» Articles » PMID: 12459628

Weiss System Revisited: a Clinicopathologic and Immunohistochemical Study of 49 Adrenocortical Tumors

Overview
Date 2002 Dec 3
PMID 12459628
Citations 109
Authors
Affiliations
Soon will be listed here.
Abstract

The definitive diagnostic criteria for malignant adrenocortical tumors are distant metastasis and/or local invasion. The Weiss histopathologic system is the most commonly used method for assessing malignancy because of its simplicity and reliability. Unfortunately, its application remains subjective. This current retrospective study evaluated the Weiss system and assessed the value of MIB-1 labeling in the diagnosis of adrenocortical malignancy. Twenty-four malignant tumors with distant metastasis, gross local invasion, or recurrence were selected and matched on their functioning status to 25 benign tumors. Two independent observers delineated the Weiss criteria. An MIB-1 labeling index was determined. Presence of three or more Weiss microscopic criteria was related to malignancy (specificity 96%, sensitivity 100%), thus confirming the value of the Weiss system. Interobserver agreement for the Weiss system (total score) was excellent (r = 0.94). The lack of reliability for some Weiss criteria led us to propose a statistically modified system, based on the most reliable criteria (2.mitotic rate x 2.cytoplasm x abnormal mitoses x necrosis x capsular invasion) with a significant correlation with the Weiss system (r = 0.98). The MIB-1 labeling index was significantly higher in malignant tumors (p <0.0001). MIB1 could also help to differentiate malignant from benign adrenocortical tumors.

Citing Articles

The differential diagnosis of adrenocortical tumors: systematic review of Ki-67 and IGF2 and meta-analysis of Ki-67.

Oliveira S, Machado M, Sousa D, Pereira S, Pignatelli D Rev Endocr Metab Disord. 2025; .

PMID: 39890749 DOI: 10.1007/s11154-025-09945-w.


MAPK1IP1L::TFE3-rearranged renal cell carcinoma: a novel fusion adding to the differential diagnosis of oncocytic renal neoplasms.

Cheng A, Wu D, Friedman L, Chan E, Williamson S, Galea L Virchows Arch. 2025; .

PMID: 39862330 DOI: 10.1007/s00428-025-04031-7.


High Diagnostic Accuracy of Arterial Phase CT in Differentiating Pheochromocytoma in Good/Poor Washout Adrenal Masses.

Phadte A, Krishnappa B, Memon S, Patil V, Lila A, Badhe P J Endocr Soc. 2024; 9(1):bvae199.

PMID: 39606180 PMC: 11590661. DOI: 10.1210/jendso/bvae199.


Role of radiologists in the diagnosis and management of adrenal disorders.

Oguro S, Tannai H, Ota H, Seiji K, Kamada H, Toyama Y Endocr J. 2024; 72(2):131-148.

PMID: 39384399 PMC: 11850109. DOI: 10.1507/endocrj.EJ24-0156.


Pediatric Adrenocortical Carcinoma: The Nuts and Bolts of Diagnosis and Treatment and Avenues for Future Discovery.

ONeill A, Ribeiro R, Pinto E, Clay M, Zambetti G, Orr B Cancer Manag Res. 2024; 16:1141-1153.

PMID: 39263332 PMC: 11389717. DOI: 10.2147/CMAR.S348725.