Immunohistochemical distinction of endometrial stromal sarcoma and cellular leiomyoma

被引:54
作者
Agoff, SN
Grieco, VS
Garcia, R
Gown, AM
机构
[1] Univ Washington, Harborview Med Ctr, Dept Cytopathol, Seattle, WA 98104 USA
[2] Univ Washington, Harborview Med Ctr, Dept Pathol, Seattle, WA 98104 USA
[3] PhenoPath Lab & Immunocytochem Res Inst, Seattle, WA USA
来源
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY | 2001年 / 9卷 / 02期
关键词
CD10; calponin; smooth muscle myosin heavy chain; cellular leiomyoma; endometrial stromal sarcoma;
D O I
10.1097/00022744-200106000-00009
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Distinguishing low grade endometrial stromal sarcoma (ESS) from benign smooth muscle proliferations like cellular leiomyoma (CL) can bt: problematic; because of differing treatments and prognosis, this distinction is important. The authors tested the hypothesis that low grade ESS could be distinguished from CL by immunohistochemistry using a panel of antibodies that have not previously been used in this setting. Antibodies to calponin, smooth muscle myosin heavy chain (SMM-HC), the Wilms tumor gene product (WT-1), and CD10 were applied to 14 cases of ESS (10 low grade, 4 high grade) and 9 CL. Among low grade ESS, 3 of 10, 3 of 10, 9 of 10, and 10 of 10 were positive for expression of calponin, SMM-HC, WT-I, and CD10, respectively. Of CL, all 9 were positive for calponin, SMM-HC, and WT-I, whereas 3 of 9 marked with antibodies to CD10. Overall, SMM-HC and calponin were expressed strongly in CL but weakly expressed in ESS; the converse was true for CD10. Expression of WT-1 and the reticulin-staining pattern do not discriminate between these two tumors. Antibodies to SMM-HC, CD10, and calponin can reliably distinguish ESS from CL.
引用
收藏
页码:164 / 169
页数:6
相关论文
共 46 条
[11]  
CLEMENT PB, 1976, AM J CLIN PATHOL, V66, P512
[12]   The pathology of uterine smooth muscle tumors and mixed endometrial stromal-smooth muscle tumors: A selective review with emphasis on recent advances [J].
Clement, PB .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 2000, 19 (01) :39-55
[13]  
Dabbs DJ, 1999, DIAGN CYTOPATHOL, V20, P203, DOI 10.1002/(SICI)1097-0339(199904)20:4<203::AID-DC4>3.0.CO
[14]  
2-V
[15]   CD10 and BCL-6 expression in paraffin sections of normal lymphoid tissue and B-cell lymphomas [J].
Dogan, A ;
Bagdi, E ;
Munson, P ;
Isaacson, PG .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2000, 24 (06) :846-852
[16]  
EVANS HL, 1982, CANCER-AM CANCER SOC, V50, P2170, DOI 10.1002/1097-0142(19821115)50:10<2170::AID-CNCR2820501033>3.0.CO
[17]  
2-K
[18]   IMMUNOHISTOCHEMISTRY OF ENDOMETRIAL STROMAL SARCOMA [J].
FARHOOD, AI ;
ABRAMS, J .
HUMAN PATHOLOGY, 1991, 22 (03) :224-230
[19]   THE CLINICAL AND HISTOLOGIC SPECTRUM OF ENDOMETRIAL STROMAL NEOPLASMS - A REPORT OF 41 CASES [J].
FEKETE, PS ;
VELLIOS, F .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1984, 3 (02) :198-212
[20]   AN IMMUNOHISTOCHEMICAL STUDY OF NORMAL ENDOMETRIAL STROMA AND ENDOMETRIAL STROMAL NEOPLASMS - EVIDENCE FOR SMOOTH-MUSCLE DIFFERENTIATION [J].
FRANQUEMONT, DW ;
FRIERSON, HF ;
MILLS, SE .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1991, 15 (09) :861-870