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Detection of tyrosinase mRNA in the sentinel lymph nodes of melanoma patients is not a predictor of short-term disease recurrence
Sentinel lymph node evaluation has enabled identification of patients with cutaneous melanoma who might benefit from elective regional lymph node dissection. Sentinel nodes are currently assessed by histologic and reverse transcription polymerase chain reaction (RT–PCR) evaluation for melanocyte-spe...
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Published in: | Modern pathology 2007-04, Vol.20 (4), p.427-434 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Sentinel lymph node evaluation has enabled identification of patients with cutaneous melanoma who might benefit from elective regional lymph node dissection. Sentinel nodes are currently assessed by histologic and reverse transcription polymerase chain reaction (RT–PCR) evaluation for melanocyte-specific markers. The clinical significance of positive findings by RT–PCR in the absence of histologic evidence of metastasis (HISNEG/PCRPOS) remains unclear. Examination of 264 lymph nodes from 139 patients revealed histopathologic positivity in 34 patients (24.5%), in which 26 also demonstrated simultaneous RT–PCR positivity (HISPOS/PCRPOS). Of 35 HISNEG/PCRPOS patients (25.2%), five also had nodal capsular nevi. In total, capsular nevi were detected in 13 patients (9.4%). A total of 70 patients (50.4%) had negative sentinel nodes by both histopathology and RT–PCR (HISNEG/PCRNEG). Over a median follow-up of 25 months, local and/or systemic recurrence developed in 31 patients (22.3%). Recurrence rates were similar among patients with histopathologic evidence of sentinel lymph node metastasis, irrespective of RT–PCR status (HISPOS/PCRPOS 62%; HISPOS/PCRNEG 75%). In contrast, only 10% of HISNEG/PCRNEG patients developed recurrence, significantly less than those in either HISPOS group (P |
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ISSN: | 0893-3952 1530-0285 |
DOI: | 10.1038/modpathol.3800754 |