Combination of medullary thyroid cancer and renal cell carcinoma in one patient
Patients who received treatment for the first malignant neoplasm remain in the group at increased risk of developing a second primary tumor throughout their later life. A rare case of medullary thyroid cancer and renal cell carcinoma of the kidney is described in one patient. Medullary thyroid cance...
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Endocrinology Research Centre
2018-06-01
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doaj-448c7f3360ab4f80bced359c2c47a4bb2021-06-02T19:26:28ZrusEndocrinology Research CentreКлиническая и экспериментальная тиреоидология1995-54722310-37872018-06-01141343810.14341/ket92598462Combination of medullary thyroid cancer and renal cell carcinoma in one patientYuliya A. Dolinskaya0Sergey P. Shevchenko1Vladimir N. Maksimov2Elena N. Voropaeva3Oksana D. Rymar4Institution of Internal and Preventive MedicineNovosibirsk State UniversityInstitution of Internal and Preventive MedicineInstitution of Internal and Preventive MedicineInstitution of Internal and Preventive MedicinePatients who received treatment for the first malignant neoplasm remain in the group at increased risk of developing a second primary tumor throughout their later life. A rare case of medullary thyroid cancer and renal cell carcinoma of the kidney is described in one patient. Medullary thyroid cancer is an orphan disease. The patient and his first-line relatives underwent molecular-genetic testing, the presence of a hereditary form of medullary cancer was excluded. During the observation, malignant kidney formation was detected, and surgical treatment was performed. The patient because of treatment and surveillance does not have data for the progression of thyroid cancer and kidney cancer, compensation for concomitant diseases has been achieved. When observing patients with medullary thyroid cancer, it is necessary to use the existing modern diagnostic arsenal, including positron emission tomography, since patients remain in the group at increased risk of disease progression and development of the second tumor throughout the entire subsequent life. In addition, this case clearly illustrates the need for a routine study of calcitonin as a diagnostic marker for the progression of medullary thyroid cancer.https://cet-endojournals.ru/ket/article/viewFile/9259/7254medullary thyroid cancerrenal cancercase report |
collection |
DOAJ |
language |
Russian |
format |
Article |
sources |
DOAJ |
author |
Yuliya A. Dolinskaya Sergey P. Shevchenko Vladimir N. Maksimov Elena N. Voropaeva Oksana D. Rymar |
spellingShingle |
Yuliya A. Dolinskaya Sergey P. Shevchenko Vladimir N. Maksimov Elena N. Voropaeva Oksana D. Rymar Combination of medullary thyroid cancer and renal cell carcinoma in one patient Клиническая и экспериментальная тиреоидология medullary thyroid cancer renal cancer case report |
author_facet |
Yuliya A. Dolinskaya Sergey P. Shevchenko Vladimir N. Maksimov Elena N. Voropaeva Oksana D. Rymar |
author_sort |
Yuliya A. Dolinskaya |
title |
Combination of medullary thyroid cancer and renal cell carcinoma in one patient |
title_short |
Combination of medullary thyroid cancer and renal cell carcinoma in one patient |
title_full |
Combination of medullary thyroid cancer and renal cell carcinoma in one patient |
title_fullStr |
Combination of medullary thyroid cancer and renal cell carcinoma in one patient |
title_full_unstemmed |
Combination of medullary thyroid cancer and renal cell carcinoma in one patient |
title_sort |
combination of medullary thyroid cancer and renal cell carcinoma in one patient |
publisher |
Endocrinology Research Centre |
series |
Клиническая и экспериментальная тиреоидология |
issn |
1995-5472 2310-3787 |
publishDate |
2018-06-01 |
description |
Patients who received treatment for the first malignant neoplasm remain in the group at increased risk of developing a second primary tumor throughout their later life. A rare case of medullary thyroid cancer and renal cell carcinoma of the kidney is described in one patient. Medullary thyroid cancer is an orphan disease. The patient and his first-line relatives underwent molecular-genetic testing, the presence of a hereditary form of medullary cancer was excluded. During the observation, malignant kidney formation was detected, and surgical treatment was performed. The patient because of treatment and surveillance does not have data for the progression of thyroid cancer and kidney cancer, compensation for concomitant diseases has been achieved. When observing patients with medullary thyroid cancer, it is necessary to use the existing modern diagnostic arsenal, including positron emission tomography, since patients remain in the group at increased risk of disease progression and development of the second tumor throughout the entire subsequent life. In addition, this case clearly illustrates the need for a routine study of calcitonin as a diagnostic marker for the progression of medullary thyroid cancer. |
topic |
medullary thyroid cancer renal cancer case report |
url |
https://cet-endojournals.ru/ket/article/viewFile/9259/7254 |
work_keys_str_mv |
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