Author:
Chen Xueqin,Song Xiao,Huang Hui,Zhang Lian,Song Zhiqiang,Yang Xichuan,Lei Shanchuan,Zhai Zhifang
Abstract
Abstract
Purpose
Merkel cell carcinoma (MCC) is a rare neuroendocrine tumor of the skin, which mainly occurs in the sun exposed sites of white patients over 65 years, with a higher recurrence and metastasis rate. Clinically, MCC overlapping Bowen’s disease (BD) is a very rare subtype of MCC. Few cases in the literature have been described and the management is not well defined. We summarize and update the epidemiology, clinical and histopathological features, metastasis characteristics, local recurrence rate and management of it by presenting two cases of MCC overlapping BD and reviewing the literature over the last 11 years.
Design
We consulted databases from PubMed, ResearchGate and Google Scholar by MeSh “Merkel cell carcinoma” and “Bowen’s disease”, “Bowen disease” or “squamous cell carcinoma in situ”, from January 2013 to December 2023 and reviewed the literatures. We reported two additional cases.
Results
Total 13 cases of MCC overlapping BD were retrospectively analyzed, in whom mainly in elderly women over 70 years, the skin lesions were primarily located on the faces, followed by the extremities and trunk. Most of them were asymptomatic, firm, dark red nodules arising on rapidly growing red or dark brown patches, or presenting as isolated nodules. Dermoscopy evaluation was rarely performed in the pre-operative diagnostic setting. All cases were confirmed by histopathology and immunohistochemistry. The most definitive treatment was extended local excision, but local recurrences were common. Of the 13 cases, 4 cases experienced local or distant metastasis. One suffered from an in-transit recurrence of MCC on the ipsilateral leg after local excision and lymph node dissection, whose metastasis completely subsided after avelumab treatment and without recurrence or metastasis during 6 months of follow-up.
Conclusions
MCC overlapping BD is a very rare skin tumor mainly predisposed on the faces, with high misdiagnosis rate and recurrence rate. Advanced disease at diagnosis is a poor prognostic factor, suggesting that earlier detection may improve outcome. The acronym, AEIOUN, has been proposed to aid in clinical identification. Our reports and the literature review can provide a better awareness and management of it.
Publisher
Springer Science and Business Media LLC
Reference30 articles.
1. Becker JC, Stang A, Hausen AZ, Fischer N, DeCaprio JA, Tothill RW et al (2018) Epidemiology, biology and therapy of Merkel cell carcinoma: conclusions from the EU project IMMOMEC. Cancer Immunol Immunother 67(3):341–351
2. Brusasco M, Macchi S, DEG F, Mora E, Zucchi A, Feliciani C et al (2022) AEIOU not only merkel cell carcinoma. Ital J Dermatol Venerol 157(5):453–454
3. Casari A, Argenziano G, Piana S, Lallas A, Moscarella E, Lombardi M et al (2018) Merkel cell carcinoma arising on a pre-existing bowen’s disease: is it just by chance? G Ital Dermatol Venereol 153(2):273–275
4. Chattopadhyay S, Hemminki A, Forsti A, Sundquist K, Sundquist J, Hemminki K (2020) Second primary cancers in patients with invasive and in situ squamous cell skin carcinoma, kaposi sarcoma, and merkel cell carcinoma: role for immune mechanisms? J Invest Dermatol 140(1):48–55
5. Choe Y, Kim Y, Park H, Yoon H, Cho S (2014) A case of merkel cell carcinoma concurrent with bowen’s disease. Korean J Dermatol 53(2):169–171
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