Management of head and neck basal cell
carcinoma from an ENT perspective
Jacqueline SW Chan 曾詩慧
HK Pract 2024;46:96-99
Summary
This article focuses on non-melanotic skin cancer in
Hong Kong, of which, basal cell carcinoma is the most
common subtype. Risk factors include environmental
exposure, inherent skin characteristics and genetic
predisposition such as in Gorlin’s syndrome. Patients
present with a slow growing skin lesion for months
to years, 70% of those appear on the face. Basal cell
carcinoma is further risk stratified by their size, location,
and histopathological characteristics. Diagnosis is aided
by dermatoscope and confirmed by incisional biopsy. The
gold standard of treatment of basal cell carcinoma is by
MOHS Micrographic Surgery, which requires expertise
and is time and labour intensive. Another alternative
is Staged Excision and Reconstruction. Other nonsurgical
method includes Topical Therapy and Radiation,
which requires careful patient and tumour selection.
摘要
本文重點關注香港的非黑色素皮膚癌,其中基底細胞癌
(BCC)是最常見的亞型。危險因素包括環境暴露、固有的
皮膚特徵和遺傳傾向,例如戈林綜合症。患者會出現數月
至數年緩慢生長的皮損,其中70%出現在面部。基底細胞
癌根據其大小、位置和組織病理學特徵進一步進行風險分
層。一般我們可以用皮膚鏡輔助診斷,並通過切開活檢確
診。BCC治療的黃金標準是MOHS顯微手術,這需要專業
知識和人力。另一種選擇是分階段切除和重建。其他非手
術方法包括局部治療和放射治療,需要仔細選擇患者。
Introduction
Skin cancers are divided into melanoma and non-melanoma
types. In Hong Kong, the incidence of non-melanoma skin cancer ranks eighth and ninth in male
and female cancers respectively in 2019 according to
the Hong Kong Cancer Registry.1 The median age is 67
years and 75 years in male and female, respectively.
Overall, it ranks eighth among the top ten commonest
cancers in Hong Kong in 2019. The incidence rates
across age groups have been stable over the years 2011-
2020 (overall crude incidence rate 13.6 per 100,000
persons). The Hong Kong Cancer Registry does not
record the incidence of basal cell carcinoma (BCC) and
squamous cell carcinoma (SCC) individually.
In a 10-year retrospective study of non-melanoma
skin cancer in Hong Kong Chinese patients published in
2001, it was found that pigmented basal cell carcinoma
was the most common type of non-melanoma skin
cancer (60.1%) in Chinese patients, in contrast with
rodent ulceration in Caucasians. The head and neck
region was the most common site of BCC and SCC
occurrence.2 This article will thereafter focus on basal
cell carcinoma of the head and neck region
Risk factors and genetics
The incidence of basal cell carcinoma is associated
with increasing age, fair skin, ultraviolet light exposure
and radiation.3 A rare germline autosomal dominant
genetic condition, naevoid basal cell carcinoma syndrome
(also known as Gorlin syndrome), is associated with
multiple (more than 5 in a lifetime) and/or early onset
(before age 30 years) BCCs and other syndromal
features.4 Other genetic syndromes associated with an
increased risk of BCC include xeroderma pigmentosum,
Bazex-Dupre–Christol syndrome and Rombo syndrome.5
Clinical presentation
Patient typically present to the medical professional
with a progressively enlarging skin lesion over a few
months to a few years. As ENT practitioners, the
lesions referred to us are usually over the nasal region, less commonly over the pinna and face in general.
Approximately 70% of BCCs appear on the face and
15% on the trunk. Very rarely is BCC diagnosed in
other areas such as the penis or perianal skin.
In general, 95% of BCCs, if recognised early,
are ‘easy to treat’, however, in the following specific
clinical scenarios BCCs might require a more
comprehensive assessment, such as a thorough search
for other coexisting skin malignancy and to arrange
imaging for any regional lymph node metastasis.:
> Locally aggressive BCCs with cosmetic and
functional deficit at baseline or anticipated after
treatment, such as at the nose and eyelids.
> BCC recurrence in previously irradiated skin
> Metachronous BCC recurrence on the face
requiring wide local excision and reconstruction
> Patient has underlying medical co-morbidities
that interfere with treatment
In general, BCC is classified into low risk and high
risk types as follow:-
Low risk BCC:
-
Tumours < 2cm in diameter on trunk and
extremities excluding the genitalia, hands and feet
-
Nodular and superficial histopathology
-
Lack of perineural invasion
-
Primary lesion
-
No prior irradiation
-
Immunocompetent patient
High risk BCC:
-
Tumours of ANY size in the head and neck region
-
Tumours > / = 2 cm in diameter on trunk and
extremities excluding the genitalia, hands and feet
-
Aggressive histological subtype: morpheaform,
sclerosing, mixed infiltrative, carcinosarcomatous
-
Perineural invasion
-
Recurrent lesions
-
Previously irradiated skin
-
Immunocompromised patients (e.g. HIV, AIDS,
congenital disorders, autoimmune disorders)
Diagnosis
BCC is usually recognised via clinical inspection,
especially for nodular, superficial, ulcerated subtypes,
but in some cases a dermatoscope may aid in the
diagnosis.6 Dermatoscopy is a non-invasive method that
helps to visualise dermatopathological features that are
otherwise not apparent to the naked eye. Examples of
these dermatopathological features include maple-leave
like area, arborising vessels and ulceration. Another
non-invasive diagnostic method is the reflectance
confocal microscopy (RCM) which has been shown to
have a higher sensitivity and specificity as compared to
visual inspection combined with dermatoscopy.7 RCM is
a non-invasive imaging of the skin that provides cellular
level magnification. With expertise the RCM images
findings can correlate with an array of histopathological
diagnoses, which, in turn, can differentiate lesion types
before a biopsy.
In my practice, I always perform an incisional
biopsy or a punch biopsy before definitive treatment,
because the histological subtype may have a bearing on
the choice of treatment. For example, high risk BCC
would not be suitable for ablative superficial treatment
that does not allow for assessment of the clearance
of margins. Another reason favouring an incisional
biopsy as opposed to excisional biopsy is that for
small tumours, if completely excised and the pathology
comes back to be malignant, it is crucial to ensure clear
resection margins. For small tumour post excisional
biopsy, owing to the rapid regeneration of the skin
especially in the head and neck region, or the uncertain
lag time between first biopsy and subsequent wide local
excision, it can be difficult to localise the initial tumour
hence the assessment of resection margin may be flawed.
For this reason, pre-operative photographs before
biopsy is an essential part of any management plan.
Management and various approaches
Surgery
In many literatures the preferred first line treatment
of BCC is often by MOHS Micrographic Surgery
(MMS), which is the gold standard for treating BCC8
especially when the location of the tumour predisposes
the patient to cosmetic and functional concerns. The
tumour is excised and immediately processed for
histological evaluation. This process is repeatedly done
until a negative margin is achieved, while minimising the amount of normal tissue to be excised. This method
spares the patient from potential functional deficit,
especially at specific regions such as the eyelid and
the lips. The downside of this method is that it is not
widely available, as it is a labour intensive procedure,
and it either requires the operating surgeon to have
specific pathological training or it requires the presence
of a dermatopathologist.
A less labour intensive method while ensuring clear
resection margins is to perform a staged excision with
complete circumferential peripheral and deep margin
assessment. The lesion is excised and the margins are
formalin fixed for pathological examination. Once the
margins are reported as clear, the skin defect can be
reconstructed at a second stage. This method is less
labour intensive and is generally available in every
practice, but the downside is that a partially healed
skin defect may present with some scarring tissue that
potentially makes mobilisation of surrounding soft
tissue for wound closure more difficult.
The excision margins depend on the risk profile of
each individual BCC case.9 For low risk BCCs, safety
margin of 3 – 4 mm is recommended while in high risk
BCCs, when MMS is not available, the safety margin
between 5mm and 15mm should be chosen based on
individual tumour characteristics, such as the location
of the tumour, medical co-morbidities, any presence of
perineural invasion etc. Previous studies have shown
that for BCCs that are less than 2 cm, a margin of
4mm would have an eradication rate of 98%, therefore
even with greater margins there would be of minimal
additional benefit.10
Topical eradication and clearance
A topical destructive tissue-removal is another but
not the primary treatment for BCCs. There are two main
reasons for this: firstly, histological examination and
controlled margin clearance is not possible with topical
or destructive treatment; secondly, the deeper part of the
tumour may not be reachable as the more superficial layer
of the tumour may be scarred during the topical treatment.
Furthermore, the efficacy of various destructive
methods is highly dependent on operator skills and
tumour characteristics, which means patient selection is
very important for achieving favourable outcome.
In a study of 284 patients whose BCCs were treated with curettage and electro-dessication, incomplete
clearance occurred in 10.3 % of the cases.11 As per the
European consensus-based interdisciplinary guidelines
published in 2019, there is a 100% consensus to avoid
topical or destructive treatment modalities in BCCs at
risk of recurrence.
In those patients where surgery is not expected to
give optimal result, radiotherapy may be a better option.
Radiotherapy
Radiotherapy is a valid alternative to surgery and
the risk of radiation induced second malignancy is
negligible. Radiotherapy is an option when the patient
is not a surgical candidate with his or her coexisting
medical comorbidities, or when the site of lesion
poses significant functional and cosmetic deficit post
excision. A systematic review has demonstrated that
the recurrence rate of primary BCCs treated with
radiotherapy has a recurrence rate of 3.5%, which is
comparable with standard surgery and MMS (3.8%).12
External beam radiotherapy (EBRT) is the most used
radiotherapy modality, while brachytherapy is an
alternative. Radiotherapy is also an option when there is
microscopic or macroscopic residual tumour and if reresection
is not the best option.
For low risk BCCs treated appropriately, the risk of
recurrence is low. Patients with high risk BCCs should
be counselled and advised to come back if they notice
any new skin lesions. Long term follow-up is sometimes
not the most pragmatic as recurrent disease may take
up to 5 years to be clinically observable. In general,
patients with high risk BCCs would benefit from
interval follow-up every 6-12 months for 3-5 years.
Last consideration
Owing to the unique anatomy and functional
concern in the head and neck region, skin lesions,
in most cases, BCCs, often require careful planning
and reconstruction. Primary closure after excision is
the ideal situation but not always the case. Healing
by secondary intent, that is, allowing the skin defect
to granulate, may predispose the patient to unsightly
scarring and distortion of facial symmetry. In many
cases of primary BCCs appearing on the nose or
pinna region, a local flap is needed for reconstruction
in order to avoid the distortion of anatomy and
function. For more complex lesions requiring extensive reconstruction, it is best dealt via a multidisciplinary
approach, such as by ENT surgeons subspecialising
in facial plastic surgery, head and neck specialists,
oncologist, and dermatopathologist.
In conclusion, BCCs are common, slow growing
skin malignancy that may first present to general
practitioners. If treated timely, the prognosis is
excellent. With careful treatment planning, there is also
minimal risk of cosmetic or functional sequalae.
References
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Peris K, Fargnoli MC, Garbe C, et al. Diagnosis and treatment of basal cell
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Rodriguez-Vigil T, Vázquez-López F, Perez-Oliva N. Recurrence rates of
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Drucker AM, Adam GP, Rofeberg V, et al. Treatments of primary basal cell
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Jacqueline SW Chan,
MBChB(CUHK), FHKCORL, FHKAM (ORL), FRCSEd (ORL)
Private Practice
Correspondence to: Dr. Jacqueline Chan, Room 1401-3, Wing On House, 71 Des Voeux
Road Central, Central, Hong Kong SAR.
E-mail: jacqie.c@gmail.com
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