Hughes J H, El-Mofty S, Sessions D, Liapis H
Department of Pathology, Washington University School of Medicine, Saint Louis, MO 63110, USA.
Pathol Res Pract. 1997;193(11-12):791-6; discussion 797-9. doi: 10.1016/S0344-0338(97)80059-3.
A case of primary intrathyroidal paraganglioma is reported, and the light microscopic and immunohistochemical findings are described. Primary paragangliomas of the thyroid region are extremely uncommon and are therefore often confused clinically and histopathologically with more common intrathyroidal mass lesions. The diagnostic difficulties are underscored by the present case, which was misdiagnosed twice, firstly as a medullary thyroid carcinoma and secondly as a follicular thyroid carcinoma. Immunohistochemistry may be very helpful in arriving at the correct diagnosis. The case was further complicated by a second neck mass contralateral to the original thyroid nodule, which was interpreted as consistent with metastasis. The second lesions was proved angiographically and histologically to be a carotid body paraganglioma.
本文报告了一例原发性甲状腺内副神经节瘤,并描述了其光镜及免疫组化结果。甲状腺区域的原发性副神经节瘤极为罕见,因此在临床和组织病理学上常与更常见的甲状腺内肿块病变相混淆。本病例凸显了诊断的困难,该病例曾被误诊两次,首先误诊为甲状腺髓样癌,其次误诊为甲状腺滤泡癌。免疫组化对做出正确诊断可能非常有帮助。该病例因在原甲状腺结节对侧出现第二个颈部肿块而进一步复杂化,该肿块被认为与转移相符。经血管造影和组织学证实,第二个病变为颈动脉体副神经节瘤。