نتایج جستجو برای: leiomyomas

تعداد نتایج: 1254  

Journal: :Cancer research 2002
Deborah S Hunter Michael Klotzbücher Hiroyuki Kugoh Sheng-Li Cai Johanna P Mullen Guidalberto Manfioletti Ulrike Fuhrman Cheryl L Walker

Unregulated proliferation of mesenchymal cells in leiomyomas, lipomas, hamartomas,and other diseases has been linked to the high mobility group (HMGA) family of DNA architectural proteins. HMGA genes are primarily expressed during embryonal development and silenced in adult tissues but can become reactivated in neoplasia as a result of chromosomal rearrangements. Although the genetic data sugge...

Ahmad Salimzadeh Ahmadreza Rajaee Fatemeh Moeineddin Hayedeh Ghaninejad Masoud Asgari

Recently multiple cutaneous leiomyomas, uterine leiomyoimatosis and renal cancer have been described as a cancer syndrome with autosomal dominant pattern of inheritance.We report a 79-year-old man who presented with multiple hyperkertotic erythematous nodules on his right leg with histological diagnosis of pilar leiomyoma. In his past medical history several systemic co...

Journal: :Japanese Journal of Gynecologic and Obstetric Endoscopy 2022

Parasitic peritoneal leiomyomatosis (PL) and disseminated (DPL) are rare medical conditions; however, cases have been widely reported in recent years. Case1: A 43-year-old woman presented at our hospital, eight years after a laparoscopic myomectomy, with anemia uterine tumor. Magnetic resonance imaging computed tomography (CT) scans revealed mass, several other pelvic masses, subcutaneous mass ...

Journal: :American journal of obstetrics and gynecology 2005
Renata A Canevari Anaglória Pontes Fabíola E Rosa Cláudia A Rainho Silvia R Rogatto

OBJECTIVE In an attempt to clarify the clonality and genetic relationships that are involved in the tumorigenesis of uterine leiomyomas, we used a total of 43 multiple leiomyomas from 14 patients and analyzed the allelic status with 15 microsatellite markers and X chromosome inactivation analysis. STUDY DESIGN We have used a set of 15 microsatellite polymorphism markers mapped on 3q, 7p, 11, ...

Journal: :Clinical science 2001
C C Gentry S O Okolo L F Fong J C Crow A B Maclean C W Perrett

Although uterine leiomyomas constitute the commonest benign tumour in women, the regulation of their growth is poorly understood. It is believed that angiogenesis, the process by which new capillaries develop from pre-existing blood vessels, may be involved. We therefore investigated the expression of vascular endothelial growth factor-A (VEGF-A), a primary regulator of angiogenesis, in leiomyo...

Journal: :Molecular human reproduction 2009
Yoshiaki Yamagata Ryo Maekawa Hiromi Asada Toshiaki Taketani Isao Tamura Hiroshi Tamura Jun Ogane Naka Hattori Kunio Shiota Norihiro Sugino

Aberrant DNA methylation has been implicated in tumorigenesis. This study was undertaken to establish the genome-wide DNA methylation profile in uterine leiomyomas and to investigate whether DNA methylation status is altered in uterine leiomyomas. For this purpose, restriction landmark genomic scanning (RLGS) was performed on a paired sample of leiomyoma and adjacent normal myometrium. The RLGS...

2017
Veronica Sarais Greta Chiara Cermisoni Matteo Schimberni Alessandra Alteri Enrico Papaleo Edgardo Somigliana Paola Vigano’

Uterine fibroids are the most common gynecologic benign tumors. Studies supporting a strong pregnancy-related growth of leiomyomas generally claimed a crucial role of sex steroid hormones. However, sex steroids are unlikely the unique actors involved as estrogen and progesterone achieve a pick serum concentration in the last trimester while leiomyomas show a typical increase during the first tr...

2014
Laura Diluvio Claudia Torti Alessandro Terrinoni Eleonora Candi Raffaella Piancatelli Emilio Piccione Evelin Jasmine Paternò Sergio Chimenti Augusto Orlandi Elena Campione Luca Bianchi

BACKGROUND Hereditary syndromes frequently need the cooperation of different specialties to increase diagnostic competence. Multiple cutaneous and uterine leiomyomatosis syndrome is a rare autosomal dominant disorder caused by the mutations of the fumarate hydratase gene, demonstrated in 80 to 100 percent of affected individuals. This can be linked to an increased risk of renal cancer in both s...

2017
Andrzej Woźniak Sławomir Woźniak

Uterine leiomyomas or uterine fibroids are the most common gynaecological tumours and occur in about 20-50% of women around the world. Ultrasonography (USG) is the first-line imaging examination in suspected fibroids and shows high sensitivity and specificity in diagnosing this condition. Ultrasound scans can be performed transvaginally (transvaginal scan - TVS) or transabdominally (transabdomi...

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