نتایج جستجو برای: adrenocortical carcinoma

تعداد نتایج: 398467  

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 1974
B H Forman M A Antar R J Touloukian P J Mulrow M Genel

F-18 FDG is the most widely used tracer in molecular imaging and it is applied for many purposes mainly in malignant diseases. Incidental finding are common in FDG-PET/CT imaging and includes benign and malignant lesions. Among the rare tumors , adrenal oncocytomas are uncommon findings and incidental findings of thyroid malignancies are not rare. Oncocytoma is a rare adrenocortical tumor and m...

Journal: :Histopathology 2009
Marco Volante Enrico Bollito Paola Sperone Veronica Tavaglione Fulvia Daffara Francesco Porpiglia Massimo Terzolo Alfredo Berruti Mauro Papotti

AIMS Pathological diagnosis of adrenocortical carcinoma relies on several microscopic features commonly used in combination in different scoring systems that are sometimes subjective and/or time consuming. The aim was to investigate the impact of individual pathological parameters in the diagnosis and prognosis of adrenocortical carcinoma. METHODS AND RESULTS The series included 92 malignant ...

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2002
E Baudin C Docao C Gicquel G Vassal A Bachelot A Penfornis M Schlumberger

BACKGROUND Complete responses are rare after medical treatment of adrenocortical tumors. We performed a single center prospective study of the antitumor effect of irinotecan (CPT-11) in patients with metastatic adrenocortical cancer. PATIENTS AND METHODS Since 1999, all patients with advanced progressive adrenocortical carcinoma, referred to the Institut Gustave-Roussy, have been enrolled pro...

Journal: :The Journal of clinical endocrinology and metabolism 2002
Zhi-He Gao Suvikki Suppola Jianqi Liu Päivi Heikkilä Juhani Jänne Raimo Voutilainen

Low H19 and abundant IGF-II expression may have a role in the development of adrenocortical carcinomas. In the mouse, the H19 promoter area has been found to be methylated when transcription of the H19 gene is silent and unmethylated when it is active. We used PCR-based methylation analysis and bisulfite genomic sequencing to study the cytosine methylation status of the H19 promoter region in 1...

2017
Minchun Jiang Huanyu Ding Cheng Li Kexu Xiang Juying Tang Ying Guo Shaoling Zhang

Adrenocortical carcinoma (ACC) is a malignant endocrine tumor. Moreover, ACC with invasion into the inferior vena cava is rare. Early diagnosis and treatment are crucial for such cases. Radical surgical resection is the key therapeutic option in ACC.

2012
Manphool Singhal Mandeep Kang Alka Khadwal Rajan Duggal Arvind Rajwanshi Niranjan Khandelwal

We describe a case of congenital non-functional adrenocortical carcinoma in a male infant who presented with recurrent pneumonia, paraparesis and sclerotic skeletal metastasis. To the best of our knowledge such presentation has never been reported.

2010
Marlon A. Guerrero Electron Kebebew

OBJECTIVE Adrenocortical carcinoma (ACC) is an aggressive tumor that accounts for 0.02% of all reported cancers. ACC commonly arises in a sporadic manner, but may also manifest as part of a familial syndrome. Regardless of the setting, ACC rarely arises concurrent with other malignant tumors. METHODS In this report we describe a 32-year-old woman who on work-up for abnormal vaginal bleeding w...

Journal: :Endocrine-related cancer 2015
T M A Kerkhofs M H T Ettaieb I G C Hermsen H R Haak

Cancer of the adrenal cortex (ACC) is a rare endocrine malignancy with limited treatment options. Patients typically present with autonomous hormonal overproduction and/or a large abdominal mass. Hormonal assays and medical imaging can be diagnostic, but urinary steroid profiling might be a more sensitive technique to assess malignancy in adrenal tumours. The stage of the disease at diagnosis i...

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