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Enterocolic granulomatous phlebitis associated with epidermal growth factor-containing fibulin-like extracellular matrix protein 1 deposition and focal amyloid properties: A case report. 肠结肠肉芽肿性静脉炎伴有含表皮生长因子的纤维蛋白样细胞外基质蛋白 1 沉积和局灶性淀粉样蛋白特性:病例报告。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-03-01 Epub Date: 2024-01-19 DOI: 10.1111/pin.13405
Shojiro Ichimata, Akane Aikawa, Naonori Sugishita, Nagaaki Katoh, Fuyuki Kametani, Hibiki Tagawa, Yusuke Handa, Masahide Yazaki, Yoshiki Sekijima, Takashi Ehara, Naoki Nishida, Shin Ishizawa

A woman in her 60s with rheumatoid arthritis was admitted with fever and abdominal pain. Laparoscopic examination with the differential diagnosis of peritoneal neoplasm and infection revealed granulomatous phlebitis in the resected greater omentum. Amorphous eosinophilic deposits observed in the resected tissue exhibited focal, weak positivity for Congo red but were strongly positive for thioflavin S, confirming their focal amyloid properties. Marked degeneration of elastic fibers was also evident. Electron microscopy revealed deposits around the affected elastic fibers. Immunohistochemistry revealed the deposition of epidermal growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1) along with T-cell-predominant lymphocytic inflammation. The definitive diagnosis was granulomatous enterocolic lymphocytic phlebitis (ELP) associated with EFEMP1 deposition exhibiting focal amyloid properties (EFEMP1/AEFEMP1), supported by proteomics analysis. This type of vasculitis is similar to amyloid-β-related angiitis of the central nervous system. Thus, we speculate that granulomatous ELP also results from an immune response that recognizes EFEMP1/AEFEMP1 deposits as foreign material and attempts to remove them. Confirmation of EFEMP1/AEFEMP1 deposition with Congo red staining is challenging, particularly in the presence of inflammation, and warrants comprehensive evaluation.

一名患有类风湿性关节炎的 60 多岁妇女因发烧和腹痛入院。腹腔镜检查发现,切除的大网膜上有肉芽肿性静脉炎,鉴别诊断为腹膜肿瘤和感染。在切除的组织中观察到无定形的嗜酸性沉积物,刚果红呈局灶性弱阳性,但硫黄素 S 呈强阳性,证实了其局灶性淀粉样变性。弹性纤维也明显退化。电子显微镜检查发现,受影响的弹性纤维周围有沉积物。免疫组化显示,含有表皮生长因子的纤维素样细胞外基质蛋白1(EFEMP1)沉积,并伴有以T细胞为主的淋巴细胞炎症。经蛋白质组学分析,最终诊断为肉芽肿性肠淋巴细胞性静脉炎(ELP),并伴有表现出局灶淀粉样特性的 EFEMP1 沉积(EFEMP1/AEFEMP1)。这种类型的血管炎与中枢神经系统的淀粉样β相关血管炎相似。因此,我们推测肉芽肿性 ELP 也是免疫反应的结果,免疫反应将 EFEMP1/AEFEMP1 沉积物识别为外来物质并试图将其清除。用刚果红染色法确认 EFEMP1/AEFEMP1 沉积具有挑战性,尤其是在存在炎症的情况下,因此需要进行全面评估。
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引用次数: 0
Alteration of small intestinal occludin and ZO-1 expession in liver cirrhosis. 肝硬化患者小肠闭塞素和 ZO-1 表达的改变
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-03-01 Epub Date: 2024-01-22 DOI: 10.1111/pin.13406
Theodoros Voulgaris, Dina Tiniakos, Dimitrios Karagiannakis, Despoina Myoteri, Despoina Karandrea, Spilios Manolakopoulos, George Papatheodoridis, Jiannis Vlachogiannakos
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引用次数: 0
Late relapsing testicle cancer identified with isochromosome 12p (i12p) fluorescence in situ hybridization (FISH) analysis. 通过 12p 异染色体(i12p)荧光原位杂交(FISH)分析确定的晚期复发性睾丸癌。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-03-01 Epub Date: 2024-02-29 DOI: 10.1111/pin.13414
Teruki Isobe, Noriyasu Kawai, Maria Aoki, Toshiharu Morikawa, Masakazu Gonda, Nami Tomiyama, Takashi Nagai, Keitaro Iida, Toshiki Etani, Taku Naiki, Toyonori Tsuzuki, Takahiro Yasui
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引用次数: 0
Abstracts of presentation by the winners of The Japanese Society of Pathology; Japan Pathology Award in 2024 (in program order). 日本病理学会 2024 年日本病理学奖获奖者演讲摘要(按节目顺序排列)。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-03-01 DOI: 10.1111/pin.13401
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引用次数: 0
Molecular pathological demonstration of an unusual angiosarcoma-like dedifferentiation pattern in hepatocellular carcinoma. 分子病理学显示肝细胞癌存在不寻常的血管肉瘤样去分化模式。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-03-01 Epub Date: 2024-02-06 DOI: 10.1111/pin.13412
Keigo Murakami, Taito Itoh, Yasunobu Okamura, Kengo Kinoshita, Hideki Ota, Michiaki Unno, Takashi Kamei, Toru Furukawa
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引用次数: 0
CSF3R-, ASXL1-, and SETBP1-mutated chronic neutrophilic leukemia with monoclonal gammopathy of undetermined significance in a patient who developed severe ascites due to sinusoidal neutrophilic infiltration. CSF3R、ASXL1 和 SETBP1 基因突变的慢性中性粒细胞白血病伴有意义不明的单克隆抗体病,患者因窦状中性粒细胞浸润而出现严重腹水。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-02-01 Epub Date: 2023-12-05 DOI: 10.1111/pin.13394
Naonori Harada, Daiki Mukai, Yuto Izuta, Ikumi Shibano, Yusuke Kizawa, Hiroshi Shiragami, Nobuhiko Ohnishi, Naoki Hosaka, Atsuko Mugitani
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引用次数: 0
HER2 staining of breast cancer is reduced under the current protocol of Ventana PATHWAY anti-HER-2/neu (4B5). 在目前的 Ventana PATHWAY 抗 HER-2/neu (4B5) 方案中,乳腺癌的 HER2 染色减少。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-02-01 Epub Date: 2024-01-10 DOI: 10.1111/pin.13404
Yoshiya Horimoto, Hiroko Onagi, Junichiro Watanabe, Takuo Hayashi
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引用次数: 0
Is the endomyocardial biopsy in giant cell myocarditis of some help for the rapid indication for heart transplantation? 巨细胞心肌炎的心内膜活检是否有助于快速确定心脏移植指征?
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-02-01 Epub Date: 2023-12-27 DOI: 10.1111/pin.13400
Andrea Marzullo, Gabriella Serio, Gerardo Cazzato, Marialessandra Capuzzolo, Carla Nardelli, Cecilia Salzillo
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引用次数: 0
Decoding the DNA methylome of central nervous system tumors: An emerging modality for integrated diagnosis. 解码中枢神经系统肿瘤的 DNA 甲基组:综合诊断的新兴模式。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-02-01 Epub Date: 2024-01-15 DOI: 10.1111/pin.13402
Kaishi Satomi, Koichi Ichimura, Junji Shibahara

The definitive diagnosis and classification of individual cancers are crucial for patient care and cancer research. To achieve a robust diagnosis of central nervous system (CNS) tumors, a genotype-phenotype integrated diagnostic approach was introduced in recent versions of the World Health Organization classification, followed by the incorporation of a genome-wide DNA methylome-based classification. Microarray-based platforms are widely used to obtain DNA methylome data, and the German Cancer Research Center (Deutsches Krebsforschungszentrum [DKFZ]) has a webtool for a DNA methylation-based classifier (DKFZ classifier). Integration of DNA methylome will further enhance the precision of CNS tumor classification, especially in diagnostically challenging cases. However, in the clinical application of DNA methylome-based classification, challenges related to data interpretation persist, in addition to technical caveats, regulations, and limited accessibility. Dimensionality reduction (DMR) can complement integrated diagnosis by visualizing a profile and comparing it with other known samples. Therefore, DNA methylome-based classification is a highly useful research tool for auxiliary analysis in challenging diagnostic and rare disease cases, and for establishing novel tumor concepts. Decoding the DNA methylome, especially by DMR in addition to DKFZ classifier, emphasizes the capability of grasping the fundamental biological principles that provide new perspectives on CNS tumors.

单个癌症的明确诊断和分类对患者护理和癌症研究至关重要。为实现对中枢神经系统(CNS)肿瘤的可靠诊断,世界卫生组织在最近的分类版本中引入了基因型-表型综合诊断方法,随后又纳入了基于全基因组 DNA 甲基组的分类。基于微阵列的平台被广泛用于获取 DNA 甲基组数据,德国癌症研究中心(Deutsches Krebsforschungszentrum [DKFZ])拥有一个基于 DNA 甲基化分类器(DKFZ classifier)的网络工具。DNA 甲基组的整合将进一步提高中枢神经系统肿瘤分类的精确度,尤其是在诊断难度较大的病例中。然而,在基于DNA甲基组的分类的临床应用中,除了技术上的注意事项、法规和有限的可及性之外,与数据解读相关的挑战依然存在。降维(DMR)可以通过可视化特征并将其与其他已知样本进行比较来补充综合诊断。因此,基于DNA甲基组的分类是一种非常有用的研究工具,可用于对具有挑战性的诊断和罕见疾病病例进行辅助分析,以及建立新的肿瘤概念。对 DNA 甲基组的解码,尤其是通过 DMR 和 DKFZ 分类器进行解码,强调了掌握基本生物学原理的能力,为中枢神经系统肿瘤提供了新的视角。
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引用次数: 0
The first autopsy case of Epstein-Barr virus-positive marginal zone lymphoma that deteriorated after COVID-19 vaccination. 首例接种 COVID-19 疫苗后病情恶化的 Epstein-Barr 病毒阳性边缘区淋巴瘤尸检病例。
IF 2.2 4区 医学 Q2 Medicine Pub Date : 2024-02-01 Epub Date: 2023-12-20 DOI: 10.1111/pin.13398
Ziyao Wang, Reiji Muto, Hiroaki Miyoshi, Mikiko Aoki, Noriko Uesugi, Hiroyuki Murayama, Kosuke Masutani, Makoto Hamasaki

This is the first autopsy case of Epstein-Barr virus-positive marginal zone lymphoma (EBV + MZL) with an other iatrogenic immunodeficiency-associated lymphoproliferative disorders (LPD) (methotrexate [MTX]-associated LPD) that deteriorated after the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine. This case had a unique immunophenotype. A 71-year-old female patient with rheumatoid arthritis receiving MTX presented with fatigue 1 week after the SARS-CoV-2 vaccination. She was hospitalized due to hepatorenal dysfunction and pancytopenia. Computed tomography revealed systemic lymphadenopathy. Her physical condition deteriorated, and the patient died. The autopsy revealed systemic lymphadenopathy comprising medium-sized atypical lymphocytes and scattered Hodgkin/Reed-Sternberg (H/RS)-like cells. An immunohistochemical examination showed that atypical lymphocytes were positive for CD79a and MUM-1 and some were positive for CD20 and IRTA-1. H/RS-like cells were immunoreactive for CD30 and CD15 and ringed by T cells. Both cell types were positive for EBV-encoded small RNA. The majority of H/RS-like cells were positive for CD20, whereas a small number of CD3-positive cells were admixed. We herein presented the first autopsy case of EBV + MZL that deteriorated after the SARS-CoV-2 vaccination.

这是第一例EB病毒阳性边缘区淋巴瘤(EB病毒+MZL)合并其他先天性免疫缺陷相关淋巴组织增生性疾病(LPD)(甲氨蝶呤[MTX]相关LPD)的尸检病例,该病例在注射严重急性呼吸系统综合征冠状病毒2型(SARS-CoV-2)疫苗后病情恶化。该病例具有独特的免疫表型。一名 71 岁的类风湿性关节炎女性患者在接种 SARS-CoV-2 疫苗一周后出现乏力症状,当时她正在接受 MTX 治疗。她因肝肾功能障碍和全血细胞减少而住院治疗。计算机断层扫描显示她患有全身淋巴结病。她的身体状况恶化,最终死亡。尸检发现全身淋巴结病变,包括中等大小的非典型淋巴细胞和散在的霍奇金/里德-斯登堡(H/RS)样细胞。免疫组化检查显示,非典型淋巴细胞的 CD79a 和 MUM-1 呈阳性,一些细胞的 CD20 和 IRTA-1 呈阳性。H/RS样细胞对CD30和CD15有免疫反应,并被T细胞环绕。两种细胞类型的 EBV 编码小 RNA 均呈阳性。大多数H/RS样细胞对CD20呈阳性,但也有少量CD3阳性细胞混杂其中。我们在此展示了首例接种 SARS-CoV-2 疫苗后病情恶化的 EBV + MZL 尸检病例。
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