Incidence of adnexal and lymph node metastases in endometrial stromal sarcoma

2009 ◽  
Vol 27 (15_suppl) ◽  
pp. 5589-5589 ◽  
Author(s):  
L. dos Santos ◽  
K. Garg ◽  
J. P. Diaz ◽  
R. A. Soslow ◽  
M. L. Hensley ◽  
...  

5589 Background: To determine the incidence of adnexal and lymph node (LN) metastases in endometrial stromal sarcoma (ESS). Methods: We identified all cases evaluated at our institution with a diagnosis of ESS from January 1, 1980 to December 31, 2007. All uterine pathology was reviewed at our center. High-grade or undifferentiated tumors and ESS arising in extrauterine sites were excluded. Pertinent clinical data were abstracted from electronic medical records. Appropriate statistical tests were performed using SPSS 15.0. Results: We identified 91 cases with ESS. All except two underwent hysterectomy. Eighty-four cases (92%) underwent salpingo-oophorectomy (bilateral in 81 [96%]). Adnexal metastases were identified in 8 (9.5%) of 84 cases. All adnexal metastases were manifested by gross adnexal tumor and occurred in patients with other gross pelvic extrauterine disease. Seven of these 8 patients also had lymph-vascular space invasion (LVSI). LVSI status was not reported in the other patient. In patients with gross pelvic extrauterine disease, adnexal metastasis did not affect survival. LN metastases were identified in 8 (24%) of the 34 patients who underwent LN evaluation. Thirty-three evaluations were performed intraoperatively and one was via postoperative CT-guided biopsy of an enlarged LN. Five of the 8 cases with LN metastases had LVSI. LVSI status was not reported in the other 3 cases. Of 20 patients with disease grossly limited to the uterus and grossly normal LN, 2 (10%) had LN metastases. Both of these cases had LVSI and extensive myoinvasion approaching the serosa. Four of the remaining 6 patients with LN metastases had grossly positive LN and other gross extrauterine disease. The final 2 patients had grossly positive LN without other extrauterine disease. Conclusions: The incidence of LN metastases in ESS is most commonly associated with gross extrauterine disease, extensive myoinvasion and LVSI. However, since myoinvasion and LVSI status often are not assessable at the time of initial hysterectomy, LN dissection remains a reasonable option at primary surgery. The rate of adnexal metastasis appears to be negligible in the absence of gross adnexal and extrauterine tumor, but there may be a role for oophorectomy in the hormonal management of ESS. No significant financial relationships to disclose.

1994 ◽  
Vol 45 (2) ◽  
pp. 203-203
Author(s):  
B.A. Goff ◽  
L.W. Rice ◽  
D. Fleischhacker ◽  
H.G. Muntz ◽  
S.S. Falkenberry ◽  
...  

1993 ◽  
Vol 50 (1) ◽  
pp. 105-109 ◽  
Author(s):  
Barbara A. Goff ◽  
Laurel W. Rice ◽  
Deborah Flelschhacker ◽  
Howard G. Muntz ◽  
Stephen S. Falkenberry ◽  
...  

2005 ◽  
Vol 96 (2) ◽  
pp. 402-406 ◽  
Author(s):  
J. Riopel ◽  
M. Plante ◽  
M.-C. Renaud ◽  
M. Roy ◽  
B. Têtu

2013 ◽  
Vol 86 (1027) ◽  
pp. 20130088 ◽  
Author(s):  
F Collettini ◽  
A C Schippers ◽  
D Schnapauff ◽  
T Denecke ◽  
B Hamm ◽  
...  

2011 ◽  
Vol 121 (2) ◽  
pp. 319-322 ◽  
Author(s):  
Lisa A. dos Santos ◽  
Karuna Garg ◽  
John P. Diaz ◽  
Robert A. Soslow ◽  
Martee L. Hensley ◽  
...  

Author(s):  
Phornsawan Wasinghon ◽  
Chyi-Long Lee

A 50-year-old woman presented with symptoms of abnormal uterine bleeding. Ultrasonography showed an intrauterine cavity nodule sized approximately 2 cm. A hysteroscopic resection was diagnosed. The histopathology revealed high-grade endometrial stromal sarcoma. The surgery was laparoscopic surgical staging with indocyanine green sentinel lymph node mapping. Two positive indocyanine green sentinel lymph node of the right and left pelvic nodes showed no nodal metastasis. Also, the five positive indocyanine green sentinel lymph node showed no nodal metastasis. The occult lymph nodes were dissected at the right and left pelvic nodes for nodes 4 and 9, respectively. Conclusively, hysteroscopic resection is beneficial for the diagnosis of uterine sarcoma. Notwithstanding, laparoscopy can be used for uterine cancer and the indocyanine green sentinel lymph node showed no false negative. The patient was stage IA.


2012 ◽  
Vol 30 (15_suppl) ◽  
pp. e15522-e15522
Author(s):  
Mylene Sy Go ◽  
Le Wang ◽  
Michael Styler ◽  
Stephanie King

e15522 Background: Uterine sarcomas behave aggressively and are associated with poor prognosis. Carcinosarcomas was re-classified as more akin to endometrial adenocarcinomas. The objective was to analyze the survival outcomes of all uterine sarcomas treated with various combinations of chemotherapy, radiation, and lymph node dissections. Methods: 60 patients with proven uterine sarcomas were treated at Hahnemann Hospital from 2002-2011. Survival analyses in each treatment group were performed by Kaplan- Meier method Results: Among the 60 women examined, 51% were carcinosarcoma, 25% leiomyosarcoma, 20% endometrial stromal sarcoma, and 4% adenosarcoma. 27% presented with stage I disease, 20% stage II, 13% stage III, and 40% with metastatic disease at diagnosis. One third of the leiomyosarcomas and endometrial stromal sarcomas have advanced disease at diagnosis. Median survival of all patients was 26 months, 20 months for carcinosarcoma, 25 months for high grade endometrial stromal sarcoma, and a trend toward superior overall survival at 73 months for leiomyosarcoma. After surgery, 51% of patients mostly carcinosarcomas received carboplatin and paclitaxel as adjuvant chemotherapy and 66% of leiomyosarcomas received gemcitabine and docetaxel. However, the survival analysis showed no statistically significant benefit in disease progression free survival. On the other hand, 50% of patients were also treated with adjunctive pelvic external beam radiation and 21% received additional vaginal brachytherapy. Our results demonstrated a small but clear survival benefit after pelvic radiation therapy. Pelvic lymphadenectomy was performed in 55% of these patients and lymph node involvement was found in 30% of uterine sarcomas mostly carcinosarcomas. Survival analysis indicated that pelvic lymphadenectomy was associated with significant survival benefit. Conclusions: Size, stage, nodal involvement, and histology are independent prognostic factors. Complete cytoreduction followed by lymph node dissection, and radiation therapy offered a survival advantage than surgery alone. However, the role of adjuvant chemotherapy remains uncertain.


2018 ◽  
Vol 31 (Supplement_1) ◽  
pp. 85-85
Author(s):  
Kiyoto Shiga ◽  
Katsunori Katagiri ◽  
Daisuke Saito

Abstract Background Cervical esophageal cancer (CEC) is a relatively rare disease but the outcomes of the patients with CEC are often poor. Lymph node metastases in the neck sometimes play a crucial role to treat the patients. The aim of this study is to evaluate the lymph node metastases and neck dissection for the patients with CEC. Methods Retrospective review of the records of the patients. Five patients with CEC who underwent total pahryngo-laryngectomy plus cervical esophagectomy were enrolled in this study. We analyzed the places of lymph node metastases of the patients and the relationship of the patients’ outcome. Results Four of the patients underwent free jejunum flap reconstruction after total pahryngo-laryngectomy plus cervical esophagectomy and the other one underwent gastric tube plus free jejunum flap reconstruction after the pahryngo-laryngectomy plus total esophagectomy. All patients underwent bilateral neck dissection. One patient underwent chemoradiotherapy as an initial treatment and he had no lymph node metastasis by pathological examination. The other four patients had neck metastases to some extent. Three of them had bilateral lymph node metastases and the other had one metastatic lymph node. Especially one patient had left upper lateral neck metastasis and right Rouvier lymph node metastasis. Conclusion These results indicated that patients with CEC should undergo bilateral neck dissection and if possible, Rouvier lymph node should also be resected during radical surgery. Disclosure All authors have declared no conflicts of interest.


Author(s):  
Shinichi Aishima ◽  
Shinnosuke Fukushima ◽  
Yukihiko Nakayama ◽  
Katsuyuki Hanashima ◽  
Mariko Hashiguchi ◽  
...  

Ovarian carcinosarcoma (OCS) is a rare malignancy accounting for only 1‒4% of all ovarian cancers. A 44-year-old premenopausal woman presented at the Obstetrics and Gynecology Department of the University Hospital of Saga, with the chief complaint of sudden abdominal pain. Tumor markers present in her serum were cancer antigen (CA) 19-9 (103U/mL), and CA 125 (114U/mL). Transvaginal ultrasound examination showed a complex mass (74×71×67mm) with solid and cystic components in the left abdominal area. Abdominopelvic computed tomography images showed a polycystic mass with a long diameter of 94 mm in the left adnexal area. The patient underwent a laparotomy immediately after the appropriate evaluation of examinations, leading to total abdominal hysterectomy, bilateral salpingo-oophorectomy and partial omentectomy. Due to the emergency surgery, intraoperative histological diagnosis for ovarian tumor was not performed. The preoperative evaluation of radiological imaging revealed no evidence of lymph node swelling, therefore lymph node resection was omitted. The left ovarian tumor already showed a partial rupture. Pathological examination following surgery revealed tubular and solid growth of the epithelial component and fascicular growth of spindle-shaped mesenchymal cells. Immunohistochemistry identified the epithelial component as endometrioid carcinoma (EC) and the mesenchymal component as endometrial stromal sarcoma (ESS). Endometriotic tissue was attached to the malignant tumor. The patient was successfully treated with adjuvant chemotherapy (paclitaxel plus carboplatin) after surgery. The patient is still alive without recurrence at 9 months after surgery. Considering the rarity of OCS with EC and ESS, we present an overview of the literature and discuss several histological and clinical issues. The etiology and pathogenesis of such tumors require further investigation (words; 228).


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