Department of Pathology, The University of Chicago, Chicago, IL, USA.
Department of Pathology and Laboratory Medicine, The University of Wisconsin, L5/185 - MC8550, 600 Highland Ave, Madison, WI, 53792, USA.
Head Neck Pathol. 2021 Sep;15(3):727-736. doi: 10.1007/s12105-020-01281-6. Epub 2021 Jan 4.
Parathyromatosis is displaced parathyroid tissue in the neck and mediastinum related to prior surgery. Parathyromatosis can be difficult to distinguish from atypical adenoma and parathyroid carcinoma. The aim of this study is to evaluate clinical and morphologic features that may differentiate parathyromatosis, atypical adenoma, and parathyroid carcinoma. Cases of parathyromatosis, atypical adenoma, and parathyroid carcinoma were identified. Index cases were reviewed by consensus for histologic features, including stromal, cytologic/architectural, and invasive features. Ki67 was performed on index cases and scored using the Adsay method. Clinical information was gathered from the electronic medical record. 4 parathyromatosis, 17 atypical adenoma, and 6 parathyroid carcinoma were included. Parathyroid carcinomas were more likely to display coarse chromatin with nucleoli (P = 0.04), infiltrative invasion (P < 0.01), and metastasis (P < 0.01). Only parathyromatosis showed circumscribed invasion. Infiltrative invasion was more common in cases with progression (P = 0.046) and metastasis (P < 0.001). Necrosis and perineural invasion were only present in cases with progression and were more frequent in cases with metastasis (P = 0.079 and P = 0.19, respectively). There were no differences in presence of a fibrous capsule, capsular invasion, intralesional fibrous bands, random endocrine atypia, solid growth, Ki67 index, gland size/weight, serum PTH/calcium levels, and locoregional recurrence rates. There is overlap in the histologic features in parathyromatosis, atypical adenoma, and parathyroid carcinoma. While perineural, vascular, and infiltrative soft tissue invasion should remain diagnostic of malignancy, other atypical features such as solid growth, coarse chromatin with nucleoli, and necrosis should raise concern for recurrence and/or metastasis, and can be present in parathyroid lesions with and without recurrence.
甲状旁腺瘤病是颈部和纵隔中与先前手术相关的异位甲状旁腺组织。甲状旁腺瘤病很难与不典型腺瘤和甲状旁腺癌区分。本研究旨在评估可能有助于区分甲状旁腺瘤病、不典型腺瘤和甲状旁腺癌的临床和形态学特征。鉴定出甲状旁腺瘤病、不典型腺瘤和甲状旁腺癌病例。通过共识对索引病例进行了组织学特征回顾,包括基质、细胞学/结构和浸润特征。对索引病例进行了 Ki67 检测,并采用 Adsay 方法进行评分。从电子病历中收集临床信息。纳入 4 例甲状旁腺瘤病、17 例不典型腺瘤和 6 例甲状旁腺癌。甲状旁腺癌更可能表现为粗染色质伴核仁(P = 0.04)、浸润性侵犯(P < 0.01)和转移(P < 0.01)。只有甲状旁腺瘤病显示局限性侵犯。进展病例和转移病例中更常见浸润性侵犯(P = 0.046 和 P < 0.001)。坏死和神经周围侵犯仅见于进展病例,且在转移病例中更为常见(P = 0.079 和 P = 0.19)。纤维囊、囊内侵犯、瘤内纤维带、随机内分泌异型性、实性生长、Ki67 指数、腺体大小/重量、血清 PTH/钙水平和局部区域复发率在存在差异方面没有差异。甲状旁腺瘤病、不典型腺瘤和甲状旁腺癌的组织学特征存在重叠。虽然神经周围、血管和浸润性软组织侵犯仍然是恶性肿瘤的诊断标准,但其他不典型特征,如实性生长、粗染色质伴核仁、坏死等,应引起对复发和/或转移的关注,并可能存在于有或无复发的甲状旁腺病变中。