The article by Bisseck and colleagues
highlights an important
issue encountered increasingly
by physicians-melanoma in children
and adolescents. The incidence and
mortality of melanoma continues to
rise.[1] It is now the fifth most common
cancer in men and the seventh
most common cancer in women. In
our practice at the Johns Hopkins
Melanoma Center, we have treated a
growing number of children and adolescents
with melanoma, including
many with stage III disease identified
by sentinel node technology, similar
to that described by Bisseck and
colleagues.
Staging Issues
There are three teaching points
from this article that we would like to
emphasize: (1) the role of the sentinel
node in staging melanoma, (2) the
clinical characteristics of melanoma
in children and adolescents, and (3)
the pathologic diagnosis of melanoma
in children and adolescents.
The sentinel node technique, pioneered
by Dr. Donald Morton, has
become a standard approach in the
staging of melanoma at most centers.
The Melanoma Staging Committee of
the American Joint Commission on
Cancer has recommended that all patients
who potentially would be entered
into melanoma clinical trials
have their sentinel lymph nodes staged
as an entry requirement.[2] Otherwise,
it is difficult to distinguish between
the impact of the natural history of
melanoma in understaged patients (ie,
those who do not have a sentinel node
excision) from the treatment effect
being evaluated in a clinical trial.
At Johns Hopkins, patients with
clinically negative nodes and whose
melanoma is greater than 1 mm usually
undergo excision of their sentinel
node for staging purposes. In addition,
patients with high-risk T1 melanoma
(level IV invasion or ulcerated
melanomas) are also considered for
the sentinel lymph node staging.
Whether survival is improved by the
more accurate staging and early intervention
with complete lymphectomy
in patients with a clinically occult nodal
metastasis must await the results of
the international multi-institutional
melanoma surgery trial.
Treatment Issues
It is alarming to see the increasing
number of children and adolescents who
present with melanoma today. Several
decades ago, this was a rare event. Major
melanoma centers are now regularly
encountering children and
adolescents with invasive melanoma,
including some with lymph node metastasis.
Many of the children treated at
our center do not have the usual risk
factors associated with melanoma, such
as family history, dysplastic nevi,
congenital nevi, or multiple moles.
No evidence to date demonstrates that
survival rates in these younger populations
are different from those in
adults, using the standardized tumor,
node, metastasis (TNM) prognostic
and staging criteria.[2]
In our practice at the Johns Hopkins
Melanoma Center, we treat children,
adolescents, and adults with
melanoma in essentially the same way.
This includes offering the sentinel
node staging technique to patients who
meet the criteria described above under
Staging Issues. We agree with the
treatment approach described by Bisseck
et al. Many clinical protocols
exclude melanoma patients who are
less than 18 years old so that followup
or high-dose interferon-alpha are
the only options after surgery.
The Spitz Nevus Factor
The pathologic diagnosis of melanoma
can be problematic. As pointed
out in this article, the Spitz nevus that
can arise in children and adolescents
has many of the histologic features of
melanoma but is not a malignancy. Conversely,
amelanotic melanomas are
sometimes diagnosed as benign Spitz
nevi and are undertreated until patients
relapse with metastatic melanoma. Because
of the overlapping histopathologic
features of invasive melanoma
and Spitz nevus in children and adolescents,
we highly recommend that an
experienced melanoma pathologist review
the pathologic slides of these individuals
so that they will be accurately
diagnosed, staged, and treated.
We commend Drs. Bisseck, Shen,
and Pranikoff for highlighting their
approach to this difficult clinical presentation
and hope their patient has a
successful clinical outcome.
