Histopathology最新文献

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Sinonasal adenosquamous carcinomas arising in seromucinous hamartoma or respiratory epithelial adenomatoid hamartoma with atypical features: Report of five detailed clinicopathological and molecular characterisation of rare entity 鼻窦腺鳞癌产生于血清粘液性火腿状瘤或具有非典型特征的呼吸道上皮腺瘤样火腿状瘤:报告五例罕见病例的详细临床病理学和分子特征。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-20 DOI: 10.1111/his.15369
Martina Bradová, Valerie Costes-Martineau, Jan Laco, Tomáš Vaněček, Petr Grossmann, Jana Němcová, Zdeněk Pavlovský, Alena Skálová, Michal Michal
{"title":"Sinonasal adenosquamous carcinomas arising in seromucinous hamartoma or respiratory epithelial adenomatoid hamartoma with atypical features: Report of five detailed clinicopathological and molecular characterisation of rare entity","authors":"Martina Bradová,&nbsp;Valerie Costes-Martineau,&nbsp;Jan Laco,&nbsp;Tomáš Vaněček,&nbsp;Petr Grossmann,&nbsp;Jana Němcová,&nbsp;Zdeněk Pavlovský,&nbsp;Alena Skálová,&nbsp;Michal Michal","doi":"10.1111/his.15369","DOIUrl":"10.1111/his.15369","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aims</h3>\u0000 \u0000 <p>Sinonasal adenosquamous carcinoma (ASC) is a rare tumour classified as a variant of squamous cell carcinoma, exhibiting both squamous and glandular differentiation. ASC has a poorer prognosis compared to sinonasal mucoepidermoid carcinoma (MEC), another uncommon tumour in this region. ASC is believed to originate from metaplastic squamous epithelium, though it may also arise from respiratory epithelium in respiratory epithelial adenomatoid hamartoma (REAH) or seromucinous glands in seromucinous hamartoma (SH).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods and results</h3>\u0000 \u0000 <p>Five cases of sinonasal ASC were retrieved from our registry. Initially, they were classified as sinonasal MEC (<i>n</i> = 3), ASC (<i>n</i> = 2), and carcinoma ex REAH (<i>n</i> = 1). All cases showed adenosquamous malignant proliferation beneath the surface respiratory epithelium with occasional squamous metaplasia, except for one case that showed dysplasia. The respiratory epithelium exhibited an inverted growth pattern consistent with REAH/SH, and displayed atypical sinonasal glands (ASGSH) arising within seromucinous hamartoma. Next-generation sequencing (NGS) revealed multiple pathogenic mutations in two cases, and in case 4 <i>GGA2::PRKCB</i> and <i>EYA2::SERINC3</i> gene fusions. One case was positive for high-risk HPV. None of the cases exhibited <i>CRTC1/3::MAML2</i> gene fusion.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The connection between ASGSH and ASC has not been described in the literature. There is a growing need for additional studies on the morphological, immunohistochemical, and genetic aspects of these tumours. SH/REAH may serve as precursor lesions in the progression of atypical sinonasal glands to malignancy, and their role in tumour development deserves further investigation.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"585-602"},"PeriodicalIF":3.9,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/his.15369","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142675743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Shared immunohistochemical and genomic features of the low- and high-grade components of a cutaneous secretory carcinoma with epidermotrophism and lymph node involvement 伴有表皮营养不良和淋巴结受累的皮肤分泌癌的低级别和高级别组成部分的共同免疫组化和基因组特征。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-18 DOI: 10.1111/his.15351
Zlatko Marusic, Louise van der Weyden, Dimas Suárez Vilela, Faustino Suárez Sánchez, Jose Ramón Méndez Álvarez, Martin Del Castillo Velasco-Herrera, Ingrid Ferreira, David J Adams, Eduardo Calonje
{"title":"Shared immunohistochemical and genomic features of the low- and high-grade components of a cutaneous secretory carcinoma with epidermotrophism and lymph node involvement","authors":"Zlatko Marusic,&nbsp;Louise van der Weyden,&nbsp;Dimas Suárez Vilela,&nbsp;Faustino Suárez Sánchez,&nbsp;Jose Ramón Méndez Álvarez,&nbsp;Martin Del Castillo Velasco-Herrera,&nbsp;Ingrid Ferreira,&nbsp;David J Adams,&nbsp;Eduardo Calonje","doi":"10.1111/his.15351","DOIUrl":"10.1111/his.15351","url":null,"abstract":"","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"656-659"},"PeriodicalIF":3.9,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142667603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evolving molecular classification of aggressive B-cell lymphoma 侵袭性 B 细胞淋巴瘤分子分类的演变。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-15 DOI: 10.1111/his.15350
Stefan K Alig, Björn Chapuy, Daisuke Ennishi, Kieron Dunleavy, Daniel J Hodson
{"title":"Evolving molecular classification of aggressive B-cell lymphoma","authors":"Stefan K Alig,&nbsp;Björn Chapuy,&nbsp;Daisuke Ennishi,&nbsp;Kieron Dunleavy,&nbsp;Daniel J Hodson","doi":"10.1111/his.15350","DOIUrl":"10.1111/his.15350","url":null,"abstract":"<p>This review aims to provide an overview of the latest developments in the classification and molecular understanding of aggressive B-cell lymphomas, specifically focusing on diffuse large B-cell lymphoma (DLBCL) and high-grade B-cell lymphoma (HGBL). Advances in molecular techniques have led to novel ways to classify these lymphomas based on clinical, histological, transcriptional, and genetic properties. While these methods have predominantly focused on the malignant compartment, recent studies emphasize the value of profiling the tumour microenvironment for a more comprehensive disease classification. Additionally, the integration of liquid biopsies represents a promising advancement, offering less invasive and dynamic insights into tumour characteristics and treatment response. Although molecular profiles are not yet routinely used to guide therapy, emerging data highlight their potential to predict responses to novel treatments. It is our belief that integrating molecular profiling and liquid biopsies into clinical practice and research now will pave the way for more personalized and effective therapies in the future.</p>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 1","pages":"94-105"},"PeriodicalIF":3.9,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/his.15350","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619330","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correlation between CTNNB1 mutation status and tumour phenotype in hepatitis B virus-related hepatocellular carcinoma 乙型肝炎病毒相关肝细胞癌中 CTNNB1 突变状态与肿瘤表型之间的相关性。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-11 DOI: 10.1111/his.15363
Yoon Jung Hwang, Yangkyu Lee, Su Jong Yu, Suk Kyun Hong, Nam-Joon Yi, YoungRok Choi, Hyejung Lee, Wonju Chung, Haeryoung Kim
{"title":"Correlation between CTNNB1 mutation status and tumour phenotype in hepatitis B virus-related hepatocellular carcinoma","authors":"Yoon Jung Hwang,&nbsp;Yangkyu Lee,&nbsp;Su Jong Yu,&nbsp;Suk Kyun Hong,&nbsp;Nam-Joon Yi,&nbsp;YoungRok Choi,&nbsp;Hyejung Lee,&nbsp;Wonju Chung,&nbsp;Haeryoung Kim","doi":"10.1111/his.15363","DOIUrl":"10.1111/his.15363","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aims</h3>\u0000 \u0000 <p>The frequency of <i>CTNNB1</i> mutation, one of the most frequent genetic events in hepatocellular carcinoma (HCC), is lower in Asian countries and in hepatitis B virus (HBV)-related HCCs. In this study, we evaluated the prevalence and types of <i>CTNNB1</i>-mutation in HBV-related HCC and correlated the molecular status with the histomorphological and immunohistochemical features.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods and results</h3>\u0000 \u0000 <p>A total of 108 consecutive cases of treatment-naïve, surgically resected HBV-related HCCs were selected. Targeted sequencing for <i>CTNNB1</i> exons 3, 7 and 8 was performed, and the results were correlated with the expression pattern of glutamine synthetase (GS), nuclear β-catenin expression status and the histomorphological characteristics of the tumour. <i>CTNNB1</i> mutations were identified in 13% of HBV-related HCCs; of these cases, mutations were found in D32-S37 (7%), T41 (4%) and S45 (2%) of exon 3. None of the HCCs demonstrated alterations in exons 7 and 8. <i>CTNNB1</i> mutation was strongly associated with diffuse strong GS expression (<i>P</i> &lt; 0.001), nuclear β-catenin expression (<i>P</i> &lt; 0.001) and the classic <i>CTNNB1</i> morphology (<i>P</i> = 0.038). Diffuse strong GS expression was observed in 78.6% of the <i>CTNNB1</i>-mutated HCCs, and nuclear β-catenin expression was identified in 64.3% of these cases. The classic <i>CTNNB1</i> morphology was observed in 57% of all <i>CTNNB1</i>-mutated HCCs. Furthermore, programmed death-ligand 1 (PD-L1) was less frequently expressed in HCCs with classic <i>CTNNB1</i> morphology.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p><i>CTNNB1</i> mutation was observed in 13% of HBV-related HCCs in this Korean cohort, and was associated with diffuse strong GS expression, nuclear β-catenin expression and classic <i>CTNNB1</i> morphology.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"547-558"},"PeriodicalIF":3.9,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multi-neoplastic potentials including metachronous clonally unrelated nodal T-follicular helper cell lymphomas in clonal haematopoiesis 克隆性造血中的多瘤性潜能,包括克隆无关的结节性 T 滤泡辅助细胞淋巴瘤。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-11 DOI: 10.1111/his.15367
Ayoma D Attygalle, Pui Kwan Chak, Ewelina Madej, Maria-Myrsini Tzioni, Zi Chen, Ming-Qing Du
{"title":"Multi-neoplastic potentials including metachronous clonally unrelated nodal T-follicular helper cell lymphomas in clonal haematopoiesis","authors":"Ayoma D Attygalle,&nbsp;Pui Kwan Chak,&nbsp;Ewelina Madej,&nbsp;Maria-Myrsini Tzioni,&nbsp;Zi Chen,&nbsp;Ming-Qing Du","doi":"10.1111/his.15367","DOIUrl":"10.1111/his.15367","url":null,"abstract":"","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"652-656"},"PeriodicalIF":3.9,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neuroendocrine differentiation and serotonin expression in oesophageal adenocarcinomas after neoadjuvant therapy: correlation with clinicopathological features and outcome 新辅助治疗后食管腺癌的神经内分泌分化和血清素表达:与临床病理特征和预后的相关性。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-11 DOI: 10.1111/his.15364
David W. Dodington, Stefano Serra, Tim Bracey, Runjan Chetty, Klaudia M. Nowak
{"title":"Neuroendocrine differentiation and serotonin expression in oesophageal adenocarcinomas after neoadjuvant therapy: correlation with clinicopathological features and outcome","authors":"David W. Dodington,&nbsp;Stefano Serra,&nbsp;Tim Bracey,&nbsp;Runjan Chetty,&nbsp;Klaudia M. Nowak","doi":"10.1111/his.15364","DOIUrl":"10.1111/his.15364","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aims</h3>\u0000 \u0000 <p>Oesophageal adenocarcinoma (EAC) is a glandular or mucinous epithelial malignancy that can show immunohistochemical evidence of neuroendocrine differentiation (NED) and express the hormone serotonin. The objective of this study was to correlate the presence of NED and serotonin with clinicopathological characteristics and patient outcome after neoadjuvant chemoradiation.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods and results</h3>\u0000 \u0000 <p>A retrospective cohort of patients treated between 2002 and 2021 was established and included 218 oesophagectomy specimens with residual tumour. Representative full-face sections of tumour were stained for synaptophysin, chromogranin-A and serotonin by immunohistochemistry, and staining results were correlated with disease-free survival (DFS) and overall survival (OS). In total, 129 (59%) tumours showed evidence of NED, defined as immunohistochemical expression of synaptophysin or chromogranin-A, while 40 (18%) showed evidence of NED and expressed serotonin. Patients with neuroendocrine-positive tumours had significantly shorter median OS compared to those with neuroendocrine-negative tumours (22.5 versus 48.8 months, <i>P</i> = 0.006), but similar median DFS (13.3 versus 17.8 months, <i>P</i> = 0.34). Using Cox regression, the association between NED and OS was significant in univariate [hazard ratio (HR) = 1.68, 95% confidence interval (CI) = 1.16–2.45] and multivariate (HR = 1.65, 95% CI = 1.08–2.52) analysis. Patients with serotonin-expressing tumours had similar median OS (21.7 versus 25.9 months, <i>P</i> = 0.24) and DFS (7.3 versus 15.6 months, <i>P</i> = 0.12) compared to those with NED but lacking serotonin. Using Cox regression, serotonin expression was associated with reduced OS in univariate (HR = 1.62, 95% CI = 1.06–2.47) but not multivariate (HR = 1.03, 95% CI = 0.64–1.65) analysis.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Our findings support NED as independent predictor of OS in EAC after neoadjuvant chemoradiation. While a subset of tumours with NED expressed serotonin, this did not provide additional prognostic information.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"559-570"},"PeriodicalIF":3.9,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/his.15364","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142619311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
First report of SMARCA4-deficient carcinoma ex-pleomorphic adenoma in salivary glands 首次报道唾液腺中的SMARCA4缺陷癌前多形性腺瘤。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-06 DOI: 10.1111/his.15359
Munita Bal, Parvathy Shree Nath, Amit Janu, Shivakumar Thiagarajan, Gouri Pantavaidya
{"title":"First report of SMARCA4-deficient carcinoma ex-pleomorphic adenoma in salivary glands","authors":"Munita Bal,&nbsp;Parvathy Shree Nath,&nbsp;Amit Janu,&nbsp;Shivakumar Thiagarajan,&nbsp;Gouri Pantavaidya","doi":"10.1111/his.15359","DOIUrl":"10.1111/his.15359","url":null,"abstract":"","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 3","pages":"480-482"},"PeriodicalIF":3.9,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142582944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mixed germ cell-sex cord stromal tumour of the testis, further evidence supporting similarity of the germ cell component to spermatocytic tumour: case report 睾丸生殖细胞-性索间质混合瘤:病例报告,进一步证明生殖细胞成分与精原细胞瘤相似。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-11-06 DOI: 10.1111/his.15360
Sarwat Gilani, Sounak Gupta, Patricia T Greipp, Sunil Patel, Rafael E Jimenez, Loren P Herrera Hernandez
{"title":"Mixed germ cell-sex cord stromal tumour of the testis, further evidence supporting similarity of the germ cell component to spermatocytic tumour: case report","authors":"Sarwat Gilani,&nbsp;Sounak Gupta,&nbsp;Patricia T Greipp,&nbsp;Sunil Patel,&nbsp;Rafael E Jimenez,&nbsp;Loren P Herrera Hernandez","doi":"10.1111/his.15360","DOIUrl":"10.1111/his.15360","url":null,"abstract":"","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"650-652"},"PeriodicalIF":3.9,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142582946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fat embolism: a systematic review to facilitate the development of standardised procedures in pathology. 脂肪栓塞:促进病理学标准化程序发展的系统回顾。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-10-31 DOI: 10.1111/his.15355
Donato Morena, Matteo Scopetti, Martina Padovano, Emanuela Turillazzi, Vittorio Fineschi
{"title":"Fat embolism: a systematic review to facilitate the development of standardised procedures in pathology.","authors":"Donato Morena, Matteo Scopetti, Martina Padovano, Emanuela Turillazzi, Vittorio Fineschi","doi":"10.1111/his.15355","DOIUrl":"https://doi.org/10.1111/his.15355","url":null,"abstract":"<p><p>Fat embolism (FE) is a historically recognised but still actively researched topic in forensic pathology. Several aspects remain not fully elucidated, such as its aetiopathogenesis, its causal role in death determination, the impact of interfering factors (e.g. cardiopulmonary resuscitation or other medical procedures) and both qualitative and quantitative diagnostic methodologies in clinical and forensic contexts. These issues are further underscored by the potential involvement of FE in the causal determination of non-traumatic deaths, which often raises questions of professional liability. The present study aims to provide a comprehensive and up-to-date overview of the most recent scientific evidence relevant to forensic pathology. Our systematic research has included 58 articles from 1990 to the present on the topic of FE and fat embolism syndrome (FES). From these articles, we identified 45 case reports, from which the authors' descriptions were extracted to provide information on individual cases and the operational methods of forensic pathologists. Additionally, 21 experimental studies were identified, and their key findings have been summarised narratively. It has emerged that both traumatic and non-traumatic cases are frequently reported in the forensic context, with orthopaedic and cosmetic surgery being among the highest-risk specialities. Experimental studies have re-evaluated the role of a patent foramen ovale in the pathogenesis of FE, as well as the impact of cardiopulmonary resuscitation in causing FE severe enough to result in death. Additionally, there are new findings regarding diagnostic techniques, including radiological and immunohistological methods; however, they have not yet fully bridged the reliability gap compared to an accurate autopsy-histological evaluation. The major critical points that emerged include the lack of complete and detailed information on premortem clinical conditions, the underutilisation of grading systems and the methodological heterogeneity applied, resulting in considerable variability regarding the organs studied histologically and the diagnostic techniques used. Despite the limitations associated with the analysis of case reports and the heterogeneity of included experimental studies, we believe that this study can provide a comprehensive overview of the FE topic. It furnishes pathologists with an updated overview useful for clinical practice and guiding future research trends, as well as facilitating the development of standardised procedures.</p>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142545185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinicopathologic features and outcomes of hepatic inflammatory pseudotumour (IPT) and hepatic IPT-like lesions 肝脏炎性假瘤(IPT)和肝脏炎性假瘤样病变的临床病理特征和预后。
IF 3.9 2区 医学
Histopathology Pub Date : 2024-10-31 DOI: 10.1111/his.15357
Eric D Nguyen, Kwun Wah Wen, Sanjay Kakar, Dana J Balitzer
{"title":"Clinicopathologic features and outcomes of hepatic inflammatory pseudotumour (IPT) and hepatic IPT-like lesions","authors":"Eric D Nguyen,&nbsp;Kwun Wah Wen,&nbsp;Sanjay Kakar,&nbsp;Dana J Balitzer","doi":"10.1111/his.15357","DOIUrl":"10.1111/his.15357","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aims</h3>\u0000 \u0000 <p>Hepatic inflammatory pseudotumours (IPTs) are nonneoplastic hepatic masses characterized by variably fibroblastic stroma and inflammatory infiltrate, hypothesized to arise as part of a response to infection or prior surgery. The aim of this study was to evaluate the clinicopathologic features and outcomes of biopsy-proven hepatic IPT as well as other cases with IPT-like histologic features.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods and Results</h3>\u0000 \u0000 <p>A database search at our institution identified cases with a pathologic diagnosis of hepatic IPT (<i>n</i> = 80) between 2000 and 2023. Histologic features (stromal quality, inflammatory cell components, granulomas, and necrosis) were evaluated. Past medical and surgical history, microbiologic studies, and outcomes were reviewed retrospectively. Patients frequently had a past medical history of malignancy (34%), biliary disease (15%), or prior intraabdominal surgery (24%), and often presented with multifocal hepatic lesions (36%). Variable inflammatory backgrounds were present, including histiocytic (36%), lymphoplasmacytic (34%), or neutrophilic (24%). Specific organisms were identified in 15% of cases, most commonly <i>Klebsiella</i> and <i>Staphylococcus</i> species. Most patients with available clinical follow-up demonstrated radiologic resolution and/or had repeat negative biopsy; a minority of patients (8%) were subsequently diagnosed with neoplastic hepatic lesions. No significant association was seen between histologic features and the subsequent clinical or pathologic diagnosis of hepatic neoplastic lesions.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Hepatic IPT is a heterogeneous entity that can present in a variety of clinical scenarios and show a wide morphologic spectrum. These lesions often regress spontaneously or with antibiotics. A subset of cases with hepatic IPT-like histologic features were subsequently diagnosed with malignancy, emphasizing the need for continued follow-up and repeat biopsy depending on clinical and radiologic features.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":"86 4","pages":"525-535"},"PeriodicalIF":3.9,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/his.15357","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142545183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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