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Rare diagnosis of an Epstein-Barr virus-positive extracavitary/solid variant of primary effusion lymphoma by duodenal endoscopic biopsy in a human immunodeficiency virus-seronegative and immunocompetent patient: A case report. 通过十二指肠内窥镜活检,在一名人类免疫缺陷病毒阴性且免疫功能正常的患者身上罕见地诊断出了爱泼斯坦-巴氏病毒阳性的腔外/固体变异型原发性渗出淋巴瘤:病例报告。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_955_22
Beril Guler, Guven Cetin

Primary effusion lymphoma and its tissue-based subtype extracavitary/solid variant was first described in human immunodeficiency virus (HIV)-seropositive patients. We report the case of a 50-year-old HIV-seronegative male patient who presented with icterus and cholestasis. Computed tomography revealed a 80 × 56 mm abdominal mass. Fine-needle aspiration biopsy was performed from the celiac lymph nodes and pancreatic head, under endoscopic ultrasonography guidance. A duodenal endoscopic biopsy was taken from the infiltration area, and a core biopsy was performed for the portal hilar mass. All biopsies showed similar cytohistopathological features. LCA-positive lymphoid neoplasia had a plasmacytoid/anaplastic morphology and null cell phenotype. HHV-8 and Epstein-Barr virus-encoded small RNAs (EBER) were diffuse positive. The patient, who did not have an effusion, was diagnosed with an extracavitary/solid variant of primary effusion lymphoma. Virus-associated lymphoproliferative disorders should be considered in the differential diagnosis of patients without a history of immunosuppression or HIV infection.

原发性渗出淋巴瘤及其组织亚型空腔外/实体变异型最早出现在人类免疫缺陷病毒(HIV)血清反应阳性的患者中。我们报告了一例 50 岁 HIV 阴性男性患者的病例,该患者出现黄疸和胆汁淤积。计算机断层扫描显示其腹部有一个 80 × 56 毫米的肿块。在内镜超声引导下,对腹腔淋巴结和胰头进行了细针穿刺活检。在浸润区进行了十二指肠内镜活检,并对门静脉肿块进行了核心活检。所有活检均显示出相似的细胞病理学特征。LCA阳性淋巴肿瘤具有浆细胞/无细胞形态和空细胞表型。HHV-8和Epstein-Barr病毒编码的小RNA(EBER)呈弥漫性阳性。患者没有渗出,被诊断为腔外/实变型原发性渗出淋巴瘤。对于无免疫抑制或艾滋病病毒感染史的患者,在鉴别诊断时应考虑病毒相关淋巴组织增生性疾病。
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引用次数: 0
Extranodal natural killer/T cell lymphoma nasal type simulating osteoradionecrosis with metachronic B lymphoma in the pelvis: Case report. 鼻腔外结节型自然杀伤/T细胞淋巴瘤模拟骨软化症并伴有骨盆中的并发B淋巴瘤:病例报告。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_296_22
Frida S Colín-Guadarrama, Violeta E Flores-Solano, Argelia Berenice-Rodríguez, Víctor H Toral-Rizo

Extranodal Natural Killer/T Cell Lymphoma Nasal Type (EN-NK/T-CL-NT) is a non-Hodgkin extranodal lymphoma of unfavorable prognosis due to its aggressive nature. This neoplasm mainly affects the paranasal sinuses, nasopharynx, oropharynx, oral cavity, palate, and rarely intestinal, gastric and skin regions. 50-year-old female with a history of lymphoma in nasal and pelvic region. At four years of tumors-free, has facial asymmetry, accompanied by sub-palpebral, nasal and lip edema. Intraoral examination revealed a large ulceration suggestive of osteoradionecrosis. Gum biopsy shows Extranodal NK/T Cell Lymphoma Nasal Type (EN-NK/T-CL-NT). In this case we highlight the characteristics of EN-NK/T-CL-NT with a presentation of osteoradionecrosis-like. Unfortunately, the nature of this tumor led to the patient's death. Clinical follow-up of patients with cancer is imperative to mend and/or decrease treatment complications, as well as to identify second primary tumors or the spread of the underlying disease.

鼻腔外结节自然杀伤细胞/T细胞淋巴瘤(EN-NK/T-CL-NT)是一种非霍奇金外结节淋巴瘤,因其侵袭性而预后不良。这种肿瘤主要侵犯鼻旁窦、鼻咽、口咽、口腔、上颚,很少侵犯肠、胃和皮肤区域。50 岁女性,曾患鼻腔和盆腔淋巴瘤。无肿瘤四年后,面部不对称,伴有睑下、鼻和唇水肿。口腔内检查发现大面积溃疡,提示骨坏死。牙龈活检显示鼻腔外结节性 NK/T 细胞淋巴瘤(EN-NK/T-CL-NT)。在这个病例中,我们突出了EN-NK/T-CL-NT的特征,表现为类似骨坏死。不幸的是,这种肿瘤的性质导致了患者的死亡。对癌症患者进行临床随访,对于弥补和/或减少治疗并发症,以及识别第二原发性肿瘤或潜在疾病的扩散至关重要。
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引用次数: 0
First isolation and characterization of SARS-CoV-2 from COVID-19 patient of North East India. 首次从印度东北部 COVID-19 患者体内分离出 SARS-CoV-2 并确定其特征。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_748_21
Aniruddha Jakharia, Biswajyoti Borkakoty, Sumi Pait, Gautam Baruah, Rahul Hazarika, Dipankar Biswas

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) responsible for the current pandemic has resulted in over 5 million deaths globally. More than a year has passed, still SARS-CoV-2 panic the public life. Virus isolation is of paramount importance for development of vaccines, in-vitro screening of antiviral compounds, pathogenesis studies, etc., Many cell lines were studied for amplification and replication of SARS-CoV-2 and Vero cells were found to be ideal cell lines for isolation. In May 2020, ICMR-Regional Medical Research Centre, NE region, India, successfully established the SARS-CoV-2 culture system in Vero CCL-81 cell lines. Phylogenetic analyses of the whole genome sequences of the SARS-CoV-2 isolate (EPI_ISL_2501532 | 2020-05-19) showed monophyletic clade G and lineage B.1.1.

严重急性呼吸系统综合症冠状病毒-2(SARS-CoV-2)是造成当前大流行病的罪魁祸首,已导致全球 500 多万人死亡。一年多过去了,SARS-CoV-2 依然肆虐公众生活。病毒分离对于疫苗开发、抗病毒化合物体外筛选、发病机理研究等至关重要,许多细胞系都对 SARS-CoV-2 的扩增和复制进行了研究,发现 Vero 细胞是分离病毒的理想细胞系。2020 年 5 月,印度东北部地区的 ICMR 区域医学研究中心成功地在 Vero CCL-81 细胞系中建立了 SARS-CoV-2 培养系统。对 SARS-CoV-2 分离物(EPI_ISL_2501532 | 2020-05-19)的全基因组序列进行的系统发生学分析表明,该分离物属于单系 G 支系和 B.1.1 系。
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引用次数: 0
Human dirofilariasis - Unforeseen lesion in subcutaneous nodules: Case series from a tertiary care hospital, Wayanad. 人类丝虫病--皮下结节中的意外病变:瓦尼亚德一家三级医院的病例系列。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_1051_21
M M Gitanjali, Prasannakumar G Konapur, Hasaf Kolakkadan, K Nabeel Azeez

Human dirofilariasis is a type of zoonotic infection caused by the Dirofilarial species. It is a type of roundworm which is commonly seen in dogs, cats and is transmitted to humans by mosquito bite. Microfilaria is rarely produced in humans. Although clinically they can have varied presentations, it usually presents as ocular or subcutaneous nodules. Definitive diagnosis requires histopathological findings of this worm. We hereby report three cases of Dirofilariasis from a tertiary care hospital in Wayanad.

人类双鞭毛虫病是一种由双鞭毛虫引起的人畜共患传染病。它是一种蛔虫,常见于狗和猫,通过蚊虫叮咬传播给人类。人类很少产生微丝蚴。虽然临床表现多种多样,但通常表现为眼部或皮下结节。明确诊断需要这种蠕虫的组织病理学结果。我们在此报告了来自瓦尼亚德一家三级医院的三例丝虫病病例。
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引用次数: 0
Comparison of Clinico-pathologic features and outcomes of ANCA negative and ANCA positive pauci immune crescentic glomerulonephritis: A single centre study. ANCA阴性和ANCA阳性免疫性新月体肾小球肾炎的临床病理特征和预后比较:单中心研究。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_604_22
Pallav Gupta, Vinant Bhargava, Manish Malik, Anurag Gupta, Anil K Bhalla, Ashwini Gupta, Vaibhav Tiwari, Devinder S Rana, Ramesh L Sapra

Introduction: Pauci-immune crescentic glomerulonephritis (PICN) is an important cause of rapidly progressive renal failure. 10-40% of PICN cases have ANCA (antineutrophil cytoplasmic antibody) negative serology. The present study compared clinico-pathologic features, Brix's renal risk score, Berden's histopathological classes and differences in outcome between ANCAnegative vs ANCA positive PICN patients.

Materials and methods: Sixty-one patients of biopsy-proven PICN were studied. Biochemical findings and ANCA serology were recorded. Renal biopsy slides were reviewed along with direct immunofluorescence. Clinical and histological features were compared between ANCA negative and positive PICN using the Man Whitney U test and Chi-square test. Patients were compared for distribution in Berden's histological classes and Brix's renal risk categories. Patient and renal survival were compared using Kaplan-Meier survival analysis.

Results: ANCA negative PICN patients were younger (44.9 ± 16.5 years vs 53.6 ± 15.1 years, P = 0.049). Nasal (0 vs 18%, P = 0.035) and pulmonary involvement (9% vs 38%, P = 0.014) were lower in ANCA negative group. Both ANCA groups had similar renal biochemical profiles, percentage normal glomeruli, 16.3 ± 18.2 vs 21.7 ± 20.4 and percentage glomeruli with crescents, 64.5 ± 28.1 vs 64.3 ± 27.1. Twenty-seven per cent of ANCA negative cases fell in the sclerotic class in Berden's classification vs just 2.5% in ANCA positive group (p = 0.037) without significant difference in Brix's renal risk categories (p = 0.329). Thirteen per cent of ANCA negative patients achieved complete remission on treatment compared to 33% in ANCA positive patients. Patient survival and overall probability of progressing to ESRD were similar in the two groups.

Conclusion: ANCA negative PICN cases present at younger ages. Nasal and pulmonary involvement is uncommon in these patients. Patient survival and progression to ESRD are similar in both ANCA groups.

简介保济免疫性新月体肾小球肾炎(PICN)是导致快速进展性肾功能衰竭的一个重要原因。10%-40%的 PICN 病例血清 ANCA(抗中性粒细胞胞浆抗体)阴性。本研究比较了 ANCA 阴性与 ANCA 阳性 PICN 患者的临床病理特征、Brix 肾脏风险评分、Berden 组织病理学分级和预后差异:研究对象为61例经活检证实的PICN患者。记录生化检查结果和 ANCA 血清学检查结果。对肾活检切片进行了直接免疫荧光检查。使用 Man Whitney U 检验和 Chi-square 检验比较了 ANCA 阴性和阳性 PICN 的临床和组织学特征。比较患者在 Berden 组织学分级和 Brix 肾脏风险分级中的分布情况。采用 Kaplan-Meier 存活率分析比较患者和肾脏的存活率:结果:ANCA阴性的PICN患者更年轻(44.9 ± 16.5岁 vs 53.6 ± 15.1岁,P = 0.049)。ANCA阴性组鼻腔受累(0 vs 18%,P = 0.035)和肺部受累(9% vs 38%,P = 0.014)的比例较低。两组ANCA患者的肾脏生化指标相似,正常肾小球(16.3 ± 18.2 vs 21.7 ± 20.4)和有新月体的肾小球(64.5 ± 28.1 vs 64.3 ± 27.1)的比例均为16.3 ± 18.2 vs 21.7 ± 20.4。27%的ANCA阴性病例属于伯登分级中的硬化级,而ANCA阳性组仅为2.5%(p = 0.037),在布里克斯肾脏风险分级中无显著差异(p = 0.329)。13%的ANCA阴性患者在治疗后获得完全缓解,而ANCA阳性患者的这一比例为33%。两组患者的存活率和进展为 ESRD 的总概率相似:结论:ANCA阴性的PICN病例发病年龄较小。结论:ANCA 阴性的 PICN 患者年龄较轻,鼻部和肺部受累在这些患者中并不常见。两组 ANCA 患者的存活率和进展为 ESRD 的概率相似。
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引用次数: 0
To study the expression of estrogen, progesterone receptor and p53 immunohistochemistry markers in subtyping endometrial carcinoma. 研究雌激素、孕激素受体和 p53 免疫组化标记物在子宫内膜癌亚型中的表达。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_568_22
Anuja Yadav, Anuradha Sistla, Meenakshi Swain, Swarnalata Gowrishankar, Michelle de Padua, Tejal Modi, Rallabandi Himabindu, Neha Agarwal, Aditya Kulkarni, Trilok Bhandari, Hemanth Vudayaraju, Chinnababu, Vijay A Reddy

Background: Endometrial cancer is one of the most commonly diagnosed cancers in women worldwide.

Aim and objectives: To study the expression of estrogen receptor (ER), progesterone receptor (PR) and p53 immunohistochemistry (IHC) markers in subtyping endometrial carcinoma. Materials and Methods: A total of 100 cases of carcinoma endometrium submitted during January 2016 to October 2018 were included in our study. The ER, PR and p53 expressions were scored as per the adopted scoring system. Agreement between ER, PR and p53 IHC expression and the consensus HE diagnosis, FIGO grading and tumour staging were assessed using Chi square tests.

Results: There was a statistical association between ER, PR and p53 status and tumour histologic type with a P value < 0.01. There was no statistical significance observed between ER and PR expressions and different FIGO grades. Statistical significance (P = 0.036) between p53 and different FIGO grades seen. No statistical significance was observed between ER, PR and p53 expressions and different tumour stages and tumour invasiveness. There was a statistical association between ER and PR status and lymph node metastasis. p53 did not show a statistical significance.

Conclusion: Combination of ER, PR and p53 IHC markers can be used to distinguish type 1 and type 2 endometrial cancers. PR expression is more specific than ER in endometrioid carcinomas. p53 expression is more specific in serous carcinoma, however, p53 IHC alone cannot be used to distinguish different grades of endometrioid carcinomas as there is variability of staining in endometrioid carcinomas.

背景:子宫内膜癌是全球妇女最常见的癌症之一:目的和目标:研究雌激素受体(ER)、孕激素受体(PR)和 p53 免疫组织化学(IHC)标记物在子宫内膜癌亚型中的表达:研究雌激素受体(ER)、孕激素受体(PR)和p53免疫组化(IHC)标记物在子宫内膜癌亚型中的表达。材料与方法:本研究共纳入2016年1月至2018年10月期间提交的100例子宫内膜癌病例。按照采用的评分系统对ER、PR和p53的表达进行评分。ER、PR和p53 IHC表达与HE共识诊断、FIGO分级和肿瘤分期之间的一致性采用Chi square检验进行评估:结果:ER、PR 和 p53 状态与肿瘤组织学类型之间存在统计学关联,P 值小于 0.01。ER和PR的表达与不同的FIGO分级之间没有统计学意义。p53 与不同 FIGO 分级之间存在统计学意义(P = 0.036)。ER、PR 和 p53 表达与不同肿瘤分期和肿瘤侵袭性之间无统计学意义。ER和PR状态与淋巴结转移之间存在统计学关联,而p53则没有统计学意义:结论:结合ER、PR和p53 IHC标记可用于区分1型和2型子宫内膜癌。在浆液性癌中,p53 的表达更具特异性,但由于子宫内膜样癌的染色存在变异性,因此不能单独使用 p53 IHC 来区分不同等级的子宫内膜样癌。
{"title":"To study the expression of estrogen, progesterone receptor and p53 immunohistochemistry markers in subtyping endometrial carcinoma.","authors":"Anuja Yadav, Anuradha Sistla, Meenakshi Swain, Swarnalata Gowrishankar, Michelle de Padua, Tejal Modi, Rallabandi Himabindu, Neha Agarwal, Aditya Kulkarni, Trilok Bhandari, Hemanth Vudayaraju, Chinnababu, Vijay A Reddy","doi":"10.4103/ijpm.ijpm_568_22","DOIUrl":"10.4103/ijpm.ijpm_568_22","url":null,"abstract":"<p><strong>Background: </strong>Endometrial cancer is one of the most commonly diagnosed cancers in women worldwide.</p><p><strong>Aim and objectives: </strong>To study the expression of estrogen receptor (ER), progesterone receptor (PR) and p53 immunohistochemistry (IHC) markers in subtyping endometrial carcinoma. Materials and Methods: A total of 100 cases of carcinoma endometrium submitted during January 2016 to October 2018 were included in our study. The ER, PR and p53 expressions were scored as per the adopted scoring system. Agreement between ER, PR and p53 IHC expression and the consensus HE diagnosis, FIGO grading and tumour staging were assessed using Chi square tests.</p><p><strong>Results: </strong>There was a statistical association between ER, PR and p53 status and tumour histologic type with a P value < 0.01. There was no statistical significance observed between ER and PR expressions and different FIGO grades. Statistical significance (P = 0.036) between p53 and different FIGO grades seen. No statistical significance was observed between ER, PR and p53 expressions and different tumour stages and tumour invasiveness. There was a statistical association between ER and PR status and lymph node metastasis. p53 did not show a statistical significance.</p><p><strong>Conclusion: </strong>Combination of ER, PR and p53 IHC markers can be used to distinguish type 1 and type 2 endometrial cancers. PR expression is more specific than ER in endometrioid carcinomas. p53 expression is more specific in serous carcinoma, however, p53 IHC alone cannot be used to distinguish different grades of endometrioid carcinomas as there is variability of staining in endometrioid carcinomas.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70762882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Interfollicular Hodgkin's lymphoma: A diagnostic challenge for pathologists. 叶间霍奇金淋巴瘤:病理学家面临的诊断挑战。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_641_22
Maneesh K Vijay, Neha Sethi

Interfollicular Hodgkin's lymphoma (IFHL) is a rare pattern of classical Hodgkin's lymphoma (CHL) showing reactive follicular hyperplasia with involvement of the interfollicular area by HL. Two cases are reported in this study having primary IFHL out of total of 500 cases of CHL reported at our center. Diagnosis of IFHL was made on the basis of morphological and immunohistochemical features. As they represent an early stage of the disease, their identification and awareness s very important to get proper treatment at its earliest. This variant is very unusual and is diagnostically challenging for pathologists.

小叶间霍奇金淋巴瘤(IFHL)是经典霍奇金淋巴瘤(CHL)的一种罕见类型,表现为反应性滤泡增生,小叶间区受累于霍奇金淋巴瘤。在本中心报告的500例CHL病例中,有两例原发性IFHL。IFHL的诊断依据形态学和免疫组化特征。由于它们代表了疾病的早期阶段,因此识别和认识它们对于尽早获得适当治疗非常重要。这种变异非常不寻常,对病理学家的诊断具有挑战性。
{"title":"Interfollicular Hodgkin's lymphoma: A diagnostic challenge for pathologists.","authors":"Maneesh K Vijay, Neha Sethi","doi":"10.4103/ijpm.ijpm_641_22","DOIUrl":"10.4103/ijpm.ijpm_641_22","url":null,"abstract":"<p><p>Interfollicular Hodgkin's lymphoma (IFHL) is a rare pattern of classical Hodgkin's lymphoma (CHL) showing reactive follicular hyperplasia with involvement of the interfollicular area by HL. Two cases are reported in this study having primary IFHL out of total of 500 cases of CHL reported at our center. Diagnosis of IFHL was made on the basis of morphological and immunohistochemical features. As they represent an early stage of the disease, their identification and awareness s very important to get proper treatment at its earliest. This variant is very unusual and is diagnostically challenging for pathologists.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70763099","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Assessment of endometrial carcinoma on biopsy as a predictor of final surgical pathology: Are we doing it right? A completed audit cycle and recommendations. 活检子宫内膜癌评估作为最终手术病理的预测指标:我们做得对吗?已完成的审计周期和建议。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_748_22
Aneeta Jassar, Nour Hemali, Anjali Bhatnagar

Background: Typing and grading of endometrial carcinomas (ECs) on small biopsy specimens is crucial to determine the need for full surgical staging. Histological subtype and grade are key factors available for risk stratification before surgery. However, this can be diagnostically challenging on small biopsy specimens, especially when morphologic features are subtle or overlapping.

Aims: The aims of this audit were to assess concordance of endometrial carcinomas on biopsy specimens with hysterectomy specimens and to determine if the immunohistochemistry (IHC) panel being used in our practice was adequately subtyping ECs.

Settings and design: The audit was approved by the Clinical Effectiveness Team of the Royal College of Pathologists (UK) as meeting all the criteria and standards set out by the College.

Materials and methods: Biopsies from 67 cases of EC were compared for histological subtype and grade of endometrioid carcinoma with resection specimens. A re-audit was carried out on 59 cases after implementation of changes recommended by the initial audit.

Results: Two of 35 (6%) tumours defined as G1 on biopsy were upgraded (to G2) on final pathology, as was one of 7 (14%) G2 tumours (to G3). One of these cases had solid areas just amounting to more than 6% on resection. In the second case, a comment was made that assessment had been difficult as the specimen was suboptimally fixed, but nuclei appeared atypical. Of seven G2 biopsies, one case was upgraded to grade 3 on final pathology based on proportion of solid areas. Our data show lower rates of discordance as compared to previous studies and on re-audit, the concordance between endometrioid and nonendometrioid serous carcinoma improved with the addition of immunohistochemistry (IHC) for Phosphatase and tensin homolog (PTEN) to biopsies.

Conclusions: PTEN IHC can complement other stains and aid in the distinction of grade 3 endometrioid carcinoma from serous carcinoma on endometrial biopsies.

背景:子宫内膜癌(EC)小活检标本的分型和分级对于确定是否需要进行全面手术分期至关重要。组织学亚型和分级是手术前进行风险分层的关键因素。目的:本次审核的目的是评估活检标本上的子宫内膜癌与子宫切除标本的一致性,并确定我们在实践中使用的免疫组化(IHC)小组是否能对EC进行充分的亚型分型:材料与方法:将67例EC活检组织学亚型和子宫内膜样癌等级与切除标本进行比较。结果:35 例中有 2 例(6%)肿瘤的组织学亚型和分级与切除标本的组织学亚型和分级不同:结果:35 例活检确定为 G1 级的肿瘤中,有 2 例(6%)在最终病理检查中升级(为 G2 级);7 例 G2 级肿瘤中,有 1 例(14%)升级(为 G3 级)。其中一个病例的实变区切除率刚刚超过 6%。在第二个病例中,由于标本固定不够理想,因此很难进行评估,但细胞核似乎不典型。在 7 例 G2 活检病例中,有 1 例在最终病理检查中根据实变区的比例升为 3 级。我们的数据显示,与之前的研究相比,不一致率较低,而且在重新审核时,活检样本中加入磷酸酶和天丝同源物(PTEN)免疫组化(IHC)后,子宫内膜样浆液性癌和非子宫内膜样浆液性癌的一致性有所提高:结论:PTEN IHC 可补充其他染色,有助于区分子宫内膜活检组织中的 3 级子宫内膜样癌和浆液性癌。
{"title":"Assessment of endometrial carcinoma on biopsy as a predictor of final surgical pathology: Are we doing it right? A completed audit cycle and recommendations.","authors":"Aneeta Jassar, Nour Hemali, Anjali Bhatnagar","doi":"10.4103/ijpm.ijpm_748_22","DOIUrl":"10.4103/ijpm.ijpm_748_22","url":null,"abstract":"<p><strong>Background: </strong>Typing and grading of endometrial carcinomas (ECs) on small biopsy specimens is crucial to determine the need for full surgical staging. Histological subtype and grade are key factors available for risk stratification before surgery. However, this can be diagnostically challenging on small biopsy specimens, especially when morphologic features are subtle or overlapping.</p><p><strong>Aims: </strong>The aims of this audit were to assess concordance of endometrial carcinomas on biopsy specimens with hysterectomy specimens and to determine if the immunohistochemistry (IHC) panel being used in our practice was adequately subtyping ECs.</p><p><strong>Settings and design: </strong>The audit was approved by the Clinical Effectiveness Team of the Royal College of Pathologists (UK) as meeting all the criteria and standards set out by the College.</p><p><strong>Materials and methods: </strong>Biopsies from 67 cases of EC were compared for histological subtype and grade of endometrioid carcinoma with resection specimens. A re-audit was carried out on 59 cases after implementation of changes recommended by the initial audit.</p><p><strong>Results: </strong>Two of 35 (6%) tumours defined as G1 on biopsy were upgraded (to G2) on final pathology, as was one of 7 (14%) G2 tumours (to G3). One of these cases had solid areas just amounting to more than 6% on resection. In the second case, a comment was made that assessment had been difficult as the specimen was suboptimally fixed, but nuclei appeared atypical. Of seven G2 biopsies, one case was upgraded to grade 3 on final pathology based on proportion of solid areas. Our data show lower rates of discordance as compared to previous studies and on re-audit, the concordance between endometrioid and nonendometrioid serous carcinoma improved with the addition of immunohistochemistry (IHC) for Phosphatase and tensin homolog (PTEN) to biopsies.</p><p><strong>Conclusions: </strong>PTEN IHC can complement other stains and aid in the distinction of grade 3 endometrioid carcinoma from serous carcinoma on endometrial biopsies.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70763323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Small cell conversion complicated with hypertrophic pulmonary osteoarthropathy after targeted therapy for advanced EGFR-mutated lung adenocarcinoma: A case report. 晚期表皮生长因子受体突变肺腺癌靶向治疗后小细胞转化并发肥厚性肺骨关节病:病例报告。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_280_22
Sijia Zhang, Leichong Chen, Kuikui Zhu, Rui Meng

In recent years, with the opening of the era of precision therapy, the treatment of patients with positive driver genes is a hot issue in global research. EGFR is the most common driver gene in NSCLC, with a positivity rate of 17%. Although targeted drugs for EGFR mutations can benefit this population with efficacy, target therapy resistance inevitably occurs. The presented case suggests that a patient with advanced lung adenocarcinoma with EGFR mutation who developed pathological-type conversion of small cell lung cancer complicated with the development of hypertropic pulmonary osteoarthropathy (HPOA) after 6 months of targeted therapy. This case demonstrates that early diagnosis of HPOA can predict the occurrence of target resistance and pathologic conversion in patients with positive driver genes, providing new clues for the clinical management of lung cancer.

近年来,随着精准治疗时代的开启,驱动基因阳性患者的治疗成为全球研究的热点问题。表皮生长因子受体(EGFR)是 NSCLC 中最常见的驱动基因,阳性率高达 17%。尽管针对表皮生长因子受体突变的靶向药物能使这一人群获益并取得疗效,但靶向治疗耐药的情况不可避免地会发生。本病例显示,一名表皮生长因子受体(EGFR)突变的晚期肺腺癌患者在接受了 6 个月的靶向治疗后,出现了小细胞肺癌的病理类型转换,并并发了肥厚性肺骨关节病(HPOA)。该病例表明,HPOA的早期诊断可预测驱动基因阳性患者靶向耐药和病理型转化的发生,为肺癌的临床治疗提供了新的线索。
{"title":"Small cell conversion complicated with hypertrophic pulmonary osteoarthropathy after targeted therapy for advanced EGFR-mutated lung adenocarcinoma: A case report.","authors":"Sijia Zhang, Leichong Chen, Kuikui Zhu, Rui Meng","doi":"10.4103/ijpm.ijpm_280_22","DOIUrl":"10.4103/ijpm.ijpm_280_22","url":null,"abstract":"<p><p>In recent years, with the opening of the era of precision therapy, the treatment of patients with positive driver genes is a hot issue in global research. EGFR is the most common driver gene in NSCLC, with a positivity rate of 17%. Although targeted drugs for EGFR mutations can benefit this population with efficacy, target therapy resistance inevitably occurs. The presented case suggests that a patient with advanced lung adenocarcinoma with EGFR mutation who developed pathological-type conversion of small cell lung cancer complicated with the development of hypertropic pulmonary osteoarthropathy (HPOA) after 6 months of targeted therapy. This case demonstrates that early diagnosis of HPOA can predict the occurrence of target resistance and pathologic conversion in patients with positive driver genes, providing new clues for the clinical management of lung cancer.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70761965","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Pigmented medulloepithelioma of the optic nerve: A challenging diagnostic entity. 视神经色素髓上皮瘤:具有挑战性的诊断实体。
IF 1 4区 医学 Q3 Medicine Pub Date : 2024-01-01 DOI: 10.4103/ijpm.ijpm_116_22
Tiabi El Mehdi, Chariba Siham, Kamaoui Imane, Benajiba Noufissa, Bennani Amal

Because of its rarity, the diagnosis of optic nerve medulloepithelioma poses a real diagnostic challenge. Medulloepithelioma is a congenital tumor that derives from the primitive medullary epithelium present in the neural tube and the optic vesicle. Its classical location is the ciliary body. Cases of retinal or optic nerve locations have been rarely reported in the literature. Only 11 cases have been published in the English literature. Herein, we report the case of a 2-year-old boy who underwent enucleation of the right eye for a presumed diagnosis of right-eye retinoblastoma, based on the presence of leukocoria on ophthalmological examination. Pathological examination showed an optic nerve medulloepithelioma. A review of the literature is also discussed in our work.

由于其罕见性,视神经髓上皮瘤的诊断确实是一项挑战。髓上皮瘤是一种先天性肿瘤,来源于神经管和视囊中的原始髓质上皮。其典型位置是睫状体。视网膜或视神经位置的病例在文献中鲜有报道。英文文献中仅发表过 11 例。在此,我们报告了一例 2 岁男童的病例。根据眼科检查发现的白眼球,推测诊断为右眼视网膜母细胞瘤,因此对其右眼进行了去核手术。病理检查显示患的是视神经延髓上皮瘤。我们的工作中还讨论了文献综述。
{"title":"Pigmented medulloepithelioma of the optic nerve: A challenging diagnostic entity.","authors":"Tiabi El Mehdi, Chariba Siham, Kamaoui Imane, Benajiba Noufissa, Bennani Amal","doi":"10.4103/ijpm.ijpm_116_22","DOIUrl":"10.4103/ijpm.ijpm_116_22","url":null,"abstract":"<p><p>Because of its rarity, the diagnosis of optic nerve medulloepithelioma poses a real diagnostic challenge. Medulloepithelioma is a congenital tumor that derives from the primitive medullary epithelium present in the neural tube and the optic vesicle. Its classical location is the ciliary body. Cases of retinal or optic nerve locations have been rarely reported in the literature. Only 11 cases have been published in the English literature. Herein, we report the case of a 2-year-old boy who underwent enucleation of the right eye for a presumed diagnosis of right-eye retinoblastoma, based on the presence of leukocoria on ophthalmological examination. Pathological examination showed an optic nerve medulloepithelioma. A review of the literature is also discussed in our work.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70762413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
期刊
Indian Journal of Pathology and Microbiology
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