alone is limited but can be improved with knowledge of some key features.
Journal ArticleDOI
Usefulness of serum IgG4 in the diagnosis and follow-up of autoimmune pancreatitis: a systematic literature review and meta-analysis
TL;DR: The heterogeneity of the studies published until now means that more studies are necessary in order to better evaluate the true accuracy of IgG4 in discriminating AIP versus other autoimmune diseases, and its determination should be included in the diagnostic workup of this disease.
Journal ArticleDOI
IgG4-related sclerosing disease, an emerging entity: a review of a multi-system disease.
TL;DR: The principal histopathologic findings in several extranodal sites include lymphoplasmacytic infiltration, lymphoid follicle formation, sclerosis and obliterative phlebitis, along with atrophy and destruction of tissues.