نتایج جستجو برای: mixed tumor

تعداد نتایج: 641555  

2013
S. Berrettini S. Fortunato A. De Vito L. Bruschini

Salivary gland tumors are rare. The majority of these tumors are benign and about 70% are pleomorphic adenomas (PA). Nasopharynx is an unusual site for the PA tumor. Only six cases are presented in the literature from 1990 to 2011. The diagnosis of this disease is linked to the sum of imaging tests, clinical and histological study of the mass of the above. The radiologic features of noninvasion...

2014
Fatemeh Homaei Shandiz Sima Kadkhodayan Malihe Hsanzade Mofrad Zohre Yousefi Roodsari Noorieh Sharifi Sistani Majid Nabizadeh Marvast Mahbobe Sadeghei

INTRODUCTION Malignant Mixed Mullerian Tumor (MMMT) is a very rare tumor, accounting for less than 1% of all ovarian cancers. CASE PRESENTATION We present a 64-year-old woman with stage III MMMT of ovary that was treated with platinum-based chemotherapy after optimal cytoreductive surgery. After 25 months of being disease free, she had a pelvic recurrence and a good response to chemoradiother...

2017
Venkatkiran Kanchustambham Swetha Saladi Setu Patolia Sara Mahmoud Assaf David Stoeckel

Salivary gland tumors (SGT) constitute a small proportion of primary respiratory system neoplasms. Benign SGT comprises pleomorphic adenoma and is exceedingly rare in the lungs. We hereby present a rare case of a benign primary pleomorphic adenoma of the lung. The histological pattern of the tumor was indistinguishable from the head and neck SGT counterparts and showed biphasic morphology. Mali...

Journal: :Kulak burun bogaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2006
Abhishek Karnwal Shanthi Pakalapati Konstance Tzifa Vivek Raut

Chondroid syringoma of the external ear canal is a rare, usually firm or polypoid tumor, representing the cutaneous counterpart of pleomorphic adenoma of salivary glands. We report a very rare case of chondroid syringoma in a 40-year-old man who presented with a fluid-containing cyst in the external ear canal. Clinical and radiological examinations showed involvement of the whole external canal...

2014
Su-Ying Wen

Chondroid syringoma is a rare benign, skin appendageal tumor, also known as mixed tumors of the skin. The clinical presentation of chondroid syringoma is non-specific, and the diagnosis is made histopathologically. A case of a 74-year-old man presented with an asymptomatic 1.3-cmsized, firm, skin-colored, subcutaneous nodule of 8 years’ duration on the superior helical rim of the left ear. Stre...

2012
Jesse Courtier Elizabeth Robbins Bruno Soares Andrew Horvai John D. Mackenzie

We report a case of primary malignant mixed tumor (MMT) of bone in an 18-year-old boy with X-ray, CT, MR, scintigraphic, FDG PET, and pathologic correlation. Primary MMT of bone is a highly aggressive tumor and presents both a diagnostic and clinical treatment challenge. This tumor is extremely rare and to the best of our knowledge, this is the first report of the diagnostic imaging findings fo...

2013
Yanzuo Chen Xianyi Sha Wei Zhang Weitong Zhong Zhuoyang Fan Qiuyue Ren Liangcen Chen Xiaoling Fang

A Pluronic polymeric mixed micelle delivery system was developed in this study by using Pluronic P105 and F127 block copolymers to encapsulate the antitumor compound, methotrexate (MTX). The MTX-loaded Pluronic P105/F127 mixed micelle exhibited the spherical shape with about 22 nm in diameter, high encapsulation efficiency (about 85%) and pH-dependent in vitro drug release. In this study, A-549...

2012
Kotb Abbass Metwalley Dalia Ahmed Elsers Hekma Saad Farghaly Hanaa Abdel-Lateif Mohamed Abdel-Kader

INTRODUCTION Ovarian tumors are the least common cause of sexual precocity in girls. Mixed germ cell-sex cord-stromal tumors associated with a yolk sac tumor of the ovary are rare neoplasms, of which only a small number of well-documented cases have been described so far. Here, we report precocious puberty in a four-year-old Egyptian girl caused by a mixed germ cell-sex cord-stromal tumor assoc...

2017
Rachel E. Beard Sydney D. Finkelstein Amir A. Borhani Marta I. Minervini J. Wallis Marsh

INTRODUCTION Mixed hepatocellular and cholangiocarcinoma tumors (MHCC) are described in the literature, as are the more rare mixed adenoneuroendocrine carcinomas (MANC) of hepatobiliary origin. Only two cases of tumors with characteristics of all three histologies/phenotypes have been previously described in one Chinese study. PRESENTATION OF CASE Herein we report clinical, microscopic and mo...

2015
Min Yu Quanbo Zhou Yu Zhou Zhiqiang Fu Langping Tan Xiao Ye Bing Zeng Wenchao Gao Jiajia Zhou Yimin Liu Zhihua Li Ye Lin Qing Lin Rufu Chen

INTRODUCTION The aim of present study was to profile the glucose-dependent and glutamine- dependent metabolism in pancreatic cancer. METHODS We performed Immunohistochemical staining of GLUT1, CAIX, BNIP3, p62, LC3, GLUD1, and GOT1. Based on the expression of metabolism-related proteins, the metabolic phenotypes of tumors were classified into two categories, including glucose- and glutamine-d...

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