Thyroid carcinoma presenting as a regional neck mass

Head & Neck ◽  
1990 ◽  
Vol 12 (2) ◽  
pp. 114-117 ◽  
Author(s):  
Moses Nussbaum ◽  
Roman Bukachevsky
Keyword(s):  
1999 ◽  
Vol 4 (2) ◽  
pp. 118-120 ◽  
Author(s):  
T. Kobayashi ◽  
Hideki Asakawa ◽  
Kazunori Taniguchi ◽  
Yoshifumi Komoike ◽  
Yasuhiro Tamaki ◽  
...  

2018 ◽  
Vol 47 (4) ◽  
pp. 334-336 ◽  
Author(s):  
Khaled Murshed ◽  
Issam Al-Bozom ◽  
Surjith Vattoth ◽  
Mohammed Akhtar

1970 ◽  
Vol 1 (1) ◽  
pp. 45-48 ◽  
Author(s):  
A Ghosh ◽  
N Nepal ◽  
MD Gharti ◽  
S Basnet ◽  
M Baxi ◽  
...  

Background: Thyroid cancer is fairly common. The worldwide annual incidence ranges from 0.5 to 10 cases per 100,000 people. Anaplastic thyroid carcinoma, comprising less than 10% of all thyroid carcinomas, remains one of the most virulent of all cancers in humans with a 10 year survival rate of only 0.1 %. In the present study we looked into the clinical, cytological and histological spectrum of anaplastic carcinoma and compared our experience with recent literature. Materials and Methods: This was a hospital based retrospective study from January 2000 to November 2010. Clinical, cytological and histopathological data of all the diagnosed anaplastic thyroid carcinoma cases were reviewed and analyzed. Results: Of the 59 thyroid malignancies diagnosed in the same period, 7 cases were anaplastic carcinoma. The mean age was 63 years and was predominantly found in females. All of the cases presented with a neck mass that lasted for a mean of 5.7 months. The mean tumor size was 14.9 cm and the most common sub-type was the spindle cell type. Atypical mitosis of more than 5 per high power field and necrosis was noted in all cases. Conclusion: Due to the markedly aggressive nature of this tumor and its association with areas of endemic thyroid disease, early diagnosis and aggressive therapy is essential, especially in the Himalayan and Sub-Himalayan belt. Keywords: Anaplastic carcinoma; Thyroid carcinoma; Spindle cell variant DOI: 10.3126/jpn.v1i1.4451 Journal of Pathology of Nepal (2011) Vol.1, 45-48


2019 ◽  
Vol 8 (4) ◽  
pp. 261
Author(s):  
InugantiVenkata Renuka ◽  
Chitturi Ramya ◽  
Sripriya Krishnan ◽  
SowjanyaKrishna Sree Kesaboyina

2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Jennifer Walsh ◽  
Tomas P. Griffin ◽  
Carmel B. Ryan ◽  
James Fitzgibbon ◽  
Patrick Sheahan ◽  
...  

A 44-year-old female presented with a two-month history of a neck mass, sore throat, hoarseness, and intermittent dysphagia. Examination revealed a “woody” hard swelling arising from the right lobe of the thyroid. Clinically this was felt to be classical Riedel’s thyroiditis (RT). Thyroid ultrasound showed a diffusely enlarged, low echogenicity thyroid with a multinodular goitre. An abnormal nodule extending across the isthmus was noted. Following a nondiagnostic fine needle aspiration, an open core biopsy was performed. This showed dense sclerotic fibrosis punctuated by nodular mononuclear inflammatory cells, which obscured follicular epithelial cells consistent with a fibrosing thyroiditis (Riedel’s thyroiditis). A biopsy of pretracheal lymph nodes showed a sclerotic process throughout the lymph nodes and nests of epithelium bands with squamous differentiation obscured by a fibrous process. These findings raised the differential diagnosis of diffuse sclerosing variant of papillary thyroid carcinoma (DSV-PTC) with metastasis to lymph nodes. A total thyroidectomy and pretracheal lymph node dissection were performed. The final histological diagnosis was DSV-PTC. When managing a patient with presumed RT it is important to consider malignancy in the differential. DSV-PTC is one of the more aggressive forms of thyroid cancer but with early diagnosis and appropriate treatment patients may have excellent outcomes.


2000 ◽  
Vol 110 (2) ◽  
pp. 204-204 ◽  
Author(s):  
Sean C. Coleman ◽  
Jonathan C. Smith ◽  
Brian B. Burkey ◽  
Terrence A. Day ◽  
Robert N. Page ◽  
...  

2020 ◽  
Vol 4 (3) ◽  
pp. 226
Author(s):  
Lo Ren Hui ◽  
Fairuz Mohd Ibrahim ◽  
Khairudin Abdullah ◽  
Nasriah Ahmad ◽  
Fazilah Hassan ◽  
...  

Anaplastic thyroid carcinoma (ATC) is uncommon but deadly. It is typically presented with fast growing neck mass, hoarseness or dysphagia. We report an extremely rare presentation of ATC in an elderly lady, with expanding ecchymosis involving laryngopharynx, neck and upper chest region, which causing upper airway obstruction. The rarity of presentation and the management dilemma were discussed.International Journal of Human and Health Sciences Vol. 04 No. 03 July’20 Page : 226-228


2018 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Gokhan Tazegul ◽  
Hümeyra Bozoğlan ◽  
Özlem Doğan ◽  
Ramazan Sari ◽  
HasanAli Altunbaş ◽  
...  

2014 ◽  
Vol 14 (1) ◽  
pp. 25-30
Author(s):  
Archimedes Lee Agahan ◽  
Ryner Jose Carrillo ◽  
Peter Mark Chao ◽  
Ramil Lising

Objective: To report a case of primary thyroid carcinoma with ocular metastasis.Methods: This is a case report of a 39-year-old male, who initially presented with a sudden painless loss of vision in the left eye and an anterior neck mass. He was initially diagnosed to have retinal detachment with vitreous hemorrhage based on ocular ultrasound. Fine Needle Aspiration Biopsy of the neck mass initially revealed medullary thyroid carcinoma. Computed topography of the chest and abdominal ultrasound revealed lung and liver metastasis. Whole body bone scintigraphy also revealed bone metastasis.Results: Patient underwent total thyroidectomy with bilateral modified radical neck dissection of the neck mass and vitreous biopsy of the left eye. Histopathology report revealed malignant carcinoma of the thyroid, medullary type while vitreous showed malignant cells from the thyroid. Patient was scheduled to undergo chemotherapy for the widespread metastasis.Conclusions: Ocular malignancy can present in many ways, thus it is necessary to consider it as a differential for cases of retinal detachment and vitreous hemorrhage. Choroidal metastasis from malignant thyroid carcinoma is rare, more so the medullary type.


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