[Sarcomatoid variant of adrenocortical carcinoma].

Authors: Silvina Fili, Daniel Moncet, Jorge A. Zoppi
Cited by: 0

Abstract

Adrenocortical carcinoma (ACC) is a rare malignancy with poor prognosis and limited response to current therapies. The sarcomatoid subtype represents the rarest and most aggressive form of ACC, with very few cases reported in the literature. We present the case of a 62-year-old male with a history of an untreated left adrenal incidentaloma, who was diagnosed four years later with advanced-stage sarcomatoid ACC. Despite surgical and oncologic treatment, the disease progressed rapidly with systemic involvement and limited survival. The histopathological diagnosis is particularly challenging, as this subtype is characterized by the coexistence of epithelial and fusocelular/pleomorphic components with sarcomatoid differentiation, which may hinder its distinction from other primary or metastatic neoplasms. This case underscores the importance of appropriate initial evaluation of adrenal incidentalomas and highlights the highly malignant behavior of this rare variant, emphasizing the need for early diagnosis and timely intervention.

Fields of Study & Subjects

Adrenal and Paraganglionic Tumors Sarcoma Diagnosis and Treatment Cardiac tumors and thrombi

Publication details

Journal / source
PubMed
Volume
86
Issue
1
Pages
229–233
Publication date
1 January 2026
Language
ES