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Interleukin-6-producing pheochromocytoma presenting with fever of unknown origin.

作者信息

Yarman Sema, Soyluk Ozlem, Altunoglu Esma, Tanakol Refik

机构信息

Division of Endocrinology and Metabolic Diseases, Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.

出版信息

Clinics (Sao Paulo). 2011;66(10):1843-5. doi: 10.1590/s1807-59322011001000028.

DOI:10.1590/s1807-59322011001000028
PMID:22012062
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3180162/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae30/3180162/97af1dc19ac3/cln-66-10-1843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae30/3180162/60f4d2d2d5ce/cln-66-10-1843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae30/3180162/97af1dc19ac3/cln-66-10-1843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae30/3180162/60f4d2d2d5ce/cln-66-10-1843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae30/3180162/97af1dc19ac3/cln-66-10-1843-g002.jpg

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2
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Pheochromocytoma presenting as fever of unknown origin.表现为不明原因发热的嗜铬细胞瘤。
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Pheochromocytoma with pyrexia and marked inflammatory signs: a paraneoplastic syndrome with possible relation to interleukin-6 production.伴有发热和明显炎症体征的嗜铬细胞瘤：一种可能与白细胞介素-6产生有关的副肿瘤综合征。
J Clin Endocrinol Metab. 1991 Oct;73(4):877-81. doi: 10.1210/jcem-73-4-877.
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本文引用的文献

1
Overexpression of protein kinase C-delta plays a crucial role in interleukin-6-producing pheochromocytoma presenting with acute inflammatory syndrome: a case report.蛋白激酶C-δ的过表达在伴有急性炎症综合征的产白细胞介素-6嗜铬细胞瘤中起关键作用：一例报告
Horm Metab Res. 2009 Apr;41(4):333-8. doi: 10.1055/s-0028-1103300. Epub 2008 Dec 1.
2
Systemic inflammatory syndrome and hepatic inflammatory cell infiltration caused by an interleukin-6 producing pheochromocytoma.由产生白细胞介素-6的嗜铬细胞瘤引起的全身炎症综合征和肝脏炎症细胞浸润。
Endocr J. 2005 Apr;52(2):193-8. doi: 10.1507/endocrj.52.193.
3
Interleukin-6 producing pheochromocytoma presenting with acute inflammatory syndrome.
患者嗜铬细胞瘤伴白细胞介素 6 水平升高。
BMJ Case Rep. 2024 Apr 25;17(4):e256410. doi: 10.1136/bcr-2023-256410.
4
IL-6-Producing Pheochromocytoma Associated With Von Hippel Lindau Disease: A Case Report With Literature Review.与冯·希佩尔-林道病相关的产生白细胞介素-6的嗜铬细胞瘤：一例病例报告及文献复习
Cureus. 2024 Jan 22;16(1):e52760. doi: 10.7759/cureus.52760. eCollection 2024 Jan.
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Acquisition of Interleukin-6 Production Ability Over Time With Pheochromocytoma.嗜铬细胞瘤随时间推移获得白细胞介素-6产生能力。
JCEM Case Rep. 2023 Sep 2;1(5):luad106. doi: 10.1210/jcemcr/luad106. eCollection 2023 Sep.
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Case Report: A 65-year-old man with paraganglioma accompanied by elevated interleukin-6 levels and KIF1B single gene mutation.病例报告：一名 65 岁男性患有副神经节瘤，伴有白细胞介素-6 水平升高和 KIF1B 单基因突变。
Front Endocrinol (Lausanne). 2023 Sep 14;14:1226468. doi: 10.3389/fendo.2023.1226468. eCollection 2023.
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JA Clin Rep. 2021 Jun 11;7(1):49. doi: 10.1186/s40981-021-00449-5.
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Clin Endocrinol (Oxf). 2001 Mar;54(3):405-10. doi: 10.1046/j.1365-2265.2001.01082.x.
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Urology. 1998 Aug;52(2):331-5. doi: 10.1016/s0090-4295(98)00192-7.
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Interleukin-6 in the fever and multiorgan crisis of pheochromocytoma.白细胞介素-6在嗜铬细胞瘤发热及多器官危象中的作用
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J Clin Endocrinol Metab. 1997 Jul;82(7):2343-9. doi: 10.1210/jcem.82.7.4072.
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Interleukin-6 secreting phaeochromocytoma associated with clinical markers of inflammation.与炎症临床标志物相关的分泌白细胞介素-6的嗜铬细胞瘤
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Biochem Biophys Res Commun. 1988 Aug 30;155(1):112-7. doi: 10.1016/s0006-291x(88)81056-8.