具有胸腺样成分的纺锤形上皮肿瘤(SETTLE):诊断难题与独特的治疗意义;病例报告。

IF 2.4 3区 医学 Q2 PATHOLOGY
Prerna Chadha, Meenakshi Kamboj, Sunil Pasricha, Vikas Arora, Vishal Yadav, Manoj Gupta, Anurag Mehta
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引用次数: 0

摘要

具有胸腺样成分的纺锤形上皮瘤(SETTLE)是一种罕见的甲状腺恶性肿瘤,据信它是由甲状腺内胸腺组织引起的。它主要影响青壮年和儿童,表现为持续时间不等的甲状腺肿块,很少发生在成年人身上。它的总生存率较高,但有延迟转移的倾向。SETTLE是一种双相分叶状肿瘤,由纺锤形细胞组成,组织病理学检查可见腺体形成。尽管它具有典型的形态,但由于其罕见性以及与其他近似肿瘤(如癌、滑膜肉瘤和胸腺瘤)的形态重叠,在组织病理学上常被误诊。在此,我们报告了这样一个病例:一名中年女性出现颈部肿块。鉴于免疫组化中 CK、p40 和 p16 的共同表达,她被初步诊断为转移性分化不良鳞状细胞癌,原发可能为口咽癌。患者接受了改良颈部切除术。在我院复查时被诊断为 SETTLE,随访 1 年后仍未复发。严谨的组织病理学检查与明智的 IHC 标志物组合相结合,并结合临床放射学检查结果,构成了诊断的主要依据。迄今为止,文献中尚未记录或评估过弥漫性和强p16免疫表达,因此需要对其在这一罕见病例中的诊断作用进行探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spindle epithelial tumor with thymus-like elements (SETTLE): a diagnostic challenge with distinct therapeutic implication; case report.

Spindle epithelial tumor with thymus-like elements (SETTLE) is a rare malignant neoplasm of the thyroid gland which is believed to arise from intrathyroidal thymic tissue. It predominantly affects young adults and children presenting with a thyroid mass of variable duration and rarely occurs in adults. It has a high overall survival with a tendency for delayed metastasis. SETTLE is a biphasic lobulated tumor composed of spindle shaped cells along with glandular formations seen on histopathological examination. Despite its typical morphology it is commonly misdiagnosed on histopathology due to its rarity and overlapping morphology with other close mimics such as a carcinoma, synovial sarcoma and thymoma. Herein we report such a case occurring in a middle aged female presenting with a neck mass. She had an initial diagnosis of metastatic poorly differentiated squamous cell carcinoma possibly with an orophayngeal primary in view of co expression of CK, p40 and p16 on immunohistochemistry. The patient underwent surgical resection with modified neck dissection. On review at our hospital it was diagnosed as SETTLE and she remains disease free after a follow-up period of 1 year. Diligent histopathological examination espoused with a judicious panel of IHC markers in conjunction with clinicoradiological findings forms the mainstay of diagnosis. Diffuse and strong p16 immunoexpression has not been documented or evaluated in literature so far, and needs to be explored for its diagnostic utility in this rare entity.

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来源期刊
Diagnostic Pathology
Diagnostic Pathology 医学-病理学
CiteScore
4.60
自引率
0.00%
发文量
93
审稿时长
1 months
期刊介绍: Diagnostic Pathology is an open access, peer-reviewed, online journal that considers research in surgical and clinical pathology, immunology, and biology, with a special focus on cutting-edge approaches in diagnostic pathology and tissue-based therapy. The journal covers all aspects of surgical pathology, including classic diagnostic pathology, prognosis-related diagnosis (tumor stages, prognosis markers, such as MIB-percentage, hormone receptors, etc.), and therapy-related findings. The journal also focuses on the technological aspects of pathology, including molecular biology techniques, morphometry aspects (stereology, DNA analysis, syntactic structure analysis), communication aspects (telecommunication, virtual microscopy, virtual pathology institutions, etc.), and electronic education and quality assurance (for example interactive publication, on-line references with automated updating, etc.).
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