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食管贲门交界处病变

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简要病史:
食管与贲门交界处有1.5X1厘米隆起性病变,活检。
肉眼检查:  
 
CK7 (-) ,CK20 (-) ,34BE12(-),
P63(+),SYN(+),BCL-2(+)KI-67(+)
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×参考诊断
形态学结合免疫组化标记,考虑小细胞癌,食管原发可能性大。

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1 楼    发表于2011-04-21 23:50:00举报|引用
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 小细胞鳞癌伴神经内分泌分化

鉴别:复合性小细胞癌,小细胞癌。

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2 楼    发表于2011-04-23 07:41:00举报|引用
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本例我们拟诊断基底细胞样鳞癌,请指导!

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3 楼    发表于2011-04-23 08:46:00举报|引用
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 同意楼主诊断
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4 楼    发表于2011-04-23 19:15:00举报|引用
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 Basaloid squamous cell carcinoma of the head and neck: role of HPV and implication in treatment and prognosis    J Clin Pathol 2010;63:857-866 doi:10.1136/jcp.2010.078154

Abstract
Basaloid squamous cell carcinoma (BSCC) is a rare variant of squamous cell carcinoma (SCC) of the head and neck. Wain's criteria (peripheral palisading, association with SCC, high nuclear-cytoplasmic ratio, high mitotic rate, solid growth), anti-34BE12 and CK 5/6 staining, and absence of neuroendocrine markers are mandatory for the diagnosis of BSCC. Its increasing incidence parallels that of human papilloma virus (HPV)-positive tumours for the oropharyngeal subsite. On the other hand, BSCC is frequently considered a high-grade carcinoma of poorer prognosis than its SCC counterparts, mostly due to a higher rate of distant metastases. However, BSCC has similar or better locoregional control rates and a relatively better radiosensitivity than SCC. BSCC seems to have a dual behaviour depending, at least partly, on its recently described association with HPV. The basaloid subtype of SCC, owing to its particular behaviour, should be systematically investigated along with HPV and smoking status, as those factors may be determinant in the response to treatment.
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5 楼    发表于2011-04-24 02:35:00举报|引用
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 以下文献是一篇对本例具有启示的资料。文中提及:

原发性食管小细胞癌Primary esophageal small cell carcinoma,  PESCC)是相当少见的侵袭性肿瘤,预后差。作者用IHC检测了15例浅表性PESCC,八个标志物的阳性结果如下:NSE 100%,Syn 100% AE1/AE3 100%,CD56 93.3%,TTF-1 60%,CgA 53.3%,CK34betaE12 6.7%,而 CK 10/13 全为阴性。随访5年生存率为6.7%,提示生存率很低。

本文献读后思考两个问题:(1PESCC可表达34betaE12,尽管表达率仅为6.7%,那么要问:表达34betaE12这样的病例是不是也表达P63呢?其他文献提示消化道腺癌有的可表达P63,就是食管腺的腺泡也可表达P63(表达在腺周边)。(2PESCC患者的生存期这么短,那要不要与食管浅表型低分化鳞癌相鉴别?因为其他文献报道食管浅表型低分化鳞癌的5年生存率是86.1%,所以本例很有必要鉴别PESCC和低分化鳞癌。所以说,还要进一步做工作将二者加以区分。

Dis Esophagus. 2010 Feb;23(2):153-9. Epub 2009 Jun 9.
   

Superficial primary small cell carcinoma of the esophagus: clinicopathological and immunohistochemical analysis of 15 cases.
   

Lu J, Xue LY, Lu N, Zou SM, Liu XY, Wen P.
   

Department of Pathology, Cancer Institute/Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100021, China.
   

Abstract
   

Primary esophageal small cell carcinoma (PESCC) is a relatively rare and aggressive tumor with poor prognosis. Systemic spreading and metastasis often occur at diagnosis. Although 5-year survival rate of superficial squamous cell carcinoma of the esophagus can be 86.1%, 5-year survival rate of superficial PESCC is still relatively low. This study mainly retrospectively analyzed clinicopathological and immunohistochemical features of 15 cases of superficial PESCC in our hospital from 1990 to 2004, in order to find suitable diagnostic markers and applicable therapies for this disease. The records mainly included presenting symptoms, demographics, diagnostic method, histopathology, follow-up, and therapy. Immunohistochemical staining of chromogranin A (CgA), neuron-specific enolase (NSE), synaptophysin (Syn), neuronal cell adhesion molecules (CD56), thyroid transc ription factor-1 (TTF-1), cytokeration 34betaE12 (CK34betaE12), cytokeratin (AE1/AE3), and cytokeratin 10/13 was performed. Incidence of superficial PESCC accounted for 4.8% of that of superficial carcinoma of the esophagus during the same period. Initial symptoms of all patients were dysphagia or accompanied with retrosternal pain and upper abdominal pain, and duration of these symptoms was 75 days averagely. Mean age of patients was 58.8 years old, and the male-to-female ratio was 2.75 : 1. Lesions were mainly located at middle thoracic esophagus. One, 2, and 5-year survival rates were 66.7, 33.3, and 6.7%, respectively. The median survival time was 19 months and mean survival time was 23.7 months after diagnosis. The percentages of PESCC samples with positive immunoreactivity were NSE 100%, Syn 100%, AE1/AE3 100%, CD56 93.3%, TTF-1 60%, CgA 53.3%, CK34betaE12 6.7%, and cytokeratin 10/13 0%, respectively. Our study suggested that PESCC was a rare and aggressive tumor with high malignancy. Superficial PESCC had rapid progression and poor prognosis compared with superficial squamous cell carcinoma of the esophagus at the same stage. The systemic therapy based on combination of postoperative chemotherapy and radiotherapy might be an effective approach for the treatment of superficial PESCC as a systemic disease. Higher proportion of positive labeling of NSE, Syn, AE1/AE3, CD56, TTF-1, and CgA in PESCC was valuably applied in diagnosis and differential diagnosis.

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6 楼    发表于2011-04-24 02:46:00举报|引用
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 从HE组织学形态和部分IHC标记看,需要考虑食管小细胞癌,而且有可能是浅表型。即便是浅表型食管小细胞癌,预后将很不好。因此一定要与预后相对好的浅表型低分化鳞癌鉴别。

从增殖活性看,Ki-67标记指数达到 90%以上,应该是高度恶性的肿瘤。形态结合IHC部分指标,很大可能是高级别神经内分泌癌,极有可能是上述的PESCC。

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7 楼    发表于2011-04-24 10:17:00举报|引用
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感谢王老师精彩点评!

患者目前情况是影像学检查提示胸腔广泛转移,胸膜、肺表面布满结节,已失去手术机会,患者放弃治疗已经出院。遗憾!

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8 楼    发表于2011-04-24 12:03:00举报|引用
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 这一例还可做一点标记,小细胞癌是首选。

谢谢提供好病例给我们分享。谢谢!

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9 楼    发表于2011-04-24 12:16:00举报|引用
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TTF-1、CgA、CD56、S-100、NSE是否阳性?需要鉴别肺外小细胞癌或转移性肺小细胞癌。

问题是:小细胞癌是否表达P63阳性?

补做一个广谱CK,看是否阳性。如果明显阳性,可否考虑小细胞鳞癌伴神经内分泌分化。

然而,更进一步,鳞状细胞癌怎么会伴神经内分泌分化呢?

如果广谱CK弱阳性或阴性,则需要考虑小细胞癌。

看看其他还有什么肿瘤像这样的免疫表型。

需要进一步查阅文献,参阅他人研究的文献报道,看如何理解这些矛盾。

谢谢!

 
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10 楼    发表于2011-04-24 12:48:00举报|引用
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以下文献采用样本配对评价了TTF-1和P63表达对小细胞性肺癌(13例)和肺低分化鳞状细胞癌(13例)的鉴别诊断意义。免疫组化标记结果显示,所有小细胞癌表达P63阴性(13/13),而表达TTF-1呈阳性(12/13,即阳性率达92%)。相反,所有低分化鳞癌(13/13)表达P63阳性,不表达TTF-1。
结合这一文献,我们是不是要看看TTF-1的表达情况。如果本例TTF-1也是阳性,那我们还要进一步做工作来鉴别诊断。
Mod Pathol. 2006 Aug;19(8):1117-23. Epub 2006 May 5.

TTF-1 and p63 for distinguishing pulmonary small-cell carcinoma from poorly differentiated squamous cell carcinoma in previously pap-stained cytologic material.

Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at Houston Medical School, Houston, 77030, USA.

Abstract

In histology and cell block sections, antibodies to thyroid transcription factor-1 (TTF-1) and p63 have been demonstrated to be useful markers for distinguishing between small-cell lung carcinoma and poorly differentiated pulmonary squamous cell carcinoma. In this study, we assessed the utility of TTF-1 and p63, as an antibody panel, for differentiating between these two neoplasms in previously Papanicolaou (Pap)-stained cytologic smears and cytospin slides. Twenty-six lung carcinomas (13 small-cell lung carcinomas, 13 poorly differentiated pulmonary squamous cell carcinomas) were evaluated. One or two previously 95% ethanol-fixed, Pap-stained smears or cytospin slides were selected from each case. The cytologic material from these slides was transferred to positively charged slides. Unstained recuts were obtained from the corresponding histologic specimens or cell blocks. Immunohistochemical staining for TTF-1 and p63 was performed on the paired samples from each tumor. All (13/13) small-cell lung carcinomas were negative for p63 and 92% (12/13) were positive for TTF-1. Conversely, all (13/13) poorly differentiated pulmonary squamous cell carcinomas expressed p63 and did not express TTF-1. Immunoreactivity for p63 was also noted in bronchial reserve cells and metaplastic squamous cells. The immunostaining results obtained from the cytology slides were concordant with those of the histology or cell block sections in all cases. The results of this study show that TTF-1 and p63 immunostaining can be successfully applied to previously Pap-stained cytologic material, as an antibody panel, to facilitate pathologic differentiation between small-cell lung carcinomas and poorly differentiated pulmonary squamous cell carcinomas. p63 immunostaining, however, must be interpreted in conjunction with cytomorphology to distinguish between poorly differentiated pulmonary squamous cell carcinomas and benign cellular constituents of the lung

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11 楼    发表于2011-04-26 12:32:00举报|引用
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以下是引用xclbljys在2011-4-24 10:17:00的发言:

 

感谢王老师精彩点评!

患者目前情况是影像学检查提示胸腔广泛转移,胸膜、肺表面布满结节,已失去手术机会,患者放弃治疗已经出院。遗憾!

谢谢楼主对本栏目的大力支持!

这个病例广泛转移,更说明本例是一个高度恶性的肿瘤,更应该考虑小细胞癌。

剩下的问题是:究竟是食管的癌来自于肺还是肺的肿瘤来自于食管?

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12 楼    发表于2011-04-27 22:00:00举报|引用
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 征询意见:

1)本例究竟是诊断为小细胞癌还是基底样鳞癌?

2)本例癌是食管原发还是肺原发?

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13 楼    发表于2011-04-29 17:27:00举报|引用
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还是想诊断为小细胞癌,倾向食管原发。请发表意见,好结束本例讨论。谢谢!
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14 楼    发表于2011-04-30 01:56:00举报|引用
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 若Syn弥漫阳性,而非局灶或散在阳性,且Ki67指数很高,支持小细胞癌,而非基底样鳞癌伴神经内分泌分化。
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15 楼    发表于2011-04-30 09:51:00举报|引用
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 本例选用的神经内分泌标记物为syn,应该来说,还是比较特异的,其他几种标记物如bcl-2、P63的标记结果只是作为参考,个人认为,诊断小细胞癌是成立的,如不放心,可加作其他标记如NSE、CgA、CD56或CD57

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The More We See, The Less We Know!

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16 楼    发表于2011-05-10 11:27:00举报|引用
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 符合小细胞癌
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17 楼    发表于2011-05-10 18:48:00举报|引用
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学习

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18 楼    发表于2011-05-10 19:02:00举报|引用
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 学习
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19 楼    发表于2011-05-11 02:46:00举报|引用
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小细胞癌是可以p63阳性的,我们昨天还有一例肺的小细胞癌是弥漫性的p63阳性。basaloid squamous cell carcinoma 不会是34be12 和ck5/6 阴性。

其实还有一个简单的IHC可做:就是pan-cytokeratin (AE1/3), 小细胞癌会出现perinuclear dot-like 染色。

至于是原发还是肺来源的,形态学本身和免疫组化学无法解决,因为其他部位的小细胞癌也可以TTF1阳性,当然TTF1阴性则更倾向于原发于食管的,因为肺的小细胞癌症是90%以上TTF1阳性。
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20 楼    发表于2011-05-13 01:06:00举报|引用
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以下是引用曹大夫在2011-5-11 2:46:00的发言:

小细胞癌是可以p63阳性的,我们昨天还有一例肺的小细胞癌是弥漫性的p63阳性。basaloid squamous cell carcinoma 不会是34be12 和ck5/6 阴性。

其实还有一个简单的IHC可做:就是pan-cytokeratin (AE1/3), 小细胞癌会出现perinuclear dot-like 染色。

至于是原发还是肺来源的,形态学本身和免疫组化学无法解决,因为其他部位的小细胞癌也可以TTF1阳性,当然TTF1阴性则更倾向于原发于食管的,因为肺的小细胞癌症是90%以上TTF1阳性。

 

谢谢曹大夫的精辟点评!

欢迎曹大夫加盟国内!

欢迎来本专栏!

谢谢!

 

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