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Application of Different Staining Methods in the Diagnosis of Pigment-Rich Melanoma.

Authors :
Chengmin Z
Jiayu L
Jun H
Yang L
Zhou Y
Source :
Journal of clinical laboratory analysis [J Clin Lab Anal] 2024 Oct; Vol. 38 (19-20), pp. e25106. Date of Electronic Publication: 2024 Sep 24.
Publication Year :
2024

Abstract

Objective: To compare the application of different treatments in the diagnosis of melanoma with severe pigment interference, to solve the problem of pigment interference with immunohistochemical interpretation.<br />Methods: The pigment-rich melanomas were first depigmented with potassium permanganate using a concentration gradient (0.1%, 0.5%, 1%) and a time gradient (1, 5, 10, 15, 30 min, 6 h), and the optimal concentration and time were found. Then, 12 cases of pigment-rich melanoma tissues were collected, and the tissues were stained with diaminobenzidine (DAB), alkaline phosphatase-fast red (AP red), multiplex immunofluorescence (MIF), and 3-amino-9-ethylcarbazole (AEC), and ferrous sulfate, comparing different methods, positive expression of HMB45, MelanA, S100, SOX10, ki67.<br />Results: First, the concentration of 0.5% potassium permanganate after 15 min treatment of the pigment significantly faded, and the intensity of antibody positivity was better than other concentrations and time. Second, after depigmentation treatment, the antibody positivity rate was 41.7%-66.7% for DAB, 66.7%-91.7% for AP red, 83.3%-100% for multiplex immunofluorescence, 25%-33.3% for AEC, and 33.3% for ferrous sulfate.<br />Conclusion: AP red staining and mIF are more suitable for the diagnosis of melanoma with severe pigment interference, and AP red staining is more economical and practical.<br /> (© 2024 The Author(s). Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1098-2825
Volume :
38
Issue :
19-20
Database :
MEDLINE
Journal :
Journal of clinical laboratory analysis
Publication Type :
Academic Journal
Accession number :
39315764
Full Text :
https://doi.org/10.1002/jcla.25106