Zhou R
The Second People's Hospital of Yibin, Yibin, China.
Acta Endocrinol (Buchar). 2024 Jan-Mar;20(1):103-106. doi: 10.4183/aeb.2024.103. Epub 2024 Oct 3.
Parathyroid carcinomas (PC) are rare. Imaging and laboratory tests can suggest a diagnosis of PC, but pathological examination is ultimately required to confirm the diagnosis.
The clinicopathologic data, diagnosis, and treatment of a case of PC diagnosed in our hospital in 2022 are retrospectively summarized in this case report to improve the understanding, diagnosis, and differential diagnosis of this disease.
Case report.
Herein, we present the case of a 35-year-old man who presented with imaging and laboratory findings suggestive of a parathyroid neoplasm.
The patient underwent radical resection of the tumor, which was histopathologically diagnosed as PC.
In this case, the clinical manifestations of PC were insidious, and the histological features had to be differentiated from tumors, such as parathyroid adenoma, clear cell renal cell carcinoma, and medullary thyroid carcinoma; thus, its diagnosis was challenging.
甲状旁腺癌(PC)较为罕见。影像学和实验室检查可提示PC的诊断,但最终确诊仍需病理检查。
本病例报告回顾性总结了2022年我院诊断的1例PC的临床病理资料、诊断及治疗情况,以提高对该病的认识、诊断及鉴别诊断能力。
病例报告。
本文报告1例35岁男性患者,其影像学和实验室检查结果提示甲状旁腺肿瘤。
患者接受了肿瘤根治性切除术,术后病理诊断为PC。
本例中,PC的临床表现隐匿,其组织学特征必须与甲状旁腺腺瘤、透明细胞肾细胞癌和甲状腺髓样癌等肿瘤相鉴别,因此其诊断具有挑战性。