[1]申金付 蒋瑞妹 谢树永 张琴 李娟.以尿崩症就诊的IgG4相关性垂体炎1例[J].国际内分泌代谢杂志,2018,38(02):143-144.[doi:10.3760/cma.j.issn.1673-4157.2018.02.019]
 Shen Jinfu,Jiang Ruimei,Xie Shuyong,et al.One case of IgG4-related pituitaryitis presenting as diabetes insipidus[J].International Journal of Endocrinology and Metabolism,2018,38(02):143-144.[doi:10.3760/cma.j.issn.1673-4157.2018.02.019]
点击复制

以尿崩症就诊的IgG4相关性垂体炎1例()
分享到:

《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
38
期数:
2018年02期
页码:
143-144
栏目:
病例报告
出版日期:
2018-03-20

文章信息/Info

Title:
One case of IgG4-related pituitaryitis presenting as diabetes insipidus
作者:
申金付 蒋瑞妹 谢树永 张琴 李娟
236003 安徽省阜阳市人民医院内分泌科
Author(s):
Shen Jinfu Jiang Ruimei Xie Shuyong Zhang Qin Li Juan
Depaertment of Endocrinology, Fuyang People's Hospital, Anhui 236003, China
DOI:
10.3760/cma.j.issn.1673-4157.2018.02.019

参考文献/References:


[1] Carmichael JD. Update on the diagnosis and management of hypophysitis[J].Curr Opin Endocrinol Diabetes Obes,2012,19(4):314-321.DOI:10.1097/MED.0b013e32835430ed.
[2] 廖若西,幸兵.IgG4相关性垂体炎研究进展[J]. 中华内分泌外科杂志, 2014,(4):339-341.DOI:10.3760/cma.j.issn.1674-6090.2014.04.024.
[3] 杨祖威,孙守悦.自身免疫性垂体炎[J]. 中华内分泌代谢杂志, 2015, 31(11):1008-1012.DOI:10.3760/cma.j.issn.1000-6699.2015.11.020.
[4] Howlett TA,Levy MJ,Robertson IJ.How reliably can autoimmune hypophysitis be diagnosed without pituitary biopsy[J].Clin Endocrinol(Oxf),2010,73(1):18-21.DOI:10.1111/j.1365-2265.2009.03765.x.
[5] Bando H,Iguchi G,Fukuoka H,et al.The prevalence of IgG4-related hypophysitis in 170 consecutive patients with hypopituitarism and/or central diabetes insipidus and review of the literature[J].Eur J Endocrinol,2013,170(2):161-172.DOI:10.1530/EJE-13-0642.
[6] van der Vliet HJ,Perenboom RM.Multiple pseudotumors in IgG4-associated multifocal systemic fibrosis[J].Ann Intern Med,2004,141(11):896-897.
[7] 侯文芳, 肖文华, 洪天配. 表现为中枢性尿崩症和肺部病变的IgG4相关性疾病的临诊应对[J]. 中华内分泌代谢杂志, 2017, 33(2):141-144. DOI:10.3760/cma.j.issn.1000-6699.2017.02.010.
[8] Leporati P,Landek-Salgado MA,Lupi I,et al.IgG4-related hypophysitis: a new addition to the hypophysitis spectrum[J].J Clin Endocrinol Metab,2011,96(7):1971-1980.DOI:10.1210/jc.2010-2970.
[9] Kamisawa T,Zen Y,Pillai S,et al.IgG4-related disease[J].Lancet,2015,385(9976):1460-1471.DOI:10.1016/S0140-6736(14)60720-0.
[10] Cheuk W,Chan JK.IgG4-related sclerosing disease: a critical appraisal of an evolving clinicopathologic entity[J].Adv Anat Pathol,2010,17(5):303-332.DOI:10.1097/PAP.0b013e3181ee63ce.
[11] Cortazar FB,Stone JH.IgG4-related disease and the kidney[J].Nat Rev Nephrol,2015,11(10):599-609.DOI:10.1038/nrneph.2015.95.
[12] Anno T,Kawasaki F,Takai M,et al.Clinical course of pituitary function and image in IgG4-related hypophysitis[J].Endocrinol Diabetes Metab Case Rep,2017,2017.pii:16-0148.DOI:10.1530/EDM-16-0148.
[13] Sato Y,Notohara K,Kojima M,et al.IgG4-related disease: historical overview and pathology of hematological disorders[J].Pathol Int,2010,60(4):247-258.DOI:10.1111/j.1440-1827.2010.02524.x.
[14] Hamano H,Kawa S,Uehara T,et al.Immunoglobulin G4-related lymphoplasmacytic sclerosing cholangitis that mimics infiltrating hilar cholangiocarcinoma: part of a spectrum of autoimmune pancreatitis [J].Gastrointest Endosc,2005,62(1):152-157.

备注/Memo

备注/Memo:

通信作者:申金付,Email:shenjinfu263@sina.com
更新日期/Last Update: 1900-01-01