JAK2 mutation–positive polycythaemia vera associated with IgA vasculitis and nephrotic syndrome: a case report-Reference-Cited by-同舟云学术

JAK2 mutation–positive polycythaemia vera associated with IgA vasculitis and nephrotic syndrome: a case report

Published:2020-02-13 Issue:2 Volume:4 Page:289-295
ISSN:2472-5625
Container-title:Modern Rheumatology Case Reports
language:en
Short-container-title:Modern Rheumatology Case Reports

Author:

Kondo Hinako¹,Watanabe Ryu¹²^ORCID,Okazaki Soshi¹,Kuriyama Kaori¹,Ochi Tetsuro²,Yamada Gen³,Sugiura Akira³,Chiba Hiromu⁴,Tsukada Akira⁴,Taniuchi Shinji⁵,Igarashi Takehiko⁶,Kudo Masataka³,Harigae Hideo²,Fujii Hiroshi²

Affiliation:

1. Department of Rheumatology, Osaki Citizen Hospital, Osaki, Japan;

2. Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan;

3. Department of Nephrology and Endocrinology, Osaki Citizen Hospital, Osaki, Japan;

4. Department of Dermatology, Osaki Citizen Hospital, Osaki, Japan;

5. Department of Pathology, Osaki Citizen Hospital, Osaki, Japan;

6. Department of Gastroenterology, Osaki Citizen Hospital, Osaki, Japan

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/24725625.2020.1728061

Reference31 articles.

1. 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides

2. Patient age, gender and extent of purpura may suggest short-term outcomes in adults with IgA vasculitis: Table 1

3. Cardiovascular, thromboembolic and renal outcomes in IgA vasculitis (Henoch-Schönlein purpura): a retrospective cohort study using routinely collected primary care data

4. Myeloproliferative neoplasms: from origins to outcomes

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