# Ultrasound Assessment in Merkel Cell Carcinoma: Case Report and Narrative Literature Review

**Authors:** Vincenza Amoruso, Letizia Castelli, Anastasia Mercurio, Patrizia Matano, Giacomo Montaldi

PMC · DOI: 10.3390/reports9010043 · Reports - Clinical Practice and Surgical Cases · 2026-01-29

## TL;DR

This paper presents a case where ultrasound helped diagnose and monitor a rare skin cancer called Merkel cell carcinoma, suggesting it could improve early detection and treatment planning.

## Contribution

The paper demonstrates the underutilized potential of high-frequency ultrasound in the diagnosis and follow-up of Merkel cell carcinoma.

## Key findings

- High-frequency ultrasound revealed a hypoechoic subdermal lesion with vascularity, leading to the diagnosis of Merkel cell carcinoma.
- A structured sonographic follow-up protocol was established postoperatively, aiding in longitudinal monitoring of the patient.

## Abstract

Background and Clinical Significance Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine skin malignancy. Early diagnosis is essential to optimize therapeutic strategies and improve prognosis. However, the role of high-frequency ultrasound (HFUS) in the diagnostic and follow-up phases of MCC remains under-investigated and underutilized in clinical practice. Case Presentation We present a case of MCC initially referred to a physiatric outpatient clinic for a functional disorder of the third finger, where HFUS revealed a well-circumscribed, hypoechoic subdermal lesion with central and peripheral vascularity. Surgical excision, histopathology, and immunohistochemistry confirmed the diagnosis of Merkel cell carcinoma. The HFUS findings were correlated with histological features, and a structured sonographic follow-up protocol was established postoperatively. Conclusions This case highlights the diagnostic and prognostic potential of HFUS in MCC, especially in early detection, surgical planning, and longitudinal follow-up. A multidisciplinary approach integrating ultrasound imaging, surgery, and pathology may enhance diagnostic accuracy and patient management.

## Linked entities

- **Diseases:** Merkel cell carcinoma (MONDO:0019210)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}, SYP (synaptophysin) [NCBI Gene 6855] {aka MRX96, MRXSYP, XLID96}, TTF1 (transcription termination factor 1) [NCBI Gene 7270] {aka TTF-1, TTF-I}, CHGA (chromogranin A) [NCBI Gene 1113] {aka CGA, PHE5, PHES}, PIEZO2 (piezo type mechanosensitive ion channel component 2) [NCBI Gene 63895] {aka C18orf30, C18orf58, DA3, DA5, DAIPT, FAM38B}
- **Diseases:** melanoma (MESH:D008545), metastasis (MESH:D009362), epidermal inclusion cysts (MESH:D004814), injury to (MESH:D014947), inflammatory (MESH:D007249), inflammatory dermatoses (MESH:D012871), pain (MESH:D010146), benign (MESH:D009369), actinic damage (MESH:D010787), nodal (MESH:D013611), lesions (MESH:D009059), neuroendocrine skin tumour (MESH:D012878), fibromas (MESH:D005350), cutaneous lymphomas (MESH:D008223), benign adnexal tumors (MESH:D000292), cutaneous malignancies (MESH:C562393), functional disorder (MESH:D003291), neuroendocrine malignancy (MESH:D018358), necrosis (MESH:D009336), MCC (MESH:D015266), inclusion cyst (MESH:D003560), ganglion cysts (MESH:D045888)
- **Chemicals:** Hematoxylin (MESH:D006416), -FDG (MESH:D019788), Eosin (MESH:D004801)
- **Species:** Homo sapiens (human, species) [taxon 9606], Merkel cell polyomavirus (no rank) [taxon 493803]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12921774/full.md

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921774/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921774/full.md

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Source: https://tomesphere.com/paper/PMC12921774