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胃肠粘膜活检上皮瘤变诊断标准讨论 Padova / Vienna Classifications(8个病例/一个提问)

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本帖最后由 于 2010-02-24 04:38:00 编辑

The Padova classification of gastric dysplasia and related lesion.

Negative for dysplasia
  Reactive foveolar heperplasia
Intestinal metaplasia (IM)
  IM, complete type
  IM, incomplete type
Indefinite for dysplasia
  Foveolar hyperproliferation
  Hyperproliferative IM
Noninvasive neoplasia ( flat or elevated [synonym, adenoma])
  Low grade
  High grade
    Including suspicious for carcinoma without invasion

      (intraglandular)
    Including carcinoma without invasion (intraglandular)
  Suspicious for invasive carcinoma
Invasive carcinoma

   


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本帖最后由 于 2010-02-24 20:06:00 编辑

Padova胃异型增生和相关病变分类

1、无异型增生

     1.1反应性小凹上皮增生

2、肠腺化生(IM

     2.1 IM 完全型

     2,2 IM 不完全型

3、异型增生不能确定

     3.1 小凹上皮增殖

     3.2 增殖型IM

4、非浸润性瘤变

     4.1 低级别

     4.2 高级别

      4.2.1包括癌疑无浸润(腺体内)

      4.2.2包括癌无浸润(腺体内)

      4.2.3可疑浸润性癌

5、浸润性癌

 

 


Vienna胃肠上皮内肿瘤分类

1、无上皮内肿瘤/异型增生
2
、不能确定上皮内肿瘤/异型增生
3
低级别上皮内肿瘤 /异型增生
  
(低级别腺瘤/异型增生)
4
、高级别上皮内肿瘤/异型增生-非浸润性
   4.1
高级别腺瘤/异型增生
   4.2
非浸润性癌(原位癌)*
   4.3
可疑浸润性癌
5
、上皮内肿瘤-浸润性
   5.1
粘膜内癌#
   5.2
粘膜下层癌或超过粘膜肌层

备注:* 非浸润性指无浸润依据; # 粘膜内指浸润固有膜 或粘膜肌层。

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3 楼    发表于2010-02-27 16:13:00举报|引用
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5 楼    发表于2010-02-27 21:46:00举报|引用
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 谢谢Dr.jin!非常好的提议!有价值的资料!
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6 楼    发表于2010-02-27 22:48:00举报|引用
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  Padova / Vienna Classifications 分类出现在WHO分类之前,个人的理解这个分类是将胃黏膜的病变轻重细分,意义在于指导临床医生依据疾病的轻重程度采用不同的干预措施,但是WHO并没有采用该分类。其原因并非是该分类不好,而是目前西方的保险制度所决定的。该分类是联系欧美与日本胃黏膜诊断标准的一个桥梁,具有一定的可重复性。目前推广存在困难,因为这个需要胃黏膜切除手术的推广才行,否则没有任何意义。

仅仅是个人理解!

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7 楼    发表于2010-02-28 04:13:00举报|引用
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本帖最后由 于 2010-02-28 07:57:00 编辑

 

1)Am J Surg Pathol. 2000;24:167-76.

Gastric dysplasia: the Padova international classification.

Rugge M, Correa P, Dixon MF, Hattori T, Leandro G, Lewin K, Riddell RH, Sipponen P, Watanabe H.

Department of Surgical and Oncological Sciences, Università degli Studi di Padova, Italy.

Comment in: Am J Surg Pathol. 2001 May;25(5):694.

 A worldwide-accepted histologic, classification of the gastric carcinomatous and precancerous lesions is a prerequisite for a consistent recording of epidemiologic data and for both developing and evaluating primary and secondary preventive efforts. Different nomenclatures have been proposed for gastric precancerous lesions in eastern countries and in Japan. This article presents a classification of gastric precancerous lesions resulting from an international consensus conference involving pathologists of different countries. Five main diagnostic categories are identified. To allow comparisons with the nomenclature proposed by the Japanese Research Society for Gastric Cancer, each category was also assigned a numeric identification: 1 = normal, 2 = indefinite for dysplasia,3 = noninvasive neoplasia, 4 = suspicious for invasive cancer, and 5 = cancer.The interobserver reproducibility of the histologic classification was tested in a series of 46 cases. By collapsing benign alterations (categories 1+2) versus noninvasive neoplasia (category 3) versus suspicious for invasive cancer and fully appearing carcinomatous lesions (categories 4+5), the general agreement value was 77.7%, whereas kappa coefficient was 0.63. By examining gastric precancerous lesions from diverse populations, the authors agreed that the gastric precancerous process is universal and the differences in nomenclatures are merely semantics. The international Padova classification of the gastric precancerous lesions is submitted to the attention of the international scientific community, which is invited to test and to improve on it.

 


2)Gut. 1999 Jul;45 Suppl 1:I5-8.

Gastric precancerous lesions: heading for an international consensus.

 Genta RM, Rugge M.

 Departments of Pathology and Medicine, Baylor College of Medicine and Veterans Affairs Medical Centre, Houston, Texas, USA.

As pathological criteria lie at the foundation for the classification of many diseases, a crucial requisite for such classifications to be valid is that their morphological basis be standardised. Inadequately standardised diagnostic criteria result in unacceptable interobserver variation, a factor that may influence both individual patient care and the evaluation of clinical protocols. One of the most important goals in gastric diseases today is to establish whether cure of Helicobacter pylori is an effective preventive measure against gastric cancer. To tackle this issue it is necessary to measure reliably intermediate outcomes, specifically gastric atrophy and dysplasia. However, there is little agreement on what gastric atrophy and atrophic gastritis are, and treatment and follow up results obtained at one clinical centre are often radically different from those obtained at another. Similarly, studies that examine the fate of dysplastic lesions in the stomach show a great divergence of outcomes between Europe and North America and Japan, where the concept of dysplasia has different connotations. To reach a consensus on the definitions and diagnostic criteria for atrophy and atrophic gastritis, a group of gastrointestinal pathologists and gastroenterologists met in Houston, Texas, USA, in February 1998. Substantive progress was made, but several problems remained, and a study aimed at resolving the issues that seem to stand in the way of an international agreement is currently underway. To fulfil the need for a broad discussion on the diagnostic differences of gastric dysplasia and cancer between East and West, an international group of pathologists gathered in Padova, Italy, in the spring of 1998. Their main objectives were: (1) to agree on the definitions of the spectrum of gastric preneoplastic lesions; (2) to establish an international glossary for gastric precancerous lesions; and (3) to test the consensus and eventually generate guidelines useful to clinicians for the development of management strategies. A consensus was achieved on the definition of gastric dysplasia as preinvasive neoplasia. Other validation studies are underway. The experiences achieved in the search for an international consensus on the phenotypes of atrophic gastritis and gastric dysplasia may represent a model in dealing with the new scenario of a modern evidence-based pathology.

 


3)Lancet. 1997;349:1725-9.

Differences in diagnostic criteria for gastric carcinoma between Japanese and western pathologists.

Schlemper RJ, Itabashi M, Kato Y, Lewin KJ, Riddell RH, Shimoda T, Sipponen P, Stolte M, Watanabe H, Takahashi H, Fujita R.

Department of Gastroenterology, Showa University Fujigaoka Hospital,

Yokohama-shi, Japan.

 Erratum in: Lancet 1997 Aug 16;350(9076):524.

 Comment in:Lancet. 1997 Aug 9;350(9075):448.

                    Lancet. 1997 Aug 9;350(9075):448.

                    Lancet. 1997 Jun 14;349(9067):1711-2.

 

BACKGROUND: There have been many studies on gastric carcinoma in populations with contrasting cancer risks. We aimed to find out whether the criteria for the histological diagnosis of early gastric carcinoma were comparable in Western countries and Japan. METHODS: Eight pathologists from Japan, North America, and Europe individually reviewed 35 microscope slides: 17 gastric biopsy samples and 18 endoscopic mucosal resections taken from 17 Japanese patients with lesions ranging from early gastric cancer to adenoma, dysplasia, and reactive atypia. The pathologists were given a list of pathological criteria and a form on which they were asked to indicate the criteria on which they based each diagnosis. FINDINGS: For seven slides most Western pathologists diagnosed low-grade adenoma/dysplasia, whereas the Japanese diagnosed definite carcinoma in four slides, suspected carcinoma in one, and adenoma in only two. Of 12 slides with high-grade adenoma/dysplasia according to most Western pathologists the Japanese gave the diagnosis of definite carcinoma in 11 and suspected in one. Of six slides showing high-grade adenoma/dysplasia with suspected carcinoma according to most Western pathologists the Japanese diagnosed definite carcinoma in all. There were no major differences in the diagnoses of three slides showing reactive epithelium

and seven slides with clearly invasive carcinoma. When the opinion of the majority of the pathologists was taken as the final diagnosis there was agreement between Western and japanese in 11 of the 35 slides (kappa coefficient 0.15 [95% CI 0.01-0.29]). Presence of invasion was the most important diagnostic criterion for most Western pathologists whereas for the Japanese nuclear features and glandular structures were more important. INTERPRETATION: In Japan, gastric carcinoma is diagnosed on nuclear and structural criteria even when invasion is absent according to the Western viewpoint. This diagnostic practice results in almost no discrepancy between the diagnosis of a superficial biopsy sample and that of the final resection specimen. This may also contribute to the relatively high incidence and good prognosis of gastric carcinoma in Japan when compared with Western countries.

 

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8 楼    发表于2010-02-28 05:24:00举报|引用
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本帖最后由 于 2010-02-28 09:39:00 编辑
上为3篇在胃粘膜癌前病变研究中为解决:1)胃粘膜异型增生3度分级在不同观察者间的差异;2)统一东西方对早期胃癌诊断标准;试图达到共识的重要文章。发表在1980年前后。非常有助于我们全面理解为什么会有“Padova胃异型增生和相关病变的分类”?为什么又出现“Vienna 胃肠上皮瘤变分类”。
1、Padova胃异型增生和相关病变分类是对胃异型增生进行定义,它是按照胃粘膜有无异型增生-异型增生的程度(上皮瘤变 低级别-高级别)- 浸润性癌的主线进行。
2、Vienna 胃肠上皮瘤变分类是对整个胃肠道( 食管、胃、肠)的分类, 它是按照食管、胃和肠有无上皮瘤形成-上皮瘤形成的程度(低级别-高级别)和有无浸润的主线进行,同时考虑到解剖学上结直肠粘膜固有层内无淋巴管的特定,不同于食管和胃。因为当食管和胃的肿瘤细胞突破上皮基底膜就有可能通过淋巴管转移危险性;而结直肠肿瘤细胞即使突破基底膜,也无通过淋巴管转移的危险性。
3、既然形态学上的“结直肠粘膜内癌”,并没有通过淋巴管转移的恶性肿瘤生物学特征,为什么要诊断为“癌”?
4、最后,还是要强调:Padova 胃异型增生和相关病变的分类和Vienna胃肠上皮瘤形成分类都是为了解决癌前期病变的诊断标准,国际胃肠研究协会在形态学上达成的共识。
5、病理科医生对于胃肠粘膜活检的病人有三种情况:1)癌前病变;2)早期浸润癌;3)进展期癌。 诊断时必须 “临床-内镜-病理” 三结合, 一旦诊断为上皮瘤变高级别,还要按Vienna标准亚分类:1)
腺瘤/异型增生;.2 非浸润性癌(原位癌);3 可疑浸润性癌。
6、在Padova分类和Vienna分类中没有“癌变”的病理学诊断名称,尽量避免使用。

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9 楼    发表于2010-02-28 08:02:00举报|引用
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本帖最后由 于 2010-02-28 08:08:00 编辑
Cancer杂志1984年的一篇重要文章的摘要,供参考:

Ming SC, Bajtai A, Correa P, Elster K, Jarvi OH, Munoz N, Nagayo T, Stemmerman
GN. Gastric dysplasia. Significance and pathologic criteria.
Cancer. 1984;54:1794-801.


1984
年国际胃癌研究协会病理组专家在复习了93例不同程度异常的胃粘膜后,达成共识:
1)未成熟和增殖性粘膜异常可分成2类,增生性和异型增生性;
2)异型增生的术语,特别是高级别型,必须限制于癌前病变,增生用于再生性改变;
3)再生性增生可以是单纯性或者不典型性,而异型增生包括中度和重度异常。由于再生性增生和异型增生常常同时存在,所以有时不能被明确的区分。
4)偶尔,不能除外重度异型增生中存在癌的可能,对这种病例必须重复活检和勤随访以确定诊断。
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10 楼    发表于2010-02-28 15:30:00举报|引用
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学习,谢谢。

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11 楼    发表于2010-03-01 23:30:00举报|引用
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 学习了,谢谢金老师!
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12 楼    发表于2010-03-02 15:40:00举报|引用
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   谢谢金老师!我正准备做一个讲座,请贴一些图!!
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13 楼    发表于2010-03-02 20:28:00举报|引用
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谢谢Dr.dytok 为华夏病理网的网友准备有关的讲座。需要什么,尽管开口,一定尽力而为。越具体,越好!

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16 楼    发表于2010-03-03 08:20:00举报|引用
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 谢谢,学习了!
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17 楼    发表于2010-03-03 13:18:00举报|引用
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 谢谢,学习
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 谢谢,学习
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