Epithelial differentiation in medulloblastoma: Comparison with other embryonal tumors of neuroectodermal origin

被引:3
作者
Sugita, Y
Tokunaga, O
Terasaki, M
Morimatsu, M
Shigemori, M
机构
[1] Saga Med Sch, Dept Pathol & Biodef, Saga 8498501, Japan
[2] Kurume Univ, Sch Med, Dept Neurosurg & Pathol, Kurume, Fukuoka 830, Japan
关键词
atypical teratoid; rhabdoid tumor; epithelial differentiation; medulloblastoma; melanotic medulloblastoma;
D O I
10.1046/j.1440-1827.2003.01572.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Three cases of medulloblastoma characterized by epithelial differentiation are described in patients 6-months-, 1-month- and 8-years-old. Histologically, tumors from the two infant patients showed a perivascular arrangement without apparent radiated cytoplasmic processes from the vessels. Tumor cells displayed round and/or pleomorphic vesicular nuclei and a more abundant eosinophilic cytoplasm than that found in classic medulloblastoma. Neither Homer-Wright rosettes nor ependymal or ependymoblastic rosettes were noted in these tumors. The tumor in the 8-year-old patient exhibited a classic medulloblastoma component intermingled with abundant eosinophilic cytoplasm forming a tubular structure. Immunohistochemically, tumor cells in all cases were positive for cytokeratin, synaptophysin, and vimentin. In the third case involving the 8-year-old patient, epithelial tumor cells were positive for cytokeratin, whereas classic medulloblastoma components were negative for cytokeratin. Positive staining for melanoma-specific antigen was seen only in the third case, where strong reactivity of tumor cells formed a tubulus. However, the classic medulloblastoma component was negative for melanoma-specific antigen. Ultrastructurally, basal laminae were observed around tumor cells in the 6-month-old patient. These morphological and immunohistochemical features suggest that medulloblastoma with epithelial differentiation is a rare but distinct variant of medulloblastoma, and that some of these tumors should show differentiation in ocular pigment epithelium.
引用
收藏
页码:858 / 864
页数:7
相关论文
共 21 条
[1]   MEDULLOBLASTOMA (QUESTIONABLE) WITH EPITHELIOID FEATURES [J].
AZZARELLI, B ;
MULLER, J ;
MIRKIN, LD .
ACTA NEUROPATHOLOGICA, 1983, 61 (02) :109-115
[2]  
BECKER LE, 2000, WHO CLASSIFICATION T, P124
[3]  
BECKER LE, 2000, WHO CLASSIFICATION T, P127
[4]   MONOSOMY-22 IN RHABDOID OR ATYPICAL TUMORS OF THE BRAIN [J].
BIEGEL, JA ;
RORKE, LB ;
PACKER, RJ ;
EMANUEL, BS .
JOURNAL OF NEUROSURGERY, 1990, 73 (05) :710-714
[5]   Atypical teratoid/rhabdoid tumor of the central nervous system: A highly malignant tumor of infancy and childhood frequently mistaken for medulloblastoma - A pediatric oncology group study [J].
Burger, PC ;
Yu, IT ;
Tihan, T ;
Friedman, HS ;
Strother, DR ;
Kepner, JL ;
Duffner, PK ;
Kun, LE ;
Perlman, EJ .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (09) :1083-1092
[6]   DIFFERENTIATION IN THE MEDULLOBLASTOMA - A HISTOLOGICAL AND IMMUNOHISTOCHEMICAL STUDY [J].
BURGER, PC ;
GRAHMANN, FC ;
BLIESTLE, A ;
KLEIHUES, P .
ACTA NEUROPATHOLOGICA, 1987, 73 (02) :115-123
[7]  
BURGER PC, 1993, ATLAS TUMOR PATHOL, P193
[8]  
CHOWDHURY C, 1985, CANCER, V55, P1495, DOI 10.1002/1097-0142(19850401)55:7<1495::AID-CNCR2820550713>3.0.CO
[9]  
2-5
[10]   MELANOTIC MEDULLOBLASTOMA - A CASE-REPORT WITH IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL EXAMINATION [J].
DOLMAN, CL .
ACTA NEUROPATHOLOGICA, 1988, 76 (05) :528-531