نتایج جستجو برای: pelvic neoplasm lipid

تعداد نتایج: 371645  

Journal: :journal of midwifery and reproductive health 0
sima kadkhodayan associate professor, department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran zohreh yousefi professor, department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran malihe hasanzadeh associate professor, department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran *, noorieh sharifi sistani professor, department of pathology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran fatemeh homaee associate professor, department of radiation oncology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran

uterine sarcoma is a rare tumor of mesodermal origin, accounting for 2-6% of uterine malignancies. leiomyosarcoma (lms) has been reported in only 1% of all uterine malignancies and is regarded as the most common primary uterine sarcoma. herein, we present a case of lms with unusual macroscopic features. the patient was a 61-year-old woman with lms, which consisted of a large cystic mass (88×136...

*, Noorieh Sharifi Sistani Fatemeh Homaee Malihe Hasanzadeh Sima Kadkhodayan Zohreh Yousefi

Uterine sarcoma is a rare tumor of mesodermal origin, accounting for 2-6% of uterine malignancies. Leiomyosarcoma (LMS) has been reported in only 1% of all uterine malignancies and is regarded as the most common primary uterine sarcoma. Herein, we present a case of LMS with unusual macroscopic features. The patient was a 61-year-old woman with LMS, which consisted of a large cystic mass (88×136...

Journal: :Infectious Diseases in Obstetrics and Gynecology 2011

Journal: :GSC Advanced Research and Reviews 2021

Leiomyosarcoma is a rare neoplasm with poor survival rate. Between June 2018 to January 2019 we treated case of Prostate initially metastatic the lung and liver multiple pelviclymph nodes. Five cycles chemotherapy palliative radiotherapy have been delivered mean follow up 1 year .Chestabdominal-pelvic CT scan MRI bone are necessarily assess clinical staging. The objective this study review our ...

Journal: :Journal of radiology case reports 2010
Justin Boe A Rao Chimpiri Cheng Z Liu

A 52 year old male presented with changes in bowel movements, and a mass was detected on digital rectal exam. Both CT and MRI revealed a large pelvic and gluteal mass filling the pelvic cavity displacing the adjacent pelvic structures. After surgical removal, pathology revealed solitary fibrous tumor; a rare neoplasm uncommonly discovered in the thorax, and even less commonly in extrapleural lo...

2011
Teresa Pusiol Doriana Morichetti Corrado Pedrazzani Francesco Ricci

Abdominal-pelvic actinomycosis is often mistaken for other conditions, presenting a preoperative diagnostic challenge. In a 46-year-old female, computed tomography showed an abdominal-pelvic retroperitoneal mass extending from the lower pole of the right kidney to the lower pelvis. The patient had a 3-year history of intrauterine device. The mass appeared to involve the ascending colon, cecum, ...

Journal: :Annals of the Academy of Medicine, Singapore 1998
A Khalid F Lawton

A case of a 53-year-old perimenopausal woman who presented with an 18-month history of irregular vaginal bleeding is reported. Vaginal ultrasonography revealed a 10 x 7 cm pelvic mass with an increased blood flow. Her serum CA125 was within the normal range. At laparotomy a normal spleen was found within the pelvic cavity.

2006
Sean D. Beaty Alvin C. Silva Giovanni De Petris

Bladder endometriosis is a rare cause of a localized bladder mass, potentially mimicking a neoplasm at cross-sectional imaging. We present the case of a patient with cyclic pelvic pain and urinary symptoms secondary to bladder endometriosis, with characteristic pelvic ultrasound and magnetic resonance imaging findings. Potential pathological mechanisms are discussed.

Journal: :iranian journal of medical sciences 0
zohreh yousefi cancer research center, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran nourieh sharifhi department of pathology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran malihe hasanzadeh department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran mansoureh mottaghi gynecologist, mashhad, iran somayeh bolandy department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran

the primitive neuroectodermal tumor (pnet) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin. categorized in the same tumor family as ewing sarcoma, the pnet is most likely to occur in bones and soft tissues. however, a small number of pnet cases arising in the pelvis have been reported as well. we present three cases of pelvic pnet: ...

Journal: :Taiwanese journal of obstetrics & gynecology 2015
Jian-song Zhou Xi Chen Tao Zhu Guo-jun Ding Ping Zhang

Accessory spleens (AS) are congenital malformations defined as additional ectopic splenic parenchyma. Most of them are innocent until found, and do not usually require treatment. They may have clinical significance since theymay be confused for enlarged lymph nodes or have a neoplastic appearance; therefore, accurate preoperative diagnosis is important to avoid unnecessary surgical management. ...

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