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甲状腺乳头状癌转移性鞋钉样变体:细胞块制备中的诊断挑战。

Metastatic hobnail variant of papillary thyroid carcinoma: A diagnostic challenge in cell block preparation.

作者信息

Mohapatra Debahuti, Naik Sujata, Das Prateek, Agrawala Sunil

机构信息

Department of Pathology, IMS and SUM Hospital, Bhubaneswar, Odisha, India.

Department of Oncosurgery, IMS and SUM Hospital, Bhubaneswar, Odisha, India.

出版信息

Indian J Pathol Microbiol. 2021 Apr-Jun;64(2):358-361. doi: 10.4103/IJPM.IJPM_381_20.

Abstract

Hobnail variant of papillary thyroid carcinoma (HV-PTC) is an unusual entity recently included in WHO classification of endocrine tumors (2017) and proposed as an aggressive variant of PTC. Compared to patients of classical counterparts, HV-PTC frequently has extrathyroidal extension, exhibits nodal or distant metastasis, and responds poorly to radioiodine treatment, leading to increased mortality. We hereby describe the cytohistological and immunohistochemical features of a metastatic HV-PTC in 55-year-old male, previously diagnosed as poorly differentiated papillary thyroid carcinoma in thyroidectomy specimen. Five years after total thyroidectomy with radical neck dissection the patient presented with gross pleural effusion showing multiple lung parenchymal and pleural based lesions with complete collapse of lung on computed tomography scan. The conventional cytology of pleural fluid showed dyscohesive cells arranged in micropapillary form gave the suggestion of metastatic papillary carcinoma. But the cell block preparation highlighted >30% hobnail cells arranged in micropapillary pattern showing increased atypical mitosis and occasional pseudoinclusions. Supplemented with immunohistochemistry (CK19, TTF-1, and p53), final diagnosis HV-PTC was made.

摘要

甲状腺乳头状癌的鞋钉样变体(HV-PTC)是一种不常见的实体,最近被纳入世界卫生组织内分泌肿瘤分类(2017年),并被提议作为PTC的侵袭性变体。与经典类型的患者相比,HV-PTC经常有甲状腺外浸润,表现为淋巴结或远处转移,对放射性碘治疗反应不佳,导致死亡率增加。我们在此描述了一名55岁男性转移性HV-PTC的细胞组织学和免疫组化特征,该患者在甲状腺切除标本中先前被诊断为低分化乳头状甲状腺癌。全甲状腺切除加根治性颈清扫术后五年,患者出现大量胸腔积液,计算机断层扫描显示肺部实质和胸膜有多处病变,肺完全萎陷。胸腔积液的传统细胞学检查显示,细胞排列成微乳头形式,提示转移性乳头状癌。但细胞块制备显示,超过30%的鞋钉样细胞排列成微乳头模式,显示非典型有丝分裂增加,偶尔有假包涵体。结合免疫组化(CK19、TTF-1和p53),最终诊断为HV-PTC。

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