罕见的高级别非肠鼻窦腺癌1例

Vanessa Gehrke, B. Beraldin, J. L. Lubianca Neto, M. Barra, Jéssica De Castro Viga, Marina Zottis De Deus Vieira, Iazmim Samih Hamed Moh´D Houdali, Marcelo Assis Moro da Rocha Filho
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摘要

鼻窦区常与恶性肿瘤相关,但腺癌极为罕见,尤其是非肠型。一种疾病的症状通常是非特异性的,在疾病发展到晚期之前很难做出诊断。放射学研究对于确定疾病的分期和计划手术是必不可少的。鼻内手术入路近年来越来越受欢迎。这个病例报告描述了一个49岁男性的病例,他患有左鼻塞,头痛,复发性鼻出血,低视力和突出。磁共振图像显示一个对比度增强的大块病变,占据了左侧小窦腔,一直到脊柱的水平。患者接受了内窥镜手术,采用向心技术,在肿瘤完全切除的同时,眼眶内侧壁和颅骨前基底得以保留。经复查病理报告,肿瘤被确定为高级别非肠腺癌。这种类型的肿瘤在男性中更常见,可以影响从青少年到老年人的任何人。鼻塞是最常见的症状,但肿胀和面部畸形也可能存在。该肿瘤以实性形态为特征,是一种具有侵袭性的侵袭性癌症。多形性程度为中度至重度,有丝分裂指数高,不典型有丝分裂和坏死。免疫组化表现为CK7阳性,CK20和CDX-2阴性。这种诊断带来了许多挑战。为了证实这些发现,免疫组织化学研究和组织学检查是必不可少的。疾病的准确分类对于确定其预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of High-Grade Non-intestinal Sinonasal Adenocarcinoma
The sinonasal region is frequently associated with malignancies, but adenocarcinomas are extremely rare, especially the non-intestinal type. The symptoms of a disease are usually non-specific, making a diagnosis difficult until the disease has reached a late stage. Radiographic studies are essential for determining the stage of the disease and planning the surgical procedure. The endonasal surgical approach has gained popu-larity in recent years. This case report describes the case of a 49-year-old male who suffered from left nasal obstruction, headaches, recurrent epistaxis, low visual acuity, and proptosis. A magnetic resonance image revealed a contrast-enhancing bulky lesion that occupied the left sinona sal cavity up to the level of the choana. The patient was subjected to an endoscopic procedure employing a centripetal technique, which allowed the medial wall of the orbit and the anterior base of the skull to be preserved while the tumor was completely removed. Upon review of the pathology report, the tumor was identified as a high grade non-intestinal adenocarcinoma. Tumors of this type are more common in men and can affect anyone from teenagers to older adults. A nasal obstruction is the most common symptom, but swelling and facial deformity may also be present. This tumor is characterized by a solid pattern and is an invasive cancer that has an aggressive nature. The level of pleomorphism is moderate to severe, with a high mitotic index and atypical mitoses as well as necrosis. There is CK7 positivity in the immunohistochemistry pattern, while CK20 and CDX-2 are negative. The diagnosis poses a number of challenges. An immunohistochemical study and a histological examination are essential in order to confirm these findings. An accurate classification of the disease is critical for determining its prognosis.
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