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Histopathological characteristics of Epstein-Barr virus (EBV)-associated encephalitis and colitis in chronic active EBV infection. 慢性活动性EBV感染中eb病毒相关脑炎和结肠炎的组织病理学特征
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-05-01 Epub Date: 2025-04-16 DOI: 10.4132/jptm.2025.02.21
Betty A Kasimo, James J Yahaya, Sun Och Yoon, Se Hoon Kim, Minsun Jung

Chronic active Epstein-Barr virus (CAEBV) can induce complications in various organs, including the brain and gastrointestinal tract. A 3-year-old boy was referred to the hospital with a history of fever and seizures for 15 days. A diagnosis of encephalitis based on computed tomography (CT) and magnetic resonance imaging findings and clinical correlation was made. Laboratory tests showed positive serology for Epstein-Barr virus (EBV) and negative for Rotavirus antigen and IgG and IgM antibodies for cytomegalovirus, herpes simplex virus, and varicella zoster virus, respectively. Abdominal CT showed diffuse wall thickening with fluid distension of small bowel loops, lower abdomen wall thickening, and a small amount of ascites. The biopsy demonstrated positive Epstein-Barr encoding region in situ hybridization in cells within the crypts and lamina propria. The patient was managed with steroids and hematopoietic stem cell transplantation (HSCT). This case showed histopathological characteristics of concurrent EBV-associated encephalitis and colitis in CAEBV infection. The three-step strategy of immunosuppressive therapy, chemotherapy, and allogeneic HSCT should be always be considered for prevention of disease progression.

慢性活动性爱泼斯坦-巴尔病毒(CAEBV)可引起多种器官的并发症,包括大脑和胃肠道。一名三岁男童因发烧及癫痫发作15天被转介至医院。根据计算机断层扫描(CT)和磁共振成像的表现和临床相关性诊断脑炎。实验室检查显示eb病毒(EBV)血清学阳性,轮状病毒抗原阴性,巨细胞病毒、单纯疱疹病毒和水痘带状疱疹病毒IgG和IgM抗体阴性。腹部CT示弥漫性肠壁增厚伴小肠袢液体膨胀,下腹壁增厚,少量腹水。活检显示隐窝和固有层内细胞的Epstein-Barr编码区原位杂交阳性。患者接受类固醇和造血干细胞移植(HSCT)治疗。本病例表现出eb病毒感染并发脑炎和结肠炎的组织病理学特征。免疫抑制治疗、化疗和同种异体造血干细胞移植三步策略应始终被考虑用于预防疾病进展。
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引用次数: 0
Lessons learned from the first 2 years of experience with thyroid core needle biopsy at an Indonesian national referral hospital. 印度尼西亚一家国家转诊医院头两年甲状腺核心针活检经验的教训。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-05-01 Epub Date: 2025-04-25 DOI: 10.4132/jptm.2025.02.19
Agnes Stephanie Harahap, Maria Francisca Ham, Retno Asti Werdhani, Erwin Danil Julian, Rafi Ilmansyah, Chloe Indira Arfelita Mangunkusumso, Tri Juli Edi Tarigan

Background: Core needle biopsy (CNB) improves diagnostic accuracy by providing precise tissue sampling for histopathological evaluation, overcoming the limitation of inconclusive fine-needle aspiration results. This study evaluated the diagnostic performance of CNB in assessing thyroid nodules, with additional analysis of the benefits of BRAF V600E and RAS Q61R immunohistochemical (IHC) markers.

Methods: This retrospective study enrolled patients with thyroid nodules who underwent CNB at Dr. Cipto Mangunkusumo Hospital, Jakarta, from July 2022 to July 2024. CNB diagnoses were classified using the Korean Thyroid Association Criteria. Diagnostic efficacy was evaluated for neoplastic and malignant lesions, both independently and with BRAF V600E and RAS Q61R IHC. The correlation between nodule size and postoperative diagnosis was also analyzed.

Results: A total of 338 thyroid nodule samples was included, and 52.7% were classified as CNB category II. In the 104 samples with postoperative diagnoses, category IV was the most prevalent (39.4%). CNB demonstrated a sensitivity of 74% and a specificity of 100% for neoplastic lesions and 23.8% sensitivity and 100% specificity for malignant lesions. Combining CNB with BRAF V600E and RAS Q1R IHC increased the sensitivity to 77% for neoplastic lesions and 28.8% for malignant lesions. Larger nodules (>3 cm) were significantly associated with neoplastic (p = .005) and malignant lesions (p = .004).

Conclusions: CNB performs well in identifying neoplastic lesions, with or without BRAF V600E and RAS Q61R IHC, but its low sensitivity for malignant lesions warrants caution. While CNB categories V-VI indicate malignancy, the possibility of malignancy in categories I-IV should not be overlooked.

背景:核心针活检(CNB)通过提供精确的组织取样进行组织病理学评估来提高诊断准确性,克服了细针穿刺结果不确定的局限性。本研究评估了CNB在评估甲状腺结节中的诊断性能,并分析了BRAF V600E和RAS Q61R免疫组化(IHC)标志物的益处。方法:这项回顾性研究纳入了2022年7月至2024年7月在雅加达Dr. Cipto Mangunkusumo医院接受CNB治疗的甲状腺结节患者。CNB诊断采用韩国甲状腺协会标准进行分类。对肿瘤和恶性病变的诊断效果进行评估,包括单独评估和使用BRAF V600E和RAS Q61R IHC。分析结节大小与术后诊断的相关性。结果:共纳入338例甲状腺结节,其中52.7%归为CNB II类。在104例术后诊断的样本中,IV类最常见(39.4%)。CNB对肿瘤病变的敏感性为74%,特异性为100%,对恶性病变的敏感性为23.8%,特异性为100%。CNB联合BRAF V600E和RAS Q1R IHC对肿瘤病变的敏感性提高了77%,对恶性病变的敏感性提高了28.8%。较大的结节(bbb3cm)与肿瘤(p = 0.005)和恶性病变(p = 0.004)显著相关。结论:CNB在识别肿瘤病变方面表现良好,无论是否有BRAF V600E和RAS Q61R IHC,但其对恶性病变的敏感性较低,值得谨慎。虽然CNB分类V-VI为恶性,但不应忽视分类I-IV为恶性的可能性。
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引用次数: 0
Cytological features of atypical adenomatous hyperplasia and adenocarcinoma in situ of the lung: a case report. 肺非典型腺瘤性增生和原位腺癌的细胞学特征:1例报告。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-05-01 Epub Date: 2025-05-09 DOI: 10.4132/jptm.2025.04.09
Misa Takahashi, Seiya Homma, Chisato Setoguchi, Yoko Umezawa, Atsuhiko Sakamoto

Atypical adenomatous hyperplasia (AAH) and adenocarcinoma in situ (AIS) are generally treated as different lesions, depending on the differences in lesion size and histological findings. However, these differences are not absolute; thus, AAH and AIS are often difficult to distinguish. Moreover, whether AAH and AIS can be regarded as different lesions remains unknown because cytological specimens, especially those of AAH, are rare. In this study, we examined these uncommon cytological specimens and compared the cytological findings between AAH and AIS. We observed many common cytological features with no obvious differences between AAH and AIS. These findings suggest that these two distinct lesions can be grouped into a single category. Therefore, we propose creating a new cytological category.

非典型腺瘤性增生(AAH)和原位腺癌(AIS)通常被视为不同的病变,取决于病变大小和组织学表现的差异。然而,这些差异并不是绝对的;因此,AAH和AIS通常难以区分。此外,由于细胞学标本,特别是AAH的细胞学标本很少,因此AAH和AIS是否可以视为不同的病变尚不清楚。在这项研究中,我们检查了这些罕见的细胞学标本,并比较了AAH和AIS的细胞学结果。我们观察到许多常见的细胞学特征,AAH和AIS之间没有明显差异。这些发现表明这两种不同的病变可以归为一类。因此,我们建议创建一个新的细胞学分类。
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引用次数: 0
Primary Merkel cell carcinoma of the salivary gland: a clinicopathologic study of four cases with a review of literature. 原发性唾液腺默克尔细胞癌:四例临床病理研究并文献复习。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-05-01 Epub Date: 2025-04-30 DOI: 10.4132/jptm.2025.03.25
Gyuheon Choi, Joon Seon Song, Hee Jin Lee, Gi Hwan Kim, Young Ho Jung, Yoon Se Lee, Kyung-Ja Cho

Background: Primary Merkel cell carcinoma of the salivary gland is currently not listed in the World Health Organization classification. However, cases of Merkel cell type neuroendocrine carcinomas of the salivary gland with perinuclear cytokeratin 20 positivity have been intermittently reported. We here investigated the clinicopathologic features of additional cases.

Methods: Data of four cases of Merkel cell type small cell neuroendocrine carcinoma of the salivary gland were retrieved. To confirm the tumors' primary nature, clinical records and pathologic materials were reviewed. Optimal immunohistochemical staining was performed to support the diagnosis.

Results: All tumors were located in the parotid gland. Possibilities of metastasis were excluded in all cases through a meticulous clinicopathological review. Tumor histology was consistent with the diagnosis of small cell neuroendocrine carcinoma. Tumors' immunohistochemical phenotypes were consistent with Merkel cell carcinoma, including Merkel cell polyomavirus large T antigen positivity in two of the four cases.

Conclusions: Merkel cell carcinomas can originate in salivary glands and are partly associated with Merkel cell polyomavirus infection as in cutaneous Merkel cell carcinomas.

背景:原发性唾液腺默克尔细胞癌目前未列入世界卫生组织分类。然而,核周细胞角蛋白20阳性的唾液腺默克尔细胞型神经内分泌癌病例已被间歇性报道。我们在此研究了其他病例的临床病理特征。方法:回顾性分析4例涎腺默克尔细胞型小细胞神经内分泌癌的资料。为了确认肿瘤的原发性,我们回顾了临床记录和病理资料。最佳免疫组织化学染色支持诊断。结果:所有肿瘤均位于腮腺。通过细致的临床病理检查,排除了所有病例转移的可能性。肿瘤组织学符合小细胞神经内分泌癌的诊断。肿瘤免疫组化表型与默克尔细胞癌一致,包括4例中2例默克尔细胞多瘤病毒大T抗原阳性。结论:梅克尔细胞癌可起源于唾液腺,并与皮肤梅克尔细胞癌中梅克尔细胞多瘤病毒感染部分相关。
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引用次数: 0
Erratum: Diagnostic challenges in the assessment of thyroid neoplasms using nuclear features and vascular and capsular invasion: a multi-center interobserver agreement study. 勘误:使用核特征和血管及囊膜侵犯评估甲状腺肿瘤的诊断挑战:一项多中心观察者间一致研究。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-05-01 Epub Date: 2025-03-31 DOI: 10.4132/jptm.2024.07.25.r
Agnes Stephanie Harahap, Mutiah Mutmainnah, Maria Francisca Ham, Dina Khoirunnisa, Abdillah Hasbi Assadyk, Husni Cangara, Aswiyanti Asri, Diah Prabawati Retnani, Fairuz Quzwain, Hasrayati Agustina, Hermawan Istiadi, Indri Windarti, Krisna Murti, Muhammad Takbir, Ni Made Mahastuti, Nila Kurniasari, Nungki Anggorowati, Pamela Abineno, Yulita Pundewi Setyorini, Kennichi Kakudo
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引用次数: 0
Categorizing high-grade serous ovarian carcinoma into clinically relevant subgroups using deep learning-based histomic clusters. 使用基于深度学习的组织簇将高级别浆液性卵巢癌分类为临床相关亚组。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-03-01 Epub Date: 2025-02-18 DOI: 10.4132/jptm.2024.10.23
Byungsoo Ahn, Eunhyang Park

Background: High-grade serous ovarian carcinoma (HGSC) exhibits significant heterogeneity, posing challenges for effective clinical categorization. Understanding the histomorphological diversity within HGSC could lead to improved prognostic stratification and personalized treatment approaches.

Methods: We applied the Histomic Atlases of Variation Of Cancers model to whole slide images from The Cancer Genome Atlas dataset for ovarian cancer. Histologically distinct tumor clones were grouped into common histomic clusters. Principal component analysis and K-means clustering classified HGSC samples into three groups: highly differentiated (HD), intermediately differentiated (ID), and lowly differentiated (LD).

Results: HD tumors showed diverse patterns, lower densities, and stronger eosin staining. ID tumors had intermediate densities and balanced staining, while LD tumors were dense, patternless, and strongly hematoxylin-stained. RNA sequencing revealed distinct patterns in mitochondrial oxidative phosphorylation and energy metabolism, with upregulation in the HD, downregulation in the LD, and the ID positioned in between. Survival analysis showed significantly lower overall survival for the LD compared to the HD and ID, underscoring the critical role of mitochondrial dynamics and energy metabolism in HGSC progression.

Conclusions: Deep learning-based histologic analysis effectively stratifies HGSC into clinically relevant prognostic groups, highlighting the role of mitochondrial dynamics and energy metabolism in disease progression. This method offers a novel approach to HGSC categorization.

背景:高级别浆液性卵巢癌(HGSC)表现出显著的异质性,这对有效的临床分类提出了挑战。了解HGSC内的组织形态学多样性可以改善预后分层和个性化治疗方法。方法:我们将癌症变异的组织图谱模型应用于来自癌症基因组图谱数据集的卵巢癌全幻灯片图像。组织学上不同的肿瘤克隆被归为共同的组织簇。主成分分析和K-means聚类将HGSC样本分为三类:高分化(HD)、中等分化(ID)和低分化(LD)。结果:HD肿瘤形态多样,密度低,伊红染色强。ID肿瘤密度中等,染色均衡;LD肿瘤致密,无模式,苏木精染色强烈。RNA测序揭示了线粒体氧化磷酸化和能量代谢的不同模式,HD上调,LD下调,ID位于两者之间。生存分析显示,与HD和ID相比,LD的总生存期明显较低,这强调了线粒体动力学和能量代谢在HGSC进展中的关键作用。结论:基于深度学习的组织学分析有效地将HGSC划分为临床相关的预后组,突出了线粒体动力学和能量代谢在疾病进展中的作用。该方法为HGSC分类提供了一种新的方法。
{"title":"Categorizing high-grade serous ovarian carcinoma into clinically relevant subgroups using deep learning-based histomic clusters.","authors":"Byungsoo Ahn, Eunhyang Park","doi":"10.4132/jptm.2024.10.23","DOIUrl":"10.4132/jptm.2024.10.23","url":null,"abstract":"<p><strong>Background: </strong>High-grade serous ovarian carcinoma (HGSC) exhibits significant heterogeneity, posing challenges for effective clinical categorization. Understanding the histomorphological diversity within HGSC could lead to improved prognostic stratification and personalized treatment approaches.</p><p><strong>Methods: </strong>We applied the Histomic Atlases of Variation Of Cancers model to whole slide images from The Cancer Genome Atlas dataset for ovarian cancer. Histologically distinct tumor clones were grouped into common histomic clusters. Principal component analysis and K-means clustering classified HGSC samples into three groups: highly differentiated (HD), intermediately differentiated (ID), and lowly differentiated (LD).</p><p><strong>Results: </strong>HD tumors showed diverse patterns, lower densities, and stronger eosin staining. ID tumors had intermediate densities and balanced staining, while LD tumors were dense, patternless, and strongly hematoxylin-stained. RNA sequencing revealed distinct patterns in mitochondrial oxidative phosphorylation and energy metabolism, with upregulation in the HD, downregulation in the LD, and the ID positioned in between. Survival analysis showed significantly lower overall survival for the LD compared to the HD and ID, underscoring the critical role of mitochondrial dynamics and energy metabolism in HGSC progression.</p><p><strong>Conclusions: </strong>Deep learning-based histologic analysis effectively stratifies HGSC into clinically relevant prognostic groups, highlighting the role of mitochondrial dynamics and energy metabolism in disease progression. This method offers a novel approach to HGSC categorization.</p>","PeriodicalId":46933,"journal":{"name":"Journal of Pathology and Translational Medicine","volume":" ","pages":"91-104"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12010873/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143442304","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Erratum: Breast fine-needle aspiration cytology in the era of core-needle biopsy: what is its role? 勘误:乳腺细针穿刺细胞学在核心针活检时代:它的作用是什么?
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-03-01 Epub Date: 2025-03-14 DOI: 10.4132/jptm.2024.11.01.r
Ahrong Kim, Hyun Jung Lee, Jee Yeon Kim
{"title":"Erratum: Breast fine-needle aspiration cytology in the era of core-needle biopsy: what is its role?","authors":"Ahrong Kim, Hyun Jung Lee, Jee Yeon Kim","doi":"10.4132/jptm.2024.11.01.r","DOIUrl":"10.4132/jptm.2024.11.01.r","url":null,"abstract":"","PeriodicalId":46933,"journal":{"name":"Journal of Pathology and Translational Medicine","volume":"59 2","pages":"147"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12026265/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143804352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mucocele of the rectal stump: mucinous cystic neoplasm with low-grade dysplasia simulating low-grade appendiceal mucinous neoplasm. 直肠残端黏液囊肿:黏液囊性肿瘤伴低级别发育不良,类似低级别阑尾黏液性肿瘤。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-03-01 Epub Date: 2025-02-26 DOI: 10.4132/jptm.2024.12.27
Hasan Basri Aydin, Maria Faraz, A David Chismark, Haiyan Qiu, Hwajeong Lee

Mucoceles, commonly observed in the appendix, are mucin-filled, dilated structures arising from a range of etiologies. Cases associated with dysplastic or neoplastic epithelium can rupture and disseminate within the abdominopelvic cavity. Similar lesions in other parts of the colon are exceedingly rare, with only 16 colonic mucoceles having been reported. The first case of a colonic mucinous neoplasm with dysplasia resembling a low-grade appendiceal mucinous neoplasm involving rectal stump was described in 2016. Here, we present the second such case arising in the rectal stump, identified in a 44-year-old male with extensive surgical history. Microscopic examination revealed low-grade dysplastic epithelium lining the cyst and mucin dissecting into the stroma, without evidence of rupture or extramural mucin. The patient was followed for 16 months without recurrence or peritoneal disease. The exact etiology and outcome of these rare lesions remain unknown, requiring close follow-up.

粘液囊肿,常见于阑尾,是由多种病因引起的充满粘液的扩张结构。与发育不良或肿瘤上皮相关的病例可在腹腔内破裂和扩散。结肠其他部位的类似病变极为罕见,仅报道了16例结肠粘液囊肿。首例结肠黏液性肿瘤伴不典型增生,类似低级别阑尾黏液性肿瘤累及直肠残端,于2016年报道。在这里,我们提出的第二个这样的情况下,出现在直肠残端,确定在一个44岁的男性有广泛的手术史。显微镜检查显示,囊肿内有低级别发育不良的上皮,黏液进入间质,未见破裂或外膜黏液。患者随访16个月,无复发或腹膜疾病。这些罕见病变的确切病因和结果尚不清楚,需要密切随访。
{"title":"Mucocele of the rectal stump: mucinous cystic neoplasm with low-grade dysplasia simulating low-grade appendiceal mucinous neoplasm.","authors":"Hasan Basri Aydin, Maria Faraz, A David Chismark, Haiyan Qiu, Hwajeong Lee","doi":"10.4132/jptm.2024.12.27","DOIUrl":"10.4132/jptm.2024.12.27","url":null,"abstract":"<p><p>Mucoceles, commonly observed in the appendix, are mucin-filled, dilated structures arising from a range of etiologies. Cases associated with dysplastic or neoplastic epithelium can rupture and disseminate within the abdominopelvic cavity. Similar lesions in other parts of the colon are exceedingly rare, with only 16 colonic mucoceles having been reported. The first case of a colonic mucinous neoplasm with dysplasia resembling a low-grade appendiceal mucinous neoplasm involving rectal stump was described in 2016. Here, we present the second such case arising in the rectal stump, identified in a 44-year-old male with extensive surgical history. Microscopic examination revealed low-grade dysplastic epithelium lining the cyst and mucin dissecting into the stroma, without evidence of rupture or extramural mucin. The patient was followed for 16 months without recurrence or peritoneal disease. The exact etiology and outcome of these rare lesions remain unknown, requiring close follow-up.</p>","PeriodicalId":46933,"journal":{"name":"Journal of Pathology and Translational Medicine","volume":"59 2","pages":"139-146"},"PeriodicalIF":1.7,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12010871/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143804353","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association study of TYMS gene expression with TYMS and ENOSF1 genetic variants in neoadjuvant chemotherapy response of gastric cancer. TYMS基因表达与TYMS和ENOSF1基因变异在胃癌新辅助化疗反应中的相关性研究。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-03-01 Epub Date: 2025-02-25 DOI: 10.4132/jptm.2024.11.05
Khadijeh Arjmandi, Iman Salahshourifar, Shiva Irani, Fereshteh Ameli, Mohsen Esfandbod

Background: The present research was designed to study the associations between genetic variants of TYMS and ENOSF1 genes with TYMS and ENOSF1 gene expression in neoadjuvant chemotherapy response among patients with gastric cancer.

Methods: Formalin-embedded and paraffin-fixed matched tumor and normal gastric cancer tissue samples from patients who received neoadjuvant 5-fluorouracil (5-FU) treatment were obtained. DNA and RNA were extracted for all samples. A 28-bp variable number tandem repeat (VNTR) at the 5' untranslated region of TYMS gene and rs2612091 and rs2741171 variants in the ENOSF1 gene were genotyped for normal tissue samples. The real-time polymerase chain reaction method was used to study the expression of ENOSF1 and TYMS genes in both normal and tumor tissues. Data were analyzed using REST 2000 and SPSS ver. 26.0 software programs.

Results: A significant association between TYMS 2R3R VNTR genotypes and 5-FU therapy was found (p = .032). The 3R3R and 2R2R genotypes were significantly associated with increased and decreased survival time, respectively (p = .003). The 3R3R genotype was significantly associated with TYMS overexpression (p < .001). Moreover, a significant association was found between the rs2612091 genotype and treatment outcome (p = .017).

Conclusions: This study highlights the impact of TYMS and ENOSF1 genes as predictive indicators for survival and response to 5-FU-based neoadjuvant chemotherapy in gastric cancer patients.

背景:本研究旨在研究TYMS和ENOSF1基因的遗传变异与TYMS和ENOSF1基因表达在胃癌患者新辅助化疗反应中的关系。方法:对接受5-氟尿嘧啶(5-FU)新辅助治疗的胃癌患者进行福尔马林包埋和石蜡固定相匹配的肿瘤和正常胃癌组织标本。提取所有样品的DNA和RNA。在正常组织样本中,对TYMS基因5'非翻译区28bp可变数串联重复序列(VNTR)和ENOSF1基因rs2612091和rs2741171变异进行了基因分型。采用实时聚合酶链反应法研究ENOSF1和TYMS基因在正常组织和肿瘤组织中的表达。数据分析采用REST 2000和SPSS ver。26.0软件程序。结果:TYMS 2R3R VNTR基因型与5-FU治疗有显著相关性(p = 0.032)。3R3R和2R2R基因型分别与生存时间增加和减少显著相关(p = 0.003)。3R3R基因型与TYMS过表达显著相关(p < 0.001)。此外,rs2612091基因型与治疗结果之间存在显著相关性(p = 0.017)。结论:本研究强调了TYMS和ENOSF1基因作为胃癌患者生存和对5- fu新辅助化疗反应的预测指标的影响。
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引用次数: 0
Uncommon granulomatous manifestation in Epstein-Barr virus-positive follicular dendritic cell sarcoma: a case report. 爱泼斯坦-巴氏病毒阳性滤泡树突状细胞肉瘤的罕见肉芽肿表现:病例报告。
IF 1.7 Q3 PATHOLOGY Pub Date : 2025-03-01 Epub Date: 2024-10-31 DOI: 10.4132/jptm.2024.09.27
Henry Goh Di Shen, Yue Zhang, Wei Qiang Leow

Hepatic Epstein-Barr virus-positive inflammatory follicular dendritic cell sarcoma (EBV+ IFDCS) represents a rare form of liver malignancy. The absence of distinct clinical and radiological characteristics, compounded by its rare occurrence, contributes to a challenging diagnosis. Here, we report a case of a 54-year-old Chinese female with a background of chronic hepatitis B virus treated with entecavir and complicated by advanced fibrosis presenting with a liver mass found on her annual surveillance ultrasound. Hepatectomy was performed under clinical suspicion of hepatocellular carcinoma. Immunomorphologic characteristics of the tumor were consistent with EBV+ IFDCS with distinct non-caseating granulomatous inflammation. Our case illustrates the importance of considering EBV+ IFDCS in the differential diagnosis of hepatic inflammatory lesions. Awareness of this entity and its characteristic features is essential for accurately diagnosing and managing this rare neoplasm.

肝脏爱泼斯坦-巴氏病毒阳性炎性滤泡树突状细胞肉瘤(EBV+ IFDCS)是一种罕见的肝脏恶性肿瘤。由于缺乏明显的临床和放射学特征,加之其罕见的发生率,导致其诊断极具挑战性。在此,我们报告了一例 54 岁的中国女性病例,她患有慢性乙型肝炎病毒,曾接受恩替卡韦治疗,并并发晚期肝纤维化,在年度监测超声检查中发现肝脏肿块。在临床怀疑为肝细胞癌的情况下进行了肝切除术。肿瘤的免疫形态学特征与 EBV+ IFDCS 一致,并伴有明显的非酪氨酸肉芽肿性炎症。我们的病例说明了在肝脏炎症病变的鉴别诊断中考虑 EBV+ IFDCS 的重要性。了解这种肿瘤及其特征对于准确诊断和处理这种罕见肿瘤至关重要。
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引用次数: 0
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Journal of Pathology and Translational Medicine
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