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POEMS syndrome: A rare entity. POEMS综合征:一种罕见的疾病。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_857_21
Chaganti P Devi, Basimalla R Stephenson, P Ramana Kumari, Panchakarla G Vani, Swargam P Madhooli

POEMS syndrome is a rare paraneoplastic syndrome due to an underlying plasma cell disorder. The diagnosis of POEMS syndrome can be a challenge. A good history, physical examination, and appropriate testing can aid in establishing its diagnosis. We are presenting the case of a 75-year-old man who was diagnosed with POEMS syndrome.

POEMS综合征是一种罕见的副肿瘤综合征,由潜在的浆细胞紊乱引起。POEMS综合征的诊断可能是一个挑战。良好的病史、身体检查和适当的检测可以帮助确定其诊断。我们介绍一例75岁的男性患者,他被诊断为POEMS综合征。
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引用次数: 0
Comparative evaluation of histopathological analysis, KOH wet mount and fungal culture to diagnose fungal infections in post-COVID patients. 组织病理学分析、KOH湿悬和真菌培养诊断新冠肺炎后患者真菌感染的比较评估。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_663_21
Seema N Baxi, Mayuri R Gohil, Anamika J Navadiya, Mayuri K Bapodra, Hiral R Patel

Context and aim: There is increasing prevalence of post-COVID fungal infection of rhinoorbitocerebral region especially mucormycosis and aspergillosis in India.[1] Early diagnosis of these fungal infections are of utmost importance, since it may improve outcome and survival.[2],[3],[4],[5],[6],[7],[8] The objective of this study was to evaluate and compare routine laboratory diagnostic methods, that is, histopathological examination, KOH wet mount and fungal culture in the diagnosis of post-COVID fungal infections.

Materials and methods: A total of 106 specimens of clinically suspected patients of post-COVID fungal infection of rhinoorbitocerebral region received in histopathology department were included in this study. The data of KOH wet mount and culture were acquired from the microbiology department after histopathological examination.

Result: Approximately 88.68% of patients were diagnosed having fungal infections by one of the laboratory methods. The sensitivity of histopathological examination was highest (79.78%), followed by KOH wet mount (58.51%) and fungal culture (35.10%). Rhizopus species of zygomycetes group were the most common isolate (24.24%) on SDA culture. Overall 76% concordance was found between histopathological examination and fungal culture report for morphological identification of fungi.

Conclusion: For the diagnosis of post-COVID fungal infection of Rhino-orbito-cerebral region, histopathological examination is was found to be more sensitive and rapid method to detect fungal hyphae. It leads to early treatment, prevents morbidity and mortality.

背景和目的:在印度,鼻眶脑区新冠肺炎后真菌感染的患病率越来越高,尤其是毛霉菌病和曲霉菌病。[1] 这些真菌感染的早期诊断至关重要,因为它可以改善预后和生存率。[2] ,[3],[4],[5],[6],[7],[8]本研究的目的是评估和比较常规实验室诊断方法,即组织病理学检查、KOH湿悬和真菌培养在诊断新冠肺炎后真菌感染中的作用。材料和方法:本研究共纳入组织病理学部门接受的106例临床疑似新冠肺炎后鼻眶椎区真菌感染患者的标本。KOH湿悬和培养的数据在组织病理学检查后从微生物学部门获得。结果:约88.68%的患者通过一种实验室方法被诊断为真菌感染。组织病理学检查的敏感性最高(79.78%),其次是KOH湿悬法(58.51%)和真菌培养法(35.10%)。在真菌形态学鉴定方面,组织病理学检查和真菌培养报告之间的一致性为76%。结论:对于诊断新冠肺炎后鼻眶脑区真菌感染,组织病理学检查是检测真菌菌丝更灵敏、快速的方法。它可以早期治疗,预防发病率和死亡率。
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引用次数: 1
Teratoid Wilm's tumor with Cryptorchidism. Teratoid Wilm肿瘤伴隐睾。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_1084_21
Nishav Garg, Pavneet K Selhi, Ankita Soni
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引用次数: 0
Expression of protein phosphatase 4 in different tissues under hypoxia. 缺氧条件下不同组织中蛋白磷酸酶4的表达。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_1179_21
Yanyan Ma, Jing Hou, Dengliang Huang, Yaogang Zhang, Zhe Liu, Meiyuan Tian

Relevant research data shows that there is a certain degree of energy metabolism imbalance in highland residents. Protein phosphatase 4 (PP4) has been found as a new factor in the regulation of sugar and lipid metabolism. Here, we investigate the differential expression of PP4 at a simulated altitude of 4,500 m in the heart, lung, and brain tissues of rats. A hypoxic plateau rat model was established using an animal decompression chamber. A blood routine test was performed by an animal blood cell analyzer on rats cultured for different hypoxia periods at 4,500 m above sea level. Quantitative polymerase chain reaction (qPCR) and western blot were used to detect the changes of protein phosphatase 4 catalytic subunit (PP4C) gene and protein in heart, lung, and brain tissues. The PP4C gene with the highest expression level found in rats slowly entering the high altitude area (20 m-2200 m-7 d-4500 m-3 d) was about twice as high as the low elevation group (20 m above sea level). The simulated high-altitude hypoxia induced an increase of PP4C expression level in all tissues, and the expression in the lung tissue was twice as expressed as heart and brain tissue at high altitude (P < 0.05). These results suggest that the PP4 phosphatase complex is ubiquitously expressed in rat tissues and likely involved in adaptation to or disease associated with high-altitude hypoxia.

相关研究数据表明,高原居民存在一定程度的能量代谢失衡。蛋白磷酸酶4(PP4)已被发现是调节糖和脂质代谢的一个新因素。在这里,我们研究了PP4在模拟海拔4500米的大鼠心脏、肺和脑组织中的差异表达。采用动物减压室建立缺氧高原大鼠模型。通过动物血细胞分析仪对在海拔4500米培养不同缺氧期的大鼠进行血常规测试。采用定量聚合酶链式反应(qPCR)和蛋白质印迹法检测心、肺和脑组织中蛋白磷酸酶4催化亚基(PP4C)基因和蛋白的变化。在缓慢进入高海拔地区(20 m-2200 m-7 d-4500 m-3 d)的大鼠中发现的表达水平最高的PP4C基因大约是低海拔组(海拔20 m)的两倍。模拟高海拔缺氧可使PP4C在所有组织中的表达水平升高,肺组织中PP4C的表达水平是高海拔心脑组织的两倍(P<0.05)。这些结果表明,PP4磷酸酶复合物在大鼠组织中普遍表达,可能参与高海拔缺氧的适应或与高海拔缺氧相关的疾病。
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引用次数: 1
Diagnostic utility of special stains in defining the spectrum of maxillofacial pathologies. 特殊污渍在确定颌面部病理谱中的诊断作用。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_1254_21
Akshay Gupta, Ankita Tandon, Saurabh Juneja, Nikita Gulati, Devi Charan Shetty

Background: The Fine needle aspiration cytology (FNAC) is considered as a valuable and distinguished diagnostic test in the initial assessment of the patients presenting with a mass in the head and neck region or when a recurrence is suspected after previous treatment.

Aims: This study was therefore designed to elucidate the efficacy of FNAC as an alternate diagnostic tool to histopathology in head and neck swellings and evaluation of staining efficacy of PAP and MGG stain over Haematoxylin and eosin (H and E) in routine cytopathological smears.

Settings and design: The study was conducted in the Department of Oral and Maxillofacial Pathology, where FNAC samples were collected from 150 patients with head and neck swellings.

Materials and methods: All the slides were stained with H and E, Papanicolaou (PAP), and May Grunewald Giemsa (MGG) stains. The cytopathological diagnosis was compared with histopathological diagnosis based on H and E stained sections obtained from paraffin-embedded formalin-fixed biopsy specimen of benign and malignant neoplasms.

Statistical analysis used: The resulting data were analyzed using SPSS software version 19. Differences between the variables were analyzed using Pearson Chi-square test and Kruskal-Wallis test wherever applicable.

Results: The FNAC as a diagnostic tool has sensitivity of 84.8%, 72.72%, and 78.78%, specificity of 62.5%, 75%, and 75%, and accuracy of 80.48%, 73.14%, and 78.04% in H and E, MGG, and PAP stain, respectively. PAP stain was the most efficient stain when all qualitative parameters are taken into consideration with maximum sensitivity and specificity for achieving definitive cytodiagnosis.

Conclusions: The FNAC is an inexpensive and minimally invasive technique to diagnose different types of head and neck swellings and complement histopathological diagnosis.

背景:细针抽吸细胞学检查(FNAC)被认为是一种有价值和独特的诊断测试,用于对头颈部肿块患者的初步评估,或在既往治疗后怀疑复发时。因此,本研究旨在阐明FNAC作为头颈部肿胀组织病理学的替代诊断工具的疗效,并评估PAP和MGG染色在常规细胞病理学涂片中对苏木精和伊红(H和E)的染色效果。设置和设计:这项研究在口腔颌面病理科进行,从150名头颈部肿胀患者身上采集了FNAC样本。材料和方法:所有载玻片均用H和E、Papanicolaou(PAP)和May-Grunewald Giemsa(MGG)染色。将细胞病理学诊断与基于从石蜡包埋的福尔马林固定的良性和恶性肿瘤活检标本中获得的H和E染色切片的组织病理学诊断进行比较。使用统计分析:使用SPSS软件19版对所得数据进行分析。在适用的情况下,使用Pearson卡方检验和Kruskal-Wallis检验分析变量之间的差异。结果:FNAC作为一种诊断工具,在H和E、MGG和PAP染色中的敏感性分别为84.8%、72.72%和78.78%,特异性分别为62.5%、75%和75%,准确率分别为80.48%、73.14%和78.04%。当考虑到所有定性参数时,PAP染色是最有效的染色,具有最大的敏感性和特异性,以实现最终的细胞诊断。结论:FNAC是一种廉价、微创的技术,可以诊断不同类型的头颈部肿胀,并补充组织病理学诊断。
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引用次数: 0
A novel case of left atrial and right lung mass turned out to be unconventional metastasis of uterine leiomyosarcoma with a review of literature. 一例新的左心房和右肺肿块是子宫平滑肌肉瘤的非常规转移,并文献复习。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_577_21
Tarang Patel, Priyanka Aswal, Ashish Jakhetiya, Virendrakumar Meena, Arun Pandey

Uterine leiomyosarcoma (ULMS) is a rare malignancy arising from the myometrial smooth muscle wall, and cardiac metastases are extremely rare. Metastasis to the heart is a very unusual finding, and atrial metastasis is even rarer. Here, we report a case of a 45 year old woman who presented with dyspnea and pleural effusion and had a significant history of hysterectomy done for ULMS. Magnetic resonance imaging revealed a left atrial mass, which was resected and revealed to be a metastasis of leiomyosarcoma on histopathology and immunohistochemistry. Metastatic ULMS may rarely present as a left atrial mass with acute clinical presentation. Detailed clinical history and accurate diagnosis are vital for further management.

子宫平滑肌肉瘤(ULMS)是一种罕见的恶性肿瘤,起源于子宫肌层平滑肌壁,心脏转移极为罕见。转移到心脏是一个非常不寻常的发现,心房转移更为罕见。在这里,我们报告了一例45岁的女性,她出现呼吸困难和胸腔积液,并有为ULMS做子宫切除术的重要历史。磁共振成像显示左心房肿块被切除,组织病理学和免疫组织化学显示为平滑肌肉瘤转移。转移性ULMS可能很少表现为急性临床表现的左心房肿块。详细的临床病史和准确的诊断对进一步的管理至关重要。
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引用次数: 0
Pediatric and adolescent chronic myeloid leukemia: A follow-up study in Western India. 儿童和青少年慢性粒细胞白血病:印度西部的一项随访研究。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_462_21
Sangita A Vanik, Dhaval Jetly, Biren Parikh, Karthik Dhandapani, Rukmini Bezbaruah

Background: Chronic myeloid leukemia (CML) is relatively rare in pediatric and adolescent age groups. The purpose of this study was to evaluate the clinical, hematopathological, and biochemical parameters of CML in pediatric and adolescent age groups, along with an assessment of the treatment response with first-line tyrosine kinase inhibitors (TKI) and its correlation with the prognostic scoring systems of adults.

Materials and methods: A retrospective study of 44 Breakpoint Cluster Region-Abelson leukemia virus (BCR-ABL1)-positive pediatric and adolescent CML cases registered at our hospital was done. The clinical and laboratory parameters were evaluated using hospital software. The treatment response was monitored and scoring was performed using mathematical calculations.

Results: The mean age was 11.6 (±4.7) years. The median hemoglobin was 8.4 g/dL and 63.6% of the cases showed white blood cell (WBC) counts >250,000/μL. The average follow-up was 21 months. A total of 97.7 and 78.1% cases achieved complete hematological response (CHR) and molecular response, respectively, during the treatment course. The maximum number of patients had low Sokal and European treatment and Outcomes Study (EUTOS) scores. Seventy-five per cent of the cases achieved CHR at 3 months, while 73.6 and 78.6% CML-Chronic phase (CP) cases with low Sokal and EUTOS scores achieved CHR at 3 months, respectively.

Conclusion: This study revealed that the CML cases in pediatric and adolescent age groups are normally present with higher WBC counts at the time of diagnosis. The association of the prognostic scoring system with treatment response was statistically insignificant. However, a larger cohort study is needed to determine the treatment response of TKI in children and adolescent CML and its correlation with the prognostic scoring systems.

背景:慢性粒细胞白血病(CML)在儿童和青少年年龄组中相对罕见。本研究的目的是评估儿童和青少年年龄组慢性粒细胞白血病的临床、血液病理学和生化参数,并评估一线酪氨酸激酶抑制剂(TKI)的治疗反应及其与成人预后评分系统的相关性。材料和方法:对我院登记的44例BCR-ABL1阳性儿童和青少年慢性粒细胞白血病病例进行回顾性研究。使用医院软件评估临床和实验室参数。监测治疗反应,并使用数学计算进行评分。结果:平均年龄11.6(±4.7)岁。血红蛋白中位数为8.4 g/dL,63.6%的病例显示白细胞计数>250000/μL。平均随访21个月。在治疗过程中,共有97.7%和78.1%的病例分别获得了完全血液学反应(CHR)和分子反应。Sokal和欧洲治疗和结果研究(EUTOS)评分较低的患者人数最多。75%的病例在3个月时达到CHR,而Sokal和EUTOS评分较低的慢性粒细胞白血病慢性期(CP)病例分别有73.6%和78.6%在3个月中达到CHR。结论:本研究表明,儿童和青少年年龄组的慢性粒细胞白血病患者在诊断时通常存在较高的白细胞计数。预后评分系统与治疗反应的相关性在统计学上不显著。然而,需要进行更大规模的队列研究来确定TKI在儿童和青少年CML中的治疗反应及其与预后评分系统的相关性。
{"title":"Pediatric and adolescent chronic myeloid leukemia: A follow-up study in Western India.","authors":"Sangita A Vanik,&nbsp;Dhaval Jetly,&nbsp;Biren Parikh,&nbsp;Karthik Dhandapani,&nbsp;Rukmini Bezbaruah","doi":"10.4103/ijpm.ijpm_462_21","DOIUrl":"10.4103/ijpm.ijpm_462_21","url":null,"abstract":"<p><strong>Background: </strong>Chronic myeloid leukemia (CML) is relatively rare in pediatric and adolescent age groups. The purpose of this study was to evaluate the clinical, hematopathological, and biochemical parameters of CML in pediatric and adolescent age groups, along with an assessment of the treatment response with first-line tyrosine kinase inhibitors (TKI) and its correlation with the prognostic scoring systems of adults.</p><p><strong>Materials and methods: </strong>A retrospective study of 44 Breakpoint Cluster Region-Abelson leukemia virus (BCR-ABL1)-positive pediatric and adolescent CML cases registered at our hospital was done. The clinical and laboratory parameters were evaluated using hospital software. The treatment response was monitored and scoring was performed using mathematical calculations.</p><p><strong>Results: </strong>The mean age was 11.6 (±4.7) years. The median hemoglobin was 8.4 g/dL and 63.6% of the cases showed white blood cell (WBC) counts >250,000/μL. The average follow-up was 21 months. A total of 97.7 and 78.1% cases achieved complete hematological response (CHR) and molecular response, respectively, during the treatment course. The maximum number of patients had low Sokal and European treatment and Outcomes Study (EUTOS) scores. Seventy-five per cent of the cases achieved CHR at 3 months, while 73.6 and 78.6% CML-Chronic phase (CP) cases with low Sokal and EUTOS scores achieved CHR at 3 months, respectively.</p><p><strong>Conclusion: </strong>This study revealed that the CML cases in pediatric and adolescent age groups are normally present with higher WBC counts at the time of diagnosis. The association of the prognostic scoring system with treatment response was statistically insignificant. However, a larger cohort study is needed to determine the treatment response of TKI in children and adolescent CML and its correlation with the prognostic scoring systems.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9921062","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
A unique coexistence of a plurihormonal pituitary adenoma with granulomatous hypophysitis. 多激素性垂体腺瘤与肉芽肿性垂体炎的独特共存。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_439_21
Sanjiban Patra, Priti Trivedi

Dual pathology in the pituitary gland is a unique phenomenon. Coexistence of a pituitary adenoma with primary hypophysitis has been reported rarely with very few cases in the literature. Among the primary hypophysitis, primary granulomatous subtype has been proposed to be idiopathic and autoimmune in nature. Plurihormonal pituitary adenomas produce hormones of more than one different pituitary cell lineage. Pituitary adenoma with a single hormonal content has been documented with concurrent primary granulomatous hypophysitis. The present case describes the unique coexistence of a plurihormonal adenoma showing somatotroph, lactotroph, and corticotroph lineage with primary granulomatous inflammation in the sellar region in a 36-year-old woman.

垂体的双重病理是一种独特的现象。垂体腺瘤与原发性垂体炎并存的报道很少,文献中很少有病例。在原发性垂体炎中,原发性肉芽肿亚型被认为是特发性和自身免疫性的。多发性垂体腺瘤产生一种以上不同垂体细胞谱系的激素。单一激素含量的垂体腺瘤已被记录为并发原发性肉芽肿性垂体炎。本病例描述了一名36岁女性鞍区多激素腺瘤与原发性肉芽肿性炎症的独特共存,该腺瘤表现为生长激素、乳细胞和促皮质激素谱系。
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引用次数: 0
Chrysosporium: A rare cause of allergic fungal rhinosinusitis. 金孢菌:一种罕见的过敏性真菌性鼻窦炎病因。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_555_21
Juhi Shrivastava, Kinal Shah, Navin Shah

Allergic fungal rhinosinusitis (AFRS) forms a significant group of patients presenting with the commonest health problem encountered in rhinology. Patients commonly present with typical symptoms of sinusitis, and the diagnosis is often made after imaging and/or intraoperatively. Infections caused by Chrysosporium species are very rare and are very rarely been reported to cause sinusitis in humans. Usually, human chrysosporial infections are mild and unmarked by symptoms. We report a rare case of allergic fungal sinusitis (AFS) caused by Chrysosporium species in a 41-year-old male with the history of diabetes mellitus.

过敏性真菌性鼻窦炎(AFRS)是鼻科最常见的健康问题患者群体。患者通常表现出典型的鼻窦炎症状,通常在影像学和/或术中诊断。由金孢菌引起的感染非常罕见,很少有报道称会导致人类鼻窦炎。通常,人类黄孢子虫感染是轻微的,没有任何症状。我们报告了一例罕见的由金孢菌引起的过敏性真菌性鼻窦炎(AFS)病例,该病例发生在一名有糖尿病病史的41岁男性中。
{"title":"Chrysosporium: A rare cause of allergic fungal rhinosinusitis.","authors":"Juhi Shrivastava,&nbsp;Kinal Shah,&nbsp;Navin Shah","doi":"10.4103/ijpm.ijpm_555_21","DOIUrl":"10.4103/ijpm.ijpm_555_21","url":null,"abstract":"<p><p>Allergic fungal rhinosinusitis (AFRS) forms a significant group of patients presenting with the commonest health problem encountered in rhinology. Patients commonly present with typical symptoms of sinusitis, and the diagnosis is often made after imaging and/or intraoperatively. Infections caused by Chrysosporium species are very rare and are very rarely been reported to cause sinusitis in humans. Usually, human chrysosporial infections are mild and unmarked by symptoms. We report a rare case of allergic fungal sinusitis (AFS) caused by Chrysosporium species in a 41-year-old male with the history of diabetes mellitus.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9923495","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
Anaplastic (undifferentiated) carcinoma of pancreas, an uncommon variant: Diagnosed on endoscopic-guided fine needle aspiration. 胰腺无定形(未分化)癌,一种罕见的变体:经内镜引导细针抽吸诊断。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-07-01 DOI: 10.4103/ijpm.ijpm_538_21
Md Ali Osama, Pooja Bakshi, Kusum Verma

Anaplastic carcinoma of pancreas (ACP) are rare pancreatic neoplasms. They are well known to be associated with more aggressive tumor behavior and less favorable prognosis than usual pancreatic ductal adenocarcinoma. Endoscopic-guided fine needle aspiration (EUS-FNA) is now a widely accepted modality in diagnosis of pancreatic lesions. However, only a few reports are available describing cytological features of anaplastic carcinoma. Here, we report two cases of ACP diagnosed on EUS-FNA.

胰腺无定形癌(ACP)是一种罕见的胰腺肿瘤。众所周知,与通常的胰腺导管腺癌相比,它们与更具侵袭性的肿瘤行为和较差的预后有关。内镜引导下细针抽吸(EUS-FNA)是目前广泛接受的胰腺病变诊断方法。然而,只有少数报道可以描述间变性癌的细胞学特征。在此,我们报告两例经EUS-FNA诊断为ACP的病例。
{"title":"Anaplastic (undifferentiated) carcinoma of pancreas, an uncommon variant: Diagnosed on endoscopic-guided fine needle aspiration.","authors":"Md Ali Osama, Pooja Bakshi, Kusum Verma","doi":"10.4103/ijpm.ijpm_538_21","DOIUrl":"10.4103/ijpm.ijpm_538_21","url":null,"abstract":"<p><p>Anaplastic carcinoma of pancreas (ACP) are rare pancreatic neoplasms. They are well known to be associated with more aggressive tumor behavior and less favorable prognosis than usual pancreatic ductal adenocarcinoma. Endoscopic-guided fine needle aspiration (EUS-FNA) is now a widely accepted modality in diagnosis of pancreatic lesions. However, only a few reports are available describing cytological features of anaplastic carcinoma. Here, we report two cases of ACP diagnosed on EUS-FNA.</p>","PeriodicalId":13488,"journal":{"name":"Indian Journal of Pathology and Microbiology","volume":null,"pages":null},"PeriodicalIF":1.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9923497","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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