A case of nevoid basal cell carcinoma syndrome dominated by facial basal cell carcinoma.
10.11817/j.issn.1672-7347.2022.200925
- Author:
Fengzhen QIU
1
;
Shaorong LEI
2
;
Lifang ZHANG
2
;
Xulei JIANG
2
;
Chenchen ZUO
3
Author Information
1. Department of Plastic and Cosmetic Surgery, Xiangya Hospital, Central South University, Changsha 410008. 735899356@qq.com.
2. Department of Plastic and Cosmetic Surgery, Xiangya Hospital, Central South University, Changsha 410008.
3. Department of Plastic and Cosmetic Surgery, Xiangya Hospital, Central South University, Changsha 410008. zuochenchen83@163.com.
- Publication Type:Journal Article
- Keywords:
basal cell carcinoma;
multiple maxillofacial keratocysts;
nevoid basal cell carcinoma syndrome
- MeSH:
Aged;
Basal Cell Nevus Syndrome/surgery*;
Carcinoma, Basal Cell/surgery*;
Child;
Female;
Hamartoma Syndrome, Multiple;
Humans;
Magnetic Resonance Imaging
- From:
Journal of Central South University(Medical Sciences)
2022;47(3):384-389
- CountryChina
- Language:English
-
Abstract:
Nevus-like basal cell carcinoma syndrome (NBCCS) is a rare autosomal dominant disease characterized by the occurrence of multiple maxillofacial keratocysts, basal cell carcinoma, child medulloblastoma, and various skeletal and soft tissue dysplasia. In 2020, a patient with NBCCS dominated by facial basal cell carcinoma was admitted to Xiangya Hospital of Central South University. The patient was an elderly woman. Ten years ago, the systemic mass appeared, especially on the face, but it was not treated. Later, these masses gradually increased in volume and number, and showed invasive properties. The nasal mass was broken and suppurated, seriously affecting the patient's life quality. The patient came to the hospital to improve the symptoms. Staphylococcus aureus and Providencia rettgeri were cultured in the patient's nasal secretions. Nasal sinus enhanced MRI showed that the subcutaneous soft tissue of the right cheek and the anterolateral mucosa of the left nasal cavity were invaded, indicating multiple malignant skin lesions. After admission, local anesthesia was performed and some masses were removed. Pathological examination of the mass showed basal cell carcinoma. After general anesthesia, multiple masses were resected. The postoperative pathological examination showed that multiple basal cell carcinoma invaded the deep dermis near subcutaneous fat layer. Combined with the results of clinical and immunohistochemical examination, the patient was diagnosed as NBCCS. There were no clear tumor thrombus in the vessel and no nerve invasion. No recurrence or new tumor was found after 1 year follow-up. The incidence rate of NBCCS is low and clinical symptoms are different. The patient's life quality is poor and the patient needs long-term individualized treatment.
