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Letters to the Editor

A rare case of TEMPI syndrome (telangiectasias, erythrocytosis, monoclonal gammopathy and ascites) associated with IgM monoclonal gammopathy

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Pages 857-859 | Received 22 Jan 2024, Accepted 20 Feb 2024, Published online: 28 Feb 2024
 

Author contributions

All authors equally contributed to this paper with conception and design of the study, literature review and analysis, drafting and critical revision and editing, and final approval of the final version.

Disclosure statement

The study did not receive ethical approval by the local Institutional Review Board. Research ethics and patients’ sensitive personal data were protected according to the 2017 Declaration of Helsinki.

Data availability statement

The data are available; Patient consent was received.

Additional information

Funding

The author(s) reported there is no funding associated with the work featured in this article.

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