scholarly journals Intrathyroidal Clear Cell Tumor of Parathyroid Origin with Review of Literature

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Daniela Pirela ◽  
Daniela Treitl ◽  
Siba El Hussein ◽  
Robert Poppiti ◽  
Thomas Mesko ◽  
...  

Water-clear cell adenoma (WCCA) of the parathyroid gland is an exceedingly rare neoplasm. To date, 17 cases have been reported in the literature, with only one of them being intrathyroidal. Here we report a case of a 34-year-old woman who presented for evaluation of a goiter and was found to have a thyroid nodule and abnormal thyroid function tests (TFT). Fine needle aspiration biopsy of the nodule revealed thyroid follicular cells without atypia and subsequent Afirma® Gene Expression Classifier (GEC) testing results were suspicious for malignancy. As a result, the patient underwent a right thyroid lobectomy and isthmusectomy. Histological sections revealed an intrathyroidal nodule consistent with a clear cell neoplasm of parathyroid origin. The histologic appearance together with the immune profile was diagnostic of WCCA, with diffuse positivity for GATA3, focal weak positivity for parathyroid hormone, and negativity for PAX8, thyroglobulin, TTF1, synaptophysin, chromogranin, and S100p. Our study focuses on the clinical presentation, current management strategies, and review of the available literature surrounding this rare diagnosis. The ultimate goal is to help endocrinologists and surgeons establish a foundational treatment plan for intrathyroidal clear cell tumor cases.

2020 ◽  
Author(s):  
leilei shen ◽  
Jixing LIN ◽  
Zhipeng REN ◽  
Bailin WANG ◽  
You Liu ◽  
...  

Abstract Background: Clear cell tumor of the lung (CCTL) is a rare and mostly benign pulmonary neoplasm arising from perivascular epithelioid cells. Only about 100 cases have been reported and half of them were in China. Limited details about CCTL often cause diagnostic or therapeutic problems. Case presentation: We describe a case of 28-year-old woman with gradually increased and enlarged multiple nodules in the left lower lobe. The patient underwent a fine-needle aspiration biopsy and was considered as CCTL. A left lower lobectomy and mediastinal lymph node dissection was performed. The gradual changes in size (1.4 cm to 2.8 cm) and quantity (10 to 49) of CCTL in this case was the biggest difference from previously reported cases. Conclusions: CCTL is a very uncommon and mostly benign PEComatous tumor with no specific morphologic features. We present a case of CCTL with multiplicity and rapid growth, which may indicate its aggressive nature. The accumulation of similar cases will help clarify its exact disease nature and to improve our understanding of such tumor.


2004 ◽  
Vol 25 (4) ◽  
pp. 652-654 ◽  
Author(s):  
A SANTANA ◽  
F NUNES ◽  
N HO ◽  
T TAKAGAKI

2011 ◽  
Vol 91 (2) ◽  
pp. 588-591 ◽  
Author(s):  
Alexandros Kalkanis ◽  
Myrto Trianti ◽  
Kostas Psathakis ◽  
Charalampos Mermigkis ◽  
Dimitrios Kalkanis ◽  
...  

2001 ◽  
Vol 33 (2) ◽  
pp. 196-199
Author(s):  
Vicky Zolota ◽  
Anna Batistatou ◽  
Maria Melachrinou ◽  
Evangelos Tzorakoeleftherakis ◽  
Vassilios Pastromas ◽  
...  

1981 ◽  
Vol 5 (6) ◽  
pp. 581-586 ◽  
Author(s):  
Alan D. Glick ◽  
Kyi Toe Tham ◽  
Nai Kwong Leung ◽  
Song Win Wong

2013 ◽  
Vol 5 (1) ◽  
pp. e2013021
Author(s):  
Volkan Yazak ◽  
Gokhan Sargin ◽  
Irfan Yavasoglu ◽  
Gurhan Kadikoylu ◽  
Canten Tataroglu ◽  
...  

The primary clear cell tumor of the lung is an extremely rare benign tumor, which is called “sugar tumor”, because of the large content of glycogen. Here we are presenting essential thrombocythemia and lung clear cell tumor which was not reported before to the best of our knowledge.A 44 years old woman admitted to the clinic with complaint of lassitude lasting for 2 months. In her physical examination the spleen was 3 cm palpable from the costa arch In laboratory findings number of platelet was 1014000 mm³. A 3.5 cm in diameter pulmonary nodule is detected in right upper lobe in the graphy of the lungs. Subsequently  computed tomography  (CT ) of thorax was carried out. Due to the benign features in the display of  the detected nodule, a total excision with curative and diagnostic intentions was performed. Microscopically the tumor were composed of nests of rounded or oval cells with distinct cell borders and optically clear cytoplasm. The nuclei were small. Immunohistochemically the tumor cells expressed HMB-45, NSE and focal S100 antigen. It was diagnosed as clear  “sugar” cell tumor. In conclusion, in lung clear cell tumor, it is important to make evaluation in terms of myeloproliferative disease in adults whose thrombocytosis continue after the treatment.


Author(s):  
Yasunori SHIKADA ◽  
Masakazu KATSURA ◽  
Sadanori TAKEO

2020 ◽  
Vol 15 (1) ◽  
Author(s):  
Leilei Shen ◽  
Jixing Lin ◽  
Zhipeng Ren ◽  
Bailin Wang ◽  
You Liu ◽  
...  

2017 ◽  
Vol 8 (5) ◽  
pp. 530-534 ◽  
Author(s):  
Yinghua Song ◽  
Fangfang Chen ◽  
Caiqing Zhang ◽  
Xiaoyan Lin

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