Papillary carcinoma in thyroglossal duct remnants: presentation of four cases and decision procedure for prophylactic thyroid gland dissection.

Author(s):  
N Tradati ◽  
F DePaoli ◽  
M Benazzo ◽  
J Andrle ◽  
L Calabrese ◽  
...  
2005 ◽  
Vol 26 (5) ◽  
pp. 348-350 ◽  
Author(s):  
William J. Kim ◽  
Raphaelle Souillard ◽  
Margaret S. Brandwein ◽  
William Lawson ◽  
Peter M. Som

1993 ◽  
Vol 107 (12) ◽  
pp. 1174-1176 ◽  
Author(s):  
Kadriye Yildiz ◽  
Haydar Köksal ◽  
Yavuz Özoran ◽  
Hayrettin Muhtar ◽  
Münir Telatar

Carcinoma in the thyroglossal duct remnant is relatively uncommon. Since the first report by Uchermann (1915), more than 150 cases of carcinoma have been reported, and the majority have been papillary thyroid carcinomas (Li Volsi etal., 1974; McNicol etal., 1988). In this report, we present a case of papillary carcinoma in the thyroglossal duct with a normal thyroid gland


2016 ◽  
Vol 6 (2) ◽  
pp. 172
Author(s):  
Ashim Kumar Biswas ◽  
Kazi Shameemus Salam ◽  
Md. Mosleb Uddin ◽  
Kanu Lal Saha ◽  
Belayat Hossain Siddiquee ◽  
...  

Thyroglossal duct cyst carcinoma in a rare condition. Only around 250 cases of malignant thyroglossal cyst have been reported as far. We report a 45 years old women presenting with a painless swelling in the midline in the upper part of front of neck for 1 yr. This swelling moves with deglutition, multilobulated moves up on protrusion of tongue. FNAC revealed cystic lesion compatible with thyroglossal duct cyst. Ultrasonogram revealed mass is separated from thyroid gland. Patient underwent sistnmk's operation and tissue was sent for histopathological examination and report reveled papillary carcinoma of thyroglossal duct cyst.


Head & Neck ◽  
2009 ◽  
Vol 31 (10) ◽  
pp. 1387-1391 ◽  
Author(s):  
Mathew Pynumootil Cherian ◽  
Balakrishnan Nair ◽  
Shaji Thomas ◽  
Thara Somanathan ◽  
Paul Sebastian

2011 ◽  
Vol 64 (5) ◽  
pp. 445
Author(s):  
Kyoung Tae Kim ◽  
Yeo Ju Kim ◽  
Sei Joong Kim ◽  
Young Up Cho ◽  
Yong Sun Jeon ◽  
...  

2007 ◽  
Vol 64 (10) ◽  
pp. 714-718
Author(s):  
Milica Cizmic ◽  
Mile Ignjatovic ◽  
Snezana Cerovic ◽  
Boris Ajdinovic

Background. Simultaneous presence of Hashimoto's thyroiditis and papillary thyroidal carcinoma in thyroidal gland with papillary carcinoma association in thyroglossal duct is quite rare. The questions like where the original site of primary process, is where metastasis is, what the cause of coexisting of these diseasesis present a diagnostic dilemma. Case report. We presented a case of a 53-year old female patient, with the diagnosis of Hashimoto's thyroiditis and symptoms of subclinical hypothyreosis and nodal changes in the right lobe of thyroidal gland, according to clinical investigation. Morphological examination of thyroidal gland, ultrasound examination and scintigraphy with technetium (Tc) confirmed the existence of nonhomogenic tissue with parenchyma nodular changes in the right lobe of thyroidal gland that weakly bonded Tc. Fine needle biopsy in nodal changes, with cytological analyses showed no evidence of atypical thyreocites. Hashimoto's thyroiditis was confirmed on the basis of the increased values of anti-microsomal antibodies, the high levels of thyreogobulin 117 ng/ml and TSH 6.29 ?IU/ml. The operation near by the nodular change in the right lobe of thyroidal gland revealed pyramidal lobe spread in the thyroglossal duct. Total thyroidectomia was done with the elimination of thyroglossal duct. Final patohystological findings showed papillary carcinoma in the nodal changes pT2, N0 and in the thyroglossal duct with the presence of Hashimoto's thyroiditis in the residual parenchyme of the thyroid gland. After the surgery the whole body scintigraphy with iodine 131 (131I) did not reveal accumulation of 131I in the body, while the fixation in the neck was 1%. After that, the patient was treated with thyroxin with suppressionsubstitution doses. Conclusion. Abnormality in embrional development of thyroidal tissue might be the source of thyroidal carcinoma or the way of spreading of metastasis of primary thyroidal carcinoma from thyroid gland. The cause of this process is most probably a hereditary mutation in RET oncogenes.


2012 ◽  
Vol 4 (1) ◽  
pp. 30-33 ◽  
Author(s):  
Zeynep Şıklar ◽  
Merih Berberoğlu ◽  
Aydın Yağmurlu ◽  
Bülent Hacıhamdioğlu ◽  
Şenay Savaş Erdeve ◽  
...  

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