Ureteral carcinoid tumor

Most ureteral tumors are transitional cell neoplasms. Neuroendocrine tumors of the genitourinary tract are extremely rare. To our knowledge, only one ureteral carcinoid tumor has been reported before. We report a second case of ureteral carcinoid tumor found in a 70-year-old female.     

胸部类癌

本文报道了３１例胸部类癌，其中胸腺类癌１４例，支气管类癌１７例，伴有异位ＡＣＴＨ综合征者１７例。１２例患者发生转移（３９％），２４例行原发肿瘤全部或部分切除，术后放疗或化疗或两者均有者１７例，４例仅行探查并取活检，２８例经手术及病理证实。     

Clinicopathologic analysis of eight cases of pancreatic carcinoid tumors

Carcinoids of the pancreas are exceedingly rare tumors that orieinate from the enterochromaffin cells of the gastroenteropancreatic neuroendocrine system. According to a recent report,1 pancreatic carcinoids are found in only 0.58% (79/13 715 cases) of the entire carcinoid group. Todate, very limited information regarding the detection and diagnosis of this entity has been reported in the available literature. Although pancreatic carcinoid tumors grow.     

肺类癌12例临床分析

为了探讨肺类癌的临床特点、诊疗方法与预后的影响因素,对12例肺类癌病例进行回顾性研究。12例患者中2例伴有类癌综合征,2例术前经纤支镜确诊。术式包括肺叶切除9例,开胸探查1例,全肺切除2例,无手术期死亡和并发症。全组5年生存率为72.65%,类癌5年生存率为84.23%,不典型类癌为66.68%。初步研究结果提示,肺类癌属低度恶性肿瘤;影像学及纤维支气管镜检查对诊断具有重要价值;光镜HE染色常可诊断,但嗜银染色及电镜确定特征性嗜银性神经内分泌颗粒是确诊的可靠标准;治疗应以保守性外科手术切除为主,尽量保留肺功能为手术原则;手术切除后预后良好,远期疗效明显优于肺癌。     

Carcinoid tumors and inflammatory bowel disease.

Three cases are described in which carcinoid tumors arose in previously established inflammatory bowel disease: two were in the ileum in cases of Crohn's disease, and one was in the rectum in a case of ulcerative colitis. Review of this association in the literature suggests that it may be more than fortuitous.     

内镜黏膜下剥离术治疗直肠类癌

目的探讨内镜黏膜下剥离术（ESD）治疗直肠类癌的应用价值。方法肠镜发现直肠黏膜下肿块后进行微探头超声检查，对诊断为类癌者应用头端弯曲的针形切开刀进行内镜黏膜下剥离术治疗：（1）黏膜下注射生理盐水抬高病灶，使病灶与肌层分离；（2）预切开病灶周围黏膜；（3）剥离病变下方黏膜下层结缔组织，完整切除病灶。结果5例直肠类癌患者，肿瘤直径0.4～1.2（平均1．1）cm，均成功完成ESD治疗。ESD手术时间（自黏膜下注射至完整剥离病变）20-45（平均35）min；术中创面少量出血，均经电凝、氩离子血浆凝固和止血夹成功止血。不需再次肠镜下止血。1例剥离深至肌层，出现皮下气肿，保守治疗好转。术后全部经病理确诊。基底和切缘未见病变累及。1个月后肠镜复查，创面基本愈合。结论ESD是治疗直肠类癌的新方法．以往需要外科手术切除的肿瘤通过ESD可以达到同样的治疗效果。     

胸腺类癌外科治疗的长期结果

目的探讨胸腺类癌的临床表现,分类与预后的关系,以及手术方式及术后辅助治疗特点,以提高对该病的认识。方法回顾性分析北京协和医院1980年1月至2006年1月18例胸腺类癌的外科治疗和随诊结果。开胸探查活检2例,姑息性切除2例,完整切除14例,包括2例上腔静脉系统切除移植人工血管。采用寿命表法计算生存率,用Cox单因素回归模型分析胸腺类癌预后的影响因素。结果2例行开胸探查患者分别于术后1年和2年死亡;2例姑息性切除术后患者症状暂时缓解;完整切除患者除1例合并柯兴综合征术后2周死于败血症,其余13例术后完全恢复,随诊5个月至15年良好。全组3年、5年、10年生存率分别为72.6%、60.5%和40.3%。经Cox单因素分析结果:纵隔淋巴结转移(P=0.047)、病理类型(P=0.000)、手术方式(P=0.000)和术后综合治疗(P=0.018)是影响预后的因素。结论胸腺类癌不同于胸腺瘤、胸腺癌,临床诊断困难;病理学分典型和不典型胸腺类癌,两者临床表现和预后明显不同。不典型类癌恶性程度高,切除后容易复发和转移,预后较差。彻底切除肿瘤以及受侵的组织和器官,可以明显提高长期生存率。术后放疗、化疗有一定辅助作用。     

Gastrointestinal manifestations of type 1 neurofibromatosis (von Recklinghausen''s disease)

Gastrointestinal involvement in von Recklinghausen's disease occurs in three principal forms: hyperplasia of the submucosal and myenteric nerve plexuses and mucosal ganglioneuromatosis which leads to disordered gut motility; gastrointestinal stromal tumours showing varying degrees of neural or smooth muscle differentiation; and a distinctive glandular, somatostatin-rich carcinoid of the periampullary region of the duodenum that contains psammoma bodies and which may be associated with phaeochromocytoma. This review describes the histopathological features of these lesions and discusses potential pitfalls in their differential diagnosis. Their accurate identification has significant implications for clinical management and may even provide the first pointer to the diagnosis of neurofibromatosis.     

胃肠道类癌临床病理与免疫组织化学研究

应用免疫组织化学ＡＢＣ法，对５２例胃肠道类癌进行８种多肽／胺类神经内分泌激素、２ 种上皮细胞性标记物的研究。结果：胃肠原位激素胰多肽、生长抑素、蛙皮素、胃泌素、五羟色胺较多 表达于组织形态分化好的类型。血管活性肽的表达随肿瘤组织形态分化降低而上升显著（１５．０％、 ２５．０％、５８．３％、Ｐ＜０．０５），并与肿瘤的浸润和转移有关（Ｐ＜０．０５）。异位激素降钙素的表达主要分 布于肿瘤组织形态分化较低的类型（２０．０％、５０．０％、６６．７％、Ｐ＜０．０５）。癌胚抗原的表达随肿瘤组 织形态分化的降低呈大幅度上升（１０．０％、５５．０％、８３．３％、Ｐ＜０．００１），且与肿瘤的浸润有关（Ｐ＜ ０．０５）；神经特异性烯醇化酶与角蛋白的表达与组织分化无相关性。提示应用多种抗原标记对胃肠 道类癌的良恶性判断很有帮助。