IJCEMR
A Case Report and Literature Review of a 33-year-old Female with Youthful RS3PE Syndrome
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Abstract
This paper presents the clinical diagnosis and management of a 33-year-old female diagnosed with young-onset RS3PE syndrome. The patient received appropriate treatment and was subsequently discharged from the Department of General Practice. She has been recovering well and has undergone continuous follow-up for six months without any recurrence. RS3PE syndrome is predominantly observed in elderly males, making it challenging to differentiate from other rheumatic immune disorders during clinical diagnosis. Additionally, it has been associated with tumor development. Currently, there is a lack of consensus both domestically and internationally regarding its pathogenesis, treatment, and diagnostic gold standard. Due to the limited sample sizes and short durations of existing studies, clinicians often exhibit habitual thinking patterns when diagnosing and treating such rare cases, leading to potential misdiagnosis. Consequently, it is essential to conduct necessary aux-iliary examinations to gather additional diagnostic information, facilitate early differential diagnosis, enhance prognosis, and improve the quality of life for patients.
References
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How to cite this paper
A Case Report and Literature Review of a 33-year-old Female with Youthful RS3PE Syndrome
How to cite this paper: Chan Cai, Yinghua Li, Mammillan, Rong Yang, Yunchun Zhou. (2025) A Case Report and Literature Review of a 33-year-old Female with Youthful RS3PE Syndrome. International Journal of Clinical and Experimental Medicine Research, 9(1), 51-55.
DOI: http://dx.doi.org/10.26855/ijcemr.2025.01.010
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