The recent development of high-frequency ultrasound, associated with the improved sensitivity in color Doppler, enabled the identification of various skin structures and layers. In basal cell carcinoma, the 22 MHz frequency ultrasound permits the delimitation of tumor margins, while color Doppler, determines its vascularization. We present two cases in which the association of both exams allowed an in vivo analysis of the tumor's morphology, size, thickness and vascularization, thus contributing to a better pre-operative evaluation.
The recent development of high-frequency ultrasound, associated with the improved sensitivity in color Doppler, enabled the identification of various skin structures and layers. In basal cell carcinoma, the 22 MHz frequency ultrasound permits the delimitation of tumor margins, while color Doppler, determines its vascularization. We present two cases in which the association of both exams allowed an in vivo analysis of the tumor's morphology, size, thickness and vascularization, thus contributing to a better pre-operative evaluation.
Used since the 70s in dermatology, ultrasonography is based on the reflection of sound
waves throughout the tissues.[1,2] According to the anatomical structure,
its vascularization and density, the ultrasound waves are reflected back to the
transducer that converts them into a gray scale, observed on the monitor.[3] The higher the frequency of the waves
emitted by the transducer, the better the spatial resolution and subsequent
visualization of structures near it. The introduction of transducers with frequency
higher than 15 MHz produced the high-frequency ultrasound (HFUS). The shortest
wavelength obtained by this frequency allowed a better assessment of superficial
structures, significantly expanding its use in cutaneous diseases.[4]In normal skin, the echogenicity of each layer depends on its main component, which in
the epidermis is represented by keratin, in the dermis by collagen and in the
subcutaneous tissue by fat lobules. In the ultrasound image, the epidermis appears as a
hyperechoic line, the dermis as a hyperechoic band less bright than the epidermis and
the subcutaneous tissue as a hypoechoic layer with hyperechoic fibrous septa in
between.[3]Dermoscopy is a complementary exam of great impact in dermatological practice that
permits an early differentiation between malignant and benign cutaneous lesions. A study
by Altamura et al, aimed at determining the accuracy of this method in
the diagnosis of basal cell carcinoma, demonstrated a high sensitivity rate
(87%).[5]Basal Cell Carcinoma (BCC) is an epithelial neoplasm, which corresponds to approximately
7580% of cutaneous tumors in middle-aged individuals with fair skin. It usually affects
areas exposed to solar radiation, with the highest incidence rate in the face.[6] Overestimation of the tumor area can lead
to unnecessary aesthetic problems. On the other hand, incomplete excisions are charged
with changing the tumor structure, thus generating a more aggressive behavior.[7,8]
Sartore et al reports that 5 to 50% of BCC are incompletely
excised.[7,9]The determination of the tumor extent and the adequate safety margins are of paramount
importance for surgical intervention.[9]
With dermoscopy, it is possible to assess the extension of the lesion in the
longitudinal and horizontal axes. However, it is not feasible to determine its depth and
the potential invasion of adjacent structures, such as cartilage and muscle, based only
on clinical and dermoscopic evaluation. With HFUS, it is possible to delimit the tumoral
margin based on the difference in refraction between the hypoechoic tumor area and the
hyperechoic perilesional region. In parallel, it is possible to assess tumor
vascularization, its nature and distribution with color Doppler exams.[7]
CASES REPORT
Two patients, one male and one female, aged 67 and 73 years presented lesions on the
nose and right flank, respectively (Figures 1 and
2). Dermoscopy (DermLite DL3, 3rd Gen, USA) and
22MHz HFUS (Esaote, My Lab Touch, Italy) were performed in both patients. The male
patient reported a past medical history of having one lesion removed in the same
location, three years ago. Dermoscopic examination showed, in both cases, the presence
of arborizing telangiectasias and ovoid nests (Figures
3 and 4). HFUS (22 MHz) demonstrated a
hypoechoic lesion in the dermis of the first patient, measuring 1mm deep by 1.9 mm in
its largest diameter, surrounded by a slightly less echogenic area consistent with
fibrosis (Figure 5A). Color Doppler exam showed
the presence of blood vessels permeating the tumor (Figure 5B). Hypoechoic lesions measuring 1 x 3.5 mm, delimitated by the
hyperechoic surrounding dermis were observed on the second patient; color Doppler
aspects were similar to those of the previous exam (Figure 6A and 6B). Patients underwent
excision of the lesions after adequate delineation of tumoral margins, guided by
dermoscopy and HFUS. Histopathological examination revealed, in the first case, nests of
basaloid cells amidst old scarring, reaching 1 mm deep and 1.8 mm laterally (Figure 7). The second patient had a similar
histopathological result, with the lesion measuring 1 mm deep and 3.5 mm laterally
(Figure 8).
FIGURE 1
Normochrom ic papular lesion, on the nose, over prior surgical scar
FIGURE 2
Erythematou s papule on the right flank
FIGURE 3
Dermoscopy showing classic arborizing telangiectasias and slightly pigmented
amorphous area
FIGURE 4
Dermoscopy presenting white - reddish glossy areas and fine telangiectasias.
Discrete ovoid nests
FIGURE 5
A. Gray scale in the ultrasound shows well delimited, hypoechoic oval
lesion, involving the dermis. B. Color Doppler shows increased
vascularity on the tumor
FIGURE 6
A. 22 MHz HFUS showing hypoechoic tumoral lesion. B.
Color Doppler shows blood vessels positioned in the inferior portion of the
lesion
FIGURE 7
Histopathological exam shows a basaloid epithelial tumor. H&E 10X
FIGURE 8
Histopathological exam: basaloid lesion infiltrating the dermis. H&E, 40X
Normochrom ic papular lesion, on the nose, over prior surgical scarErythematou s papule on the right flankDermoscopy showing classic arborizing telangiectasias and slightly pigmented
amorphous areaDermoscopy presenting white - reddish glossy areas and fine telangiectasias.
Discrete ovoid nestsA. Gray scale in the ultrasound shows well delimited, hypoechoic oval
lesion, involving the dermis. B. Color Doppler shows increased
vascularity on the tumorA. 22 MHz HFUS showing hypoechoic tumoral lesion. B.
Color Doppler shows blood vessels positioned in the inferior portion of the
lesionHistopathological exam shows a basaloid epithelial tumor. H&E 10XHistopathological exam: basaloid lesion infiltrating the dermis. H&E, 40X
DISCUSSION
Currently, histopathological examination is the gold standard for diagnosis and
morphological and structural assessment of BCC. However, new techniques for in
vivo investigation have been used to expedite diagnosis and optimize
pre-operative evaluation.Studies indicate that HFUS represents an innovative method for exploring cutaneous
tumors, including BCC. Unfit to assess tumor cellularity, this exam cannot be used to
confirm diagnosis, but it enables a detailed preoperative study: by assessing the
different skin layers and their respective thicknesses, the tumor size and involvement
of deep planes. Color Doppler exam can estimate the blood flow on the lesion and its
surroundings.Histopathological analysis confirmed the assessment of pre-operative tests.In summary, we report two cases that exemplify how the association of HFUS with
dermoscopy adds substantial value to the analysis of tumoral dimensions, which also
permits the safe determination of their margins and vascularization patterns prior to
tumor excision.
Authors: Davide Altamura; Scott W Menzies; Giuseppe Argenziano; Iris Zalaudek; H Peter Soyer; Francesco Sera; Michelle Avramidis; Kathryn DeAmbrosis; Maria Concetta Fargnoli; Ketty Peris Journal: J Am Acad Dermatol Date: 2009-10-13 Impact factor: 11.527
Authors: Pedro Andrade; Maria Manuel Brites; Ricardo Vieira; Angelina Mariano; José Pedro Reis; Oscar Tellechea; Américo Figueiredo Journal: An Bras Dermatol Date: 2012 Mar-Apr Impact factor: 1.896
Authors: Elisa de Oliveira Barcaui; Antonio Carlos Pires Carvalho; Flavia Paiva Proença Lobo Lopes; Juan Piñeiro-Maceira; Carlos Baptista Barcaui Journal: An Bras Dermatol Date: 2016 May-Jun Impact factor: 1.896