scholarly journals A case of thyroglossal duct carcinoma with bone metastasis in late elderly person

2019 ◽  
Vol 29 (2) ◽  
pp. 185-191
Author(s):  
Kaori Kayano ◽  
Shota Kinoshita
1997 ◽  
Vol 72 (4) ◽  
pp. 315-319 ◽  
Author(s):  
Hassan M. Heshmati ◽  
Vahab Fatourechi ◽  
Jon A. van Heerden ◽  
Ian D. Hay ◽  
John R. Goellner

2020 ◽  
Vol 35 (1) ◽  
pp. 63-65
Author(s):  
Anna Claudine Lahoz ◽  
Precious Eunice Grullo ◽  
Ryner Jose Carrillo

ABSTRACT Objective: To report a case of thyroglossal duct carcinoma with concurrent papillary thyroid carcinoma Methods: Design: Case Report Setting: Tertiary National University Hospital Patient: One Results: A 46-year-old woman was diagnosed with thyroglossal duct carcinoma after undergoing a Sistrunk procedure. Due to presence of thyroid nodules, the patient underwent second stage thyroidectomy with central neck dissection which revealed papillary thyroid carcinoma. Conclusion: Thyroglossal duct carcinomas are rare entities and there is no current consensus regarding their management. Difficulties arise in the diagnosis of these tumors as they present similarly to benign thyroglossal duct cysts. Most cases are diagnosed postoperatively. Proper preoperative assessment including head and neck examination, biopsy, and radiologic imaging is necessary to recognize patients who could benefit from more aggressive management. Keywords: thyroglossal carcinoma; thyroglossal duct cyst; papillary thyroid carcinoma


2001 ◽  
Vol 110 (8) ◽  
pp. 734-738 ◽  
Author(s):  
Salil V. Doshi ◽  
Raul M. Cruz ◽  
Raymond L. Hilsinger

JAMA ◽  
1982 ◽  
Vol 248 (8) ◽  
pp. 924b-924 ◽  
Author(s):  
M. Blum

2015 ◽  
Vol 81 (1) ◽  
pp. 25-27 ◽  
Author(s):  
Angela Pezzolla ◽  
Daniele Paradies ◽  
Serafina Lattarulo ◽  
Anna Ciampolillo ◽  
Luigi Madami

2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Naoki Kunitomo ◽  
Hiroyuki Fujii ◽  
Akifumi Fujita ◽  
Yumiko Hamano ◽  
Minako Takanosawa ◽  
...  

Thyroglossal duct (TGD) carcinoma is a rare malignant tumor arising from remnants of thyroid tissue or the wall of the duct and generally occurs along the anatomic course of the TGD. TGD carcinoma originating in the hyoid bone is extremely rare but can occur since the TGD penetrates the hyoid bone on rare occasions. This report describes the case of a 30-year-old man with TGD carcinoma originating in the hyoid bone. Computed tomography demonstrated a mass in the hyoid bone that expanded the cortical bone of the hyoid. The mass had a central solid component with calcification and a marginal cystic component. When we encounter a calcified mass in the hyoid bone, we should consider TGD carcinoma among the differential diagnoses.


1995 ◽  
Vol 109 (11) ◽  
pp. 1124-1127 ◽  
Author(s):  
Andreas W. Hilger ◽  
Stuart D. Thompson ◽  
Lesley A. Smallman ◽  
John C. Watkinson

AbstractPapillary carcinoma arising in a thyroglossal duct cyst is a rare finding. Less than 100 cases have been reported in the English literature. In most cases the diagnosis is only established after excision of a clinically benign thyroglossal duct cyst. The aetiology of such tumours is unclear but de novo origin and spread from a primary thyroid gland tumour has been suggested. This has important implications for therapeutic approaches. A further case of thyroglossal duct carcinoma is presented and the management is discussed on the basis of the current rationale for treatment of thyroid cancer.


JAMA ◽  
1982 ◽  
Vol 248 (8) ◽  
pp. 924
Author(s):  
Parakrama Chandrasoma

1998 ◽  
Vol 108 (8) ◽  
pp. 1154-1158 ◽  
Author(s):  
Thomas L. Kennedy ◽  
Mark Whitaker ◽  
George Wadih

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