Sun-Exposed versus Sun-Protected Cutaneous Basal Cell Carcinoma: Clinico-Pathological Profile and p16 Immunostaining

Author:

Hasan Abdulkarim1ORCID,Kandil Ahmad M.1,Al-Ghamdi Hasan S.2,Alghamdi Mohammad A.2,Nasr Mohamed3,Naeem Suhaib Alsayed3,Abd-Elhay Wagih M.3,Mohamed Osama Khalil E.4,Ibrahim Hany Sabry A.5,Ahmed Eman Mohamed6,Abdrabo Ahmed Elsayed M.7,Elgohary Shimaa Abdelraouf8

Affiliation:

1. Pathology Department, Faculty of Medicine, Al-Azhar University, Cairo 11884, Egypt

2. Internal Medicine Department, Division of Dermatology, Faculty of Medicine, Albaha University, Albaha 65799, Saudi Arabia

3. Histology Department, Faculty of Medicine, Al-Azhar University, Cairo 11884, Egypt

4. Dermatology, Venerology and Andrology Department, Faculty of Medicine, Al-Azhar University, Cairo 11884, Egypt

5. Dermatology, Venerology and Andrology Department, International Islamic Center of Population Studies and Research, Al-Azhar University, Cairo 11651, Egypt

6. Pathology Department, Faculty of Medicine for Girls, Al-Azhar University, Cairo 11884, Egypt

7. Community and Industrial Medicine Department, Faculty of Medicine, Al-Azhar University, Cairo 11884, Egypt

8. Pathology Department, Faculty of Medicine, Ain Shams University, Cairo 11517, Egypt

Abstract

Introduction: Although widespread, BCC is still relatively poorly understood in regards to pathogenesis and prognosis, particularly the lesions formed on anatomical sites away from sun exposure. With the aim of deepening our understanding of the pathogenesis and clinico-pathological correlations of BCCs, we conducted this study. Methods: Tissue blocks and data of 52 Egyptian patients diagnosed with BCC were retrieved for clinical information and inclusion criteria, then re-examined histologically; p16 immunostaining was carried out and evaluated for analysis and comparison between the two groups, i.e., sun-exposed and sun-protected. Results: Sex, age, clinical suspicion, tumor size, recurrence status, and histologic variants did not show a significant difference between the sun-protected and sun-exposed groups; however, the mean ages recorded were 67.2 vs. 62.7 for the sun-protected and sun-exposed groups, respectively. A total of 52% of BCCs were positive for p16. The sun-protected lesions showed p16 positivity in 61% of cases, whereas 49% of the sun-exposed lesions were positive with no significant difference. There was a significant difference in p16 expression between the recurrent and non-recurrent lesions. Conclusions: A significant difference was seen in the case of cancer recurrence, where all the recurrent BCCs in this study demonstrated negative p16 immunostaining of the primary lesions; however, the positively stained cases in total were 52% of BCCs. The mean patient age of the sun-protected group was much higher than in previous peer studies. We assume that the biological, prognostic, and clinical aspects of p16 protein expression in BCCs are still far from being clearly understood. Further studies are highly recommended, with more focus on its role in the pathogenesis and the prognostic factors.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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