解开谜团:从泪腺中分化较差的原发性导管腺癌,具有侵袭性特征。案例报告和文献综述

Q3 Medicine
S. Malik, C. Ahluwalia, A. Aziz Khan
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引用次数: 0

摘要

摘要原发性泪腺导管腺癌(PDA)是一种罕见的起源于导管上皮细胞的侵袭性恶性肿瘤。其罕见性和多样化的临床表现构成了重大的诊断挑战,强调需要准确的诊断和适当的管理策略。该研究报告了一个有趣的病例,一名50岁男性患有巨大的原发性泪腺导管腺癌,最初因其非典型临床表现为“向下和向外”突出而误诊为脑膜孤立性纤维性肿瘤。该病例强调了组织病理学对实现正确诊断和指导管理决策的重要性。尽管采用积极的治疗方法,但原发性导管腺癌患者的预后仍然严峻,因为其具有侵袭性和复发转移的倾向。本病例研究强调,尽管存在异常的临床和放射表现,原发性导管腺癌的鉴别应予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Desvelando el enigma: gigantesco adenocarcinoma ductal primario de novo pobremente diferenciado de la glándula lagrimal con características agresivas. Informe de un caso y revisión de la literatura
Primary ductal adenocarcinoma (PDA) of the lacrimal gland is a rare and aggressive malignancy originating from ductal epithelial cells. Its rarity and diverse clinical presentations pose significant diagnostic challenges, emphasizing the need for accurate diagnosis and appropriate management strategies. The study presents an intriguing case of a 50-year-old man with a large de novo primary ductal adenocarcinoma of the lacrimal gland, initially misdiagnosed as a meningeal solitary fibrous tumor due to its atypical clinical presentation of «down and out» proptosis. The case underscores the importance of histopathology to achieve a correct diagnosis and guide management decisions. Despite aggressive treatment approaches, the prognosis of primary ductal adenocarcinoma patients remains grim due to its aggressive behavior and tendency for recurrence and metastasis. The present case study emphasizes that a differential of primary ductal adenocarcinoma should be considered despite the presence of anomalous clinical and radiological presentation.
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
109
审稿时长
78 days
期刊介绍: La revista Archivos de la Sociedad Española de Oftalmología, editada mensualmente por la propia Sociedad, tiene como objetivo publicar trabajos de investigación básica y clínica como artículos originales; casos clínicos, innovaciones técnicas y correlaciones clinicopatológicas en forma de comunicaciones cortas; editoriales; revisiones; cartas al editor; comentarios de libros; información de eventos; noticias personales y anuncios comerciales, así como trabajos de temas históricos y motivos inconográficos relacionados con la Oftalmología. El título abreviado es Arch Soc Esp Oftalmol, y debe ser utilizado en bibliografías, notas a pie de página y referencias bibliográficas.
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