Case Report: Challenging diagnostic of an accessory spleen mimicking a retroperitoneal tumor: A case report and review of the literature [version 1; peer review: 1 approved with reservations]
Background: The accessory spleen is a congenital defect with an additional splenic tissue to the native spleen due to an incomplete fusion of splenic masses during the embryologic period. The preoperative diagnosis is usually mistaken for a retroperitoneal neoplasm. The aim of the present manuscript...
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Published in: | F1000 research Vol. 12; p. 491 |
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Abstract | Background: The accessory spleen is a congenital defect with an additional splenic tissue to the native spleen due to an incomplete fusion of splenic masses during the embryologic period. The preoperative diagnosis is usually mistaken for a retroperitoneal neoplasm. The aim of the present manuscript is to highlight the diagnostic difficulties of a retroperitoneal spleen.
Case presentation: A 41-year-old woman was admitted to the surgical department of Habib Thameur Hospital, Tunis, for an abdominal mass discovered by auto palpation associated with a left lower quadrant pain. The computed tomographic scan showed a heterogeneous and partially necrotic retroperitoneal mass located along the left primitive iliac vessels . Arterial supply to the mass arose from the aorta and the left iliac vessel. The spleen was normal. MRI examination showed a left retroperitoneal heterogeneous and necrotic mass, surrounding the iliac vessels extended from the aortic to the left iliac bifurcation, hyper vascularized at the arterial time with a peripheral capsule intensely enhanced, and there were two other lateroaortic vascularized masses. The patient had a laparotomy resection of the retroperitoneal mass. The result of the specimen examination was an accessory spleen. The postoperative outcome was uneventful.
Conclusion: An accessory spleen on the retroperitoneal position is extremely uncommon. Preoperative diagnosis is still challenging. The main misdiagnosis was neoplastic disease. |
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AbstractList | Background: The accessory spleen is a congenital defect with an additional splenic tissue to the native spleen due to an incomplete fusion of splenic masses during the embryologic period. The preoperative diagnosis is usually mistaken for a retroperitoneal neoplasm. The aim of the present manuscript is to highlight the diagnostic difficulties of a retroperitoneal spleen.
Case presentation: A 41-year-old woman was admitted to the surgical department of Habib Thameur Hospital, Tunis, for an abdominal mass discovered by auto palpation associated with a left lower quadrant pain. The computed tomographic scan showed a heterogeneous and partially necrotic retroperitoneal mass located along the left primitive iliac vessels . Arterial supply to the mass arose from the aorta and the left iliac vessel. The spleen was normal. MRI examination showed a left retroperitoneal heterogeneous and necrotic mass, surrounding the iliac vessels extended from the aortic to the left iliac bifurcation, hyper vascularized at the arterial time with a peripheral capsule intensely enhanced, and there were two other lateroaortic vascularized masses. The patient had a laparotomy resection of the retroperitoneal mass. The result of the specimen examination was an accessory spleen. The postoperative outcome was uneventful.
Conclusion: An accessory spleen on the retroperitoneal position is extremely uncommon. Preoperative diagnosis is still challenging. The main misdiagnosis was neoplastic disease. Background: The accessory spleen is a congenital defect with an additional splenic tissue to the native spleen due to an incomplete fusion of splenic masses during the embryologic period. The preoperative diagnosis is usually mistaken for a retroperitoneal neoplasm. The aim of the present manuscript is to highlight the diagnostic difficulties of a retroperitoneal spleen. Case presentation: A 41-year-old woman was admitted to the surgical department of Habib Thameur Hospital, Tunis, for an abdominal mass discovered by auto palpation associated with a left lower quadrant pain. The computed tomographic scan showed a heterogeneous and partially necrotic retroperitoneal mass located along the left primitive iliac vessels . Arterial supply to the mass arose from the aorta and the left iliac vessel. The spleen was normal. MRI examination showed a left retroperitoneal heterogeneous and necrotic mass, surrounding the iliac vessels extended from the aortic to the left iliac bifurcation, hyper vascularized at the arterial time with a peripheral capsule intensely enhanced, and there were two other lateroaortic vascularized masses. The patient had a laparotomy resection of the retroperitoneal mass. The result of the specimen examination was an accessory spleen. The postoperative outcome was uneventful. Conclusion: An accessory spleen on the retroperitoneal position is extremely uncommon. Preoperative diagnosis is still challenging. The main misdiagnosis was neoplastic disease. |
Author | Chamekhi, Chiraz Hadded, Dhafer Benzarti, Yazid Zouaghi, Alia Mesbahi, Meryam Zaafouri, Haithem Riahi, Wassim Miri, Rim Khanchel, Fatma Cherif, Mona Mleyhi, Sobhi Ghedira, Faker Souli, Aslam Ben Maamer, Aniss |
Author_xml | – sequence: 1 givenname: Alia orcidid: 0000-0003-4489-3384 surname: Zouaghi fullname: Zouaghi, Alia organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 2 givenname: Rim surname: Miri fullname: Miri, Rim organization: Cardio-vascular Surgery Department, La Rabta Hospital, Tunis, 1000, Tunisia – sequence: 3 givenname: Dhafer orcidid: 0000-0002-6732-6879 surname: Hadded fullname: Hadded, Dhafer organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 4 givenname: Meryam orcidid: 0000-0001-7035-7820 surname: Mesbahi fullname: Mesbahi, Meryam email: meryam.mesbahi@gmail.com organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 5 givenname: Haithem orcidid: 0000-0002-6355-1059 surname: Zaafouri fullname: Zaafouri, Haithem organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 6 givenname: Mona surname: Cherif fullname: Cherif, Mona organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 7 givenname: Wassim surname: Riahi fullname: Riahi, Wassim organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 8 givenname: Yazid surname: Benzarti fullname: Benzarti, Yazid organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 9 givenname: Sobhi surname: Mleyhi fullname: Mleyhi, Sobhi organization: Cardio-vascular Surgery Department, La Rabta Hospital, Tunis, 1000, Tunisia – sequence: 10 givenname: Faker surname: Ghedira fullname: Ghedira, Faker organization: Cardio-vascular Surgery Department, La Rabta Hospital, Tunis, 1000, Tunisia – sequence: 11 givenname: Aslam surname: Souli fullname: Souli, Aslam organization: Radiology Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 12 givenname: Chiraz orcidid: 0000-0003-3612-6978 surname: Chamekhi fullname: Chamekhi, Chiraz organization: Radiology Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 13 givenname: Fatma surname: Khanchel fullname: Khanchel, Fatma organization: Anatomic Pathology Department, Habib Thameur Hospital, Tunis, 1000, Tunisia – sequence: 14 givenname: Aniss surname: Ben Maamer fullname: Ben Maamer, Aniss organization: General Surgery Department, Habib Thameur Hospital, Tunis, 1000, Tunisia |
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Cites_doi | 10.1111/j.1442-2042.2008.02078.x 10.1016/j.ejrex.2010.07.003 10.1148/rg.314095132 10.1186/s12893-019-0510-z 10.1093/jscr/rjx195 10.1016/j.diii.2016.03.008 10.1159/000473248 10.1177/0300060519875898 10.1016/S0022-5347(17)42313-5 10.3892/ol.2015.3622 10.1016/j.eucr.2017.08.006 10.1259/0007-1285-42-504-939 10.1007/s12149-007-0122-z 10.1016/j.ijscr.2018.10.056 10.1016/j.jmig.2007.04.016 10.1016/S1015-9584(11)60019-5 10.7860/JCDR/2015/13229.6120 |
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Copyright | Copyright: © 2023 Zouaghi A et al. |
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Keywords | retroperitoneal spleen case report accessory spleen retroperitoneal neoplasm retroperitoneal mass |
Language | English |
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References | P Rajiah (ref1) juill 2011; 31 A Chhaidar (ref15) 2018; 53 H Amer (ref4) sept 2007; 14 R Porwal (ref7) 2015 Y Li (ref11) févr 2020; 48 M Kim (ref6) août 2008; 15 R Maharaj (ref8) 2016; 6 M Felice (ref12) janv 2018; 16 C Rosenthal (ref19) 1981; 7 W Lily (ref10) oct 2010; 76 E Bergeron (ref13) mai 2008; 22 M Ronot (ref9) sept 2016; 97 T Ch (ref14) 2013; 17 F Sbrana (ref16) 1 oct 2017; 2017 V Palumbo (ref3) déc 2019; 19 C Tjaden (ref17) janv 2011; 34 J Zhou (ref5) oct 2015; 10 A Kapoor (ref18) 2004; 66 W Rosenkranz (ref20) déc 1969; 42 D Bartkowski (ref2) janv 1988; 139 |
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Snippet | Background: The accessory spleen is a congenital defect with an additional splenic tissue to the native spleen due to an incomplete fusion of splenic masses... Background: The accessory spleen is a congenital defect with an additional splenic tissue to the native spleen due to an incomplete fusion of splenic masses... |
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Title | Case Report: Challenging diagnostic of an accessory spleen mimicking a retroperitoneal tumor: A case report and review of the literature [version 1; peer review: 1 approved with reservations] |
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