Journal Article10.1080/03009740500499484
A case of IgG4-related autoimmune disease with multiple organ involvement.
Hideki Nakamura,H Wada,Tomoki Origuchi,A. Kawakami,Naota Taura,Toshiyuki Aramaki,Keita Fujikawa,Nozomi Iwanaga,Yasumori Izumi,Kouichiro Aratake,Hiroaki Ida,Takashi Taguchi,J Irie,M Akiyama,Akinari Mizokami,T Tsutsumi,K Eguchi +16 more
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Citations
Proposal for diagnostic criteria for IgG4-related kidney disease
Mitsuhiro Kawano,Takako Saeki,Hitoshi Nakashima,Shinichi Nishi,Yutaka Yamaguchi,Satoshi Hisano,Nobuaki Yamanaka,Dai Inoue,Motohisa Yamamoto,Hiroki Takahashi,Hideki Nomura,Takashi Taguchi,Hisanori Umehara,Hirofumi Makino,Takao Saito +14 more
TL;DR: The provisional criteria and algorithm appear to be useful for clarifying the entity of IgG 4-RKD and seeking underlying IgG4- RKD cases; however, further experience is needed to confirm the validity of these criteria.
431
Clinicopathological characteristics of patients with IgG4-related tubulointerstitial nephritis
Takako Saeki,Shinichi Nishi,Naofumi Imai,Tomoyuki Ito,Hajime Yamazaki,Mitsuhiro Kawano,Motohisa Yamamoto,Hiroki Takahashi,Shoko Matsui,Shinji Nakada,Tomoki Origuchi,Akira Hirabayashi,Noriyuki Homma,Yutaka Tsubata,Takuma Takata,Yoko Wada,Akihiko Saito,Sachiko Fukase,Kunihiro Ishioka,Kana Miyazaki,Yasufumi Masaki,Hisanori Umehara,Susumu Sugai,Ichiei Narita +23 more
TL;DR: It is suggested that renal parenchymal lesions actually develop in association with IgG4-related disease, for which the term 'IgG 4-related tubulointerstitial nephritis' is proposed.
403
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.
132
Characteristic tubulointerstitial nephritis in IgG4-related disease.
Yutaka Yamaguchi,Yukiko Kanetsuna,Kazuho Honda,Nobuaki Yamanaka,Mitsuhiro Kawano,Michio Nagata +5 more
TL;DR: The distinctive histologic features of IgG4-related tubuloInterstitial nephritis can facilitate the differential diagnosis of tubulointerstitial nephitis, even without autoimmune pancreatitis or an abnormal computed tomography suggesting a renal tumor.
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Membranoproliferative glomerulonephritis-like glomerular disease and concurrent tubulointerstitial nephritis complicating IgG4-related autoimmune pancreatitis.
Junko Morimoto,Yoshiyuki Hasegawa,Hirofumi Fukushima,Noriko Uesugi,Satoshi Hisano,Takao Saito,Hidetoshi Kaneoka +6 more
TL;DR: An 80-year-old Japanese man was referred to the authors' hospital with a 14-month history of proteinuria, and a progressively rising serum creatinine level, andRenal biopsy revealed membranoproliferative glomerulonephritis-like glomerular disease and concurrent tubulointerstitial nephritis.
74
References
A new clinicopathological entity of IgG4-related autoimmune disease
Terumi Kamisawa,Nobuaki Funata,Yukiko K. Hayashi,Yoshinobu Eishi,Morio Koike,Kouji Tsuruta,Atsutake Okamoto,Naoto Egawa,Hitoshi Nakajima +8 more
TL;DR: It is suggested that AIP is not simply pancreatitis but that it is a pancreatic lesion involved in IgG4-related systemic disease with extensive organ involvement, and a new clinicopathological entity is proposed.
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Clinical and pathological differences between Mikulicz's disease and Sjögren's syndrome
Motohisa Yamamoto,S. Harada,Mikiko Ohara,Chisako Suzuki,Yasuyoshi Naishiro,Hiroyuki Yamamoto,Hiroki Takahashi,Kohzoh Imai +7 more
TL;DR: Mikulicz's disease is suggested to be an IgG4-related systemic disease and Histopathologically, only MD was associated with prominent infiltration of IgG 4-positive plasmacytes into lachrymal and salivary glands.
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Elevated IgG4 concentrations in serum of patients with Mikulicz's disease
Motohisa Yamamoto,M Ohara,Chisako Suzuki,Y Naishiro,Hiroyuki Yamamoto,Hiroki Takahashi,Kohzoh Imai +6 more
TL;DR: It was showed that serum IgG4 concentrations are elevated in patients with Mikulicz's disease, but not in those with Sjögren's syndrome, which is responsive to glucocorticoid treatment.
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The probable systemic nature of Mikulicz's disease and its relation to Sjögren's syndrome.
TL;DR: In 1892 Mikulicz described a case of benign, asymptomatic, symmetric enlargement of the lacrimal and salivary glands.
176
Clinical and pathological characteristics of Mikulicz's disease (IgG4-related plasmacytic exocrinopathy).
TL;DR: This work proposes the new entity "IgG4-related plasmacytic exocrinopathy" and expects future development with regard to its relationship with autoimmune pancreatitis, which similarly presents elevated serum IgG4 levels.
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