Mixed tumors, myoepitheliomas, and oncocytomas of the soft tissues are likely members of the same family: A clinicopathologic and ultrastructural study

被引:15
作者
Bisceglia, M
Cardone, M
Fantasia, L
Cenacchi, G
Pasquinelli, G
机构
[1] Osped Casa Sollievo Sofferenza, IRCCS, Serv Anat Patol, I-71013 San Giovanni Rotondo, FG, Italy
[2] Osped Casa Sollievo Sofferenza, IRCCS, Div Ortopedia, I-71013 San Giovanni Rotondo, FG, Italy
[3] Policlin S Orsola Malpighi, Ist Anat Patol, Bologna, Italy
关键词
immunohistochemistry; mixed tumor; myoepithelioma; oncocytoma; soft tissue tumors; ultrastructure;
D O I
10.1080/019131201317101270
中图分类号
TH742 [显微镜];
学科分类号
摘要
Four diagnostically unusual soft tissue tumors are presented. All lesions were of consistent size and long duration. Histologically, one lesion was analogous to mixed tumors of the usual sites (i.e., salivary glands), one lesion was totally spindled, and the two other lesions both had oncocytic appearances (epithelioid and spindle biphasic pattern in a case, purely epithelioid in the other). Immunohistochemically, the mixed tumor was positive for vimentin, cytokeratins, S-100 protein, and focally for EMA. The purely spindled tumor exhibited immunoreactivity for vimentin, actins, S-100 protein, EMA (focally), and GFAP. The oncocytic biphasic tumor was positive for mitochondrial antigen, vimentin, and actins. The purely epithelioid oncocytic neoplasm was immunoreactive only for mitochondrial antigen and vimentin. Ultrastructurally, in the epithelial-like portion of the first (mixed) tumor, peripheral arrays of contractile filaments were detected along with well-developed desmosomes. In the second (spindled) case, peripheral contractile filaments and attenuated desmosomes were also seen. In the third case, a huge number of mitochondria, some desmosomes, and actin-type microfilaments were found. In the fourth case, desmosomes and punctate subplasmalemmal densities, in addition to numerous mitochondria, were documented. In all cases an external basal lamina were present, which was discontinuous in the first three cases and almost continuous in the fourth. These tumors were respectively designated as mixed tumor, myoepithelioma of the classic type, myoepithelioma of oncocytic type with biphasic cell architecture, and true oncocytoma. So far, all tumors have followed benign clinical courses (median follow up: 12 months). Comparisons with similar tumors of other sites are drawn, and suggestions for considering all of them as members of the same myoepithelial-derived tumor family are given.
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页码:399 / 418
页数:20
相关论文
共 12 条
[1]  
BISCEGLIA M, 1998, PATHOLOGICA, V90, P201
[2]  
Bosman C, 1996, ACTA HAEMATOL-BASEL, V96, P50
[3]   MYOEPITHELIOMA OF THE RETROPERITONEUM [J].
BURKE, T ;
SAHIN, A ;
JOHNSON, DE ;
ORDONEZ, NG ;
MACKAY, B .
ULTRASTRUCTURAL PATHOLOGY, 1995, 19 (04) :269-274
[4]  
d'Amore ESG, 1999, SEMIN DIAGN PATHOL, V16, P178
[5]   MYOEPITHELIOMA - DEFINITIONS AND DIAGNOSTIC-CRITERIA [J].
DARDICK, I .
ULTRASTRUCTURAL PATHOLOGY, 1995, 19 (05) :335-345
[6]  
ERLANDSON RA, 1994, DIAGNOSTIC TRANSMISS, P162
[7]   Mixed tumors and myoepitheliomas of soft tissue - A clinicopathologic study of 19 cases with a unifying concept [J].
Kilpatrick, SE ;
Hitchcock, MG ;
Kraus, MD ;
Calonje, E ;
Fletcher, CDM .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (01) :13-22
[8]  
MARTINEZMADRIGA.F, 1997, HISTOLOGY PATHOLOGIS, P415
[9]   Myoepitheliomas of the skin and soft tissues - Report of 12 cases [J].
Michal, M ;
Miettinen, M .
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY, 1999, 434 (05) :393-400
[10]   Soft tissue oncocytoma [J].
Polk, P ;
Parker, KM ;
Biggs, PJ .
HUMAN PATHOLOGY, 1996, 27 (02) :206-208