DermKnowledgeBASE: Malignant Mixed Tumor

Malignant Mixed Tumor

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The text is the summary of recent articles on Malignant Mixed Tumor at 75 thresold from National Library of Medicine (NLM). This information is subject to NCBI's Disclaimer and Copyright notice.

Focally, there was sebaceous differentiation identified, in the form of prominent multivacuolated cytoplasm, with nuclear indentations [1]. There was strong and Diffuse staining of the Sebaceous Cells by cytokeratin (CK) 7, epithelial membrane antigen (EMA), and androgen receptor (AR) [2]. Myoepithelial cell proliferation with osteocartilaginous metaplasia was observed in this area [3]. Hereditary syndromes, including Multiple endocrine neoplasia type 1 syndrome, von Hippel-Lindau syndrome, neurofibromatosis 1, and tuberous sclerosis, are related to NETs of the GI and pancreatobiliary tracts [4]. A retrospective clinical and histopathologic review with immunohistochemical staining for HB-EGF, EGFR, and integrin-α5 was performed for 62 surgically staged MMMT cases [5].

However, baboon syndrome has not previously been observed in patients receiving zoledronic acid [6]. Preoperative Pap tests were correlated with histological findings [7]. The Pleomorphic adenoma with osteosarcomatous change is extremely rare and appropriate treatment is not clearly established [8]. Five months postoperatively, the patient developed Metastasis to the Lungs and right hilar lymph node region [9].

References: 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 ,

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I have varied research interests ranging from eHealth, Health Information Exchange, Clinical Trials and Research, Contact Dermatitis, Bioinformatics, and Cosmetic Dermatology. I have work experience in Canada as an eHealth analyst, and in Dubai and India as a Specialist Dermatologist.


Bell Raj Eapen
Hamilton, ON