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Facial Merkel cell carcinoma in a patient with diabetes and hepatitis B: A case report.
Ren, Ming-Yang; Shi, Yun-Juan; Lu, Wei; Fan, Sha-Sha; Tao, Xiao-Hua; Ding, Yang.
Afiliação
  • Ren MY; School of Medicine, Graduate School of Bengbu Medical College, Bengbu 233030, Anhui Province, China.
  • Shi YJ; School of Medicine, Graduate School of Bengbu Medical College, Bengbu 233030, Anhui Province, China.
  • Lu W; Center for Plastic and Reconstructive Surgery, Department of Dermatology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
  • Fan SS; Center for Plastic and Reconstructive Surgery, Department of Dermatology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
  • Tao XH; Center for Plastic and Reconstructive Surgery, Department of Dermatology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China.
  • Ding Y; Center for Plastic and Reconstructive Surgery, Department of Dermatology, Zhejiang Provincial People's Hospital, Hangzhou 310014, Zhejiang Province, China. dingyangdoctor@163.com.
World J Clin Cases ; 11(17): 4179-4186, 2023 Jun 16.
Article em En | MEDLINE | ID: mdl-37388796
ABSTRACT

BACKGROUND:

Patients with chronic inflammatory disorders are at a higher risk of developing aggressive Merkel cell carcinoma (MCC). Diabetes is a common chronic inflammatory disease that is possibly associated with MCC; however, there are still no reports on the association between hepatitis B virus (HBV) infection and MCC. Whether there is an association between these three diseases and the specific mechanisms behind their effects is worth further research in the future. CASE

SUMMARY:

We herein report a rare case of MCC with extracutaneous and nodal invasion in an Asian individual with type 2 diabetes mellitus and chronic HBV infection, but no immunosuppression or other malignancies. Such cases are uncommon and have rarely been reported in the literature. A 56-year-old Asian male presented with a significant mass on his right cheek and underwent extensive resection combined with parotidectomy, neck lymphadenectomy, and split-thickness skin grafting. Based on the histopathological findings, a diagnosis of MCC involving the adipose tissue, muscle, nerve, and parotid gland with lymphovascular invasion was made. Subsequently, he received radiotherapy with no adverse reactions.

CONCLUSION:

MCC is a rare, aggressive skin cancer with frequent local recurrence, nodal invasion, and metastasis, which usually arises in older people of the white race. Patients with chronic inflammatory disorders are at a higher risk of developing aggressive MCC. The diagnosis can be confirmed with histology and immunohistochemistry. For localized MCC, surgery is the preferred treatment option. However, for advanced MCC, radiotherapy and chemotherapy have proven to be effective. In cases where chemotherapy is not effective or in the advanced stages of MCC, immune therapy plays an important role in treatment. As with any rare disease, the management of MCC remains an enormous challenge for clinicians; thus, follow-up should be individualized and future progress needs multidisciplinary collaborative efforts. Furthermore, physicians should include MCC in their list of possible diagnoses when they come across painless, rapidly growing lesions, particularly in patients with chronic HBV infection or diabetes, as these patients are more susceptible to the development of this condition and it tends to be more aggressive in them.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: World J Clin Cases Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: World J Clin Cases Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China