唐氏综合征患者无症状巨大AB型胸腺瘤1例报告。

Elisa Sicolo, Vittorio Aprile, Tommaso Ferrarello, Diana Bacchin, Maria Giovanna Mastromarino, Greta Alì, Marcello Carlo Ambrogi, Marco Lucchi, Stylianos Korasidis
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引用次数: 0

摘要

背景:纵隔肿块的管理对所有处理它的医生来说都是一个真正的挑战。纵隔,事实上,包含不同的重要结构,往往涉及到日益严重的肿瘤生长。因此,根据所涉及的结构,高达60%的纵隔肿块患者有症状。不同的肿瘤可能主要来自所有纵隔器官,而胸腺上皮肿瘤和淋巴瘤占90%以上的纵隔肿瘤。病例描述:我们报告的第一个病例描述了一个巨大的无症状纵隔肿块在一个43岁的男性患唐氏综合症(DS),原来是一个胸腺瘤,治疗完全和成功的根治性手术。尽管没有任何症状,但巨大胸腺瘤浸润膈膜、心包、左肺上叶及左膈神经,导致心脏和大血管受压。结论:迄今为止,这是第一次对退行性椎体变性患者胸腺恶性肿瘤的描述,通常以低发病率的实体瘤为特征,除了生殖细胞肿瘤。由于患者的临床状况和肿瘤特征,手术一直极具挑战性;然而,肿瘤根治性标准完全满足。手术四年后,患者仍然活着,没有疾病,这凸显了根治性手术的重要性。
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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An asymptomatic giant AB thymoma in a patient with Down syndrome: a case report.

Background: Mediastinal mass management may represent a real challenge for all the physicians who deal with it. Mediastinum, in fact, contains different vital structures which are often involved by growing neoplasms with increasing severity. Therefore, up to 60% of the patients with mediastinal mass are symptomatic, according to the structure involved. Different neoplasms may arise essentially from all mediastinal organs, whereas thymic epithelial tumors and lymphomas represent more than 90% of mediastinal tumors.

Case description: We report the first case described of a giant asymptomatic mediastinal mass in a 43-year-old male affected by Down syndrome (DS), turned out to be a thymoma, treated exclusively and successfully with radical surgery. Despite the absence of any symptoms, the giant thymoma infiltrated the diaphragm, the pericardium, the upper lobe of the left lung together with the left phrenic nerve resulting in the compression of heart and great vessels.

Conclusions: To date, this is the first description of a thymic malignancy in a patient with DS, that usually is characterized by a low-incidence of solid tumor except for germ-cells ones. Surgery has been extremely challenging, due the clinical condition of the patient together with the tumor features; nevertheless, oncological radicality criteria were completely fulfilled. After four years from surgery, the patient is alive and still disease-free, highlighting the importance of radical surgery.

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Imaging of thymic epithelial tumors-a clinical practice review. Locally advanced thymic epithelial tumors: a foreword to the special series. Genomic insights into molecular profiling of thymic carcinoma: a narrative review. Re-evaluation and operative indications after induction therapy for thymic epithelial tumors. Narrative review of indication and management of induction therapy for thymic epithelial tumors.
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