A case of IgG4-related disease with features of Mikulicz’s disease, and retroperitoneal fibrosis and lymphadenopathy mimicking Castleman’s disease

2011 ◽  
Vol 21 (4) ◽  
pp. 410-414 ◽  
Author(s):  
Kenchi Takenaka ◽  
Kazuki Takada ◽  
Daisuke Kobayashi ◽  
Masato Moriguchi ◽  
Masayoshi Harigai ◽  
...  
RMD Open ◽  
2017 ◽  
Vol 3 (1) ◽  
pp. e000432 ◽  
Author(s):  
Takanori Sasaki ◽  
Mitsuhiro Akiyama ◽  
Yuko Kaneko ◽  
Takehiko Mori ◽  
Hidekata Yasuoka ◽  
...  

2017 ◽  
Vol 56 (9) ◽  
pp. 1095-1099 ◽  
Author(s):  
Hiroki Mochizuki ◽  
Manako Kato ◽  
Takakazu Higuchi ◽  
Ryosuke Koyamada ◽  
Satoru Arai ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Yasuhiro Kinugawa ◽  
Takeshi Uehara ◽  
Mai Iwaya ◽  
Shiho Asaka ◽  
Shota Kobayashi ◽  
...  

Abstract Background It is difficult to distinguish between multicentric Castleman’s disease (MCD) and IgG4-related lung disease (IgG4-LD), an IgG4-related disease (IgG4-RD) in the lung. Methods We focused on IL-6, which is elevated in MCD, to distinguish between MCD and IgG4-LD by RNAscope, a highly sensitive RNA in situ method. Six cases of MCD and four cases of IgG4-LD were selected. Results In all cases of MCD and IgG4-LD, 10 or more IgG4-positive cells were found in one high-power field. All MCD cases were inconsistent with the pathological IgG4-related comprehensive diagnostic criteria, but 2 of 6 cases had an IgG4/IgG ratio greater than 40%. In all IgG4-LD cases, histological features were consistent with the pathological IgG4-RD comprehensive diagnostic criteria. IL-6 expression was observed in all MCD and IgG4-LD cases except for one IgG4-LD biopsy. IL-6-expressing cells were mainly identified in the stroma. Sites of IL-6 expression were not characteristic and were sparse. IL-6 expression tended to be higher in MCD compared with IgG4-LD. A positive correlation was found between the IL-6 H-score and serum IL-6 level. Conclusion Differences in IL-6 expression may help distinguish between MCD and IgG4-LD. In addition, the presence of high IL-6 levels may help elucidate the pathological mechanisms of IgG4-LD.


2016 ◽  
pp. 293-301
Author(s):  
Eiko Hasegawa ◽  
Akinari Sekine ◽  
Jun-ichi Inenaga ◽  
Takeshi Fujii ◽  
Kenichi Ohashi ◽  
...  

Oncotarget ◽  
2018 ◽  
Vol 9 (6) ◽  
pp. 6691-6706 ◽  
Author(s):  
Kyoko Otani ◽  
Dai Inoue ◽  
Kohei Fujikura ◽  
Takahiro Komori ◽  
Shiho Abe-Suzuki ◽  
...  

2012 ◽  
Vol 208 (12) ◽  
pp. 746-749 ◽  
Author(s):  
Mai Takeuchi ◽  
Yasuharu Sato ◽  
Katsuyoshi Takata ◽  
Keita Kobayashi ◽  
Kyotaro Ohno ◽  
...  

2021 ◽  
Vol 9 ◽  
pp. 2050313X2110169
Author(s):  
Kim Rouven Liedtke ◽  
Christoph Käding ◽  
Paula Döring ◽  
Sander Bekeschus ◽  
Anne Susann Glitsch

Several chronic inflammatory diseases have been found to be a subtype of IgG4-related disease, all of which have a typical clinical and histological change, which is based in particular on an overexpression of IgG4 and subsequent fibrosis. At least a part of the retroperitoneal fibrosis, which was originally classified as idiopathic, seems to be assigned to IgG4-related disease. Lymphangiomas are benign, cystic tumors that rarely occur in adults. However, there is no firm association with IgG4-related disease described in the literature to date. This report is about a patient suffering from acute renal failure due to a giant retroperitoneal cyst. Surgical resection remains incomplete in the iliac vessel area due to severe fibrosis and histology revealed features of both lymphangioma and IgG4+ fibrosis. The case description is followed by a brief overview of IgG4-related disease and a consideration of whether lymphangiomas might be assigned to this topic.


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