scholarly journals Benign Metastasizing Leiomyoma to the Lung and Spine: A Case Report and Literature Review

2019 ◽  
Vol 12 (1) ◽  
pp. 218-223 ◽  
Author(s):  
Emily Barber ◽  
Ann Eapen ◽  
Rita Mehta ◽  
Erin Lin ◽  
Karen Lane ◽  
...  

Benign metastasizing leiomyomas (BML) represent a rare phenomenon consisting of the extra-uterine spread of smooth muscle cells with similar histological, immunological, and molecular patterns to those of benign uterine leiomyomas. They are considered benign based off their low mitotic activity, lack of anaplasia or necrosis, and limited vascularization. This condition represents an interesting diagnostic and treatment challenge based on their rarity and indolent nature. Our case represents a unique finding of BML in the thoracic spine in a postmenopausal woman many years after hysterectomy and partial oophorectomy. There are currently no standard guidelines for treatment of BML, given the rare nature of this condition, with most patients treated with a combination of surgical resection and radiotherapy, followed by hormonal treatment and radiological surveillance serving as the primary backbone of current management plans. Given that these patients present a unique clinical challenge in terms of diagnosis and management, it is important to delineate and further examine these rare entities.

2018 ◽  
Vol 26 (7) ◽  
pp. 676-679 ◽  
Author(s):  
Scott Wolfe ◽  
James Sullivan ◽  
Leonard Kahn

There are 3 histologically benign smooth muscle neoplasms that have unusual growth patterns. These include intravascular leiomyomatosis, benign metastasizing leiomyoma, and leiomyomatosis peritonealis desseminata. We report a unique case of perivascular leiomyomatosis. The tumor showed multiple nodules of benign smooth muscle with some of the nodules closely associated with the periphery of the medial muscle layer of venous channels. All the neoplastic nodules were located on the outer surface of venous channels, thus precluding a diagnosis of intravascular leiomyomatosis. To the best of our knowledge, this is the first documentation of such an entity.


2007 ◽  
Vol 57 (3) ◽  
pp. 239
Author(s):  
Ji Eun Ahn ◽  
Kyung-Hyun Do ◽  
Eun Jin Chae ◽  
Joon Beom Seo ◽  
Jin Seong Lee ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-5
Author(s):  
Ryan Yu ◽  
Melanie Ferri

We report a 51-year-old woman who presented to the emergency department with left-sided pleuritic chest pain 2 weeks after subtotal hysterectomy and bilateral salpingo-oophorectomy for a leiomyomatous uterus. Computed tomography scan of the chest revealed bilateral pulmonary nodules. Biopsy showed cytologically bland spindle cells without overt malignant features. Immunohistochemistry confirmed smooth muscle phenotype, in keeping with a clinicopathologic diagnosis of benign metastasizing leiomyoma (BML). BML does not frequently come to the attention of the emergency physician because it is rare and usually asymptomatic. When symptomatic, its clinical presentation depends on the site(s) of metastasis, number, and size of the smooth muscle tumors. Emergent presentations of BML are reviewed.


2018 ◽  
Vol 18 ◽  
pp. e00061 ◽  
Author(s):  
Jennifer B. Bakkensen ◽  
Wesley Samore ◽  
Pietro Bortoletto ◽  
Cynthia C. Morton ◽  
Raymond M. Anchan

2019 ◽  
Vol 45 (10) ◽  
pp. 2132-2136 ◽  
Author(s):  
Xiong Yuan ◽  
Ying Sun ◽  
Yichao Jin ◽  
Lei Xu ◽  
Huihua Dai ◽  
...  

Author(s):  
Gennaro Scutiero ◽  
Luigi Nappi ◽  
Alessandra Spada ◽  
Pantaleo Bufo ◽  
Pantaleo Greco

1970 ◽  
Vol 2 (1) ◽  
pp. 67-70 ◽  
Author(s):  
Abhimanyu Jha ◽  
Gita Sayami ◽  
Deepti Adhikari

Uterine lipoleiomyosarcoma is a heterologous sarcoma composed of variable proportions of malignant lipoblasts histologically corresponding to well differentiated liposarcoma and malignant smooth muscle cells corresponding to leiomyosarcoma. Finding of benign lipomatous component in a typical leiomyoma (lipoleiomyoma) is not an uncommon, however, lipoleiomyosarcoma is an extremely rare malignant tumor and only very few cases have been reported so far. We report a case of lipoleiomyosarcoma of uterine corpus in a postmenopausal woman presenting with lower abdominal pain and abdominal mass. Diagnosis of lipoleiomyosarcoma was confirmed by histopathological examination of hysterectomy specimen. This is the first case of lipoleiomyosarcoma of uterus reported from Nepal. Keywords: Lipoleiomyosarcoma, uterus, histopathology, unusual case.   doi:10.3126/njog.v2i1.1482    N. J. Obstet. Gynaecol Vol. 2, No. 1, p. 67 - 70 May -June 2007


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