A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule
Objective. Marine-Lenhart Syndrome (MLS) is defined as concomitant occurrence of autonomously functioning thyroid nodule (AFTN) with Graves’ disease (GD). Malignancy in a functional nodule is rare. We aimed to present an extremely rare case of papillary thyroid cancer in a MLS nodule with lateral ly...
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doaj-bc39178e991d4600bb7efa1d3bef4b802020-11-24T23:14:31ZengHindawi LimitedCase Reports in Surgery2090-69002090-69192016-01-01201610.1155/2016/87404058740405A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome NoduleMehmet Uludag0Nurcihan Aygun1Alper Ozel2Feyza Yener Ozturk3Rabia Karasu4Banu Yilmaz Ozguven5Bulent Citgez6Mehmet Mihmanli7Adnan Isgor8Department of General Surgery, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of General Surgery, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of Radiology, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of Endocrinology and Metabolism, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of Radiology, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of Pathology, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of General Surgery, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of General Surgery, Sisli Hamidiye Etfal Training and Research Hospital, 34371 Istanbul, TurkeyDepartment of General Surgery, Bahcesehir University Medical Faculty, 34353 Istanbul, TurkeyObjective. Marine-Lenhart Syndrome (MLS) is defined as concomitant occurrence of autonomously functioning thyroid nodule (AFTN) with Graves’ disease (GD). Malignancy in a functional nodule is rare. We aimed to present an extremely rare case of papillary thyroid cancer in a MLS nodule with lateral lymph node metastases. Case. A 43-year-old male presented with hyperthyroidism and Graves’ ophthalmopathy. On Tc99m pertechnetate scintigraphy, a hyperactive nodule in the left upper thyroid pole was detected and the remaining tissue showed a mildly increased uptake. The ultrasonography demonstrated 15.5 × 13.5 × 12 mm sized hypoechoic nodule in the left upper pole of the thyroid and round lymph nodes on the left side of the neck. Fine needle aspiration biopsy (FNAB) of the nodule and lymph node revealed cytological findings consistent with papillary cancer. Total thyroidectomy with central and left modified radical neck dissection was performed. On pathologic examination, two foci of micropapillary cancer were detected. The skip metastases were present in three lymph nodes on the neck. Conclusion. AFTN can be seen rarely in association with GD. It is not possible to exclude malignancy due to the clinical and imaging findings. In the presence of suspicious clinical and sonographic features, FNAB should be performed.http://dx.doi.org/10.1155/2016/8740405 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mehmet Uludag Nurcihan Aygun Alper Ozel Feyza Yener Ozturk Rabia Karasu Banu Yilmaz Ozguven Bulent Citgez Mehmet Mihmanli Adnan Isgor |
spellingShingle |
Mehmet Uludag Nurcihan Aygun Alper Ozel Feyza Yener Ozturk Rabia Karasu Banu Yilmaz Ozguven Bulent Citgez Mehmet Mihmanli Adnan Isgor A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule Case Reports in Surgery |
author_facet |
Mehmet Uludag Nurcihan Aygun Alper Ozel Feyza Yener Ozturk Rabia Karasu Banu Yilmaz Ozguven Bulent Citgez Mehmet Mihmanli Adnan Isgor |
author_sort |
Mehmet Uludag |
title |
A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule |
title_short |
A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule |
title_full |
A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule |
title_fullStr |
A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule |
title_full_unstemmed |
A Rare Presentation of Autonomously Functioning Papillary Thyroid Cancer: Malignancy in Marine-Lenhart Syndrome Nodule |
title_sort |
rare presentation of autonomously functioning papillary thyroid cancer: malignancy in marine-lenhart syndrome nodule |
publisher |
Hindawi Limited |
series |
Case Reports in Surgery |
issn |
2090-6900 2090-6919 |
publishDate |
2016-01-01 |
description |
Objective. Marine-Lenhart Syndrome (MLS) is defined as concomitant occurrence of autonomously functioning thyroid nodule (AFTN) with Graves’ disease (GD). Malignancy in a functional nodule is rare. We aimed to present an extremely rare case of papillary thyroid cancer in a MLS nodule with lateral lymph node metastases. Case. A 43-year-old male presented with hyperthyroidism and Graves’ ophthalmopathy. On Tc99m pertechnetate scintigraphy, a hyperactive nodule in the left upper thyroid pole was detected and the remaining tissue showed a mildly increased uptake. The ultrasonography demonstrated 15.5 × 13.5 × 12 mm sized hypoechoic nodule in the left upper pole of the thyroid and round lymph nodes on the left side of the neck. Fine needle aspiration biopsy (FNAB) of the nodule and lymph node revealed cytological findings consistent with papillary cancer. Total thyroidectomy with central and left modified radical neck dissection was performed. On pathologic examination, two foci of micropapillary cancer were detected. The skip metastases were present in three lymph nodes on the neck. Conclusion. AFTN can be seen rarely in association with GD. It is not possible to exclude malignancy due to the clinical and imaging findings. In the presence of suspicious clinical and sonographic features, FNAB should be performed. |
url |
http://dx.doi.org/10.1155/2016/8740405 |
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