Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2022 Feb 11;58(2):269.
doi: 10.3390/medicina58020269.

A Challenging Nodular Lesion of the Ear

Affiliations
Case Reports

A Challenging Nodular Lesion of the Ear

Antonella Tammaro et al. Medicina (Kaunas). .

Abstract

Skin nodular lesion are really frequent, but rapidly growing ones needs to be quickly removed since they can hide really aggressive skin tumor. Among malignant lesion Merkel cell carcinoma arise. It is a rare neuroendocrine skin tumor highly aggressive, not easy to diagnose at first stage, since at first diagnosis it is already widespreading all over the body. In order to renew interest in this letal skin tumori is mandatory to remind high risk population which include elderly people, white skin, chronically exposed to UV immunocompromised. Our unhappy case was described to increase awareness on this kind of skin tumor, since new drug appeared in the market can give an hope to these patients.

Keywords: Merkel cell carcinoma; ear; nodular lesion.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Asymptomatic rapidly growing violaceous nodule on the right helix of the patient.
Figure 2
Figure 2
Histologic findings. A predominately dermal blue nodule composed of small–medium-sized round cells with a round nucleus, fine granular chromatin, inconspicuous nucleoli, and scanty cytoplasm (A) ×200, Lower insert ×20 hematoxylin-eosin, (H&E). Immunohistochemically, the neoplastic cells are positive for CD56 (B) ×200 and synaptophysin (C) ×200 and negative for chromogranin A (D) ×200.

References

    1. Yusuf M., McKenzie G., Rattani A., Tennant P., Bumpous J., Miller D., Dunlap N. Merkel Cell Carcinoma of the Head and Neck: Epidemiology, Pathogenesis, Current State of Treatment and Future Directions. Cancers. 2021;13:3506. doi: 10.3390/cancers13143506. - DOI - PMC - PubMed
    1. Heath M., Jaimes N., Lemos B., Mostaghimi A., Wang L.C., Peñas P.F., Nghiem P. Clinical characteristics of Merkel cell carcinoma at diagnosis in 195 patients: The AEIOU features. J. Am. Acad. Dermatol. 2008;58:375–381. doi: 10.1016/j.jaad.2007.11.020. - DOI - PMC - PubMed
    1. Becker J.C., Stang A., DeCaprio J.A., Cerroni L., Lebbé C., Veness M., Nghiem P. Merkel cell carcinoma. Nat. Rev. Dis. Prim. 2017;3:17077. doi: 10.1038/nrdp.2017.77. - DOI - PMC - PubMed
    1. Li J., Wang X., Diaz J., Tsang S.H., Buck C.B., You J. Merkel Cell Polyomavirus Large T Antigen Disrupts Host Genomic Integrity and Inhibits Cellular Proliferation. J. Virol. 2013;87:9173–9188. doi: 10.1128/JVI.01216-13. - DOI - PMC - PubMed
    1. Walsh N.M. Complete spontaneous regression of Merkel cell carcinoma (1986–2016): A 30 year perspective. J. Cutan. Pathol. 2016;43:1150–1154. doi: 10.1111/cup.12812. - DOI - PubMed

Publication types