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Merkel Cell Carcinosarcoma With a Bland Sarcomatous Component.
Amanda M Ireland1, Tamazin N Leecy1, Benjamin A Wood1
1Department of Anatomical Pathology, PathWest Laboratory Medicine, Queen Elizabeth II Medical Centre, Nedlands, Australia; and.
The American Journal of Dermatopathology
|September 8, 2022
Summary
Merkel cell carcinosarcoma is a rare cancer. This case highlights a unique, bland sarcomatous component that may be mistaken for a reactive process, emphasizing the need for careful diagnosis in metastatic Merkel cell carcinoma.
Area of Science:
- Oncology
- Pathology
- Dermatology
Background:
- Merkel cell carcinoma (MCC) is a rare, aggressive skin cancer.
- MCC with a sarcomatous component is exceptionally rare, with limited cases documented.
Observation:
- A case of metastatic Merkel cell carcinosarcoma presented in a lymph node.
- The metastatic lesion exhibited a biphasic morphology: neuroendocrine epithelial cells and spindle cells.
- The sarcomatous component showed mild cytological atypia and was mitotically active.
Findings:
- Immunomorphological and molecular analyses confirmed a common origin for both epithelial and mesenchymal components.
- This represents the first reported case of Merkel cell carcinosarcoma with a bland sarcomatous component.
- The bland nature of the sarcomatous element poses a diagnostic challenge, potentially mimicking reactive stromal changes.
Implications:
- Accurate diagnosis of Merkel cell carcinosarcoma is crucial for appropriate patient management.
- Awareness of this rare variant is essential for pathologists to avoid misdiagnosis.
- Further research may elucidate the behavior and treatment of this specific subtype of Merkel cell carcinoma.

