2008
DOI: 10.1016/j.urolonc.2007.02.008
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Metastatic adrenocortical oncocytoma: A case report

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Cited by 30 publications
(26 citation statements)
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“…In such cases, the lesion has been designated by some authors as an adrenocortical oncocytoma [4,5,9,11], analogous to the oncocytoma that is recognised in the kidney and salivary, thyroid and parathyroid glands [7]. However, oncocytic adrenocortical neoplasms have also presented in some cases as carcinomas with a malignant clinical course; for example, demonstrating invasion of the inferior vena cava [8,[12][13][14], local recurrence following resection [15,16] and bone, liver and lung metastases [15], with death as a reported outcome [17]. Thus, the major challenge in the management of these neoplasms is to distinguish benign from malignant lesions.…”
Section: Discussionmentioning
confidence: 99%
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“…In such cases, the lesion has been designated by some authors as an adrenocortical oncocytoma [4,5,9,11], analogous to the oncocytoma that is recognised in the kidney and salivary, thyroid and parathyroid glands [7]. However, oncocytic adrenocortical neoplasms have also presented in some cases as carcinomas with a malignant clinical course; for example, demonstrating invasion of the inferior vena cava [8,[12][13][14], local recurrence following resection [15,16] and bone, liver and lung metastases [15], with death as a reported outcome [17]. Thus, the major challenge in the management of these neoplasms is to distinguish benign from malignant lesions.…”
Section: Discussionmentioning
confidence: 99%
“…Yet, the entity remains incompletely understood, with no single clinical, histological or immunochemical feature able to predict the clinical course of an individual lesion. To assist in their categorisation, Bisceglia et al [17] proposed a classification system that divided oncocytic adrenocortical neoplasms into three broad groups on the basis of histological features with different prognostic implications; however, given the small number of lesions reported, as well as the short clinical follow-up available for most lesions, this classification system is considered controversial [15] and caution is still warranted when applying histological criteria to individual lesions [17]. Indeed, some reported cases in the literature have demonstrated a more aggressive clinical course than would be predicted using this classification system [8,12,13,17].…”
Section: Discussionmentioning
confidence: 99%
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“…Depuis, une cinquantaine de cas ont été signalés de façon sporadique [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18] . La plus grande série a été décrite par Bisceglia 1 et comprenait 10 patients.…”
Section: Discussionunclassified
“…Oncocytomas have rarely been reported in a number of distinct anatomical locations including the kidney, lung, breast, ovary, liver, gut, prostate gland and various sites in the head and neck including the pituitary, thyroid and salivary glands [2,3]. When present in the retroperitoneum, such lesions arise from either the kidney or the adrenal gland [4].…”
mentioning
confidence: 99%