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- multiple endocrine neoplasms, MEN 多发性内分泌肿瘤
- multiple endocrine neoplasm type 1 多发性内分泌肿瘤1型
- Mixed multiple endocrine neoplasms: An autopsy case report and review of literature 混合型多发性内分泌肿瘤（尸检病例报告及文献复习）
- Multiple Endocrine Neoplasm: Clinical Features and Imaging Technique Correlation 多发性内分泌肿瘤的临床特点与影像学诊断
- multiple endocrine neoplasms 多发性内分泌肿瘤
- multiple endocrine neoplasm 多发性内分泌腺肿瘤
- Luckily, most endocrine neoplasms are benign adenomas. 幸运的是，绝大部分内分泌肿瘤都是良性腺瘤。
- 9.To understand pathologic and clinical features of multiple endocrinal neoplasm syndrome. 9.;了解多发性内分泌肿瘤的临床病理特点。
- It is difficult to determine malignancy in endocrine neoplasms based upon cytology alone. 仅从内分泌肿瘤的细胞学检查很难确定为恶性。
- The familial kind are associated with multiple endocrine neoplasia syndrome. 家族发病类型与多发性内分泌瘤综合征有关系。
- Endocrine neoplasms are composed of small round cells with small round nuclei and pink to blue cytoplasm. 内分泌肿瘤由小圆形细胞构成，其内有小圆形的细胞核，细胞质呈粉蓝色。
- Both benign and malignant endocrine neoplasms demonstrate some degree of cellular pleomorphism, so it is not easy to tell benign from malignant on histologic grounds alone. 无论是良性内分泌肿瘤还是恶性内分泌肿瘤都显示一定程度的细胞异型性,因此仅从组织学上很难区分肿瘤的良恶性。
- The conditions were familial adenomatous polyposis, myotonic dystrophy, multiple endocrine neoplasia, hereditary motor and sensory neuropathy. 这些疾病包括家族腺瘤息肉
- Patients with multiple endocrine neoplasia (MEN) type II disease are predisposed to develop bilateral adrenal pheochromocytomas. 摘要第二型多发性内分泌瘤的病患多并有发生两侧嗜铬细胞瘤，传统治疗方法为两侧肾上腺切除术。
- Long-term survival is common in patients with medullary carcinoma and multiple endocrine neoplasia, type IIA, with >2/3 of affected patients alive at 10 yr. 髓样癌及多发性内分泌瘤IIA病人长期存活是常见的，2/3以上病人可存活10年。
- Long-term survival is common in patients with medullary carcinoma and multiple endocrine neoplasia, type IIA, with > 2/3 of affected patients alive at 10 yr. 髓样癌及多发性内分泌瘤IIA病人长期存活是常见的，2/3以上病人可存活10年。
- MEN, muitiple endocrine neoplasms 多发性内分泌肿瘤
- The usual presentation is that of an asymptomatic thyroid nodule, although many cases are now diagnosed during routine screening of affected kindreds with multiple endocrine neoplasia type IIA or IIB before a palpable tumor develops. 通常表现为无症状甲状腺结节，虽然很多病例在肿瘤扪及前就可通过多内分泌肿瘤IIA或IIB血缘关系的常规检查得到确诊。
- Patients with multiple endocrine neoplasia (MEN) type II disease are predisposed to develop bilateral adrenal pheochromocytomas.The standard treatment is a bilateral adrenalectomy in these patients. 摘要第二型多发性内分泌瘤的病患多并有发生两侧嗜铬细胞瘤，传统治疗方法为两侧肾上腺切除术。
- Thymic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: A Comparative Study on 21 Cases Among a Series of 761 MEN1 from the GTE (Groupe des Tumeurs Endocrines). 多发性内分泌腺瘤1型患者出现的胸腺神经内分泌肿瘤：来自GTE的761例MEN1患者中21例胸腺神经内分泌肿瘤的对比研究。
