نتایج جستجو برای: medullary thyroid cancer

تعداد نتایج: 982512  

2010
Nina Ventura Edson Marchiori Gláucia Zanetti Antonio Muccillo Mariana Leite Pereira Guilherme Abdalla Pedro Martins Carolina Lamas Constantino Rodrigo Canellas Viviane Brandão Romulo Varella de Oliveira

Medullary thyroid carcinoma is a rare malignancy that arises from calcitonin-producing C-cells and frequently metastasizes to lymph nodes in the neck. Distant metastases may involve bone, lung, and liver. The infrequent number of cases limits the clinical nature and ability to optimize diagnostic tools. Here, we present a case of a micronodular radiographic pattern in metastatic medullary thyro...

Journal: :Journal of clinical pathology 1977
J Economidou P Karacoulis O N Manousos E Manesis A Kydonakis D A Koutras

Plasma carcinoembryonic antigen (CEA) levels were measured by the Z-Gel technique in 138 patients with benign thyroidopathies, 25 patients with thyroid cancer, and 141 normal persons. Levels were raised (above 5 ng/ml) in 2% of the normal subjects, in none of the patients with benign thyroidopathies, and in 20% of the patients with thyroid cancer. They were considerably raised in all cases of m...

Journal: :Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion 2011
Juan Carlos Galofré José Manuel Gómez-Sáez Cristina Álvarez Escola Elías Álvarez García Emma Anda Apiñaniz Amparo Calleja Sergio Donnay Anna Lucas-Martin Edelmiro Menéndez Torre Elena Navarro González Vicente Pereg Begoña Pérez Corral Javier Santamaría Sandi Garcilaso Riesco Eizaguirre Carles Zafón Llopis

s/. 27. de Groot JW, Zonnenberg BA, van Ufford-Mannesse PQ, de Vries MM, Links TP, Lips CJ, et al. A phase II trial of imatinib therapy for metastatic medullary thyroid carcinoma. J Clin Endocrinol Metab. 2007;92:3466--9. 28. Cohen EE, Rosen LS, Vokes EE, Kies MS, Forastiere AA, Worden FP, et al. Axitinib is an active treatment for all histologic subtypes of advanced thyroid cancer: results fro...

2012
Ezzat Tarek Rajeev Paramesawaran Ben Phillips Greg Sadler

Patients with multiple endocrine neoplasia (MEN) type 2A develop medullary thyroid cancer, which is associated with poor prognosis in its metastatic stage. Hyperparathyroidism is a common finding in both MEN 1 and 2. We report a 68-year-old patient diagnosed clinically with MEN 1 based on the presence of hyperparathyroidism and pituitary Cushing's disease with no supporting genetic evidence. T...

2013
Yash Somnay David Schneider Haggi Mazeh

Note Medullary thyroid cancers (MTC) are rare tumors of neuroendocrine origin that arise from parafollicular C cells which secrete a variety of peptides and hormones including calcitonin. As opposed to the more common papillary and follicular thyroid cancer subtypes, MTC represents a rare and under-characterized form of cancer, and can cause death if untreated (Taccaliti et al., 2011). MTC can ...

Journal: :Endocrinology and Metabolism Clinics of North America 2007

Journal: :Memo – Magazine of European Medical Oncology 2023

Summary Established systemic treatment options for advanced thyroid cancer include the multityrosine kinase inhibitors lenvatinib and sorafenib radioactive iodine refractory differentiated (DTC) vandetanib cabozantinib medullary (MTC). Recently, COSMIC-311 study resulted in approval of DTC with progression upon and/or sorafenib; thus, first time a specific second-line therapy has been defined t...

Journal: :Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion 2014
Lynda Louhibi Amparo Marco Pedro J Pinés José C Padillo Inés Gómez Miguel A Valero Mubarak Alramadán Sandra Herranz Miguel Aguirre Antonio Hernández

OBJECTIVE Medullary thyroid cancer is a rare tumor that is more aggressive and has a worse prognosis than differentiated thyroid cancer. The purpose of this study was to report the demographic, clinical, and genetic characteristics of patients seen in the health care system of the community of Castilla-La Mancha over a 16-year period. PATIENTS AND METHODS Data were collected through a review ...

Journal: :Annals of clinical and laboratory science 1986
F J Hornicek T S Danowski S M Robinson K T Sweeney G I Malinin

Serum calcitonin was determined by RIA in 59 healthy subjects (Group 1), 49 randomly selected patients with treated or untreated thyroid disorders (Group 2), and in 12 kindred of a pheochromocytoma index case (Group 3). Although most subjects in Group 2 had normal calcitonin levels, there were significant (p less than 0.001) differences between all three groups. Of the five patients in Group 2 ...

Journal: :Journal of the Formosan Medical Association 2011

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