Protumorigenic M2-like phenotype cell infiltration in the melanotic neuroectodermal tumor of infancy

被引:7
|
作者
Strieder, Luciana [1 ]
Carlos, Roman [2 ]
Leon, Jorge Esquiche [3 ]
Ribeiro-Silva, Alfredo [4 ]
Costa, Victor [1 ]
Kaminagakura, Estela [5 ]
机构
[1] UNESP Univ Estadual Paulista, Inst Sci & Technol, Sch Dent, Oral Biopathol, Sao Jose Dos Campos, Brazil
[2] Ctr Clin Cabeza & Cuello, Guatemala City, Guatemala
[3] Univ Sao Paulo, Oral Pathol, Dept Stomatol Publ Oral Hlth & Forens Dent, Ribeirao Preto Sch Dent, BR-14049 Ribeirao Preto, Brazil
[4] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pathol, BR-14049 Ribeirao Preto, Brazil
[5] UNESP Univ Estadual Paulista, Stomatol, Dept Biosci & Oral Diag, Inst Sci & Technol,Sch Dent, Sao Jose Dos Campos, Brazil
关键词
DENDRITIC CELLS; CANCER; MACROPHAGES; SYNDECAN-1; MICROENVIRONMENT; PROGRESSION; SUBSETS;
D O I
10.1016/j.oooo.2015.09.015
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective. The aim of this study is to report 2 cases of melanotic neuroectodermal tumor of infancy (MNTI), emphasizing the analysis of intratumoral immune cells by immunohistochemistry. Study Design. Case 1: A 6-month-old girl presented with a 3-cm tumor in the anterior region of the left maxilla. Case 2: A 4-month-old boy presented with a 4-cm tumor in the anterior region of the left maxilla. Microscopically, case 1 had predominantly neuroblast-like cells supported by fibrillary neuropil-like stroma arranged in an alveolar pattern, whereas case 2 exhibited scattered melanocyte-like and neuroblast-like cells supported by fibrovascular stroma. A large immunohistochemical panel for characterizing intratumoral macrophage and dendritic cell subsets was performed. Results. Immunohistochemical analysis indicated positivity for HLA-DR, XIIIa, CD68, and CD163 (range 6%-50%) mainly on the fibrovascular stroma, suggesting M2 macrophage-like cell phenotype. CD138 was overexpressed in the tumor stroma. Conclusions. Results suggest the involvement of M2-polarized macrophages in the MNTI pathogenesis, which may act by modulating tumor growth and/or tumor stromal remodeling.
引用
收藏
页码:173 / 179
页数:7
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