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2018 | 21 |
Tytuł artykułu

Voluminous Pheochromocytoma suspected of malignancy: a difficult diagnosis and an uncertain prognosis. About a case

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Pheochromocytomas are rare tumors arising from the adrenal medulla. The diagnosis of malignancy remains a dogma between surgeon, pathologist and oncologist. We present a case of voluminous pheochromocytoma in a 53-year-old female patient, suspect of malignancy in the pathologic examination, while emphasizing the importance of the clinical and radiological long-term monitoring.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
21
Opis fizyczny
p.9-15,fig.,ref.
Twórcy
autor
  • Department of Surgery, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
autor
  • Department of Surgery, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
autor
  • Department of Surgery, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
autor
  • Department of Surgery, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
autor
  • Department of Surgery, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
autor
  • Department of Pathological Anatomy and Cytology, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
  • Department of Pathological Anatomy and Cytology, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
autor
  • Department of Pathological Anatomy and Cytology, Mohamed Tahar Maamouri Hospital, Nabeul, Tunisia
Bibliografia
  • [1] Scholz T, Eisenhofer G, Pacak K, Dralle H, Lehnert H. Clinical review: Current treatment of malignant pheochromocytoma. J Clin Endocrinol Metab. 2007; 92: 1217-25.
  • [2] Sèbe P, Rigaud J, Avancès C, Brunaud L, Caillard C, Camparoa P et al. CCAFU's contribution to the French National Cancer Institute's reference frame: Adrenal malignant tumors. Prog Urol. 2013; 23 Suppl 2: S167-74.
  • [3] Herbomez M, Rouaix N, Bauters C, Wémeau J-L. Biological diagnosis of pheochromocytomas and paragangliomas. Presse Med. 2009; 38(6): 927-34.
  • [4] Chrisoulidou A, Kaltsas G, Ilias I. The diagnosis and management of malignant pheochromocytoma and paraganglioma. Endocr Relat Cancer 2007; 14: 569–85.
  • [5] Jebbari A, Nassar I, Edderai M, Bouklata S, Hammani L, Imani F. Principles of analysis for adrenal masses: contribution of CT and MRI. Feuill de Radiol. 2008; 48: 309–15.
  • [6] Woo S, Suh CH, Kim SY, Cho JY, Kim SH. Pheochromocytoma as a frequent false-positive in adrenal washout CT: A systematic review and meta-analysis. Eur Radiol. 2018; 28(3): 1027-36.
  • [7] Huang S Q, Feng XL, Yong L. The MRI of extraadrenal pheochromocytoma in the abdominal cavity. Eur J Radiol. 2007; 62: 335–41.
  • [8] Kizu H, Takayama T, Tsushima H. Localization of metastases from malignant pheochromocytoma in patients undergoing 131I-MIBG therapy with manually fused 123I-MIBG SPECT and CT images. J Nucl Med Technol. 2008; 36(4): 186–8.
  • [9] Ilias I, Chen CC, Carrasquillo JA. Comparison of 6-18F-fluorodopamine PET with 123I-metaiodobenzylguanidine and 111in-pentetreotide scintigraphy in localization of non metastatic and metastatic pheochromocytoma. J Nucl Med. 2008; 49(10): 1613–19.
  • [10] Strong VE, Kennedy T, Al-Ahmadie H. Prognostic indicators of malignancy in adrenal pheochromocytomas: clinical, histopathologic and cell cycle/apoptosis gene expression analysis. J Surg. 2008; 143: 759–68.
  • [11] Patey M. Pheochromocytoma and the diagnosis of malignancy: recent data and the role of the pathologist. Ann Pathol. 2008 Nov; 28 Spec No 1(1): S42-4.
  • [12] Thompson LD. Pheochromocytoma of the Adrenal Gland Scaled Score (PASS) to separate benign from malignant neoplasmas: a clinicopathologic and immunophenotypic study of 100 cases. Am J Surg Pathol. 2002; 26: 551–66.
  • [13] Brauckhoff M, Gimm O, Dralle H. Preoperative and surgical therapy in sporadic and familial pheochromocytoma. Front Horm Res. 2004; 31: 121–44.
  • [14] Cheikhrouhou H, Khiari K, Chérif L, Hadj Ali I, Hèni M, Rajhi H et al. Malignant pheochromocytomas: about three cases. Ann Endocrinol. 2006; 67: 238–44.
  • [15] Takano A, Oriuchi N, Tsushima Y. Endo Detection of metastatic lesions from malignant pheochromocytoma and paraganglioma with diffusion-weighted magnetic resonance imaging: comparison with 18F-FDG positron emission tomography and 123I-MIBG scintigraphy. Ann Nucl Med. 2008; 22(5): 395–401.
  • [16] Soufi M, Mohsine R, El Malki H.O, Ifrine L, Belkouchi A. Malign adrenal pheochromocytoma: diagnosis dilemma and therapeutics procedures J Afr Cancer. 2010; 2: 275-81.
  • [17] Gao B, Meng F, Bian W. Development and validation of pheochromocytoma of the Adrenal Gland Scaled Score for predicting malignant pheochromocytomas. Urology 2006; 68: 282–286.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-06c1418a-35d1-4598-adb6-30b541dbeaf1
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