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Báo cáo khoa học: Special problems encountering surgical management of large retroperitoneal schwannomas
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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Special problems encountering surgical management of large retroperitoneal schwannomas
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Báo cáo khoa học: "Special problems encountering surgical management of large retroperitoneal schwannomas"World Journal of Surgical Oncology BioMed Central Open AccessResearchSpecial problems encountering surgical management of largeretroperitoneal schwannomasTheodosios Theodosopoulos*1, Vaia K Stafyla1, Paraskevi Tsiantoula1,Anneza Yiallourou1, Athanasios Marinis1, Agathi Kondi-Pafitis2,Achilleas Chatziioannou3, Efstathios Boviatsis4 and Dionysios Voros1Address: 1Second Department of Surgery, Areteion Hospital, University of Athens, Greece, 2Department of Pathology, Areteion Hospital,University of Athens, Greece, 3Department of Radiology, Areteion Hospital, University of Athens, Greece and 4Department of Neurosurgery,Evangelismos General Hospital, Athens, GreeceEmail: Theodosios Theodosopoulos* - theodosios@vodafone.net.gr; Vaia K Stafyla - vstafyla@hotmail.com;Paraskevi Tsiantoula - vivi_tsiantoula@yahoo.gr; Anneza Yiallourou - annyiallo@yahoo.gr; Athanasios Marinis - sakisdoc@yahoo.com;Agathi Kondi-Pafitis - akondi@med.uoa.gr; Achilleas Chatziioannou - achatzi@med.uoa.gr; Efstathios Boviatsis - eboviatsis@gmail.com;Dionysios Voros - diovoros@med.uoa.gr* Corresponding authorPublished: 3 October 2008 Received: 16 April 2008 Accepted: 3 October 2008World Journal of Surgical Oncology 2008, 6:107 doi:10.1186/1477-7819-6-107This article is available from: http://www.wjso.com/content/6/1/107© 2008 Theodosopoulos et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Retroperitoneal schwannomas are rare, usually benign tumors that originate in the neural sheath and account for only a small percentage of retroperitoneal tumors. The aim of this clinical study is to present our experience in managing retroperitoneal schwannomas with a review of the current literature and to point out the surgical technical difficulties we faced, due to the tumors strange behavior that eroded the vertebra in two cases without causing malignant invasion. Methods: We reviewed the medical files of 69 patients treated in our department for retroperitoneal tumors from January 1991 until December 2006. Five patients had retroperitoneal schwannomas according to pathology report. Results: There were two male and three female patients, with a mean age of 56 years (range 44– 67 years). All patients were asymptomatic and none suffered from von Recklinghausen disease. Imaging workup included ultrasonography, computed tomography and magnetic resonance imaging. One patient, after having a non-diagnostic computed tomography fine needle aspiration (CT-FNA), underwent exploratory laparotomy and incisional biopsy that established the diagnosis of schwannoma. After complete excision of the tumors, postoperative course was uneventful in all patients. Tumors maximum diameter was 12.7 cm (range 7–20 cm). No recurrences were detected during the follow up period (6–75 months). Conclusion: Preoperative establishment of diagnosis is difficult in case of retroperitoneal schwannomas, however close relationship of retroperitoneal tumors with adjacent neural structures in imaging studies should raise a suspicion. Complete surgical resection is the treatment of choice. Histology and Immunohistochemistry confirms the diagnosis. Page 1 of 6 (page number not for citation purposes)World Journal of Surgical Oncology 2008, 6:107 http://www.wjso.com/content/6/1/107BackgroundNeural sheath tumors are a subclass of soft tissue neo-plasms that include both benign and malignant schwan-nomas and neurofibromas. Schwannomas are foundmost commonly in cranial and peripheral nerves andoccur rarely in the retroperitoneum, the last comprisingabout 3% of all schwannomas [1]. Schwannomas consti-tute approximately 4% of all retroperitoneal tumors [2-4].They are typically solitary, circumscribed and encapsu-lated lesions on gross appearance [5]. Histologically,schwannomas are distinguished by the presence of areasof high and low cellularity, called Antoni A and B tissue,respectively [6]. They are often found incidentally, orpresent with vague, non specific symptoms. Figure side of the 4th l× 12 cm retroperitoneal mass eroding the left shows a 13.5 umbar vertebrae CT scan1In this study, clinical, imaging and histological character- CT scan shows a 13.5 × 12 cm retroperitoneal massistics, bu ...
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Báo cáo khoa học: "Special problems encountering surgical management of large retroperitoneal schwannomas"World Journal of Surgical Oncology BioMed Central Open AccessResearchSpecial problems encountering surgical management of largeretroperitoneal schwannomasTheodosios Theodosopoulos*1, Vaia K Stafyla1, Paraskevi Tsiantoula1,Anneza Yiallourou1, Athanasios Marinis1, Agathi Kondi-Pafitis2,Achilleas Chatziioannou3, Efstathios Boviatsis4 and Dionysios Voros1Address: 1Second Department of Surgery, Areteion Hospital, University of Athens, Greece, 2Department of Pathology, Areteion Hospital,University of Athens, Greece, 3Department of Radiology, Areteion Hospital, University of Athens, Greece and 4Department of Neurosurgery,Evangelismos General Hospital, Athens, GreeceEmail: Theodosios Theodosopoulos* - theodosios@vodafone.net.gr; Vaia K Stafyla - vstafyla@hotmail.com;Paraskevi Tsiantoula - vivi_tsiantoula@yahoo.gr; Anneza Yiallourou - annyiallo@yahoo.gr; Athanasios Marinis - sakisdoc@yahoo.com;Agathi Kondi-Pafitis - akondi@med.uoa.gr; Achilleas Chatziioannou - achatzi@med.uoa.gr; Efstathios Boviatsis - eboviatsis@gmail.com;Dionysios Voros - diovoros@med.uoa.gr* Corresponding authorPublished: 3 October 2008 Received: 16 April 2008 Accepted: 3 October 2008World Journal of Surgical Oncology 2008, 6:107 doi:10.1186/1477-7819-6-107This article is available from: http://www.wjso.com/content/6/1/107© 2008 Theodosopoulos et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Retroperitoneal schwannomas are rare, usually benign tumors that originate in the neural sheath and account for only a small percentage of retroperitoneal tumors. The aim of this clinical study is to present our experience in managing retroperitoneal schwannomas with a review of the current literature and to point out the surgical technical difficulties we faced, due to the tumors strange behavior that eroded the vertebra in two cases without causing malignant invasion. Methods: We reviewed the medical files of 69 patients treated in our department for retroperitoneal tumors from January 1991 until December 2006. Five patients had retroperitoneal schwannomas according to pathology report. Results: There were two male and three female patients, with a mean age of 56 years (range 44– 67 years). All patients were asymptomatic and none suffered from von Recklinghausen disease. Imaging workup included ultrasonography, computed tomography and magnetic resonance imaging. One patient, after having a non-diagnostic computed tomography fine needle aspiration (CT-FNA), underwent exploratory laparotomy and incisional biopsy that established the diagnosis of schwannoma. After complete excision of the tumors, postoperative course was uneventful in all patients. Tumors maximum diameter was 12.7 cm (range 7–20 cm). No recurrences were detected during the follow up period (6–75 months). Conclusion: Preoperative establishment of diagnosis is difficult in case of retroperitoneal schwannomas, however close relationship of retroperitoneal tumors with adjacent neural structures in imaging studies should raise a suspicion. Complete surgical resection is the treatment of choice. Histology and Immunohistochemistry confirms the diagnosis. Page 1 of 6 (page number not for citation purposes)World Journal of Surgical Oncology 2008, 6:107 http://www.wjso.com/content/6/1/107BackgroundNeural sheath tumors are a subclass of soft tissue neo-plasms that include both benign and malignant schwan-nomas and neurofibromas. Schwannomas are foundmost commonly in cranial and peripheral nerves andoccur rarely in the retroperitoneum, the last comprisingabout 3% of all schwannomas [1]. Schwannomas consti-tute approximately 4% of all retroperitoneal tumors [2-4].They are typically solitary, circumscribed and encapsu-lated lesions on gross appearance [5]. Histologically,schwannomas are distinguished by the presence of areasof high and low cellularity, called Antoni A and B tissue,respectively [6]. They are often found incidentally, orpresent with vague, non specific symptoms. Figure side of the 4th l× 12 cm retroperitoneal mass eroding the left shows a 13.5 umbar vertebrae CT scan1In this study, clinical, imaging and histological character- CT scan shows a 13.5 × 12 cm retroperitoneal massistics, bu ...
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