scholarly journals ALK-1-positive inflammatory myofibroblastic tumor of the thyroid complicated by Hashimoto’s thyroiditis: report of a rare case and a literature review

2020 ◽  
Vol 15 (1) ◽  
Author(s):  
Cheng-fang Li ◽  
Xing-long Wu ◽  
Jin-jing Wang ◽  
Kai Wang ◽  
Su-yuan Zhang ◽  
...  
2021 ◽  
Vol 4 (3) ◽  
Author(s):  
Ramesh Mahadev Tambat ◽  
Sreenivas M. D. ◽  
Tejas A. P. ◽  
Nitin Kumar K ◽  
Sadiq Nawaz F ◽  
...  

2017 ◽  
Vol 102 (5-6) ◽  
pp. 222-226
Author(s):  
Sang Yull Kang ◽  
Yo Na Kim ◽  
Seon Kwang Kim ◽  
Hyun Jo Youn ◽  
Sung Hoo Jung

Immunoglobulin (Ig) G4-related Hashimoto's thyroiditis is a newly discovered subtype of Hashimoto's thyroiditis and characterized by thyroid inflammation and marked fibrosis. IgG4-related Hashimoto's thyroiditis is very rare and there has been relatively little information available to date. A 46-year-old woman with a past history of thyroid dysfunction visited our outpatient clinic for severe anterior neck swelling. She complained of swallowing discomfort and pain due to severe goiter and was successfully treated with total thyroidectomy. Immunohistochemistry showed thyroid invasion by IgG4-positive cells and an IgG4/IgG ratio over 40%. The patient was diagnosed with IgG4-related Hashimoto's thyroiditis. We report a very rare case of IgG4-related Hashimoto's thyroiditis with severe goiter. A more comprehensive understanding of the IgG4-related Hashimoto's thyroiditis may help physicians to allow proper diagnosis and treatment of patients with severe goiter.


2020 ◽  
Vol 16 (4) ◽  
pp. 349-354
Author(s):  
V.А. Shidlovskyi ◽  
А.V. Shidlovskyi ◽  
M.I. Sheremet ◽  
L.P. Sydorchuk ◽  
I.V. Pankiv

2012 ◽  
Vol 4 (1) ◽  
pp. 15-16
Author(s):  
Bhargav PRK ◽  
V Amar ◽  
SK Uday

ABSTRACT Hashimoto's thyroiditis (HT) is the commonest cause of hypothyroidism, especially in iodine replete areas. The clinical presentation of HT is usually insidious with mild goiter and progressive hypothyroidism. But, HT presents with large goiter and compressive symptoms in some cases. The treatment of HT is mostly conservative with thyroxine treatment sooner or later. Occasionally, surgery is indicated for large goiters with persistent pressure symptoms or associated nodules. We report a rare case of unusually large goiter with compressive symptoms, hitherto unreported in literature. How to cite this article Bhargav PRK, Amar V, Uday SK. Megalo-Goitrous Form of Hashimoto's Thyroiditis: A Rare Indication for Surgery. World J Endocr Surg 2012;4(1):15-16.


2015 ◽  
Vol 7 (3) ◽  
Author(s):  
Liladhar Kashyap ◽  
Abdulhameed Alsaheel ◽  
Rohan Walvekar ◽  
Lawrence Simon ◽  
Ricardo Gomez

Hashimoto’s thyroiditis (HT) usually presents as painless thyroid swelling. Painful pediatric HT is a rare condition with limited literature on pain management. We report a 15- year-old female who presented with 4 weeks history of fatigue, malaise and progressive, painful midline thyroid swelling. There was no difficulty in swallowing, no fever or recent upper respiratory infection symptoms. Exam was remarkable for diffusely enlarged, very tender, and non-nodular thyroid. Thyroid function tests, C-reactive protein, and complete blood count were normal. Ultrasound revealed diffusely enlarged non-nodular, non-cystic gland with mild increased vascularity. Diagnosis of HT was confirmed by biopsy and thyroid antibodies. Over a 6 week period, pain management with ibuprofen, levothyroxine, corticosteroid, gabapentin and amitriptyline was unsuccessful. Ultimately, total thyroidectomy resulted in complete resolution of thyroid pain. We can conclude that thyroidectomy may be considered for the rare case of painful HT in children.


Endocrine ◽  
2014 ◽  
Vol 48 (2) ◽  
pp. 629-636 ◽  
Author(s):  
Ayman A. Zayed ◽  
Moaath K. Mustafa Ali ◽  
Omar I. Jaber ◽  
Moh’d J. Suleiman ◽  
Ashraf A. Ashhab ◽  
...  

2003 ◽  
Vol 82 (1) ◽  
pp. 64-66 ◽  
Author(s):  
Kimberly Mugler ◽  
Loretta Gaido ◽  
John Ryder ◽  
Sherif Said

As only eight cases have been previously reported in the literature, plasma cell granuloma of the thyroid gland is a rare entity. This condition can be confused with a benign or malignant neoplastic thyroid process. In this article, we describe a new case of plasma cell granuloma of the thyroid gland that occurred in a 46-year-old man who also had Hashimoto's thyroiditis. This case represents only the second documented instance of a plasma cell granuloma of the thyroid occurring in the setting of Hashimoto's thyroiditis. Moreover, it is only the second case of a plasma cell granuloma that has been reported in a male.


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