Abstract #131: Sclerosing Mucoepidermoid Carcinoma With Eosinophilia: A Rare, Difficult-to-Diagnose, Malignant Thyroid Carcinoma

2006 ◽  
Vol 12 ◽  
pp. 67-68
Author(s):  
Jane Frances Chukwu ◽  
Saleh A. Aldasouqi ◽  
Khalil Katato ◽  
Kavitha Kesari ◽  
Jamal Hammoud
Medicine ◽  
2020 ◽  
Vol 99 (42) ◽  
pp. e22783
Author(s):  
Ruiqi Mao ◽  
Lifang Shi ◽  
Wei Yan ◽  
Wenli Li ◽  
Baicheng Li ◽  
...  

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Jasmine S. Sukumar ◽  
Senthil Sukumar ◽  
Darshana Purohit ◽  
Brian J. Welch ◽  
Jyoti Balani ◽  
...  

Abstract Background Sclerosing mucoepidermoid carcinoma with eosinophilia is a rare form of thyroid carcinoma. The underlying molecular mechanisms of sclerosing mucoepidermoid carcinoma with eosinophilia tumorigenesis remain unknown. Case presentation We present two cases of sclerosing mucoepidermoid carcinoma with eosinophilia, both with a concurrent papillary thyroid carcinoma. Patient 1, a 70-year-old Caucasian woman, presented with sclerosing mucoepidermoid carcinoma with eosinophilia with distant renal metastasis and coexisting papillary thyroid carcinoma. Patient 2, a 74-year-old Caucasian woman with a remote history of thyroid cancer treated with thyroidectomy, presented with locoregionally invasive sclerosing mucoepidermoid carcinoma with eosinophilia and recurrent papillary thyroid carcinoma in the thyroid bed. BRAF mutation studies were performed on the sclerosing mucoepidermoid carcinoma with eosinophilia tumors. In both cases, sclerosing mucoepidermoid carcinoma with eosinophilia was positive for the BRAF V600E mutation by polymerase chain reaction. Patient 1 is the first reported case of sclerosing mucoepidermoid carcinoma with eosinophilia with renal metastasis, to the best of our knowledge. Conclusions Our findings suggest, for the first time, to our knowledge, involvement of the RAS-RAF-MEK-ERK signaling pathway in the pathogenesis of sclerosing mucoepidermoid carcinoma with eosinophilia. Thus, BRAF inhibitors may prove to be a useful targeted medical therapy in the treatment of a subset of patients with aggressive sclerosing mucoepidermoid carcinoma with eosinophilia tumors who exhibit BRAF activating mutation.


2015 ◽  
Vol 93 (10) ◽  
pp. e137-e138
Author(s):  
Rolando Orbeal ◽  
Jaime Jimeno ◽  
Gabriela Monroy ◽  
Francesc Badia ◽  
David Parés

2004 ◽  
Vol 128 (9) ◽  
pp. 1046-1049
Author(s):  
Oluwole Fadare ◽  
Denise Hileeto ◽  
Yves L. Gruddin ◽  
M. Rajan Mariappan

Abstract Although mucoepidermoid carcinoma is the most common primary malignancy of the salivary glands, the sclerosing morphologic variant of this tumor is extremely rare, with only 6 reported cases. As its name suggests, sclerosing mucoepidermoid carcinoma is characterized by an intense central sclerosis that occupies the entirety of an otherwise typical tumor, frequently with an inflammatory infiltrate of plasma cells, eosinophils, and/or lymphocytes at its peripheral regions. The sclerosis associated with these tumors may obscure their typical morphologic features and result in diagnostic difficulties. Tumor infarction and extravasation of mucin eventuating in reactive fibrosis are 2 mechanisms of formation that have been suggested as underlying this morphologic variant. We describe herein another case of sclerosing mucoepidermoid carcinoma that was diagnosed in a 44-year-old woman and review the relevant literature. Morphologic evidence in support of the mucin extravasation hypothesis was identified, as small pools of mucin were present throughout the tumor. However, there was no concentration of the mucin pools near the areas with the most viable tumor cells, which would have provided evidence for a temporal sequence that eventuates in lack of mucin in the most sclerotic regions.


2021 ◽  
Vol 14 (7) ◽  
pp. e241086
Author(s):  
Joseph Salem ◽  
Eamon Shamil ◽  
Lorrette Ffolkes ◽  
Enyinnaya Ofo

Sclerosing mucoepidermoid carcinoma with eosinophilia of the thyroid in a 46-year-old woman.


2006 ◽  
Vol 263 (10) ◽  
pp. 955-959 ◽  
Author(s):  
S. Brett Heavner ◽  
Rajal B. Shah ◽  
Jeffrey S. Moyer

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