Verrucous carcinoma arising from actinic keratosis: a case report

Article information

Arch Craniofac Surg. 2021;22(6):333-336
Publication date (electronic) : 2021 December 20
doi : https://doi.org/10.7181/acfs.2021.00542
1Department of Plastic and Reconstructive Surgery, National Health Insurance Service Ilsan Hospital, Goyang, Korea
2Department of Pathology, National Health Insurance Service Ilsan Hospital, Goyang, Korea
Correspondence: Seum Chung Department of Plastic and Reconstructive Surgery, National Health Insurance Service Ilsan Hospital, 100 Ilsan-ro, Ilsandong-gu, Goyang 10444, Korea E-mail: schung@nhimc.or.kr

This study was presented as a poster at the 9th R&R Forum on May 9–10, 2019 at Chonnam National University, Gwangju, Korea.

Received 2021 October 22; Revised 2021 November 10; Accepted 2021 December 9.

Abstract

Verrucous carcinoma (VC) is a rare subtype of squamous cell carcinoma that commonly occurs in the oral cavity. However, VC of the facial skin is relatively rare. We report a case of a 91-year-old woman with VC of the facial skin in the left zygoma area. She was diagnosed with actinic keratosis (4 × 3 cm) of the same site approximately 12 years previously, but declined further treatment. The mass was excised with a minimum of 0.4 cm from gross margins with the result of free from tumor of all margins by frozen section, allowing for primary closure after skin undermining. Basal resection was performed in the preplatysmal plane. The diagnosis of VC was confirmed by histopathological examination. Postoperatively, the wound healed without incident and with no signs of facial nerve injury. To our knowledge, this is the first reported case of VC of facial skin arising from actinic keratosis.

INTRODUCTION

Verrucous carcinoma (VC) is a relatively rare subtype of squamous cell carcinoma (SCC), which was first described by Ackermann in 1948 [1]. The types of skin cancer are classified into basal cell carcinoma, SCC, malignant melanoma, and others (adenocarcinoma, angiosarcoma, extramammary Paget disease, Merkel cell carcinoma, and VC). VC is known as a relatively rare subtype [2]. Chewing tobacco, poor oral hygiene, human papillomavirus (HPV), and habitual smoking are considered significant etiologic factors for VC [3,4]. VC is generally characterized by a grossly ulcerating, fungating, or polypoid wart-like mass; histologically, the tumors are composed of squamous epithelial cells with minimal cellular atypia arranged in a verrucous pattern [5]. VC can be locally destructive requiring free flap reconstruction [6]. The prognosis of VC is better than that of SCC since metastasis is extremely rare [3]. Previously, many types of VCs were diagnosed, with the majority occurring in the mucosal tissue. Some VC subtypes of the skin have been reported in the genital/perianal region, toes, and calcaneal regions; thus, most of these cases were located in regions that were protected from sunlight by clothing. Here, we report a case of VC arising from the skin of the cheek with untreated actinic keratosis (AK).

CASE REPORT

A 91-year-old woman presented with a 5 × 4 cm fungating mass that had developed approximately 2 years ago in the left zygoma area (Fig. 1). She had received a histological diagnosis of AK (mass size at biopsy: 4 × 3 cm) of the same site by punch biopsy approximately 12 years previously but had declined additional treatment after biopsy. A high probability of skin cancer was suspected; therefore, excision of the mass and surrounding AK was recommended. However, the patient refused extensive surgery and only wanted “removal of the protruding mass.” An excisional biopsy of the main mass was performed under local anesthesia. The mass was excised with a minimum of 0.4 cm from gross margins with the result of free from tumor of all margins by frozen section, allowing for primary closure after skin undermining. Basal resection was performed in the preplatysmal plane. The histology showed verrucous epidermal proliferation with marked hyperkeratosis (Fig. 2), and lack of nuclear atypia and stromal infiltration consistent with VC (Fig 3). All surgical margins were free of cancer. Evidence for HPV infection, such as viral inclusion bodies, was not observed. Postoperatively, the wound healed without incident and with no signs of facial nerve injury (Fig. 4).

Fig. 1.

Preoperative photograph of a 91-year-old woman with a protruding mass on the left zygomatic area.

Fig. 2.

Verrucous epidermal proliferation (open arrows) with marked hyperkeratosis (arrowheads) (H&E, ×40).

Fig. 3.

Lack of nuclear atypia and stromal infiltration (arrowheads) (H&E, ×200).

Fig. 4.

Postoperative photograph 4 weeks after excision with remaining actinic keratosis.

DISCUSSION

VC is a low-grade, well-differentiated SCC and extremely rare (0.075 per 100,000) [7]. Many types of VC according to the site of occurrence have been reported, such as the genital tract (Buschke-Loewenstein tumor), oral cavity and aerodigestive tract (Ackerman tumor, oral florid papillomatosis, oral florid verrucosis, giant mucocutaneous papillomatosis, nonmetastasizing papillomatosis), palmoplantar area (epithelioma cuniculatum, carcinoma cuniculatum), and cutaneous region (papillomatosis cutis carcinoides, papillomatosis cutis, giant cutaneous papilloma) [8]. Diaz-Perez et al. [9] reported a VC of the lip and several cases of VC of the lip mucosa and skin regions generally protected from sunlight by clothing (sole, genital area, etc.) have also been reported [10]. However, VC of sun-exposed facial skin is extremely rare [11,12], and to our knowledge, this is the first reported case of VC of facial skin arising from AK. This case initially presented about 12 years ago with a pruritic mass on the left zygoma of about 1-year duration. The mass was irregularly shaped, elevated and flesh colored. Punch biopsies were done from multiple sites and all showed parakeratosis, atypia of the basilar layer of the epidermis, and mild dermal lymphocytic infiltrate; consistent for AK. The patient was a farmer for more than 60 years who occasionally wore a hat but never used sunscreens for her face or other sun-exposed areas. Since she declined further treatment for her AK even after the possibility of progression to skin cancer was explained, we strongly recommended her to avoid direct sun exposure and to use sunscreen and a hat. However, during her latest presentation it was noted that she had returned to farming soon after her biopsies and only wore a hat.

The etiology of VC is not well known. Chronic inflammatory processes such as osteomyelitis scars, fistulas, ulcers, and lipoidica necrobiosis may be related to the occurrence of VC [13]. Repeated microtrauma and viral infections (especially HPV-6 and HPV-11) are also considered causative factors [14]. However, in this case, evidence of HPV infection such as viral inclusion bodies was not observed, and had no previous history of infection or trauma to the tumor area. This case suggests that the intraepidermal dysplasia characteristic of AK may progress to VC through the three stages of photocarcinogenesis: initiation (ultraviolet [UV]-light exposure, DNA damage), promotion (clonal expansion of metaplastic cells, additional UV irradiation), and progression into neoplastic cells [15]. To our knowledge, this is the first reported case of VC of facial skin arising from AK.

Notes

Conflict of interest

No potential conflict of interest relevant to this article was reported.

Ethical approval

The study was approved by the Institutional Review Board of National Insurance Service Ilsan Hospital (IRB No. 2021-09-038).

Patient consent

The patient provided written informed consent for the publication and the use of her images.

Author contribution

Conceptualization: Seum Chung. Project administration: Seum Chung. Visualization: Ji Hyuk Jung, Mi Kyung Lee. Writing - original draft: Ji Hyuk Jung. Writing - review & editing: Ji Hyuk Jung, Yeo Reum Jeon, Hyo In Kim, Seum Chung. Supervision: Seum Chung.

Abbreviations

AK

actinic keratosis

HPV

human papillomavirus

SCC

squamous cell carcinoma

UV

ultraviolet

VC

verrucous carcinoma

References

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Article information Continued

Fig. 1.

Preoperative photograph of a 91-year-old woman with a protruding mass on the left zygomatic area.

Fig. 2.

Verrucous epidermal proliferation (open arrows) with marked hyperkeratosis (arrowheads) (H&E, ×40).

Fig. 3.

Lack of nuclear atypia and stromal infiltration (arrowheads) (H&E, ×200).

Fig. 4.

Postoperative photograph 4 weeks after excision with remaining actinic keratosis.