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DOI 10.1111/cup.12966

Медицинская библиотека · Journal of cutaneous pathology · 2017

Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up.

Jour George, Aung Phyu P, Rozas-Muñoz Eduardo, Curry Johnathan L, Prieto Victor, Ivan Doina

Клинический случайСтатьяПеревод пока не подготовлен

Аннотация

BACKGROUND

Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous carcinoma. MCC typically involves dermis and although epidermotropism has been reported, MCC strictly intraepidermal or in situ (MCCIS) is exceedingly rare. Most of the cases of MCCIS described so far have other associated lesions, such as squamous or basal cell carcinoma, actinic keratosis and so on. Herein, we describe 3 patients with MCC strictly in situ, without a dermal component.

METHODS

Our patients were elderly. 2 of the lesions involved the head and neck area and 1 was on a finger. All tumors were strictly intraepidermal in the diagnostic biopsies, and had histomorphologic features and an immunohistochemical profile supporting the diagnosis of MCC. Excisional biopsies were performed in 2 cases and failed to reveal dermal involvement by MCC or other associated malignancies.

RESULTS AND

CONCLUSION

Our findings raise the awareness that MCC strictly in situ does exist and it should be included in the differential diagnosis of Paget's or extramammary Paget's disease, pagetoid squamous cell carcinoma, melanoma and other neoplasms that typically show histologically pagetoid extension of neoplastic cells. Considering the limited number of cases reported to date, the diagnosis of isolated MCCIS should not warrant a change in management from the typical MCC.

Для цитирования: Jour George, Aung Phyu P, Rozas-Muñoz Eduardo, Curry Johnathan L, Prieto Victor, Ivan Doina. Intraepidermal Merkel cell carcinoma: A case series of a rare entity with clinical follow up.. Journal of cutaneous pathology. 2017. DOI: 10.1111/cup.12966.

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