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Bilateral Adrenal Infarction That Developed in Latent Essential Thrombocythemia.

Authors :
Hada Y
Yamada A
Kobayashi T
Sugiyama T
Ishii K
Takase K
Takakubo N
Nagaoka K
Karasawa S
Kameda W
Ishizawa K
Susa S
Source :
Internal medicine (Tokyo, Japan) [Intern Med] 2024 Feb 01; Vol. 63 (3), pp. 419-423. Date of Electronic Publication: 2023 Jun 21.
Publication Year :
2024

Abstract

Bilateral adrenal infarction is an extremely rare disease, and it has been reported that some coagulation abnormalities, including essential thrombocythemia (ET), exist in the background. We herein report a 76-year-old patient in whom the platelet count had been in the normal range at the onset of adrenal infarction but subsequently increased to 102×10 <superscript>4</superscript> /μL at 7 months later, leading to the diagnosis of JAK2V617F-positive ET. As the presence of the JAK2V617F mutation increases the risk of thrombosis, Janus kinase 2 (JAK2) genetic testing should be considered in some cases of nonspecific unknown thrombosis, even if there are no obvious hematological findings, such as clonal hematopoiesis of indeterminate potential (CHIP).

Details

Language :
English
ISSN :
1349-7235
Volume :
63
Issue :
3
Database :
MEDLINE
Journal :
Internal medicine (Tokyo, Japan)
Publication Type :
Academic Journal
Accession number :
37344430
Full Text :
https://doi.org/10.2169/internalmedicine.1947-23