نتایج جستجو برای: medullary carcinoma

تعداد نتایج: 403199  

2016
Ibrahim Albalawi

Breast cancer is common worldwide, in the United States of America, 240000 new cases are diagnosed every year. Medullary breast cancer is a rare type of invasive ductal breast cancer. It accounts 1-7% of all breas 2010). Medullary breast cancer is less common carriers of the BRCA-1 genetic mutation. Moore and Foote (1947) described the unique histological features of medullary breast cancer as ...

Journal: :Journal of the National Cancer Institute 2004
Samuel A Wells Joseph R Nevins

Medullary thyroid carcinoma occurs most often as a sporadic malignancy, although in approximately 30% of cases, it occurs as part of the multiple endocrine neoplasia type 2 (MEN2) syndromes MEN2A and MEN2B or the related disease, familial medullary thyroid carcinoma. These three syndromes, inherited as autosomal dominant traits, are clinically characterized by near complete penetrance but varia...

Journal: :Indian journal of cancer 2005
Saral S Desai Suchana Sarkar Anita M Borges

BACKGROUND The microscopic features of medullary carcinoma have been described in world literature, together with its behavior and molecular biology. However, no large study has been reported from India. AIMS This study aims to analyse the clinical, and especially the pathological features of medullary carcinoma of the thyroid, and the surrounding thyroid. MATERIALS AND METHODS In this stud...

2017
Artur Kowalik Danuta Gąsior-Perczak Martyna Gromek Monika Siołek Agnieszka Walczyk Iwona Pałyga Małgorzata Chłopek Janusz Kopczyński Ryszard Mężyk Aldona Kowalska Stanisław Góźdź

Thyroid cancer is one of the most frequently diagnosed cancers of the endocrine system. There are no known genetic risk factors for non-medullary thyroid cancer, other than a small number of hereditary syndromes; however, approximately 5% of non-medullary thyroid cancer, designated familial non-medullary thyroid cancer, exhibits heritability. The p.G534E (c.1601G>A) variant of HABP2 was recentl...

Journal: :European thyroid journal 2015
Haggi Mazeh Amir Orlev Ido Mizrahi David J Gross Herbert R Freund

BACKGROUND Papillary thyroid carcinoma is the most common thyroid cancer (85%). Follicular thyroid carcinoma is the second most common type of thyroid cancer, accounting for up to 10% of all thyroid cancers. Medullary thyroid carcinoma accounts for only 5-8% of thyroid cancers. Concurrent medullary, follicular, and papillary carcinomas of the thyroid gland are extremely rare and reported scarce...

Alfred Roy Srilatha Parampalli Srinivas, Vijay kumar

Nonfunctional adrenocortical carcinoma is an extremely rare malignant tumor in children. Unlike the functional tumor which is detected early due to its hormonal presentation, nonfunctional tumor is detected at a later stage. Here we report a case of a 10 year old girl who presented with abdominal mass and symptoms of short duration. No hypertension and cushingoid features were seen. Serum alpha...

Journal: :Journal of Endocrinology and Metabolism 2022

Medullary thyroid cancer is a rare neuroendocrine tumor with aggressive behavior and an uncertain prognosis. Calcitonin the associated marker; however, tumors of lung or intestine can also present high values. We report case 53-year-old patient presenting dry cough for 3 years. Computed tomography (CT) showed 58-mm expansive lesion in right anterior mediastinum cervical ultrasound informed 9-mm...

Introduction: Medullary thyroid cancer (MTC) is an uncommon neoplasm originating from parafollicular C cells. Distant metastasis in MTC, such as axillary node involvement, is extremely rare.  Case Report: The present study describes a known case of MTC with axillary lymph node metastasis in a 31-year-old woman. In 2010, she underwent total thyroidectomy and right-sided modified radical neck dis...

Journal: :American Journal of Surgical Pathology 2014

Journal: :Pediatrics 2005
Malaka B Jackson Marta Guttenberg Holly Hedrick Thomas Moshang

Multiple endocrine neoplasia type 2A (MEN 2A) is most frequently caused by codon 634 activating mutations. Medullary thyroid carcinoma has occurred before the age of 2, with pheochromocytomas and primary hyperparathyroidism occurring later in childhood. We report cases of 4 siblings with C634Y-positive MEN 2A (all <11 years old): 3 with medullary thyroid carcinoma (1 had nodal metastasis, and a...

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