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Artykuły w czasopismach na temat „Tumors”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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1

Vladanov, Ivan, Alexei Plesacov, Artur Colta, and Vitalii Ghicavii. "Diagnostic markers of urinary bladder tumors." Moldovan Medical Journal 64(1) (February 15, 2021): 71–75. https://doi.org/10.5281/zenodo.4527239.

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<strong>Background:</strong> The perfect method for laboratory diagnosis of bladder cancer should have high sensitivity and specificity, should be easily reproducible, inexpensive, be suitable for primary diagnosis, screening, and follow-up of patients, for timely detection of recurrence. In clinical practice, for bladder cancer diagnostics has used the following markers: UBC, BTA, "ImmunoCyt", NMP22, "UroVision», and others.  Each method has relative advantages and disadvantages.  The study has demonstrated an influence on the test result of the histological str

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Deepak, Goyal, Gupta Ankur, Gupta Garima, and Agrawal Sadhana. "Types and Frequency of Ovarian Neoplasm According to Age: A 10 Year Histopathological Study." International Journal of Pharmaceutical and Clinical Research 14, no. 5 (2022): 341–46. https://doi.org/10.5281/zenodo.13825496.

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<strong>Objectives</strong>: To find Types and frequency of Ovarian Neoplasms according to age and to compare it with other studies. <strong>Methodology</strong>: A 10-year retrospective study of ovarian Neoplasms, specimens of that were received and diagnosed in the Department of Pathology, R.N.T. Medical College, Udaipur Rajasthan. This study was conducted for a period of 10 years from Jan 2004 to Dec 2013. <strong>Results:</strong> The study was carried out on 472 specimens. Maximum tumors of the ovary (26.48%) were found in age group of 31-40 years followed by age group 21-3

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Md., Akil Azher Siddique, Arundhati, and Singh Rashmi. "Histopathological Correlation with Clinico-Radiological Diagnosis of Bone Tumours." International Journal of Current Pharmaceutical Review and Research 15, no. 12 (2023): 668–73. https://doi.org/10.5281/zenodo.11526942.

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AbstractHistological examination of bone tumors is considered to be a challenging field inpathology. Bone tumors andtumor – like lesions are very rare. The low incidence of these tumors and the resulting limited experience indealing with them adds to the diagnostic difficulties.Clinico–radiological evaluation of bone tumors and tumor – like lesions is an essential part of patientmanagement. Histopathological diagnosis should be given after proper review of clinical and radiologicalfindings.There is very good correlation between clinico – radiological and histopathologic

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George-Cătălin, Moroșan, Moroșan Andreea-Cătălina, Dobrin Romeo, et al. "BRAIN. Broad Research in Artificial Intelligence and Neuroscience - Psychiatric Manifestations in the Context of Brain Tumors: Study and Findings." BRAIN. Broad Research in Artificial Intelligence and Neuroscience 15, no. 4 (2024): 231–52. https://doi.org/10.70594/brain/15.4/16.

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The increase in the frequency of psychiatric disorders is increasingly observed in patients diagnosed with cancer. Brain tumors are often associated with psychiatric symptoms such as mood symptoms, psychosis, memory problems, personality changes, anxiety, or depression. This study investigates what types of manifestations are present in patients with brain tumors, highlighting the connection with the location of the tumor. We conducted a clinical study on a sample of 91 patients diagnosed with primary brain tumors, hospitalized at the "Prof. Dr. Nicolae Oblu Emergency Clinical Hospital," Iași,

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Mathew, George, and Shwetha Jose. "PRIMARY TUMORS AND TUMOR-LIKE LESIONS OF BONE IN CHILDREN." International Journal of Integrative Medical Sciences 4, no. 6 (2017): 507–11. http://dx.doi.org/10.16965/ijims.2017.112.

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GROSU, Luminiţa-Bianca, and Camelia DIACONU. "Cardiac Tumors." Annals of the Academy of Romanian Scientists Series of Medicine 3, no. 1 (2022): 7–12. http://dx.doi.org/10.56082/annalsarscimed.2022.1.7.

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Cardiac tumors represent a rare and challenging clinical situation. They can be primary (benign or malignant) or secondary (metastatic). Secondary tumors are more frequent than the primary tumors. Most of the primary cardiac tumors are benign and originate from the endocardium or myocardium, while the metastatic tumors develop from lung, breast, kidney carcinoma, melanoma and lymphoma. The diagnosis of cardiac tumors is often difficult because of their rarity, variety and nonspecific symptoms. The clinical manifestations depend on tumor’s size, location, infiltration and consist of four catego

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O., H. Boichuk, and Y. Hulii D. "DIAGNOSTIC PECULIARITIES OF BENIGN OVARIAN TUMORS DURING PREGNANCY." REPRODUCTIVE ENDOCRINOLOGY, no. 56 (December 30, 2020): 38–42. https://doi.org/10.18370/2309-4117.2020.56.38-42.

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<strong>Objective of the study</strong>: improvement of diagnostic methods for pregnant women with tumor-like formations and ovarian tumors. <strong>Materials and methods</strong>. 60 pregnant women were examined and divided into 3 groups: group I – 28 pregnant women with ovarian tumors who underwent surgical treatment during pregnancy; group II – 21 women with ovarian tumors who underwent surgical treatment at various times after spontaneous delivery; group III (control) – 11 women with a normal course of pregnancy without ovarian tumors. Doppler ultrasound was performed on

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Vladova, Paulina, and Sergey Iliev. "Appendiceal neuroendocrine tumors - recent insights." International Journal of Surgery and Medicine 4, no. 3 (2018): 1. http://dx.doi.org/10.5455/ijsm.appendiceal-neuroendocrine-tumors.

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Stanić, Dragana, Danica Grujičić, Tatjana Pekmezović, et al. "Clinical profile, treatment and outcome of pediatric brain tumors in Serbia in a 10-year period: A national referral institution experience." PLoS One 16, no. 10 (2021): e0259095. https://doi.org/10.1371/journal.pone.0259095.

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<strong>Objective. </strong>This study aimed to evaluate the characteristics of children with primary brain tumors, the effectiveness of treatment modalities, and to detect factors related to the outcome. <strong>Methods. </strong>A detailed analysis was performed on a series of 173 pediatric patients treated in a Serbian referral oncology institution between 2007 and 2016, based on their clinical, histological, treatment, and follow-up data. <strong>Results. </strong>Mean survival time of all children was 94.5months. 2-, 5- and 10-year overall survival probabilities w

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10

Khanam, Shafeya, Maliha Rashid, Zebunnessa Parvin, et al. "Histological Variants of Ovarian Tumour in Bangladeshi Women." Ibrahim Cardiac Medical Journal 5, no. 1-2 (2017): 40–44. http://dx.doi.org/10.3329/icmj.v5i1-2.53698.

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Objective: Types of ovarian tumour are widely divergent and no age group is immune from ovarian tumour; but certain ages are more vulnerable to develop certain types of tumours. By far, very few studies describing the histological types and subtypes of ovarian tumour in the context of Bangladeshi population have been conducted. The present study was intended to find the histological variants of ovarian tumours in our women. Methods: The present study was carried out in Dhaka Medical College Hospital between July 2001 to June 2002. The total number of patients admitted with a clinical dia

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Khareba, G. G., V. M. Lisovyi, and D. V. Shchukin. "RESULTS OF NEPHRON-SPARING SURGERY OF INTRAPARENCHYMAL RENAL TUMORS." Актуальні проблеми сучасної медицини: Вісник Української медичної стоматологічної академії 20, no. 2 (2020): 96–101. http://dx.doi.org/10.31718/2077-1096.20.2.96.

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Surgical treatment is the main therapy for patients with renal cell carcinoma. The current approach in the treatment of kidney tumours has become widely introduced into nephron-sparing surgery. This approach is usually applied in cases of complex surgeries for large-size tumours with intravenous extension, multifocal, and intraparenchymal renal tumours. The purpose of the study was to investigate the results of nephron-sparing surgery for intraparenchymal renal tumours. Material and methods. The results were obtained in the process of nephron-sparing surgery treatment of 701 patients with rena

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Thakur, Ajay Singh, Renuka Gahine, and Vishal Kulkarni. "A study on morphologic and histological pattern of the central nervous system tumors." International Journal of Research in Medical Sciences 6, no. 12 (2018): 3879. http://dx.doi.org/10.18203/2320-6012.ijrms20184699.

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Background: It has been revealed by International Agency for Research on Cancer that the worldwide incidence rate of CNS tumors in 2002 was 3.7/100,000 population among males and 2.6/100,000 population among females. Central Nervous System (CNS) tumors account for 85% of brain tumors and 15 % of spinal cord tumors, however metastatic tumors are usually extradural. According to the WHO classification tumors of CNS comprise more than 50 clinico-pathological entities. The major categories include the tumors of neuroepithelial tissue, cranial and paraspinal nerves, meninges, sellar region, lymphom

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13

Mathisen, Douglas J. "Tracheal tumors." Journal of the Japanese Association for Chest Surgery 19, no. 3 (2005): 301. http://dx.doi.org/10.2995/jacsurg.19.301.

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Eviana, Norahmawati, Natania Nurasih Amelinda, Pandu Persada Isma Satria, Irmansyah Irsan Istan, and Darinafitri Irma. "A rare case malignant granular cell tumor of the thigh with radiological imaging likely rhabdomyosarcoma: A case report." GSC Biological and Pharmaceutical Sciences 27, no. 1 (2024): 247–52. https://doi.org/10.5281/zenodo.11977549.

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Granular cell tumors (GCTs) are uncommon soft tissue tumors characterized by the cytoplasmic granular appearance of the neoplastic cells. Malignant GCTs are rare neural tumors, intensely aggressive. Both the rare occurrence of malignant GCTs and its similarities in features with their benign lesions make the diagnosis of this malignancy difficult. Malignant GCTs comprise less than 2% of GCTs and are mostly found in the subcutaneous soft tissues of the lower extremities, especially the thighs. This article presents a case of a large malignant GCTs in the left thigh of a 46-year-old woman. Plain

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Sobti, Parul, Vivek Harkare, Sonali Khadakkar, Rahul Varma, and Prajakta Golhar. "Comparison between 70 degree endoscopy, direct laryngoscopy and CT scan in T staging of Laryngeal cancer." Panacea Journal of Medical Sciences 7, no. 2 (2017): 68–71. https://doi.org/10.18231/pjms.v.7.i.2.68-71.

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The purpose of the study was to study and compare the importance of 70 degree endoscopy, direct laryngoscopy and CT scan in showing the extent of laryngeal tumours which would then decide the course of treatment for the patient. A total of 25 patients were included in the study and all patients underwent 70 degree endoscopy, direct laryngoscopy and CT scan examination. The CT scan findings were taken as gold standard and the T staging of the laryngeal tumours was compared with 70 degree endoscopy and direct laryngoscopy which was done using Cohens Kappa statistics. The sensitivity of 70 degree

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Joaquim, Andrei Fernandes, Enrico Ghizoni, Marcelo Gomes Cordeiro Valadares, Simone Appenzeller, Simone dos Santos Aguiar, and Helder Tedeschi. "Spinal tumors in children." Revista da Associação Médica Brasileira 63, no. 5 (2017): 459–65. http://dx.doi.org/10.1590/1806-9282.63.05.459.

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Summary Introduction: Spinal tumors are rare in the pediatric population, presenting many specific peculiarities when compared to adults. We have performed a broad narrative review to describe the most common spinal tumors in children, discussing their main characteristics and management options. Method: The authors have performed an extensive review of the peer-reviewed literature addressing the aforementioned objectives. Results: Multimodality radiological studies (plain films, 3D computed tomography scan and magnetic resonance imaging) are necessary for proper evaluation and differential di

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Kim, Dong-Ju, Lee-Chan Jang, Jae-Woon Choi, and Jin-Woo Park. "Retroperitoneal Tumors Mimicking Adrenal Tumor." Korean Journal of Endocrine Surgery 12, no. 1 (2012): 31. http://dx.doi.org/10.16956/kjes.2012.12.1.31.

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Millichap, J. Gordon, and John J. Millichap. "Tumors and Tumor-Related Epilepsy." Pediatric Neurology Briefs 28, no. 2 (2014): 9. http://dx.doi.org/10.15844/pedneurbriefs-28-2-1.

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Eriksson, Barbro, Kjell Öberg, and Mats Stridsberg. "Tumor Markers in Neuroendocrine Tumors." Digestion 62, no. 1 (2000): 33–38. http://dx.doi.org/10.1159/000051853.

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Adashvoyev, Khusan Anvarbekovich, Jaloliddin Ibragimovich Boboyev, and Rustam Bafoevich Hazratkulov. "SURGICAL TREATMENT AND DIFFERENTIAL DIAGNOSIS OF CALVARIAL TUMORS (LITERATURE REVIEW)." Journal of neurology and neurosergery 4, no. 2 (2023): 3. https://doi.org/10.5281/zenodo.7826075.

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This article presents a review of the literature on tumors of the cranial vault, dedicated to the differential diagnosis and methods of surgical treatment. However, there are no studies with a high level of evidence base, about the significant benefits of a particular treatment method.

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Natekar, Ashwini, Shubasis Basu, Gavruv Gupta, and Maruti Pujari. "Spectrum of bone and soft tissue tumors in a tertiary cancer institute in Eastern india." International Journal of Research in Medical Sciences 6, no. 8 (2018): 2686. http://dx.doi.org/10.18203/2320-6012.ijrms20183252.

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Background: Bone and soft tissue tumours are uncommon tumours that can affect any age group. Soft tissue tumors are said to be heterogeneous group of mesenchymal malignancies. Primary bone sarcomas are rare tumors, comprising approximately 0.2% of all cancers. Their true incidence is difficult to estimate because of their rarity. The outcome of the disease depends on the age and time at diagnosis.Methods: A study was carried out in department of pathology in tertiary cancer institute in East India from December 2015 to September 2017. A total of 60 cases were included in the study. All age gro

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Welsh, Cynthia. "Glial Tumors." AJSP: Reviews and Reports 25, no. 2 (2020): 57–62. http://dx.doi.org/10.1097/pcr.0000000000000364.

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Abstract Glial tumors comprise the majority of primary intra-axial intracranial tumors. Since its introduction in 2016, the revised fourth edition of the World Health Organization (WHO) classification of central nervous system tumors has changed the diagnostic and therapeutic approach in glial tumors (WHO Classification of Tumours of the Central Nervous System [revised fourth edition]; Lyon, France: IARC; 2016). Diffuse gliomas (WHO grades II–IV) are now molecularly stratified based on isocitrate dehydrogenase 1 or 2 mutation status and classified according to 1p/19q codeletion status into ast

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Austin, Publishing Group. "A Small And a Large Solitary Fibrous Tumors of the Pleura." Austin Journal of Medical Oncology 10, no. 1 (2023): 1076. https://doi.org/10.26420/austinjmedoncol.2023.1076.

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Abstract Solitary Fibrous Tumor of the Pleura (SFTP) is an exceptionally rare mesenchymal tumor that typically originates from the visceral pleura and constitutes less than 5% of all pleural tumors. While it often displays benign histological features, the tumor’s behavior remains enigmatic and less comprehensively understood, primarily owing to its limited incidence and case studies. We present two cases of SFTP. The First one was a small pleural nodule a nodule in a 61 year old patien, confirmed as a SFTP through CT-guided biopsy. Successful tumor resection was performed, with histopat

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Galati, Melissa, Li Li, Sumedha Sudhaman, et al. "MODL-25. REPLICATION REPAIR DEFICIENT MOUSE MODELS PROVIDE INSIGHT ON HYPERMUTANT BRAIN TUMOURS, MECHANISMS OF IMMUNE EVASION, AND COMBINATORIAL IMMUNOTHERAPY." Neuro-Oncology 22, Supplement_3 (2020): iii416. http://dx.doi.org/10.1093/neuonc/noaa222.598.

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Abstract Replication repair deficiency (RRD) is the leading cause of hypermutant brain tumours in children. RRD is caused by defects in one of four mismatch repair (MMR) genes and mutations in POLE or POLD1. Such tumours are resistant to common therapeutic agents and animal models are needed to study RRD in vivo and test novel therapies like immune checkpoint inhibitors (ICIs). To model RRD brain tumours specifically, we engineered a Pole mutant mouse model harbouring the S459F mutation (PoleS459F). We combined PoleS459F mice with conditional Msh2 knockout (Msh2LoxP) and Nestin-cre mice. All N

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Abdullazade, Samir, Kemal Kosemehmetoglu, Ilknur Adanir, Lale Kutluay, and Alp Usubutun. "Uterine tumors resembling ovarian sex cord-stromal tumors: synchronous uterine tumors resembling ovarian sex cord-stromal tumors and ovarian sex cord tumor." Annals of Diagnostic Pathology 14, no. 6 (2010): 432–37. http://dx.doi.org/10.1016/j.anndiagpath.2010.07.001.

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Chen, Yanxi. "The Role of Epidemic Tumor Vaccine in Cold Tumors to Hot Tumors." Transactions on Materials, Biotechnology and Life Sciences 7 (December 24, 2024): 377–82. https://doi.org/10.62051/abrm9r87.

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Compared with hot tumors, cold tumors are a more difficult problem at present. Because cold tumors lack in congenital immunity, it is difficult for ordinary immune examination inhibitors to work. Therefore, how to "ignite" cold tumors as hot tumors is the focus of the current research. At present, scholars have proposed different and corresponding methods for various causes of T cell immunodeficiency. Among them, tumor vaccines stand out from the principle of activating the immune response of T cells and NK cells, and is currently generally recognized as a new therapy and research hotspot with

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Lekshmy, Jayan, R. Ramya, P. AHMED SAHANAZ, and M. Ramya. "Virus V/S Salivary Gland: Viral Etiology In The Pathogenesis Of Salivary Gland Tumors: A Systematic Review." International Journal of Medical Reviews and Case Reports 3, no. 9 (2019): 589–97. https://doi.org/10.5455/IJMRCR.salivary-gland-tumors.

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INTRODUCTION: salivary gland tumors a diverse group of lesions that by virtue of its rarity as well as clinical, histological and morphological diversity pose a challenge to the pathologist.The role of oncogenic viruses in the pathogenesis of salivary gland has been studied and researched from as early as 1950s.Even with the advent of newer diagnostic techniques, researches done to establish a relationship between salivary gland tumors and oncogenic viruses has reached a standstill because of the controversies in the results obtained from previous studies AIM: To critically analyse the literat

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Markam, Miss Surbhi. "Tumors of Kidney." International Journal of Trend in Scientific Research and Development Volume-3, Issue-2 (2019): 663–71. http://dx.doi.org/10.31142/ijtsrd21438.

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Novikova, Inna Arnoldovna, Galina Nerodo, and Anna Iurievna Mordan. "Comparative analysis of DNA-cytometric indices of primary and relapsing ovarian cencer." Journal of Clinical Oncology 31, no. 15_suppl (2013): e16558-e16558. http://dx.doi.org/10.1200/jco.2013.31.15_suppl.e16558.

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e16558 Background: A ploidy of an average grade of aneuploidy cells and of proliferation index in ovarian tumor was studied. Methods: 21 patients with ovarian cancer of III-IV grades and 12 patients with acknowledged relapse of the disease aged from 46 to 67 to part in the research. We used CycleTEST PLUS DNA Reagent Kit (Becton Dickinson) for the analysis of DNA in the tumor’s tissues. Preparation of the tumor’s tissues was made with the use of disaggregating device BD Medimachine; after painting with propidium iodide (PI) we analyzed at flow cytofluorimeter BD Facs CantooII. Received data wa

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Mott, Frank E., Alex Esana, Carl Chakmakjian, and Jon D. Herrington. "Tumor Lysis Syndrome in Solid Tumors." Supportive Cancer Therapy 2, no. 3 (2005): 188–91. http://dx.doi.org/10.3816/sct.2005.n.012.

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Rustin, Gordon J. S. "Circulating tumor markers in gynecological tumors." Current Opinion in Oncology 8, no. 5 (1996): 426–31. http://dx.doi.org/10.1097/00001622-199609000-00015.

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MÖBUS, VOLKER, SIGRID HORN, MICHAEL STÖCK, and VOLKER SCHIRRMACHER. "Tumor Cell Vaccination for Gynecological Tumors." Hybridoma 12, no. 5 (1993): 543–47. http://dx.doi.org/10.1089/hyb.1993.12.543.

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Massari, Francesco, Vincenzo Di Nunno, Francesca Comito, et al. "Circulating tumor cells in genitourinary tumors." Therapeutic Advances in Urology 10, no. 2 (2017): 65–77. http://dx.doi.org/10.1177/1756287217742564.

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Management of advanced urogenital malignancies has profoundly changed in recent years due to the development of novel targeted drugs that have significantly improved patient’s clinical outcomes. This process has been made possible mainly thanks to better knowledge of tumor genetic alterations and molecular altered pathways. Despite these remarkable results, several issues such as early detection of the disease as well as the research into early markers of recurrence or disease progression still remain an open challenge for clinical research. The detection of circulating tumor cells and circula

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Gemici, Cengiz. "Tumor Lysis Syndrome in Solid Tumors." Journal of Clinical Oncology 27, no. 16 (2009): 2738–39. http://dx.doi.org/10.1200/jco.2009.22.4154.

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Gnoli, Maria, Francesca Ponti, and Luca Sangiorgi. "Tumor Syndromes That Include Bone Tumors." Surgical Pathology Clinics 10, no. 3 (2017): 749–64. http://dx.doi.org/10.1016/j.path.2017.04.009.

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Wolff, J. M., and F. K. Habib. "Tumor suppressor genes in urologic tumors." Urology 42, no. 4 (1993): 461–66. http://dx.doi.org/10.1016/0090-4295(93)90389-r.

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DeLeo, Albert B. "Tumor-Specific Antigens of Mouse Tumors." Journal of Immunotherapy 12, no. 3 (1992): 194–95. http://dx.doi.org/10.1097/00002371-199210000-00010.

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Kilgore, William B., and William M. Parrish. "Calcaneal Tumors and Tumor-like Conditions." Foot and Ankle Clinics 10, no. 3 (2005): 541–65. http://dx.doi.org/10.1016/j.fcl.2005.05.002.

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Alexander, Joseph M. "Tumor Suppressor Loss in Pituitary Tumors." Brain Pathology 11, no. 3 (2006): 342–55. http://dx.doi.org/10.1111/j.1750-3639.2001.tb00404.x.

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KALLAS, ELIAS, RAFAEL DINIZ ABRANTES, and ALEXANDRE CIAPPINA HUEB. "Tumor lamination in mediastinal giant tumors." Revista do Colégio Brasileiro de Cirurgiões 44, no. 6 (2017): 655–58. http://dx.doi.org/10.1590/0100-69912017006007.

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ABSTRACT Mediastinum tumors may grow slowly and reach giant proportions without symptoms, hindering surgical removal. Tumor big dimensions difficult surgical maneuvers, with risk of uncontrollable bleeding and prejudice to surrounding structures. It may be necessary the use of exceptional measures such as venous-venous circulatory deviation, pre-operatory embolization and total extracorporeal circulation. We describe the technique of tumor lamination that allows for complete or almost complete resection of such tumors that in many occasions are not resectable. The description is based on the r

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Sarioglu, Sulen, Emel Kilicarslan, Barbaros Aydin, et al. "Tumor deposits in salivary gland tumors." Pathology International 68, no. 3 (2018): 183–89. http://dx.doi.org/10.1111/pin.12637.

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Weintraub, Steven Jay. "Dormant Tumor-Suppressor Pathways in Tumors." American Journal of Respiratory Cell and Molecular Biology 20, no. 4 (1999): 541–42. http://dx.doi.org/10.1165/ajrcmb.20.4.f147.

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Foreman, Nicholas K., and Andrew M. Donson. "Tumor vaccination for malignant brain tumors." Pediatric Blood & Cancer 54, no. 4 (2009): 495–96. http://dx.doi.org/10.1002/pbc.22388.

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Buergy, Daniel, Frederik Wenz, Christoph Groden, and Marc A. Brockmann. "Tumor-platelet interaction in solid tumors." International Journal of Cancer 130, no. 12 (2012): 2747–60. http://dx.doi.org/10.1002/ijc.27441.

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Šimkus, Donatas, Saulius Petkevičius, Gediminas Pridotkas, et al. "Histological and immunohistochemical practical studies of canine cutaneous tumors." Medycyna Weterynaryjna 72, no. 9 (2016): 571–79. http://dx.doi.org/10.21521/mw.5558.

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A total of one hundred and fifty-three canine cutaneous tumors were examined and analyzed using the standard haematoxylin-eosin staining method. Additionally, tumors were examined immunohistochemically (41.4%) with antibodies LP34, AE1/AE3, V9 and histochemically (24.8%) with toluidine blue. Epithelial and melanocytic tumors of the skin accounted for 52.3% and mesenchymal tumours constituted 47.7%. All epidermal and follicular tumors demonstrated positive immunostaining for “LP34” antibodies. Fibromas and fibrosarcomas, which were immunohistochemically positive for antibodies “V9”, demonstrate

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Sharma, Manupriya, Anjali Soni, and Rashmi Kaul. "Histopathological pattern of ovarian neoplasms in Sub-Himalayan belt of rural India: a four-year study from a tertiary care teaching hospital." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 6, no. 12 (2017): 5448. http://dx.doi.org/10.18203/2320-1770.ijrcog20175258.

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Background: Ovarian tumors are one of the ubiquitous and common forms of neoplasms in women. The aim of the study was to understand the pattern of benign and malignant ovarian neoplasms and their distribution in different age groups in rural population of India.Methods: A retrospective study conducted in the Department of Pathology in close collaboration with Department of Obstetrics and Gynecology, Dr. Rajendra Prasad Government Medical College, Kangra at Tanda (HP), India. All the patients irrespective of age group who were operated for ovarian neoplasms (benign or malignant) were included i

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Graham, Donald V., Donatella Tampieri, and Jean-Guy Villemure. "Intramedullary Dermoid Tumor Diagnosed with the Assistance of Magnetic Resonance Imaging." Neurosurgery 23, no. 6 (1988): 765–67. http://dx.doi.org/10.1227/00006123-198812000-00016.

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Abstract Intramedullary dermoid tumors are unusual. Traditional methods of diagnosing spinal tumors have included clinical suspicion, plain roentgenography, myelography, and computed tomography. A case of intramedullary tumor provisionally diagnosed preoperatively by traditional methods and specifically as dermoid tumore with the assistance of magnetic resonance imaging is presented. Diagnosis and treatment of spinal dermoid tumors with an emphasis on magnetic resonance imaging is discussed.

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Kumavat, Prashant Vijay, Nitin Gadgil, Chetan Chaudhari, Ujwal Rathod, Ganesh Kshirsagar, and Sangita Margam. "Bone Tumors and Tumor-like lesions: A study in a Tertiary Care Hospital, Mumbai." Annals of Pathology and Laboratory Medicine 4, no. 1 (2017): A10—A18. http://dx.doi.org/10.21276/apalm.2017.972.

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Nouhou Diori, A., L. Laminou, H. Amadou Bouba Traoré, et al. "Clinical, epidemiological and anatomopathological aspects of palpebral-conjunctival tumours in the Ophthalmology department of the Amirou Boubacar Diallo National Hospital in Niamey." Journal Africain des Cas Cliniques et Revues 9, no. 1 (2025): 147–56. https://doi.org/10.70065/2591.jaccrafri.008l012802.

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Palpebro-conjunctival tumors are not negligible in frequency, their clinical presentation is ambiguous, and their diagnosis relies on determination of their anatomopathological nature by biopsy. The aim was to study the clinical, epidemiological and anatomopathological aspects of palpebro-conjunctival tumours in the Ophthalmology Department of the Niamey HNABD. Methodology: this was a prospective descriptive and analytical study, conducted over a 5-year period from 01 January 2019 to 31 December 2023. Cases of palpebro-conjunctival tumors received in the ophthalmology department of the Niamey

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Reddy, Sama Snehaja, Pakam Dinusha, Viswanath Sai, V. Krishna Kumar, and G. Mahender Reddy. "Histopathological study of neuroepithelial tumors of central nervous system." Panacea Journal of Medical Sciences 13, no. 1 (2023): 120–25. http://dx.doi.org/10.18231/j.pjms.2023.025.

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Central nervous system tumours have diverse histomorphological appearances. Accurate characterization of space-occupying lesions by histology is important for appropriate treatment. The present study is an attempt to evaluate the histomorphological patterns of the neuroepithelial tumors of central nervous system in order to provide accurate pre-therapeutic neuro-anatomic data and to facilitate better therapeutic results after surgery.To study the spectrum of neuroepithelial tumors presenting as space occupying lesions in the central nervous system.This was a prospective study carried out in th

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