Literature DB >> 20703467

Size of the tumor and pheochromocytoma of the adrenal gland scaled score (PASS): can they predict malignancy?

Amit Agarwal1, Prateek K Mehrotra, Manoj Jain, Sushil K Gupta, Anjali Mishra, Gyan Chand, Gaurav Agarwal, A K Verma, S K Mishra, Uttam Singh.   

Abstract

BACKGROUND: Size can predict malignancy in adrenocortical tumors, but the same extrapolation for pheochromocytomas (PCC) is controversial. The goal of this study was to find a correlation between the tumor size and malignant potential of PCC and determine whether the "Pheochromocytoma of the adrenal gland scaled score" (PASS) proposed by Thompson can be applied to predict malignancy.
METHODS: A retrospective analysis of patients with PCC operated on from 1991 to 2007 revealed 98 PCC removed from 93 patients. Tumor size was available for 90 tumors. Six (6.4%) patients had proven malignancy. Five familial cases were excluded from the PASS analysis.
RESULTS: Of the benign cases, none developed recurrence or metastasis. There were 54 (60%) tumors > 6 cm and 36 (40%) tumors ≤ 6 cm. All 12 PASS parameters were individually present in higher frequency in the >6-cm group; but the difference was not statistically significant except cellular monotony (p = 0.02). Overall, a PASS ≤ 4 was found in 57 patients. Mean PASS was statistically significantly higher in the >6-cm group (4.4 vs. 3.3, p = 0.04). Of the sporadic benign cases, 21 (41%) patients with tumor size > 6 cm had a PASS of >4, and none of them developed metastasis. PASS ≤ 4 was found in 25 (81%) PCC in the ≤6-cm group, and none developed metastases. PASS ≥ 4 was found in six (19%) patients in the ≤6-cm group, and none developed metastases. 68 patients completed 5-year follow-up, and the remaining had a mean follow-up of 28.7 months. No correlation was found between tumor size and PASS > 4 and PASS ≤ 4 (7.8 cm vs. 7.1 cm; p = 0.23).
CONCLUSIONS: Presently there is not enough evidence to indict a large (>6 cm) PCC as malignant. Furthermore, PASS cannot be reliably applied to PCC for predicting malignancy.

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Year:  2010        PMID: 20703467     DOI: 10.1007/s00268-010-0744-5

Source DB:  PubMed          Journal:  World J Surg        ISSN: 0364-2313            Impact factor:   3.352


  17 in total

1.  Clinical experience over 48 years with pheochromocytoma.

Authors:  R E Goldstein; J A O'Neill; G W Holcomb; W M Morgan; W W Neblett; J A Oates; N Brown; J Nadeau; B Smith; D L Page; N N Abumrad; H W Scott
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2.  A comparison of open and laparoscopic approaches to adrenalectomy in patients with phaeochromocytoma.

Authors:  M J Davies; D P McGlade; S W Banting
Journal:  Anaesth Intensive Care       Date:  2004-04       Impact factor: 1.669

3.  Prognostic profile for patients with pheochromocytoma derived from clinical and pathological factors and DNA ploidy pattern.

Authors:  O Nativ; C S Grant; S G Sheps; J R O'Fallon; G M Farrow; J A van Heerden; M M Lieber
Journal:  J Surg Oncol       Date:  1992-08       Impact factor: 3.454

4.  Pheochromocytomas: can malignant potential be predicted?

Authors:  H John; W H Ziegler; D Hauri; P Jaeger
Journal:  Urology       Date:  1999-04       Impact factor: 2.649

5.  Pathologic features of prognostic significance for adrenocortical carcinoma after curative resection.

Authors:  L E Harrison; P B Gaudin; M F Brennan
Journal:  Arch Surg       Date:  1999-02

6.  Is preoperative iodine 123 meta-iodobenzylguanidine scintigraphy routinely necessary before initial adrenalectomy for pheochromocytoma?

Authors:  Judiann Miskulin; Barry L Shulkin; Gerard M Doherty; James C Sisson; Richard E Burney; Paul G Gauger
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7.  High incidence of malignant pheochromocytoma in a surgical unit. 26 cases out of 100 patients operated from 1971 to 1991.

Authors:  C Proye; M Vix; A Goropoulos; P Kerlo; M Lecomte-Houcke
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8.  Laparoscopic adrenalectomy for pheochromocytoma: comparison with conventional open adrenalectomy.

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9.  "The" pheochromocytoma: a benign, intra-adrenal, hypertensive, sporadic unilateral tumor. Does it exist?

Authors:  C A Proye; M Vix; S Jansson; L E Tisell; H Dralle; W Hiller
Journal:  World J Surg       Date:  1994 Jul-Aug       Impact factor: 3.352

10.  Long-term evaluation following resection of apparently benign pheochromocytoma(s)/paraganglioma(s).

Authors:  J A van Heerden; C F Roland; J A Carney; S G Sheps; C S Grant
Journal:  World J Surg       Date:  1990 May-Jun       Impact factor: 3.352

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  30 in total

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Review 2.  Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment.

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3.  Giant cystic pheochromocytoma.

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4.  Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma.

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Journal:  World J Surg       Date:  2016-03       Impact factor: 3.352

Review 5.  Diagnostic tests and biomarkers for pheochromocytoma and extra-adrenal paraganglioma: from routine laboratory methods to disease stratification.

Authors:  Graeme Eisenhofer; Arthur S Tischler; Ronald R de Krijger
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6.  A Case of Malignant Pheochromocytoma Presenting 7 Years After the Initial Surgery.

Authors:  Larsa Al-Omaishi; Jonathan Babin; Ralph L Corsetti
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Review 7.  Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours.

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8.  Surgical management of organ-contained unilateral pheochromocytoma: comparative outcomes of laparoscopic and conventional open surgical procedures in a large single-institution series.

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Review 9.  Malignant pheochromocytomas and paragangliomas: a diagnostic challenge.

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Journal:  Langenbecks Arch Surg       Date:  2011-11-29       Impact factor: 3.445

10.  Editorial comment.

Authors:  Brian Shuch; Karel Pacak; W Marston Linehan; Gennady Bratslavsky
Journal:  J Urol       Date:  2011-03-21       Impact factor: 7.450

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