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Merkel Cell Carcinoma: A Rare and Underdiagnosed Entity
Ronen Toledano1, Adi Maisel Lotan1, Hadas Yarimi2
1Department of Plastic and Reconstructive Surgery, Shaare Zedek Medical Center, affiliated with Hadassah-Hebrew University School of Medicine, Jerusalem, Israel.
The Israel Medical Association Journal : IMAJ
|August 17, 2025
Summary
Merkel cell carcinoma (MCC) is a rare skin cancer. This study highlights unique patient characteristics and an 82% 2-year survival rate, emphasizing early detection for better outcomes.
Area of Science:
- Oncology
- Dermatology
- Epidemiology
Background:
- Merkel cell carcinoma (MCC) is a rare, aggressive neuroendocrine skin tumor with rising incidence.
- MCC predominantly affects older individuals, accounting for less than 1% of skin malignancies.
Purpose of the Study:
- To characterize clinical presentation, treatments, and outcomes for MCC patients.
- To increase clinical awareness for early MCC recognition and diagnosis.
Main Methods:
- Retrospective cohort study of 17 MCC patients at Shaare Zedek Medical Center (2015-2022).
- Analysis of demographic, epidemiological, clinical, and pathological data.
Main Results:
- The cohort (mean age 70.06) showed predominantly female patients and Jewish origin.
- Common comorbidities included hypertension (64.7%) and diabetes (35.3%).
- 29.4% had lymph node involvement, and 23.5% presented with metastatic disease; ischemic heart disease correlated with lower survival (P=0.009).
Conclusions:
- The study identified unique MCC characteristics, including female predominance and a slightly younger average age at diagnosis.
- The 2-year survival rate was 82%, underscoring the critical role of early detection and diagnosis in improving patient outcomes.
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