Patients with high-risk (thick, deeply invasive) primary melanoma were, in
the past, managed by wide local excision and elective node dissection or wi
de local excision alone, with subsequent lymphadenectomy if the regional no
des developed clinically detectable metastases. We recently developed a mor
e logical approach called selective lymph node dissection. To be effective,
this requires close collaboration of surgeons, pathologists, and nuclear m
edicine physicians. The draining lymph node basin is identified preoperativ
ely by lymphoscintigraphy. During surgery, a marker dye (isosulfan blue) an
d radioactive technetium labeled albumin are injected intradermally around
the primary melanoma and the afferent lymphatics are followed up to the fir
st lymph nodes of the ipsilateral regional nodal basin. The surgeon excises
the blue-colored and maximally radioactive sentinel nodes and the patholog
ist critically evaluates these for the presence of a metastatic tumor. If t
he sentinel nodes are tumor free, no further nodal dissection is undertaken
; if a tumor is present, a complete dissection of the nodal basin is perfor
med. We have examined 1,119 sentinel lymph nodes from 669 patients treated
by selective lymph node dissection. We identified melanoma cells in sentine
l nodes from 126 patients (17.8%). A single node contained tumors in 67% of
patients, 2 nodes were positive in 25%, and the remaining 12% of patients
had three tumor-containing nodes. Melanoma cells were dispersed singly or i
n variably sized groups, usually in the peripheral nodal sinus. In around 4
0% of patients, immunohistochemistry is required to identify minute numbers
of tumor cells. With experience, pathologists identify tumors in hematoxyl
in and eosin (H&E) preparations in an increasing proportion of lymph nodes.
Tumor cells are more frequent in the sentinel nodes of patients with prima
ry tumors of deeper Clark level and greater Breslow thickness, Tumor cells
must be discriminated from capsular nevus cells, interdigitating dendritic
leukocytes, macrophages,and intranodal neural tissues. Copyright (C) 2000 b
y W.B. Saunders Company.