Merkel Cell Carcinoma: A Rare and Underdiagnosed Entity.

Our study reveals unique characteristics of MCC, predominance of female patients, and a slightly younger average diagnosis age compared to existing literature. The 2-year survival rate in our cohort was 82%. The study underscores the importance of early detection and diagnosis of MCC, thereby enhancing clinical awareness and improving patient outcomes.

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PubMed
Published
2025-08-01
Primary Topic
Polyomavirus and related diseases
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article
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article

Merkel Cell Carcinoma: A Rare and Underdiagnosed Entity.

Ronen Toledano, Adi Maisel Lotan, Yoav Gronovich, Hadas Yarimi
PubMed
Polyomavirus and related diseases
article

Merkel Cell Carcinoma: A Rare and Underdiagnosed Entity.

Ronen Toledano, Adi Maisel Lotan, Yoav Gronovich, Hadas Yarimi
article en

Abstract

Our study reveals unique characteristics of MCC, predominance of female patients, and a slightly younger average diagnosis age compared to existing literature. The 2-year survival rate in our cohort was 82%. The study underscores the importance of early detection and diagnosis of MCC, thereby enhancing clinical awareness and improving patient outcomes.

PubMedVol. 27(8)
Hebrew University of Jerusalem (IL), Hadassah Medical Center (IL)
Openalex Percentile: Top 70%
Polyomavirus and related diseases
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Merkel Cell Carcinoma: A Rare and Underdiagnosed Entity. — Ronen Toledano, Adi Maisel Lotan, et al. · PubMed (2025) | TGRS Research Map | TGRS