The use of synchrotron infrared microspectroscopy in the assessment of cutaneous T-cell lymphoma vs. pityriasis lichenoides chronica

被引:9
作者
El Bedewi, Ahmed [1 ,2 ]
El Anany, Galal [3 ]
El Mofty, Medhat [3 ]
Kretlow, Ariane [2 ]
Park, Simone [2 ]
Miller, Lisa M. [2 ]
机构
[1] NRRCT Dermatol, Cairo 11211, Egypt
[2] Brookhaven Natl Lab, Natl Synchrotron Light Source, Upton, NY 11973 USA
[3] Cairo Univ, Dept Dermatol, Fac Med, Cairo, Egypt
基金
美国能源部;
关键词
infrared microspectroscopy; mycosis fungoides; pityriasis lichenoides chronica; synchrotron and nucleic acids;
D O I
10.1111/j.1600-0781.2010.00498.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background The diagnosis of cutaneous lymphomas remains a challenge for both the clinician and dermatopathologist. Objectives To differentiate between frank malignant and premalignant lymphocytes within the skin. Methods This study was performed on 20 patients with a mean age of 50 years. They were divided into two groups: mycosis fungoides (MF) (stage IA, IB and IIA) and pityriasis lichenoides chronica (PLC). Immunophenotyping using antibodies CD3, CD4, CD8, CD20 and CD30 was performed. Synchrotron Fourier transform infrared microspectroscopy (S-FTIRM) was performed on cell nuclei to assess chemical differences between MF and PLC cases as a potential complementary screening tool. Dermal spectra of both MF and PLC were compared using principal components analysis (PCA) of the S-FTIRM data. Results All PLC spectra was clustered together. However, the MF spectra formed two clusters, one that grouped with the PLC and the other grouped separately. Moreover, protein and nucleic acids showed highly significant differences between MF (IIA and IB), MF (IA) and PLC. Conclusions The malignant transformation within lymphocytes was identifiable through the spectroscopic analysis of protein, RNA and DNA with S-FTIRM, making it a promising tool for classifying the progression of cutaneous T-cell lymphoma.
引用
收藏
页码:93 / 97
页数:5
相关论文
共 16 条
[1]  
Andrus PG, 2006, TECHNOL CANCER RES T, V5, P157
[2]  
Andrus PGL, 1998, BIOSPECTROSCOPY, V4, P37, DOI 10.1002/(SICI)1520-6343(1998)4:1<37::AID-BSPY4>3.0.CO
[3]  
2-P
[4]   Determination of the relative amount of nucleic acids and proteins in leukemic and normal lymphocytes by means of Fourier transform infrared microspectroscopy [J].
Benedetti, E ;
Bramanti, E ;
Papineschi, F ;
Rossi, I ;
Benedetti, E .
APPLIED SPECTROSCOPY, 1997, 51 (06) :792-797
[5]   Assessment of T-cell clonality via T-cell receptor-γ rearrangements in cutaneous T-cell-dominant infiltrates using polymerase chain reaction and single-stranded DNA conformational polymorphism assay [J].
Chen, M ;
Deng, A ;
Crowson, AN ;
Srinivasan, M ;
Yearsley, KH ;
Jewell, S ;
Morrison, C ;
Long, S ;
Werling, R ;
Magro, C .
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2004, 12 (04) :373-379
[6]  
DAOUD MS, 2003, DERMATOLOGY GEN MED, P1950
[7]  
HEALD P, 2003, DERMATOLOGY GEN MED, P2403
[8]   Diagnostic value of combining immunostaining for CD3 and nuclear morphometry in mycosis fungoides [J].
Lira, M. ;
Schenka, A. A. ;
Magna, L. A. ;
Cotta, A. C. ;
Cintra, M. L. ;
de Souza, E. M. ;
Brousset, P. ;
Vassallo, J. .
JOURNAL OF CLINICAL PATHOLOGY, 2008, 61 (02) :209-212
[9]  
MACKIE R, 1998, DERMATOLOGY GEN MED, P2350
[10]   Pityriasis lichenoides chronica: stratification by molecular and phenotypic profile [J].
Magro, Cynthia M. ;
Crowson, A. Neil ;
Morrison, Carl ;
Li, Jingwei .
HUMAN PATHOLOGY, 2007, 38 (03) :479-490