Original article 375
Digital surface microscopy analysis of conjunctival
pigmented lesions: a preliminary study
Gian Marco Tosi
a
, Pietro Rubegni
b
, Karin Schuerfeld
c
, Paolo Toti
c
,
Gabriele Cevenini
d
, Giordana Dell’Eva
e
, Lucio Andreassi
b
,
Aldo Caporossi
a
and Marco Burroni
b
The objective of this study was to investigate whether
digital surface microscopy (DSM) could be used for the
follow-up and comparison of malignant and benign con-
junctival pigmented lesions (CPLs). Thirty-nine CPLs [16 de
novo malignant melanomas (MMs), one MM arising from
primary acquired melanosis (PAM), six PAMs and 16 naevi]
were digitally analysed and biopsied. All of the PAMs and
10 naevi, which had not been surgically excised, were
followed up using DSM. Thirty parameters were evaluated
grouped into four categories: geometry, colour, texture and
islands of colour. None of the CPLs that were followed up,
which comprised 10 naevocytic naevi and seven PAMs,
showed any morphological change at DSM analysis, except
for one PAM which developed an MM 1 year later. Of the
geometric variables examined, the area, maximum dia-
meter and minimum diameter showed significantly higher
values in MMs compared with benign CPLs. With regard to
the colour of CPLs, MMs were significantly darker and bluer
than naevi. In the texture group, contrast was significantly
higher in MMs. In the islands-of-colour group, the imbal-
ance of blue–grey regions and the presence of dark areas
were significantly higher in MMs. DSM greatly simplified
the follow-up of CPLs, such as PAMs with atypia, by
providing satisfactory quality images with high reproduci-
bility; this technique is also easy to use and well accepted
by patients. Moreover, this preliminary study allowed us to
determine which objective variables could be important for
distinguishing between benign CPLs and conjunctival
MMs. Melanoma Res 14:375–380
c
2004 Lippincott
Williams & Wilkins.
Melanoma Research 2004, 14:375–380
Keywords: Computer, conjunctival melanoma, conjunctival naevus, image
analysis, primary acquired melanosis
a
Department of Ophthalmology and Neurosurgery,
b
Dermatology,
c
Human
Pathology and Oncology,
d
Thoracic Surgery and Biomedical Technologies,
University of Siena, Siena, Italy and
e
Lega Italiana Tumori Siena, Siena, Italy.
Sponsorship: This work was supported by a grant from the Italian Ministry of
Instruction, University and Research.
Correspondence and requests for reprints to Dr Pietro Rubegni, Dipartimento di
Dermatologia, Universita` di Siena, Via delle Scotte, 1, 53100 Siena, Italy.
Tel: + 39 0577585422; fax: + 39 057744238;
e-mail: rubegni@unisi.it
Received 29 April 2004 Accepted (after revision) 24 June 2004
Introduction
Conjunctival malignant melanoma (MM) is a rare
malignancy with an estimated incidence of 0.02–0.08
per 100 000 inhabitants in Western populations [1]. The
incidence of conjunctival melanoma in the white popula-
tion has increased in a similar manner to cutaneous
melanoma and, from a biological point of view, shows a
greater resemblance to its cutaneous counterpart than its
uveal counterpart [1,2]. Three clinical and histopatholo-
gical forms of conjunctival MM have been identified: MM
evolving from primary acquired melanosis (PAM), MM
with no pre-existing conjunctival pigmented lesions
(CPLs) and MM originating from a conjunctival naevus
[3,4]. Conjunctival MM is a potentially deadly tumour.
Metastases are detected in 14–27% of patients [5–7] and
mortality is 13–40% over 10 years [6–8]. According to
some authors [9], it should be managed, like all
conjunctival malignancies, with meticulous surgical plan-
ning using a wide microsurgical dissection, avoiding
incisional biopsy because of the subsequent risk of
tumour dissemination and recurrence. Early diagnosis is
of crucial importance in reducing mortality and avoiding
disfiguring surgery, which becomes mandatory at a later
stage.
In dermatology, a recent technique known as epilumines-
cence light microscopy (ELM), which magnifies lesions
and enables them to be examined down to the dermo-
epidermal junction, has led to a 5–30% increase in
diagnostic accuracy with respect to simple clinical
observation [10,11]. However, evaluation of the many
morphological characteristics of pigmented lesions by
ELM is often extremely complex and subjective. To avoid
these problems, technologies and methods have been
developed to enable an objective evaluation to be made of
the many parameters that have emerged with decades of
experience of using ELM [12]. An example is digital
surface microscopy (DSM), which gathers numerical data
and allows pigmented lesion images to be described
objectively [13–16]. In fact, DSM is a recent evolution of
0960-8931 c 2004 Lippincott Williams & Wilkins
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