Literature DB >> 30037428

Adrenocortical oncocytic neoplasm: A systematic review.

John J Kanitra1, John C Hardaway2, Tahereh Soleimani3, Tracy J Koehler4, Michael K McLeod3, Srinivas Kavuturu5.   

Abstract

BACKGROUND: Adrenocortical oncocytic neoplasms are rare tumors, generally regarded as benign and hormonally nonfunctional. We performed a systematic review to update the literature on adrenocortical oncocytic neoplasms by reviewing patient and tumor characteristics, as well as management trends, because the literature is composed of predominately single-case reports.
METHODS: A systematic search was performed in PubMed, Embase, and Cochrane Library through June 2017. Malignant potential was determined by applying the Lin-Weiss-Bisceglia criteria to cases.
RESULTS: Included for analysis were 84 citations describing 140 adrenocortical oncocytic neoplasms, including our own case. These were diagnosed predominantly in females (66%), on the left side (64%), and were nonfunctional (66%). Average age at diagnosis was 44 years (2.5-77), and median tumor size was 80 mm (16-285). A total of 35% of adrenocortical oncocytic neoplasms were benign, 41% borderline, and 24% malignant. Male patients were more likely to have a malignant tumor compared with females (36% versus 18%, P = .035). The 5-year overall survival for benign adrenocortical oncocytic neoplasms was 100%, borderline 88%, and malignant 47%. Hormonal function did not discriminate malignant from benign lesions. Adrenocortical oncocytic neoplasms that stained positive for synaptophysin (50%, P < .001) and negative for vimentin (62%, P = .009) are more often benign.
CONCLUSION: We found that the majority of adrenocortical oncocytic neoplasms (65%) were either malignant or had malignant potential, contrary to the previous literature. The Lin-Weiss-Bisceglia criteria are useful in identifying those patients for whom closer surveillance is warranted, because their prognosis is dependent on the Lin-Weiss-Bisceglia diagnosis.
Copyright © 2018 Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 30037428     DOI: 10.1016/j.surg.2018.04.044

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  6 in total

Review 1.  Overview of the 2022 WHO Classification of Neuroendocrine Neoplasms.

Authors:  Guido Rindi; Ozgur Mete; Silvia Uccella; Olca Basturk; Stefano La Rosa; Lodewijk A A Brosens; Shereen Ezzat; Wouter W de Herder; David S Klimstra; Mauro Papotti; Sylvia L Asa
Journal:  Endocr Pathol       Date:  2022-03-16       Impact factor: 3.943

2.  Case Report: Adrenocortical Oncocytoma in a Patient with a Previous Contralateral Adrenalectomy for a Cortisol-Secreting Adenoma.

Authors:  Letizia Canu; Giuliano Perigli; Benedetta Badii; Raffaella Santi; Gabriella Nesi; Silvia Pradella; Mario Maggi; Alessandro Peri
Journal:  Front Surg       Date:  2022-05-19

3.  Oncocytic adrenocortical tumor with uncertain malignant potential in pediatric population: A case report and review of literature.

Authors:  Xiao-Chun Chen; Yun-Man Tang; Yu Mao; Dao-Rui Qin
Journal:  World J Clin Cases       Date:  2021-07-16       Impact factor: 1.337

4.  A case of adrenocortical oncocytic carcinoma arising in ectopic adrenal tissue: a multidisciplinary diagnostic challenge.

Authors:  Nikita Wadhwani; Daniel Mais; Dharam Kaushik; Mio Kitano
Journal:  Ecancermedicalscience       Date:  2020-11-05

5.  Laparoscopic resection of an adrenal oncocytic neoplasm: Report of a case and review of the literature.

Authors:  P St-Amour; R Djafarrian; T Zingg; S La Rosa; N Demartines; M Matter
Journal:  Int J Surg Case Rep       Date:  2020-09-29

Review 6.  Adrenocortical Carcinoma: Updates of Clinical and Pathological Features after Renewed World Health Organisation Classification and Pathology Staging.

Authors:  Alfred King-Yin Lam
Journal:  Biomedicines       Date:  2021-02-10
  6 in total

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