Case of thyroid transcription factor-1-positive neuroendocrine carcinoma of the sphenoid sinus with bone metastases

Q4 Medicine
Kohei Inomata , Hidenori Yokoi , Masachika Fujiwara , Yasuaki Kimura , Yuma Matsumoto , Shoji Naito , Arisa Ohara , Naohiro Okano , Hiroshi Kamma , Koichiro Saito
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引用次数: 0

Abstract

Malignant tumors in the sinonasal region are rare and account for only 0.2–0.8% of all cancers and 1–3% of all head and neck carcinomas. Among the confirmed cases, the involvement of the sphenoid sinus is even rarer, accounting for only 2–3% of paranasal sinus tumors (Osguthorpe et al., 1994; Esposito et al., 2006; DeMonte et al., 2000).

Neuroendocrine carcinoma of the sphenoid sinus as a primary lesion is very rare; due to its rarity, no standard treatment has been established. Staining for thyroid transcription factor-1 (TTF-1) has been shown to be useful in the definite diagnosis of primary lung tumors. However, cases of TTF-1-positive small-cell neuroendocrine carcinomas that did not originate in the lung have been reported in the literature. Herein, we report the case of a patient with TTF-1-positive small-cell neuroendocrine carcinoma of the sphenoid sinus as the primary lesion and multiple bone metastases; to the best of our knowledge, this is the first report of such a case. A 52-year-old woman presented with complains of numbness and pain that extended from the left cheek to the lower lip and continued for 2 months. Head magnetic resonance imaging showed a neoplastic lesion in the left sphenoid sinus. We performed a transnasal endoscopic tumor biopsy; based on the results of pathological and immunohistochemical examination, a diagnosis of TTF-1-positive neuroendocrine carcinoma of the left sphenoid sinus with multiple bone metastases was made. Despite treatment with Cyberknife therapy and chemotherapy, the patient died approximately 12 months after treatment initiation. The findings of this case may help elucidate the significance of TTF-1-positive cells in small-cell neuroendocrine carcinomas.

蝶窦甲状腺转录因子-1阳性神经内分泌癌伴骨转移1例
鼻窦区的恶性肿瘤很少见,仅占所有癌症的0.2-0.8%,头颈癌的1-3%。在已证实的病例中,受累于蝶窦的病例更为罕见,仅占鼻窦肿瘤的2-3% (Osguthorpe et al., 1994;Esposito et al., 2006;DeMonte et al., 2000)。以蝶窦神经内分泌癌为原发性病变是非常罕见的;由于其罕见,没有标准的治疗方法。甲状腺转录因子-1 (TTF-1)染色已被证明对原发性肺肿瘤的明确诊断有用。然而,ttf -1阳性的小细胞神经内分泌癌并非起源于肺的病例在文献中有报道。在此,我们报告一例以蝶窦ttf -1阳性小细胞神经内分泌癌为原发病变并伴有多发性骨转移的病例;据我们所知,这是此类病例的首次报告。52岁女性,主诉从左脸颊到下唇持续2个月的麻木和疼痛。头部磁共振成像显示左侧蝶窦肿瘤病变。我们进行了经鼻内镜肿瘤活检;结合病理及免疫组化检查结果,诊断为左侧蝶窦ttf -1阳性神经内分泌癌伴多发骨转移。尽管接受了射波刀治疗和化疗,患者在治疗开始后大约12个月死亡。本病例的发现可能有助于阐明ttf -1阳性细胞在小细胞神经内分泌癌中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
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审稿时长
16 weeks
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