pelvic peritonectomy
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2020 ◽  
pp. 030089162097769
Author(s):  
Pamela Milito ◽  
Luigi Battaglia ◽  
Maurizio Cosimelli ◽  
Maria Antista ◽  
Marcello Guaglio ◽  
...  

Introduction: Surgical management of patients with multiple metastases from mucinous rectal carcinoma is feasible. Case description: We present a case of a 66-year-old woman with a late onset of peritoneal and coccygeal metastasis from a mucinous rectal carcinoma treated with cytoreductive surgery. After 30 months from rectal resection, the patient underwent exploratory laparotomy with resection of all tumor localizations by means of pelvic peritonectomy, complete supracolic omentectomy, jejuneal resection, appendectomy, and excision of the mobile part of the coccyx. Conclusion: This report aims to point out the atypical late-onset recurrence presentation and management of a mucinous carcinoma of the rectum.


2020 ◽  
Vol 5 (3) ◽  
Author(s):  
Antonio Macrì ◽  
Giorgio Badessi ◽  
Carmelo Mazzeo ◽  
Marica Galati ◽  
Eugenio Cucinotta ◽  
...  

AbstractObjectivesPelvic peritonectomy can induce anorectal and urogenital dysfunctions. To reduce this type of complications during the procedure, we propose to use intraoperative neuromonitoring (IONM).ContentStimulation with a bipolar probe allows the identification of the obturator and ilioinguinal and pudendal nerves. At the end of the cytoreductive surgery, the motor and somatosensory evoked potentials must be evaluated to confirm the preservation of pelvic innervation.SummaryThe use of IONM during pelvic peritonectomy is technically feasible, and it can help to preserve pelvic nerves.OutlookObviously, its definitive value remains to be elucidated.


2020 ◽  
Vol 24 (10) ◽  
pp. 1083-1088
Author(s):  
A. Arjona-Sánchez ◽  
D. Cortés-Guiral ◽  
M. Duran-Martínez ◽  
P. Villarejo-Campos ◽  
J. M. Sánchez-Hidalgo ◽  
...  

Medicina ◽  
2020 ◽  
Vol 56 (4) ◽  
pp. 152
Author(s):  
Nicolae Bacalbasa ◽  
Irina Cecilia Balescu ◽  
Camelia Diaconu ◽  
Simona Dima ◽  
Laura Iliescu ◽  
...  

Background/Aim: Synchronous gynecological malignancies are rarely encountered, and most often these cases are represented by synchronous ovarian and endometrial cancer. The aim of this paper is to present the case of a 53-year-old patient who was diagnosed with synchronous cervical and ovarian cancer. Case presentation: The patient had been initially investigated for vaginal bleeding and was submitted to a biopsy confirming the presence of a cervical adenocarcinoma. Once the diagnostic of malignancy was confirmed, the patient was submitted to a computed tomography which revealed the presence of large abdominal tumoral nodules of peritoneal carcinomatosis and was submitted to palliative chemotherapy with poor response. Eighteen months later she developed intestinal obstruction and was submitted to surgery. At that moment, synchronous ovarian and cervical tumors were diagnosed. Total radical hysterectomy with bilateral adnexectomy, pelvic and para-aortic lymph node dissection, omentectomy, and pelvic peritonectomy was performed; in the meantime, the histopathological studies confirmed the presence of two synchronous malignancies. Conclusion: Although synchronous lesions are rarely encountered, this eventuality should not be omitted. In such cases, surgery should be taken in consideration and the intent of radicality should regard both lesions.


2020 ◽  
Vol 222 (3) ◽  
pp. S838-S839
Author(s):  
M. Misal ◽  
R. Delara ◽  
M. Wasson
Keyword(s):  

Author(s):  
Ahmed Atef ◽  
Khaled Gaballa ◽  
Mohammad Zuhdy ◽  
Khalid Atallah ◽  
Wagdi Elkashef ◽  
...  

Abstract Background Desmoplastic small-round-cell tumor (DSRCT) is an extremely rare and highly aggressive malignancy. It is of yet unclear origin, but it is assumed to be of a mesothelial origin based on its tendency for widespread metastasis in serosal linings. Case presentation In this report, we describe a young female who presented with bilateral ovarian masses that mimicked the classic clinical picture of ovarian cancer. The patient had a cytoreductive surgery done in the form of total abdominal hysterectomy, bilateral salpingo-oophorectomy, omentectomy, pelvic peritonectomy, low para-aortic and bilateral iliac lymphadenectomy. Postoperative course was smooth with no adverse events. The final pathology report revealed desmoplastic small-round-cell tumor. Afterwards, the patient was referred to medical oncologist to receive her adjuvant therapy. Conclusions DSRCT is still an unknown disease to us given the limited number of cases and poor survival. Given the lack of clear guidelines, treatment is offered based on the best available evidence and the collaborative effort of a multi-disciplinary team.


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