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TFE3 Expression in Tumors of the Microphthalmia-Associated Transcription Factor (MiTF) Family
被引:32
作者:
Dickson, Brendan C.
[1
]
Brooks, John S.
[1
,2
]
Pasha, Theresa L.
Zhang, Paul J.
[3
]
机构:
[1] Penn Hosp, Philadelphia, PA 19107 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Hosp Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词:
TFE3;
PEComa;
melanoma;
angiomyolipoma;
clear cell sarcoma;
immunohistochemistry;
CLEAR-CELL SARCOMA;
SOFT PART SARCOMA;
MELANOCYTIC DIFFERENTIATION;
GENE FUSION;
NEOPLASMS;
CARCINOMA;
MARKERS;
PECOMA;
IMMUNOREACTIVITY;
ANGIOMYOLIPOMAS;
D O I:
10.1177/1066896909352861
中图分类号:
R36 [病理学];
学科分类号:
100104 ;
摘要:
The DNA-binding factor TFE3 is closely related to microphthalmia-associated transcription factor (MiTF) and is over-expressed in alveolar soft part sarcoma (ASPS) and select renal cell carcinomas. Reports of TFE3 expression in PEComa prompted investigation into TFE3 expression among other members of the putative MiTF group of neoplasms. The authors examined cases of PEComa (n = 6), conventional angiomyolipoma (AML; n = 22), metastatic melanoma (n = 16), and clear cell sarcoma (CCS; n = 9) for TFE3 expression. Nuclear immunostaining was observed in 74% (39/53) of cases, as follows: 5/6 PEComas, 18/22 AMLs, 10/16 metastatic melanomas, and 6/9 CCSs. However, with the exception of PEComas, compared with ASPS controls, TFE3 staining was significantly less intense in the tumors examined. These results illustrate that TFE3 immunoreactivity is detectable in other members of the MiTF family of neoplasms. For this reason, such neoplasms warrant consideration in the differential diagnosis with nuclear TFE3 immunoreactivity, particularly when staining is focal and less intense.
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页码:26 / 30
页数:5
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