Literature DB >> 11758721

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

M Bisceglia1, M Cardone, L Fantasia, G Cenacchi, G Pasquinelli.   

Abstract

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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Year:  2001        PMID: 11758721     DOI: 10.1080/019131201317101270

Source DB:  PubMed          Journal:  Ultrastruct Pathol        ISSN: 0191-3123            Impact factor:   1.094


  6 in total

1.  A case of soft tissue myoepithelial tumor arising in masticator space.

Authors:  Jai Hyang Go
Journal:  Yonsei Med J       Date:  2005-10-31       Impact factor: 2.759

Review 2.  [Myoepithelial neoplasms of skin and soft tissues].

Authors:  T Mentzel
Journal:  Pathologe       Date:  2005-09       Impact factor: 1.011

3.  Imprint cytology of soft tissue myoepithelioma: a case study.

Authors:  Seok Ju Park; Ae Ri Kim; Mi Jin Gu; Joon Hyuk Choi; Duk Seop Shin
Journal:  Korean J Pathol       Date:  2013-06-25

4.  [Myoepithelioma of soft tissue -- case report with clinicopathologic, ultrastructural, and cytogenetic findings].

Authors:  C Kuhnen; P Herter; A Kasprzynski; M Vogt; M Jaworska; G Johnen
Journal:  Pathologe       Date:  2005-09       Impact factor: 1.011

5.  Histopathological, immunohistochemical and molecular spectrum of myoepithelial tumours of soft tissues.

Authors:  Bharat Rekhi; Mukund Sable; Nirmala A Jambhekar
Journal:  Virchows Arch       Date:  2012-10-25       Impact factor: 4.064

6.  A rare myoepithelioma of the sinonasal cavity: case report.

Authors:  Suhail I Sayed; Rehan A Kazi; Mohan V Jagade; Rajan S Palav; Vinod V Shinde; Prashant V Pawar
Journal:  Cases J       Date:  2008-07-11
  6 in total

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