Gopinath Chaitra, Shekar Suman, Acharya Madan, Pattan Vishwanath, Sundaresh Vishnu
Diabetes and Endocrinology, Kansas City University, Kansas City, USA.
Medical Center Primary Care, University of Kentucky Bowling Green Campus, Bowling Green, USA.
Cureus. 2022 Jun 23;14(6):e26234. doi: 10.7759/cureus.26234. eCollection 2022 Jun.
Pure androgen-secreting adrenocortical tumors (PASATs) are rare entities. Their clinical presentations include virilizing features that vary based on age and gender. The pathogenesis of this tumor is still unclear, with around 50% of such tumors being malignant. Imaging characteristics of the tumor on CT/MRI including size, heterogenicity, and contrast wash-out time are used to predict malignancy. Surgical excision is recommended for all functional adrenal tumors. In this report, we discuss a case of a 68-year-old postmenopausal female presenting with hyperandrogenism and was found to have a 7-cm, PASAT that raised suspicion for malignancy on CT scan, but was determined to be benign on surgical pathology.
纯分泌雄激素的肾上腺皮质肿瘤(PASATs)是罕见的实体瘤。它们的临床表现包括男性化特征,这些特征会因年龄和性别而有所不同。这种肿瘤的发病机制仍不清楚,约50%的此类肿瘤为恶性。CT/MRI上肿瘤的影像学特征,包括大小、异质性和对比剂洗脱时间,用于预测恶性程度。对于所有功能性肾上腺肿瘤,建议进行手术切除。在本报告中,我们讨论了一例68岁绝经后女性,表现为雄激素过多,CT扫描发现有一个7厘米的PASAT,该肿瘤在CT扫描上引起了对恶性肿瘤的怀疑,但手术病理确定为良性。