Nodal

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  • 文章类型: Journal Article
    淋巴瘤是一类主要在淋巴结中出现的肿瘤疾病。它们主要分为霍奇金淋巴瘤和非霍奇金淋巴瘤(NHL)。NHL可以是B,T和空细胞类别具有基于其组织学特征的其他亚型。淋巴瘤可以是淋巴结和淋巴结外。头颈部区域是结外淋巴瘤的第二常见部位,扁桃体是最常见的受累部位;其他部位包括鼻咽和舌根。B-细胞类型是最常见的类型。主要发生在老年人身上。演示文稿取决于所涉及的网站。各种方式,如手术治疗,化疗(或)放疗是可用的。取决于患者因素,每个阶段具有不同的存活率和预后以及对治疗的反应。在本文中,我们报告了2例扁桃体非霍奇金淋巴瘤患者,术前临床诊断和放射学诊断尚无定论,最终诊断是根据组织病理学检查确定的。
    Lymphomas are a diverse group of neoplastic disorders arising primarily in lymph nodes. They have been majorly classified into Hodgkin and Non-Hodgkin lymphomas(NHL). NHL can be of B, T and Null cell categories having further subtypes based on their histological characteristics. Lymphomas can be nodal and extra nodal. The head and neck area are the second most common site of extra nodal lymphoma, with tonsils being the most common site of involvement; other sites include the nasopharynx and tongue base. B- Cell type being the most common type. Predominantly occurs in elderly. Presentations depends on the site involved. Various modalities like surgical treatment, chemotherapy (or) radiotherapy is available. Each stage has varied survival rates and prognosis and responses to the treat depending on the patient factors. In this paper,  we report two cases of patients with non-Hodgkin lymphoma of tonsil, where the preoperative clinical diagnosis and radiological diagnosis was inconclusive and final diagnosis was established based on histopathological examination.
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  • 文章类型: Case Reports
    我们报告了一名日本5岁男孩,患有原发性纤毛运动障碍(PCD),该男孩是由于长时间暴露于抗生素引起的艰难梭菌(CD)感染而被诊断出来的。他患有顽固性中耳炎伴积液(OME),并在开始服用抗生素后连续4个月出现腹痛和腹泻。他的粪便含有CD毒素。万古霉素治疗后,他的症状有所改善,粪便不含CD毒素。他的既往病史包括频繁的肺炎。我们,因此,对他的鼻粘膜活检标本进行电子显微镜检查和基因检测,他被诊断出患有PCD.PCD是一种罕见的遗传性遗传性疾病,可引起纤毛功能障碍。这很难诊断,因为一些没有PCD的儿童也会出现相同的症状。因此,患有棘手OME的孩子,鼻窦炎,频繁的肺炎,或支气管炎,并长期服用抗生素应检查潜在疾病,比如PCD。
    We report a Japanese 5-year-old boy with primary ciliary dyskinesia (PCD) which was diagnosed owing to Clostridium difficile (CD) infection caused by prolonged antibiotic exposure. He had intractable otitis media with effusion (OME) and had abdominal pain and diarrhea for 4 months after starting antibiotics administration. His stool contained CD toxin. After vancomycin treatment, his symptoms improved and his stools did not contain CD toxin. His past medical history included frequent pneumonia. We, therefore, performed electron microscopy of the biopsy specimen from his nasal mucosa and genetic testing, and he was diagnosed with PCD. PCD is a rare inherited genetic disease causing ciliary dysfunction, which is very difficult to diagnose because some children without PCD also develop the same symptoms. Therefore, children who have intractable OME, rhinosinusitis, frequent pneumonia, or bronchitis and are taking antibiotics for long periods of time should be checked for underlying diseases, such as PCD.
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