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Fine-needle aspiration cytology as the first pathological diagnostic modality in breast lesions: A comparison with core needle biopsy 细针穿刺细胞学作为乳腺病变的第一病理诊断方式:与核心针活检的比较
Pub Date : 2010-03-04 DOI: 10.1111/j.1755-9294.2009.01062.x
Sang-Mo Park, Dong-Wha Lee, So-Young Jin, Dong-Won Kim, Yoon-Mi Jeen, In-Ho Choi

Background and aim: Breast cancer is the second most common malignancy in Korean women. Fine needle aspiration cytology (FNAC) has been used as the first-line pathological modality; however, use of core needle biopsy (CNB) is on the increase. FNAC is a cost effective, less invasive and rapid method for evaluation of breast lesions. The limitations of FNAC, such as high false negative rates and equivocal results restrict its use. The aim of this study is to evaluate FNAC as a diagnostic tool in comparison with CNB by matching corresponding excision specimens. Methods: From May, 2003 to April, 2008, 753 cases of FNAC, 331 cases of CNB, and 98 cases of combined FNAC and CNB were collected. Diagnoses with FNAC and CNB were compared with excision. Results: Sensitivity, specificity, and diagnostic accuracy of FNAC were 93.8%, 80.8%, and 90.1%, respectively. Those of CNB were 92.1%, 90.9%, and 92.3%, and combined FNAC and CNB, 100%, 77.8%, and 98.0%. There were no false positive cases in either the FNAC or the CNB group. False negative rates were 6.2% in FNAC and 9.9% in CNB. Sampling error was the cause of error or a false negative result in all FNAC samples, and all but one CNB sample. Diagnostic accuracy of FNAC was superior to that of CNB for lesions between 1 cm and 2 cm. Conclusions: Our data suggest that FNAC is an accurate and reliable first line diagnostic tool for evaluation of breast lesions when compared with core biopsy.

背景和目的:乳腺癌是韩国女性中第二常见的恶性肿瘤。细针吸细胞学(FNAC)已被用作一线病理模式;然而,核心针活检(CNB)的使用正在增加。FNAC是一种成本效益高、侵入性小、快速的乳腺病变评估方法。FNAC的假阴性率高、结果模棱两可等局限性制约了其应用。本研究的目的是通过匹配相应的切除标本,将FNAC作为诊断工具与CNB进行比较。方法:收集2003年5月~ 2008年4月FNAC患者753例,CNB患者331例,FNAC与CNB合并患者98例。比较FNAC和CNB的诊断。结果:FNAC的敏感性为93.8%,特异性为80.8%,诊断准确率为90.1%。CNB组为92.1%、90.9%、92.3%,FNAC联合CNB组为100%、77.8%、98.0%。FNAC组和CNB组均未出现假阳性病例。FNAC组假阴性率为6.2%,CNB组为9.9%。抽样误差是导致所有FNAC样本和CNB样本出现错误或假阴性结果的原因。对于1 ~ 2 cm的病变,FNAC的诊断准确率优于CNB。结论:我们的数据表明,与核心活检相比,FNAC是评估乳腺病变的准确可靠的一线诊断工具。
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引用次数: 13
Prognostic significance of pSTAT3 and Survivin expression in diffuse large B-cell lymphoma pSTAT3和Survivin表达在弥漫性大b细胞淋巴瘤中的预后意义
Pub Date : 2010-03-04 DOI: 10.1111/j.1755-9294.2009.01063.x
Ji-Youn Sung, Sung-Jig Lim, Youn Wha Kim, Juhie Lee

Background and aim: The activated phosphorylated form of signal transducer and activator of transcription 3 (pSTAT3) up-regulates multiple downstream targets, including Survivin, which is an inhibitor of apoptosis, and has been implicated as an important process in malignant progression. The purpose of this study was to investigate the expression of pSTAT3 and Survivin in diffuse large B cell lymphomas (DLBCL) for their clinicopathological significance. Methods: Using tissue microarrays constructed from 102 DLBCLs, immunohistochemistry was done for pSTAT3 and Survivin. Results: Immunoreactivity for pSTAT3 and Survivin was seen in 41% and 46% of 102 patients of DLBCL. Patients who expressed pSTAT3 were more likely to have Survivin (p < 0.001) and p53 expressions (p= 0.002). According to the sub-groups of DLBCL, non-germinal center B cell (non-GCB) group was more likely to express pSTAT3 and Survivin. Both the pSTAT3 and Survivin expression were significantly associated with short overall survival by Kaplan–Meier survival curves and log-rank tests in both overall (p= 0.021 and p= 0.002) and non-GCB group of DLBCL (p= 0.023 and p= 0.006). Multivariate analysis confirmed that Survivin was an independent prognostic factor in both overall DLBCL (p= 0.014) and non-GCB group (p= 0.032). Conclusions: pSTAT3 and Survivin expression appear to be important prognostic factors for DLBCL patients.

背景与目的:信号转导因子和转录激活因子3 (pSTAT3)的活化磷酸化形式上调了多个下游靶标,包括Survivin,它是一种细胞凋亡抑制剂,在恶性进展中被认为是一个重要过程。本研究旨在探讨pSTAT3和Survivin在弥漫性大B细胞淋巴瘤(DLBCL)中的表达及其临床病理意义。方法:利用102例dlbcl构建的组织芯片,对pSTAT3和Survivin进行免疫组化检测。结果:102例DLBCL患者中pSTAT3和Survivin的免疫反应性分别为41%和46%。表达pSTAT3的患者更有可能有Survivin (p <0.001)和p53表达(p= 0.002)。根据DLBCL的亚组,非生发中心B细胞(non-GCB)组更容易表达pSTAT3和Survivin。Kaplan-Meier生存曲线和log-rank检验显示,pSTAT3和Survivin的表达与DLBCL总体(p= 0.021和p= 0.002)和非gcb组(p= 0.023和p= 0.006)的短总生存期显著相关。多因素分析证实,Survivin是整体DLBCL (p= 0.014)和非gcb组(p= 0.032)的独立预后因素。结论:pSTAT3和Survivin表达可能是影响DLBCL患者预后的重要因素。
{"title":"Prognostic significance of pSTAT3 and Survivin expression in diffuse large B-cell lymphoma","authors":"Ji-Youn Sung,&nbsp;Sung-Jig Lim,&nbsp;Youn Wha Kim,&nbsp;Juhie Lee","doi":"10.1111/j.1755-9294.2009.01063.x","DOIUrl":"10.1111/j.1755-9294.2009.01063.x","url":null,"abstract":"<div>\u0000 \u0000 <p> <b>Background and aim:</b> The activated phosphorylated form of signal transducer and activator of transcription 3 (pSTAT3) up-regulates multiple downstream targets, including Survivin, which is an inhibitor of apoptosis, and has been implicated as an important process in malignant progression. The purpose of this study was to investigate the expression of pSTAT3 and Survivin in diffuse large B cell lymphomas (DLBCL) for their clinicopathological significance. <b>Methods:</b> Using tissue microarrays constructed from 102 DLBCLs, immunohistochemistry was done for pSTAT3 and Survivin. <b>Results:</b> Immunoreactivity for pSTAT3 and Survivin was seen in 41% and 46% of 102 patients of DLBCL. Patients who expressed pSTAT3 were more likely to have Survivin (<i>p</i> &lt; 0.001) and p53 expressions (<i>p</i>= 0.002). According to the sub-groups of DLBCL, non-germinal center B cell (non-GCB) group was more likely to express pSTAT3 and Survivin. Both the pSTAT3 and Survivin expression were significantly associated with short overall survival by Kaplan–Meier survival curves and log-rank tests in both overall (<i>p</i>= 0.021 and <i>p</i>= 0.002) and non-GCB group of DLBCL (<i>p</i>= 0.023 and <i>p</i>= 0.006). Multivariate analysis confirmed that Survivin was an independent prognostic factor in both overall DLBCL (<i>p</i>= 0.014) and non-GCB group (<i>p</i>= 0.032). <b>Conclusions:</b> pSTAT3 and Survivin expression appear to be important prognostic factors for DLBCL patients.</p>\u0000 </div>","PeriodicalId":92990,"journal":{"name":"Basic and applied pathology","volume":"3 1","pages":"7-13"},"PeriodicalIF":0.0,"publicationDate":"2010-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1755-9294.2009.01063.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63680080","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Human neuroblastoma cell line SNU-NB1 loses sensitivity to brain-derived neurotrophic factor during establishment 人神经母细胞瘤细胞系SNU-NB1在建立过程中失去对脑源性神经营养因子的敏感性
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01056.x
Woong Jae Yun, Soo Hee Kim, Eun Shin, Ja June Jang, Kyoungbun Lee

Background and aims: The expression pattern of high affinity neurotrophin receptors dichotomizes the clinicopathologic characteristics of neuroblastoma (NB). The effects mediated by trkA have been documented in many experimental systems, whereas the effects mediated by trkB have only been investigated in limited studies. Methods: We established a new cell line of NB, “SNU-NB1”, by primary culture and the effects mediated by trkB were addressed in this cell line. Results: NB cells in primary culture showed amplification of N-myc and expression of trkB. Activation of trkB in primary culture by brain-derived neurotrophic factor (BDNF) was followed by activation of extracellular signal-regulated kinase1/2 (ERK1/2), growth inhibition, neuronal differentiation, and N-myc down-regulation. However, fully transformed SNU-NB1 cells lost BDNF sensitivity while being tumorigenic in vivo. Restoration of trkB expression in SNU-NB1 cells, by retroviral infection of trkB, induced differentiation and inhibition of growth in the cells following BDNF treatment. Although the prognosis of neuroblastomas is different according to the status of trkA and trkB mRNA expressions, the cytologic effects mediated by trkB per se are similar to those by trkA in NB. Conclusion: The patterns of trkA and trkB mRNA expression were markers for different lineages of transformed cells but were inconsistent with the clinical behavior.

背景与目的:高亲和力神经营养因子受体的表达模式区分了神经母细胞瘤(NB)的临床病理特征。trkA介导的影响已在许多实验系统中得到证实,而trkB介导的影响仅在有限的研究中得到调查。方法:采用原代培养方法建立NB细胞株“SNU-NB1”,并在该细胞株中研究trkB介导的作用。结果:原代培养NB细胞N-myc扩增,trkB表达。脑源性神经营养因子(BDNF)在原代培养中激活trkB,随后激活细胞外信号调节激酶1/2 (ERK1/2),抑制生长,神经元分化和N-myc下调。然而,完全转化的SNU-NB1细胞在体内具有致瘤性的同时失去了BDNF敏感性。通过trkB的逆转录病毒感染,恢复SNU-NB1细胞中trkB的表达,诱导BDNF处理后细胞的分化和生长抑制。虽然神经母细胞瘤的预后因trkA和trkB mRNA表达状态的不同而不同,但trkB本身介导的细胞学作用与trkA在NB中的作用相似。结论:trkA和trkB mRNA的表达模式是转化细胞不同谱系的标志,但与临床行为不一致。
{"title":"Human neuroblastoma cell line SNU-NB1 loses sensitivity to brain-derived neurotrophic factor during establishment","authors":"Woong Jae Yun,&nbsp;Soo Hee Kim,&nbsp;Eun Shin,&nbsp;Ja June Jang,&nbsp;Kyoungbun Lee","doi":"10.1111/j.1755-9294.2009.01056.x","DOIUrl":"10.1111/j.1755-9294.2009.01056.x","url":null,"abstract":"<div>\u0000 \u0000 <p> <b>Background and aims:</b> The expression pattern of high affinity neurotrophin receptors dichotomizes the clinicopathologic characteristics of neuroblastoma (NB). The effects mediated by trkA have been documented in many experimental systems, whereas the effects mediated by trkB have only been investigated in limited studies. <b>Methods:</b> We established a new cell line of NB, “SNU-NB1”, by primary culture and the effects mediated by trkB were addressed in this cell line. <b>Results:</b> NB cells in primary culture showed amplification of N-myc and expression of trkB. Activation of trkB in primary culture by brain-derived neurotrophic factor (BDNF) was followed by activation of extracellular signal-regulated kinase1/2 (ERK1/2), growth inhibition, neuronal differentiation, and N-myc down-regulation. However, fully transformed SNU-NB1 cells lost BDNF sensitivity while being tumorigenic <i>in vivo</i>. Restoration of trkB expression in SNU-NB1 cells, by retroviral infection of trkB, induced differentiation and inhibition of growth in the cells following BDNF treatment. Although the prognosis of neuroblastomas is different according to the status of trkA and trkB mRNA expressions, the cytologic effects mediated by trkB per se are similar to those by trkA in NB. <b>Conclusion:</b> The patterns of trkA and trkB mRNA expression were markers for different lineages of transformed cells but were inconsistent with the clinical behavior.</p>\u0000 </div>","PeriodicalId":92990,"journal":{"name":"Basic and applied pathology","volume":"2 4","pages":"131-136"},"PeriodicalIF":0.0,"publicationDate":"2009-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1755-9294.2009.01056.x","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63679497","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Undifferentiated carcinoma of the ascending colon with prominent rhabdoid features: A case report 升结肠未分化癌伴显著横纹肌特征1例
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01054.x
Jeana Kim, Kyungji Lee, Kyung-Jin Seo, Heejeong Lee, Tae-Eun Kim, Kyo-Young Lee, Eun Sun Jung

Colorectal adenocarcinoma with rhabdoid features is extremely rare and only three cases have been previously reported. We report a 62-year-old man who presented with general weakness and poor oral intake for 6 months, and showed multiple masses at the duodenum, jejunum, ileum and the ascending colon. The patient underwent right hemicolectomy with small bowel segmental resection. Microscopically, the tumor masses were characterized by incohesive sheet of neoplastic cells with vesicular nuclei, large nucleoli, and abundant eosinophilic cytoplasm. Immunohistochemical studies showed strong reactivity of the tumor cells for pan-cytokeratin, anti-endomysial antibodies (EMA) and vimentin. This was a case of undifferentiated carcinoma with prominent rhabdoid feautures arising in the ascending colon with multiple gastrointestinal metastases.

具有横纹肌样特征的结直肠腺癌极为罕见,以前仅报道过3例。我们报告一位62岁的男性,他表现出全身虚弱和口腔摄入不良6个月,并在十二指肠、空肠、回肠和升结肠出现多发肿块。患者行右半结肠切除术及小肠节段切除术。显微镜下,肿瘤肿块的特征是肿瘤细胞不粘连,具有泡状核、大核仁和丰富的嗜酸性细胞质。免疫组化研究显示肿瘤细胞对泛细胞角蛋白、抗肌内膜抗体(EMA)和波形蛋白有较强的反应性。这是一例未分化癌,在升结肠出现突出的横纹肌样特征,并发多发性胃肠道转移。
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引用次数: 0
Correlated expression of peroxisome proliferator-activated receptor γ with high histologic grade and basal type in invasive ductal carcinoma of the breast 乳腺浸润性导管癌中高组织学分级和基础型过氧化物酶体增殖物激活受体γ的相关表达
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01053.x
Hoiseon Jeong, Youngseok Lee, Jungsuk An, Ok Hee Woo, KyongHwa Park, Aeree Kim

Backgroud and aim: Peroxisome proliferator-activated receptor γ (PPARγ) is one of the ligand-activated transcription factors belonging to the nuclear hormone receptor family. The protein is expressed in various kinds of tumor and has been implicated as a tumor suppressor in most cancers. We aimed to understand the role of PPARγ in breast cancer. Methods: The expression of PPARγ in 288 cases of invasive ductal carcinoma was examined using tissue microarray and immunohistochemistry. Results: PPARγ immunoreactivity was detected in 21.5% of cases and significantly associated with expression of EGFR and ki-67 (P= 0.008; P= 0.046). PPARγ expression was correlated with high histological grade and basal type (P≤ 0.001; P= 0.009). Conclusions: PPARγ expression is related to poor prognostic factors of breast cancer. It is considered that PPARγ has evident tumor promoting properties in vivo, but receptor-independent effects of PPARγ ligands may compound its biologic effects in cancer. A better understanding of action mechanisms of the activated PPARγ is required.

背景与目的:过氧化物酶体增殖体激活受体γ (PPARγ)是核激素受体家族中配体激活的转录因子之一。该蛋白在多种肿瘤中表达,并在大多数癌症中被认为是肿瘤抑制因子。我们的目的是了解PPARγ在乳腺癌中的作用。方法:采用组织芯片和免疫组化技术检测288例浸润性导管癌组织中PPARγ的表达。结果:21.5%的病例检测到PPARγ免疫反应性,并与EGFR、ki-67的表达显著相关(P= 0.008;P = 0.046)。PPARγ表达与高组织学分级和基础型相关(P≤0.001;P = 0.009)。结论:PPARγ表达与乳腺癌预后不良因素有关。研究认为,PPARγ在体内具有明显的促肿瘤特性,但PPARγ配体的受体非依赖性可能会使其在癌症中的生物学效应复合。需要更好地了解活化PPARγ的作用机制。
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引用次数: 0
How overworked are pathologists? An assessment of cases for histopathology and cytopathology services 病理学家有多劳累?组织病理学和细胞病理学服务的病例评估
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01058.x
Hye Kyoung Yoon, Michele H Diwa, Youn Soo Lee, Gwangil Kim, Sang Yong Song, Kyoung Bun Lee, Han Kyeom Kim, Woon Sup Han, Jeong-Wook Seo

Background and aim: The objective of this paper is to evaluate the workload of staff in anatomic pathology (AP) laboratories in Korea. Methods: A survey was conducted at 197 AP laboratories in South Korea, these were categorized as 37 free standing laboratories, 14 laboratories in non-training hospitals (without residents), 79 in training hospitals (with residents), and 67 in university hospitals. The workloads of the staff were analyzed using the mean and standard deviation of the number of cases. Results: In total, there were 512 pathologists, 806 technicians and 205 cytopathology screeners. In a year, they processed a total of 3,150,261 histopathology cases and 4,115,420 cytopathology cases. The numbers of histopathology cases per pathologist or technician in one laboratory were 6,950 ± 6,748 and 4,074 ± 3,630, respectively. There were 109 laboratories that employed 205 cytoscreeners in addition to the 308 pathologists, where a cytoscreener read 14,780 ± 13,110 cases of cytopathology. However, in 88 laboratories, there were 132 pathologists who were not assisted by cytoscreeners, where a pathologist was reading 4,277 ± 3,033 cases of cytopathology. Conclusion: We propose a mean plus a standard deviation as a recommended guideline for staff workload at each laboratory setting to be used for a quality assurance program.

背景与目的:本文的目的是评估韩国解剖病理学(AP)实验室工作人员的工作量。方法:对韩国197家AP实验室进行调查,其中独立实验室37家,非培训医院(无住院医师)实验室14家,培训医院(有住院医师)实验室79家,大学医院实验室67家。采用病例数的平均值和标准差对工作人员的工作量进行分析。结果:共有病理医师512名,技师806名,细胞病理学筛查员205名。一年内共处理组织病理学病例3150261例,细胞病理学病例4115420例。每个实验室病理学家或技术人员的组织病理学病例数分别为6,950±6,748例和4,074±3,630例。109个实验室有205名细胞筛检员,308名病理学家,其中1名细胞筛检员有14780±13110例细胞病理。然而,在88个实验室中,有132名病理学家没有使用细胞筛检仪,其中一名病理学家阅读了4277±3033例细胞病理学。结论:我们提出一个平均值加一个标准差作为每个实验室设置的工作人员工作量的推荐指南,用于质量保证计划。
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引用次数: 2
EBM 循证医学
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01065.x
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引用次数: 0
Failure of bone regeneration after demineralized bone matrix allograft in human maxillary sinus floor elevation 脱矿化骨基质同种异体骨移植在上颌窦底抬高术后骨再生失败的研究
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01055.x
Sang Shin Lee, Jae Hyun Jang, Kwang Soo Kim, Young Jae Yoo, Yeon Sook Kim, Suk Keun Lee

Background and aims: There are a number of different commercially available demineralized bone matrix (DBM) products with significant differences between products with regard to the osteoinductive effect in bone defects. We aimed to evaluate the cellular response for the osteoinductive effect of the DBM graft materials by immunohistochemistry. Methods: Among five cases of sinus mucosa biopsy from the implant placement into the sinus floor elevation using DBM allograft, one case showed an intact sinus mucosa containing DBM inserted 4 months ago, while the others were severely infected and unable to be compared with each other for the osteoinductive effect of DBM. Immunohistochemistry investigations were undertaken. Results: The multinucleated giant cells were strongly positive for RANKL, cathepsin K, and HSP-90, and consistently positive for lysozyme, TNF-α, CD31, CD68, MMP-2, and MMP-9. The stromal cells were strongly positive for osteonectin and osteocalcin, but weak for BMP-2, BMP-4, RUNX2, TGF-β1, CTGF, and TGase-2. Conclusions: For sinus floor elevation the autogenic bone graft or osteogenic stem cell replacement is necessary, whereas DBM allograft only being insufficient.

背景和目的:有许多不同的市售脱矿骨基质(DBM)产品,在骨缺损的骨诱导作用方面,产品之间存在显著差异。我们的目的是通过免疫组织化学方法评估DBM移植材料对骨诱导作用的细胞反应。方法:在5例使用同种异体DBM移植物从种植体置入到窦底抬高处进行的窦黏膜活检中,1例为4个月前置入的含DBM的完整窦黏膜,其余为严重感染,无法比较DBM的成骨效果。进行免疫组化检查。结果:多核巨细胞RANKL、cathepsin K、HSP-90呈强阳性,溶菌酶、TNF-α、CD31、CD68、MMP-2、MMP-9呈持续阳性。基质细胞骨连接素、骨钙素呈强阳性,BMP-2、BMP-4、RUNX2、TGF-β1、CTGF、TGase-2呈弱阳性。结论:对于窦底抬高,自体骨移植或成骨干细胞置换是必要的,而DBM同种异体移植是不够的。
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引用次数: 6
Peripancreatic lymph node gastrinoma 胰周淋巴结胃原质瘤
Pub Date : 2009-12-03 DOI: 10.1111/j.1755-9294.2009.01057.x
Si-Hyong Jang, Se Min Jang, Young Jin Jun, Woong Na, Kyueng Whan Min, Ki-Seok Jang, Seung Sam Paik

Gastrinoma is one of the most symptomatic pancreatic endocrine tumors and is associated with recurrent gastric or duodenal ulcer and an induction of chronic gastric acid hypersecretion. This tumor is commonly involved within the gastrinoma triangle. Herein we report a peripancreatic lymph node gastrinoma in a 56-year-old man who was suffered from a recurrent duodenal or jejunal ulcer perforation. Octreotide scan detected a peripancreatic or periduodenal mass and the serum gastrin level was set in upper normal range (107.73 pg/mL). Whipple's procedure was performed. The resected specimen showed multiple duodenal ulcers, hypertrophic gastric body mucosa and an enlarged peripancreatic node, measured 1.5 × 1.0 cm in cross diameter. Microscopic examination revealed a single enlarged lymph node replaced by tumor cell nests with pale eosinophilic cytoplasm and ‘salt-and-pepper’ chromatin pattern. On immunohistochemical staining, the tumor cells were diffusely positive for chromogranin, synaptophysin, gastrin and focally positive for CD56. He was finally diagnosed as a primary lymph node gastrinoma. After operation, the patient revisited our hospital due to severe esophageal stricture and he underwent endoscopic esophagoplasty.

胃原质瘤是最具症状性的胰腺内分泌肿瘤之一,与胃或十二指肠溃疡复发及慢性胃酸高分泌有关。这种肿瘤通常累及胃泌素瘤三角区。在此,我们报告一个56岁男性胰脏周围淋巴结胃原质瘤,他患有复发性十二指肠或空肠溃疡穿孔。奥曲肽扫描发现胰腺周围或十二指肠周围肿块,血清胃泌素水平在正常范围上(107.73 pg/mL)。进行了惠普尔手术。切除标本显示十二指肠多发溃疡,胃体粘膜肥厚,胰周结肿大,交叉直径1.5 × 1.0 cm。镜检显示单个肿大的淋巴结被肿瘤细胞巢所取代,具有苍白的嗜酸性细胞质和“盐和胡椒”染色质模式。免疫组化染色显示肿瘤细胞嗜铬粒蛋白、突触素、胃泌素弥漫性阳性,CD56局部阳性。他最终被诊断为原发性淋巴结胃原质瘤。术后患者因严重食管狭窄再次来我院就诊,行内镜下食管成形术。
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引用次数: 1
Genetic analysis of NOD2 in patients with intestinal tuberculosis and Crohn's disease in Korea 韩国肠结核和克罗恩病患者NOD2基因分析
Pub Date : 2009-09-02 DOI: 10.1111/j.1755-9294.2009.01050.x
Yosep Chong, Mi Jung Lee, So Young Jung, Joon Mee Kim, Mee-Yon Cho

Background and aims: Nod2 is an intracellular pathogen sensor found to be associated with susceptibility to Crohn's disease (CD) in Western countries. However, the results from Asian population including Koreans showed discordant findings. Meanwhile, a recent study demonstrated significant associations between NOD2 polymorphisms and tuberculosis (TB). However, in Korea, no studies on NOD2 mutations in TB patients have been conducted as of yet. Methods: We collected the surgically resected intestines confirmed as TB with more than one positivity among TB-polymerase chain reaction, Ziehl-Neelsen stain, and culture for Mycobacterium tuberculosis. CD was confirmed on the basis of usual clinico-pathological criteria with all negativity for aforementioned tests and without other infectious causes. DNA extracted from the formalin-fixed, paraffin-embedded tissues of patients with intestinal TB (14), CD (19), and controls (18) were amplified by PCR using five primers for Ala140Thr, Pro268Ser, Arg702Trp, Arg708His, Ala725Gly, Gly908Arg, and Leu1007fs. DNA sequencing was then performed. Results: Histologically, well-defined granulomas with caseous necrosis were found in all TB but not in any CD. We found no mutations related to CD as well as TB in DNA sequencing. Conclusions: This result reconfirmed that the molecular changes associated with CD in Asian populations might differ from Western populations. Furthermore, the genetic change associated with TB in Korea is still remains to be clarified.

背景和目的:Nod2是一种细胞内病原体传感器,在西方国家被发现与克罗恩病(CD)的易感性相关。但是,对包括韩国人在内的亚洲人的调查结果却不一致。同时,最近的一项研究表明NOD2多态性与结核病(TB)之间存在显著关联。但是,在国内还没有对结核患者的NOD2突变进行研究。方法:收集经手术切除并经结核聚合酶链反应、Ziehl-Neelsen染色及结核分枝杆菌培养等多项检测呈阳性的TB肠子。根据通常的临床病理标准确诊乳糜泻,上述检查均为阴性,无其他感染原因。从肠结核患者(14例)、CD患者(19例)和对照组(18例)经福尔马林固定、石蜡包埋的组织中提取DNA,采用五种引物进行PCR扩增,引物分别为Ala140Thr、Pro268Ser、Arg702Trp、Arg708His、Ala725Gly、Gly908Arg和Leu1007fs。然后进行DNA测序。结果:组织学上,明确的肉芽肿和干酪样坏死在所有结核病中都有发现,但在任何CD中都没有发现。我们在DNA测序中没有发现与CD和TB相关的突变。结论:这一结果再次证实了亚洲人群与CD相关的分子变化可能不同于西方人群。此外,与韩国结核病相关的基因变化仍有待澄清。
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引用次数: 1
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Basic and applied pathology
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