Myoepithelial tumors of soft tissue (myoepithelioma, mixed tumor, 'parachordoma‘ and myoepithelial carcinoma)

Author(s):  
Therese Bocklage ◽  
Robert Quinn ◽  
Berndt Schmit ◽  
Claire Verschraegen
2012 ◽  
Vol 45 (1) ◽  
pp. 58-63 ◽  
Author(s):  
María Auxiliadora Aparicio ◽  
Fernando López-Barea ◽  
Juan Jesús Cruz ◽  
María del Carmen García Macías ◽  
Teresa Hernández ◽  
...  

2006 ◽  
Vol 63 (6) ◽  
pp. 611-614 ◽  
Author(s):  
Zorica Stojsic ◽  
Dimitrije Brasanac ◽  
Dragoljub Bacetic ◽  
Radmila Jankovic ◽  
Neda Drndarevic

Background. Myoepitheliomas are tumors composed predominantly or exclusively of myoepithelial cells, usually arising in salivary glands. Cutaneous/soft tissue localization is very rare, especially for the malignant myoepitheliomas. Case report. We presented a case of myoepithelial carcinoma involving subcutaneous adipose tissue of the left forearm in a woman aged 62 years. The tumor was composed of epithelioid and hyaline cell types, arranged in diffuse sheets, nests and loose clusters within hyalinized and myxoid matrix. The neoplasm displayed high-grade cytologic atypia with some cells having pleomorphic, hyperchromatic nuclei, and others showing vesicular nuclei, large nucleoli with scattered bizarre giant cells. High mean mitotic count of 7 mitoses/10 high power fields and extensive necrosis favored the diagnosis of malignancy. Immunohistochemical staining was positive for cytokeratin (AE1/AE3), epithelial membrane antigen, S-100 protein, glial fibrillary acidic protein, and vimentin. Conclusion. Considering the subcutaneous localization, myoepithelial immunophenotype and high-grade cytologic atypia the neoplasm was classified as a soft-tissue myoepithelial carcinoma.


2019 ◽  
Vol 30 ◽  
pp. ix138-ix139
Author(s):  
F.E. Chamberlain ◽  
E. Cojocaru ◽  
M. Scaranti ◽  
J. Noujaim ◽  
K. Thway ◽  
...  

2015 ◽  
Vol 01 (02) ◽  
pp. 109-111
Author(s):  
Michael Dorbad ◽  
Peter Lim ◽  
Jeffrey Taylor

ABSTRACTMyoepithelial carcinomas of soft tissue origin are rare tumors in the pediatric population. Due to the rarity of this malignancy, very few cases have been reported in the literature, and a consensus on treatment has not been established. Most myoepithelial carcinomas of soft tissue present in the extremities and are treated with surgical excision followed by adjuvant radiotherapy. We report 2 cases of pediatric myoepithelial carcinoma presenting with vertebral involvement making complete surgical removal impossible. These patients underwent chemotherapy and adjuvant radiotherapy as the main treatment for their primary tumors.


2014 ◽  
Vol 19 (6) ◽  
pp. 1051-1055 ◽  
Author(s):  
Andrés Combalía ◽  
Vicente Marco ◽  
Roberto Seijas ◽  
Rosa Domínguez

2020 ◽  
Vol 154 (Supplement_1) ◽  
pp. S50-S50
Author(s):  
F Chen ◽  
H Syed

Abstract Introduction/Objective A 38-year-old female without a history of trauma and malignancy presented with left knee pain and swelling for two weeks. MRI and PET scan find a left knee mass arising from the bone along the medial metaphysis of the distal femur. She underwent femur resection, and the specimen was sent for pathology evaluation. Methods Grossly, the cut surface of the sample revealed a 4.5 x 2 cm area of hemorrhagic softening of the bone with adjacent soft tissue nodules. Microscopically, the tumor showed biphasic or multiphase morphologic features, prominently presented with areas showing well-differentiated epithelial features and other areas with spindling and sheets of tumor cells. Areas suspicious for a vascular invasion were seen at the periphery of the soft tissue extension of the tumor. Immunohistochemistry stains showed the tumor cells are positive for vimentin, AE1/3, EMA, CK7, CK19, GATA3, and BRST2; and are negative for S100, HMB45, GFAP, Calponin, CDX2, PAX8, WT1, P63, CD34, and ER. The molecular test showed positive for the ESWR1 gene but negative for SYT gene translocation. Results A diagnosis of primary myoepithelial carcinoma of bone extension into surrounding soft tissue was made. Conclusion The most challenging differential diagnosis for this case is metastatic breast cancer. Many of the positive epithelial stains distinctly highlight the epithelial featured geographic areas sparing the background spindled stroma. The positive staining of GATA3 and BRST2, two commonly used breast linage markers, is unusual and not known in myoepithelial carcinoma. In light of the EWSR1 positive and SYT FISH negative results, combined with the morphologic features, locations as well as negative PET scan against its breast origins. Although many myoepithelial markers, such as S100, Calponin, P63, and GFAP were negative, make this case very unique. The molecular diagnosis is the mainstay for this final diagnosis.


Rare Tumors ◽  
2016 ◽  
Vol 8 (1) ◽  
pp. 20-23 ◽  
Author(s):  
Despoina Mourtzoukou ◽  
Shane Zaidi ◽  
Robin L. Jones ◽  
Cyril Fisher ◽  
Khin Thway

2005 ◽  
Vol 55 (8) ◽  
pp. 510-513 ◽  
Author(s):  
Oi Harada ◽  
Hiroyoshi Ota ◽  
Jun Nakayama

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