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Báo cáo khoa học: Adrenocortical oncocytic carcinoma with recurrent metastases: a case report and review of the literature
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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: Adrenocortical oncocytic carcinoma with recurrent metastases: a case report and review of the literature
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Báo cáo khoa học: "Adrenocortical oncocytic carcinoma with recurrent metastases: a case report and review of the literature"World Journal of Surgical Oncology BioMed Central Open AccessReviewAdrenocortical oncocytic carcinoma with recurrent metastases: acase report and review of the literaturePinelopi Argyriou*1, Charalambos Zisis2, Nektarios Alevizopoulos3,Emmanuel M Kefaloyannis2, Constantine Gennatas4 andConstantina D Petraki1Address: 1Department of Pathology, Evangelismos General Hospital, Ipsilantou Str., Athens, Greece, 2Department of Thoracic and VascularSurgery, Evangelismos General Hospital, Ipsilantou Str., Athens, Greece, 3Oncology Clinic, Evangelismos General Hospital, Ipsilantou Str., Athens,Greece and 4Oncology Clinic, Areteion Hospital, University of Athens, Vas. Sofias Av., Athens-GreeceEmail: Pinelopi Argyriou* - pa7ha7@yahoo.gr; Charalambos Zisis - chzisis@hol.gr; Nektarios Alevizopoulos - nalevizopoulos@gmail.com;Emmanuel M Kefaloyannis - mankef2004@yahoo.co.uk; Constantine Gennatas - gennatas@otenet.gr;Constantina D Petraki - nelniko@otenet.gr* Corresponding authorPublished: 17 December 2008 Received: 1 April 2008 Accepted: 17 December 2008World Journal of Surgical Oncology 2008, 6:134 doi:10.1186/1477-7819-6-134This article is available from: http://www.wjso.com/content/6/1/134© 2008 Argyriou 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: Adrenal cortex oncocytic carcinoma (AOC) represents an exceptional pathological entity, since only 22 cases have been documented in the literature so far. Case presentation: Our case concerns a 54-year-old man with past medical history of right adrenal excision with partial hepatectomy, due to an adrenocortical carcinoma. The patient was admitted in our hospital to undergo surgical resection of a left lung mass newly detected on chest Computed Tomography scan. The histological and immunohistochemical study revealed a metastatic AOC. Although the patient was given mitotane orally in adjuvant basis, he experienced relapse with multiple metastases in the thorax twice in the next year and was treated with consecutive resections. Two and a half years later, a right hip joint metastasis was found and concurrent chemoradiation was given. Finally, approximately five years post disease onset, the patient died due to massive metastatic disease. A thorough review of AOC and particularly all diagnostic difficulties are extensively stated. Conclusion: Histological classification of adrenocortical oncocytic tumours has been so far a matter of debate. There is no officially established histological scoring system regarding these rare neoplasms and therefore many diagnostic difficulties occur for pathologists. nantly or exclusively of this kind of cells are called onco-BackgroundHamperl introduced the term oncocyte in 1931 refer- cytic [2]. Such tumours have been described in thering to a cell with abundant, granular, eosinophilic cyto- overwhelming majority of organs: kidney, thyroid andplasm [1]. Electron microscopic studies revealed that this pituitary gland, salivary, adrenal, parathyroid and lac-granularity was due to mitochondria accumulation in the rimal glands, paraganglia, respiratory tract, paranasaloncocyte cytoplasm [2]. Neoplasms composed predomi- sinuses and pleura, liver, pancreatobiliary system, stom- Page 1 of 6 (page number not for citation purposes)World Journal of Surgical Oncology 2008, 6:134 http://www.wjso.com/content/6/1/134ach, colon and rectum, central nervous system, female lary growth pattern and focal necroses (Figure 2a, b). Aand male genital tracts, skin and soft tissues [2-15]. Adren- number of 4 mitotic figures/50 high power fields (HPFs)ocortical oncocytic neoplasms (AONs) represent unusual were documented. The proliferative index Ki-67 (MIB-1,lesions and three histological categories are included: 1:50, DAKO) was in a value range of 10–20% and p53oncocytoma (AO), oncocytic neoplasm of uncertain oncoprotein (DO-7, 1:20, DAKO) was weakly expressedmalignant potential (AONUMP) and oncocytic carci- in a few cells. Immunohistochemical examinationnoma (AOC) [3]. In our study, we add to the 22 cases revealed positivity for Vimentin (V9, 1:2000, DAKO),found in the literature a new AOC with peculiar clinical Melan-A (A103, 1:40, DAKO), Calretinin with a fried-egg-presentation [16-29]. ...
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Báo cáo khoa học: "Adrenocortical oncocytic carcinoma with recurrent metastases: a case report and review of the literature"World Journal of Surgical Oncology BioMed Central Open AccessReviewAdrenocortical oncocytic carcinoma with recurrent metastases: acase report and review of the literaturePinelopi Argyriou*1, Charalambos Zisis2, Nektarios Alevizopoulos3,Emmanuel M Kefaloyannis2, Constantine Gennatas4 andConstantina D Petraki1Address: 1Department of Pathology, Evangelismos General Hospital, Ipsilantou Str., Athens, Greece, 2Department of Thoracic and VascularSurgery, Evangelismos General Hospital, Ipsilantou Str., Athens, Greece, 3Oncology Clinic, Evangelismos General Hospital, Ipsilantou Str., Athens,Greece and 4Oncology Clinic, Areteion Hospital, University of Athens, Vas. Sofias Av., Athens-GreeceEmail: Pinelopi Argyriou* - pa7ha7@yahoo.gr; Charalambos Zisis - chzisis@hol.gr; Nektarios Alevizopoulos - nalevizopoulos@gmail.com;Emmanuel M Kefaloyannis - mankef2004@yahoo.co.uk; Constantine Gennatas - gennatas@otenet.gr;Constantina D Petraki - nelniko@otenet.gr* Corresponding authorPublished: 17 December 2008 Received: 1 April 2008 Accepted: 17 December 2008World Journal of Surgical Oncology 2008, 6:134 doi:10.1186/1477-7819-6-134This article is available from: http://www.wjso.com/content/6/1/134© 2008 Argyriou 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: Adrenal cortex oncocytic carcinoma (AOC) represents an exceptional pathological entity, since only 22 cases have been documented in the literature so far. Case presentation: Our case concerns a 54-year-old man with past medical history of right adrenal excision with partial hepatectomy, due to an adrenocortical carcinoma. The patient was admitted in our hospital to undergo surgical resection of a left lung mass newly detected on chest Computed Tomography scan. The histological and immunohistochemical study revealed a metastatic AOC. Although the patient was given mitotane orally in adjuvant basis, he experienced relapse with multiple metastases in the thorax twice in the next year and was treated with consecutive resections. Two and a half years later, a right hip joint metastasis was found and concurrent chemoradiation was given. Finally, approximately five years post disease onset, the patient died due to massive metastatic disease. A thorough review of AOC and particularly all diagnostic difficulties are extensively stated. Conclusion: Histological classification of adrenocortical oncocytic tumours has been so far a matter of debate. There is no officially established histological scoring system regarding these rare neoplasms and therefore many diagnostic difficulties occur for pathologists. nantly or exclusively of this kind of cells are called onco-BackgroundHamperl introduced the term oncocyte in 1931 refer- cytic [2]. Such tumours have been described in thering to a cell with abundant, granular, eosinophilic cyto- overwhelming majority of organs: kidney, thyroid andplasm [1]. Electron microscopic studies revealed that this pituitary gland, salivary, adrenal, parathyroid and lac-granularity was due to mitochondria accumulation in the rimal glands, paraganglia, respiratory tract, paranasaloncocyte cytoplasm [2]. Neoplasms composed predomi- sinuses and pleura, liver, pancreatobiliary system, stom- Page 1 of 6 (page number not for citation purposes)World Journal of Surgical Oncology 2008, 6:134 http://www.wjso.com/content/6/1/134ach, colon and rectum, central nervous system, female lary growth pattern and focal necroses (Figure 2a, b). Aand male genital tracts, skin and soft tissues [2-15]. Adren- number of 4 mitotic figures/50 high power fields (HPFs)ocortical oncocytic neoplasms (AONs) represent unusual were documented. The proliferative index Ki-67 (MIB-1,lesions and three histological categories are included: 1:50, DAKO) was in a value range of 10–20% and p53oncocytoma (AO), oncocytic neoplasm of uncertain oncoprotein (DO-7, 1:20, DAKO) was weakly expressedmalignant potential (AONUMP) and oncocytic carci- in a few cells. Immunohistochemical examinationnoma (AOC) [3]. In our study, we add to the 22 cases revealed positivity for Vimentin (V9, 1:2000, DAKO),found in the literature a new AOC with peculiar clinical Melan-A (A103, 1:40, DAKO), Calretinin with a fried-egg-presentation [16-29]. ...
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