نتایج جستجو برای: leiomyomatosis

تعداد نتایج: 634  

2017
Don Nguyen Rishi Maheshwary Cassie Tran Scott Rudkin Luke Treaster

•Leiomyomatosis following laparoscopic hysterectomy with morcellation is reported.•Parasitic myomas grow in a benign fashion but may be fatal depending on location.•Fibroids are a contraindication for laparoscopic hysterectomy with morcellation.•Containment bags may address intraperitoneal spillage of malignant tissue.

2009
Firas W. Obeidat Reinhold A. Lang Florian Löhe Christian Graeb Carsten Rist Karl–Walter Jauch Tanija K. Hüttl Thomas P. Hüttl

CASE REPORT A 42-year-old female presented with long-standing symptoms suggestive of gastroesophageal reflux disease improved after proton pump inhibitor treatment. An upper endoscopy revealed an intrathoracic position of the stomach (type 4 hiatal hernia) with no mucosal abnormality. Barium swallow demonstrated gastric herniation with gastric volvulus without stenosis. A computed tomographic s...

2013
Na Rae Kim Chan Yong Park Hyun Yee Cho

Here, we report the case of a 43-year-old female who was diagnosed with a cotyledonoid dissecting leiomyoma (CDL) of the uterus. CDL is a recently described and extremely rare variant of a benign leiomyoma that can grossly masquerade as a malignancy. The 13-cm sized tumor was located primarily on the extrauterine surface as an intrauterine continuity, which showed dark red, congested, bulbous p...

Journal: :Proceedings of the Royal Society of Medicine 1970

2008
Ercan Çaliskan Serkan Bodur Mustafa Ulubay Ibrahim Özmen Ali Fuat Çiçek Güzin Deveci Engin Kaya

Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) is an autosomal dominant manifestation of cutaneous and uterine leiomyomas together with renal cancer due to autosomal dominant germline mutations of fumarate hydratase gene. A twenty-year-old female patient presented with type-II segmental piloleiomyoma and increased menstruation due to uterine leiomyomas, with a history of bilateral n...

Journal: :Journal of cutaneous medicine and surgery 2012
David Serra Pedro Amaro Margarida Gonçalo Mário Silva Barbara Ferrando Barbara Pasini Américo Figueiredo

BACKGROUND Cutaneous leiomyomatosis has been associated with multiple uterine myomas and, more recently, with germline heterozygous mutations of the FH gene and certain types of renal cancer. Despite the growing amount of knowledge concerning this genodermatosis, its clinical spectrum remains incompletely characterized. OBJECTIVE We report the observation of a patient with multiple cutaneous ...

Journal: :Ugeskrift for laeger 1988
N Johannesen

Disseminated peritoneal leiomyomatosis (DPL) is a very rare condition that almost always occurs in young women subjected to an altered hormonal milieu, usually pregnancy. To the surgeon, DPL may appear as metastases; the possibility of DPL should be considered whenever peritoneal nodules are encountered in a young woman, particularly if she is pregnant. Here we present the case report of a 35-y...

2017
Giannos Psathas Maria Zarokosta Menelaos Zoulamoglou Dimosthenis Chrysikos Ioannis Thivaios Ioannis Kaklamanos Konstantinos Birbas Theodoros Mariolis–Sapsakos

INTRODUCTION Leiomyomatosis peritonealis disseminata (LPD) is a peculiar benign clinical disorder characterized by proliferation of peritoneal and subperitoneal nodules. LPD is a difficultly diagnosed benign disease that rarely degenerates into malignancy. PRESENTATION OF CASE A 40-year-old Caucasian female with vaginal bleeding proceeded to our institution for elective excision of abdominal ...

Journal: :Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2014
Inês Cruz Isabel João Bruno Stuart Mário Iala Luísa Bento Carlos Cotrim Angelo Nobre Hélder Pereira

Intravenous leiomyomatosis is an unusual clinical condition characterized by histologically benign smooth muscle lesions extending from the uterus into pelvic and systemic veins and, more rarely, into the right cardiac chambers. We report the case of a 45-year-old woman who presented with a three-week history of dyspnea on exertion, shortness of breath and fatigue. Echocardiography showed a lar...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید