Regression in primary cutaneous melanoma: etiopathogenesis and clinical significance

被引:66
作者
Aung, Phyu P. [1 ]
Nagarajan, Priyadharsini [1 ]
Prieto, Victor G. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
SENTINEL LYMPH-NODE; THIN MALIGNANT-MELANOMA; T-CELL RESPONSES; HISTOLOGIC REGRESSION; TUMOR-REGRESSION; PROGNOSTIC IMPLICATIONS; METASTATIC MELANOMA; PREDICTING SENTINEL; DENDRITIC CELLS; MM MELANOMAS;
D O I
10.1038/labinvest.2017.8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Though not required currently for staging, regression is a histopathologic parameter typically reported upon diagnosis of an invasive primary cutaneous melanoma. The studies examining the prognostic significance of regression in patient outcome have yielded controversial findings; likely because the definition and assessment of regression have not been consistent, in addition to subjectivity of pathologists' interpretation. Regression is histologically characterized by variable decrease in the number of melanoma cells accompanied by the presence of a host response consisting of dermal fibrosis, inflammatory infiltrate, melanophages, ectatic blood vessels, epidermal attenuation, and/or apoptosis of keratinocytes or melanocytes; the relative extent of these features depends on the stage of the regression. However, the magnitudes to which these individual changes must be present to meet the threshold of histologic regression have not been well defined or agreed upon, and thus, the definition and classification of histologic regression in melanoma varies considerably among institutions and even among individual pathologists. In order to determine the clinical significance of histologic analysis of regression, there is a compelling need for a universal scheme to objectively define and assess histologic regression in primary cutaneous melanoma, so that the biologic and prognostic significance of this process may be completely understood.
引用
收藏
页码:657 / 668
页数:12
相关论文
共 116 条
  • [1] [Anonymous], 2016, American Cancer Society: Cancer Facts and Figures 2016
  • [2] [Anonymous], 1976, NATL CANC I MONOGR, V44, P67
  • [3] MULTIFACTORIAL ANALYSIS OF MELANOMA - PROGNOSTIC HISTOPATHOLOGICAL FEATURES COMPARING CLARKS AND BRESLOWS STAGING METHODS
    BALCH, CM
    MURAD, TM
    SOONG, SJ
    INGALLS, AL
    HALPERN, NB
    MADDOX, WA
    [J]. ANNALS OF SURGERY, 1978, 188 (06) : 732 - 742
  • [4] Hypothesis: A role for telomere crisis in spontaneous regression of melanoma
    Bastian, BC
    [J]. ARCHIVES OF DERMATOLOGY, 2003, 139 (05) : 667 - 668
  • [5] Bayer-Garner Ilene B, 2004, Clin Med Res, V2, P89
  • [6] Modeling Melanoma In Vitro and In Vivo
    Beaumont, Kimberley A.
    Mohana-Kumaran, Nethia
    Haass, Nikolas K.
    [J]. HEALTHCARE, 2014, 2 (01): : 27 - 46
  • [7] Presence and localization of T-cell subsets in relation to melanocyte differentiation antigen expression and tumour regression as assessed by immunohistochemistry and molecular analysis of microdissected T cells
    Bernsen, MR
    Diepstra, JHS
    van Mil, P
    Punt, CAJ
    Figdor, CG
    van Muijen, GNP
    Adema, GJ
    Ruiter, DJ
    [J]. JOURNAL OF PATHOLOGY, 2004, 202 (01) : 70 - 79
  • [8] Evaluation of melanoma features and their relationship with nodal disease: the importance of the pathological report
    Bertolli, Eduardo
    de Macedo, Mariana Petaccia
    Lopes Pinto, Clovis Antonio
    Damascena, Aline Santos
    Molina, Andre Sapata
    Ueno, Patricia Sayuri
    Duprat Neto, Joao Pedreira
    [J]. TUMORI JOURNAL, 2015, 101 (05): : 501 - 505
  • [9] Bhatia S, 2009, ONCOLOGY-NY, V23, P488
  • [10] HISTOLOGICAL REGRESSION IN PRIMARY CUTANEOUS MELANOMA - RECOGNITION, PREVALENCE AND SIGNIFICANCE
    BLESSING, K
    MCLAREN, KM
    [J]. HISTOPATHOLOGY, 1992, 20 (04) : 315 - 322