Intraperitoneal Solitary Fibrous Tumor
Solitary fibrous tumors of the pelvis are rare. We report the case of a 32-years-old patient who presented with abdominopelvic mass. The imaging studies showed a right adnexal mass of more than 10 cm. Exploratory laparotomy revealed a 20 cm mass at the Douglas pouch which was adhered to the posterio...
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2014-01-01
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Series: | Case Reports in Obstetrics and Gynecology |
Online Access: | http://dx.doi.org/10.1155/2014/906510 |
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doaj-5f5d64f995334043ad7aca6ca62171cf2020-11-24T23:15:28ZengHindawi LimitedCase Reports in Obstetrics and Gynecology2090-66842090-66922014-01-01201410.1155/2014/906510906510Intraperitoneal Solitary Fibrous TumorYoussef Benabdejlil0Jaouad Kouach1Abdellah Babahabib2Moulay Elmehdi Elhassani3Issam Rharassi4Adil Boudhas5Hicham Bakkali6Mohammed Elmarjany7Driss Moussaoui8Mohamed Dehayni9Department of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, MoroccoDepartment of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, MoroccoDepartment of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, MoroccoDepartment of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, MoroccoDepartment of Pathological Anatomy, Military Training Hospital Med V, Rabat, MoroccoDepartment of Pathological Anatomy, Military Training Hospital Med V, Rabat, MoroccoFaculty of Medicine and Pharmacy, University Mohammed V Souissi, Rabat, MoroccoFaculty of Medicine and Pharmacy, University Mohammed V Souissi, Rabat, MoroccoDepartment of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, MoroccoDepartment of Gynecology-Obstetric, Military Training Hospital Med V, Rabat, MoroccoSolitary fibrous tumors of the pelvis are rare. We report the case of a 32-years-old patient who presented with abdominopelvic mass. The imaging studies showed a right adnexal mass of more than 10 cm. Exploratory laparotomy revealed a 20 cm mass at the Douglas pouch which was adhered to the posterior wall of the uterus. Complete resection of the mass was performed. Histological analysis showed a spindle cell undifferentiated tumor whose morphological and immunohistochemical profile are consistent with solitary fibrous tumor. It is important to know that although these tumors are rare, their evolution can be pejorative. Therefore, long-term followup should be recommended.http://dx.doi.org/10.1155/2014/906510 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Youssef Benabdejlil Jaouad Kouach Abdellah Babahabib Moulay Elmehdi Elhassani Issam Rharassi Adil Boudhas Hicham Bakkali Mohammed Elmarjany Driss Moussaoui Mohamed Dehayni |
spellingShingle |
Youssef Benabdejlil Jaouad Kouach Abdellah Babahabib Moulay Elmehdi Elhassani Issam Rharassi Adil Boudhas Hicham Bakkali Mohammed Elmarjany Driss Moussaoui Mohamed Dehayni Intraperitoneal Solitary Fibrous Tumor Case Reports in Obstetrics and Gynecology |
author_facet |
Youssef Benabdejlil Jaouad Kouach Abdellah Babahabib Moulay Elmehdi Elhassani Issam Rharassi Adil Boudhas Hicham Bakkali Mohammed Elmarjany Driss Moussaoui Mohamed Dehayni |
author_sort |
Youssef Benabdejlil |
title |
Intraperitoneal Solitary Fibrous Tumor |
title_short |
Intraperitoneal Solitary Fibrous Tumor |
title_full |
Intraperitoneal Solitary Fibrous Tumor |
title_fullStr |
Intraperitoneal Solitary Fibrous Tumor |
title_full_unstemmed |
Intraperitoneal Solitary Fibrous Tumor |
title_sort |
intraperitoneal solitary fibrous tumor |
publisher |
Hindawi Limited |
series |
Case Reports in Obstetrics and Gynecology |
issn |
2090-6684 2090-6692 |
publishDate |
2014-01-01 |
description |
Solitary fibrous tumors of the pelvis are rare. We report the case of a 32-years-old patient who presented with abdominopelvic mass. The imaging studies showed a right adnexal mass of more than 10 cm. Exploratory laparotomy revealed a 20 cm mass at the Douglas pouch which was adhered to the posterior wall of the uterus. Complete resection of the mass was performed. Histological analysis showed a spindle cell undifferentiated tumor whose morphological and immunohistochemical profile are consistent with solitary fibrous tumor. It is important to know that although these tumors are rare, their evolution can be pejorative. Therefore, long-term followup should be recommended. |
url |
http://dx.doi.org/10.1155/2014/906510 |
work_keys_str_mv |
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