Relevant bibliographies by topics / Lymphoma

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Lymphoma'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Lymphoma"

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Burke, Jerome S. "Lymphoproliferative Disorders of the Gastrointestinal Tract: A Review and Pragmatic Guide to Diagnosis." Archives of Pathology & Laboratory Medicine 135, no. 10 (2011): 1283–97. http://dx.doi.org/10.5858/arpa.2011-0145-ra.

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Context.—The gastrointestinal tract is the most common site of extranodal lymphomas. Although all histologic categories of malignant lymphoma develop in the gastrointestinal tract, large B-cell lymphomas predominate, followed by extranodal marginal zone lymphomas of mucosa-associated lymphoid tissue (MALT) type; the latter is especially prevalent in stomach. The acceptance of extranodal marginal zone lymphoma of MALT type as a clinicopathologic entity has reduced the number of cases that formerly were interpreted as florid lymphoid hyperplasia (“pseudolymphoma”). Nonetheless, the distinction o
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Elwan, Nagwa M., Dina A. Badawy, Salwa A. Atlam, and Ghada F. R. Hassan. "Prevalence profile of cutaneous T- and B-cell lymphoma in Gharbia Governorate, Egypt." Journal of the Egyptian Women's Dermatologic Society 21, no. 3 (2024): 204–12. http://dx.doi.org/10.4103/jewd.jewd_94_23.

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Background Lymphomas represent a heterogeneous group of lymphoid malignancies with varied patterns of clinical behavior and responses to treatment. The WHO classification distinguishes lymphoid neoplasms derived from precursor lymphoid cells from those derived from mature lymphoid cells and separates each group into neoplasms of B-cell or T-cell origin. T-cell lymphomas represent 82.9%, while B-cell lymphomas account for 21.3% of cutaneous lymphomas. Objective To study the prevalence of cutaneous T- and B-cell lymphomas in Gharbia Governorate, Egypt from 1999 to 2019. Patients and methods This
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Tammouch, Zoulikha, Mouna Salihoun, Fatima Chait, Rihane El Mohtarim, Sabrine Derqaoui, and Nawal Kabbaj. "Gastric Burkitt Lymphoma, an Infrequent Cause of Hematemesis." Saudi Journal of Pathology and Microbiology 9, no. 02 (2024): 37–42. http://dx.doi.org/10.36348/sjpm.2024.v09i02.003.

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Among gastric malignancies, lymphomas rank as the second most common type, following gastric adenocarcinoma. The majority of gastric lymphomas are either mucosa-associated lymphoid tissue lymphomas or diffuse large B-cell lymphomas. Primary gastric Burkitt lymphoma, is a subtype of non-Hodgkin's lymphoma, represents an exceptionally rare and aggressive malignancy, with only a limited number of reported cases globally. We present the case of a male patient with primary gastric Burkitt lymphoma revealed by digestive hemorrhage. The diagnosis was confirmed by endoscopy and gastric biopsies. The g
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Laurent, Camille, Marine Baron, Nadia Amara, et al. "Impact of Expert Pathologic Review of Lymphoma Diagnosis: Study of Patients From the French Lymphopath Network." Journal of Clinical Oncology 35, no. 18 (2017): 2008–17. http://dx.doi.org/10.1200/jco.2016.71.2083.

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Purpose To prospectively assess the clinical impact of expert review of lymphoma diagnosis in France. Materials and Methods From January 2010 to December 2013, 42,145 samples from patients with newly diagnosed or suspected lymphomas were reviewed, according to the 2008 WHO classification, in real time by experts through the Lymphopath Network. Changes in diagnosis between referral and expert review were classified as major or minor according to their potential impact on patient care. Results The 42,145 reviewed samples comprised 36,920 newly diagnosed mature lymphomas, 321 precursor lymphoid n
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Topalovski, Margarita, Domnita Crisan, and Joan C. Mattson. "Lymphoma of the Breast." Archives of Pathology & Laboratory Medicine 123, no. 12 (1999): 1208–18. http://dx.doi.org/10.5858/1999-123-1208-lotb.

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Abstract Background.—Primary lymphomas of the breast are rare, accounting for 1.7% to 2.2% of extranodal lymphomas and 0.38% to 0.7% of all non-Hodgkin lymphomas. Although secondary breast lymphomas are also rare, they represent the largest group of metastatic tumors of the breast. Objectives.—To investigate the clinicopathologic and immunophenotypic characteristics of breast lymphomas, the relative frequency of primary and secondary mammary lymphomas, and in selected cases, the role of gene rearrangement analysis in diagnosis and staging of these lymphomas. Results.—We conducted a retrospecti
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Rechal, Rinoosha, Virender Pratibh Prasad, Shweta Sethi, and Venkata Nagarjuna Maturu. "Non-resolving pneumonia: primary pulmonary MALT lymphoma." BMJ Case Reports 17, no. 3 (2024): e255075. http://dx.doi.org/10.1136/bcr-2023-255075.

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Mucosa-associated lymphoid tissue (MALT) lymphoma is an uncommon extranodal low-grade B-cell lymphoma. Pulmonary MALT lymphomas originate from bronchial MALT and are also referred to as bronchial-associated lymphoid tissue lymphomas. MALT lymphomas of the lung are slow-growing tumours and usually present as asymptomatic chronic alveolar opacities visible on chest radiographs or with non-specific pulmonary symptoms. Here we described a case of a male patient in his early 50s with cough and chest pain for 4 years. His CT chest scan showed consolidation in the lingula and left lower lobe. Histopa
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Miyake, Keitaro, Kazuhiro Hirasawa, Haruka Nishimura, and Kiyoaki Tsukahara. "Rare incidence of mucosa-associated lymphoid tissue lymphoma presenting as buccal fat pad tumor: A case report." World Journal of Clinical Cases 12, no. 31 (2024): 6506–12. http://dx.doi.org/10.12998/wjcc.v12.i31.6506.

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BACKGROUND Mucosa-associated lymphoid tissue (MALT) lymphoma, a type of non-Hodgkin lymphoma, originates in the mucosal lining of body organs and internal cavities, including the nose, mouth, lungs, and digestive tract. The lymphoma develops when the body produces abnormal B lymphocytes. These lymphomas develop at the edge of the lymphoid tissue, called the marginal zone, and, hence, are classified as a type of marginal zone lymphomas. They are the most common type of marginal zone lymphomas although their occurrence is rare. To date, no previous cases of MALT lymphoma in the buccal fat pad ha
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Mayer, Erik K., Shabnam Undre, Daniel C. Cohen, Marjorie M. Walker, Justin A. Vale, and Anup Patel. "“An Unusual Urological Tumour”: Above the Collar and below the Belt." Case Reports in Oncological Medicine 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/480826.

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Bladder lymphomas are rarely primary tumours and more commonly associated with systemic lymphoma, either as nonlocalised bladder lymphoma or as secondary bladder lymphoma. Primary bladder lymphomas (PBL) tend to be low-grade mucosa-associated lymphoid tissue (MALT) type, contrasting with diffuse large cell or follicular centre cell types more commonly seen in secondary bladder lymphoma. Bladder involvement by systemic lymphoma infers poor prognosis and patients often have no localising symptoms (typically a postmortem diagnosis). Other treatments are preferred over surgery for all bladder lymp
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Hoeller, Sylvia, and Christiane Copie-Bergman. "Grey Zone Lymphomas: Lymphomas with Intermediate Features." Advances in Hematology 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/460801.

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The current classification of lymphoid neoplasms is based on clinical information, morphology, immunophenotype, and molecular genetic characteristics. Despite technical and scientific progress, some aggressive B-cell lymphomas with features overlapping between two different types of lymphomas remain difficult to classify. The updated 2008 World Health Organization (WHO) classification of Tumours of the Hematopoietic and Lymphoid Tissues has addressed this problem by creation of two new provisional categories of B-cell lymphomas, unclassifiable; one with features intermediate between diffuse la
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Ahn, Ji Yong. "Gastrointestinal Tract Lymphoma." Korean Journal of Helicobacter and Upper Gastrointestinal Research 22, no. 1 (2022): 18–28. http://dx.doi.org/10.7704/kjhugr.2021.0064.

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The gastrointestinal tract is the most common site of extranodal lymphoma, and more than 95% of gastrointestinal lymphoma cases are of the non-Hodgkin type. The stomach is the primary site of extranodal non-Hodgkin lymphoma, and more than 98% of primary gastric lymphoma (PGL) cases are diffuse large B-cell lymphomas (DLBCL) and mucosa-associated lymphoid tissue (MALT) lymphomas. Because PGL usually presents with nonspecific clinical symptoms and various endoscopic features, its diagnosis is mainly dependent on histopathologic findings. Chemotherapy is the first-line treatment choice for gastri
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Dissertations / Theses on the topic "Lymphoma"

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Sakakibaya, Ayako, Kumi Kawai, Tetsuro Nagasaka, et al. "Molecular diagnosis of malignant lymphoma : mantle cell lymphoma, anaplastic large cell lymphoma, and marginal zone B-cell lymphoma of malt." Nagoya University School of Medicine, 2006. http://hdl.handle.net/2237/6127.

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Maesako, Yoshitomo. "Comparison of gene expression profiles of lymphoma cell lines from transformed follicular lymphoma, Burkitt's lymphoma and de novo diffuse large B-cell lymphoma." Kyoto University, 2004. http://hdl.handle.net/2433/148266.

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D'Haene, Nicky. "Implication des galectines-1 et -3 dans l'angiogenèse et en particulier en ce qui concerne les lymphomes." Doctoral thesis, Universite Libre de Bruxelles, 2011. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209900.

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Les lymphomes sont constitués de sous-groupes tumoraux définis par différents critères cliniques, morphologiques, immunophénotypiques et moléculaires. Néanmoins, même au sein d’un sous-groupe, il existe une grande hétérogénéité dans l’évolution clinique des patients, ce qui rend leur prise en charge difficile. Ceci souligne l’importance de découvrir de nouveaux biomarqueurs pronostiques qui amélioreraient l’approche thérapeutique personnalisée. <p>La revue de la littérature fait apparaitre les galectines-1 et -3 comme des protéines impliquées dans le développement des cancers ainsi que dans la
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Camilleri, Emily Therese. "The Transcriptional Role of FOXP1 in Non-Hodgkin's Lymphoma." Thesis, Griffith University, 2013. http://hdl.handle.net/10072/367974.

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Non-Hodgkin's lymphoma (NHL) is a family of lymphoid malignances that are the 6th leading cause of death in Australia. B cell lymhomas account for approximately 90% of all NHL cases, and the common subtypes Diffuse Large B cell Lymphoma (DLBCL) and Follicular Lymphoma (FL) together make uo 60% of all cases. DLBCL and FL are both germinal centre derived B cell lymphomas, however these malignancies represent opposite ends of the clinical scale, being aggressive compared to indolent disease respectively. Early detection of lymphoma is highly advantageous for aggressive subtypes like DLBCL, where
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Virginia, Mancini. "The Lymphoma Microenviroment." Doctoral thesis, Università di Siena, 2022. http://hdl.handle.net/11365/1194259.

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The study of the microenviroment, the cellular milieau in wich the neoplastic cells thrive, represents a relevant focus of investigation in order to explore potential targets for immunotherapy. Using immunohistochemistry tecnique, we analyzed the lymphoma microenviroment in particular in sampling of Primary Testicular Diffuse Large B-cells Lymphoma, an aggressive lymphoma for wich few therapeutic strategies are available.
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Sharma, Purva, Bahaaeldin Youssef, Sakshi Singal, and Devapiran Jaishankar. "In Situ Follicular Neoplasia yet another Spectrum That Extends From Normalcy to Overt Malignancy." Digital Commons @ East Tennessee State University, 2020. https://dc.etsu.edu/asrf/2020/presentations/28.

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In situ follicular neoplasia (ISFN) is defined as a monoclonal proliferation of B cells with immunophenotypic and genetic features of follicular lymphoma (FL) but confined to germinal centers of lymph nodes or other organs. It may not be associated with underlying overt lymphoma. It can be associated with lymphoproliferative disorders other than FL. A fifty-seven-year-old caucasian male initially presented with atypical chest pain, which led to cardiology evaluation. Patient underwent a coronary CT angiogram, which revealed a calcium score of 0, however also incidentally revealed mediastinal l
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Clothier, Stacy Lauren. "Immune Checkpoint Molecule Expression in Canine Lymphoma and Canine Reactive Lymphoid Hyperplasia." Thesis, Virginia Tech, 2019. http://hdl.handle.net/10919/103200.

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Background: Although lymphoma is one of the most common malignancies in dogs, remission rates and survival times remain stagnant. Treatment with a multi-agent chemotherapy protocol induces remission for less than one year and the majority of patients relapse. Fewer than 25% of dogs live longer than two years with the currently available treatments. Targeted immunotherapy using checkpoint molecule blockade of PD-1 and PD-L1 shows promise for various types of human cancer, including relapsed/refractory lymphoma; however, little is known regarding the role of these checkpoint molecules in canine
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FANGAZIO, MARCO. "Molecular Determinants of Follicular Lymphoma Transformation to Diffuse Large B cell Lymphoma." Doctoral thesis, Università del Piemonte Orientale, 2014. http://hdl.handle.net/11579/46568.

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Amini, Rose-Marie. "Hodgkin Lymphoma : Studies of Advanced Stages, Relapses and the Relation to Non-Hodgkin Lymphomas." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2002. http://publications.uu.se/theses/91-554-5265-5/.

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Majeed, Aneela, Onyee Chan, Onyemaechi Okolo, Volodymyr Shponka, Anca Georgescu, and Daniel Persky. "Hodgkin Lymphoma Mimicking Osteomyelitis." KARGER, 2017. http://hdl.handle.net/10150/625840.

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Hodgkin lymphoma with symptomatic osseous involvement can have a similar presentation to osteomyelitis. Common findings in symptoms, laboratory workup, and imaging can make it very difficult to distinguish between the two diseases. Excisional biopsy should be pursued if fine-needle biopsy is equivocal and suspicion of lymphoma is high. We report a case of a 40-year-old man who presented with a history of marine animal sting on his neck and later developed erythema in the area, chest pain, constitutional symptoms, adenopathy, and imaging classic for sternal osteomyelitis. Fortunately, initial b
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Books on the topic "Lymphoma"

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W, Hancock Barry, ed. Malignant lymphoma. Arnold, 2000.

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L, Harris Nancy, ed. Atlas of lymphoid hyperplasia and lymphoma. W.B. Saunders Co., 1997.

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Illidge, Tim, and Peter W. M. Johnson. Lymphoma. Humana Press, 2005. http://dx.doi.org/10.1385/1592599362.

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Küppers, Ralf, ed. Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-269-8.

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Younes, Anas, and Bertrand Coiffier, eds. Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1.

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Marcus, Robert, John W. Sweetenham, and Michael E. Williams, eds. Lymphoma. Cambridge University Press, 2009. http://dx.doi.org/10.1017/cbo9780511862472.

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Küppers, Ralf, ed. Lymphoma. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9151-8.

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M, Miller Thomas, and Grogan Thomas M, eds. Lymphoma. Saunders, 1997.

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C, Wotherspoon A., and Imperial Cancer Research Fund (Great Britain), eds. Lymphoma. Cold Spring Harbor Laboratory Press, 1997.

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Küppers, Ralf, ed. Lymphoma. Springer US, 2025. http://dx.doi.org/10.1007/978-1-0716-4188-0.

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Book chapters on the topic "Lymphoma"

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Kirsch, Brian James, Shu-Jyuan Chang, Michael James Betenbaugh, and Anne Le. "Non-Hodgkin Lymphoma Metabolism." In The Heterogeneity of Cancer Metabolism. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-65768-0_7.

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AbstractNon-Hodgkin lymphomas (NHLs) are a heterogeneous group of lymphoid neoplasms with different biological characteristics. About 90% of all lymphomas in the United States originate from B lymphocytes, while the remaining originate from T cells [1]. The treatment of NHLs depends on the neoplastic histology and stage of the tumor, which will indicate whether radiotherapy, chemotherapy, or a combination is the best suitable treatment [2]. The American Cancer Society describes the staging of lymphoma as follows: Stage I is lymphoma in a single node or area. Stage II is when that lymphoma has
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Bento, Leyre, Bertram Glass, and Norbert Schmitz. "Large B-Cell Lymphoma." In The EBMT Handbook. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-44080-9_86.

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AbstractThe most recent WHO classification of tumors of hematopoietic and lymphoid tissues (Alaggio et al. 2022) classifies large B cell lymphomas (LBCL) into diffuse large B cell lymphoma (DLBCL) NOS with distinct morphological and molecular (germinal center B-cell, activated B-cell) subtypes, high-grade B-cell lymphomas (with MYC and BCL2 rearrangements or NOS subtype), and other less frequent subtypes.
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Serroukh, Yasmina, and Silvia Montoto. "Indolent Lymphoma." In The EBMT Handbook. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-44080-9_84.

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AbstractIndolent lymphomas (iNHL) form an heterogenous group accounings for 1/3 of all malignant lymphomas with Follicular lymphoma (FL) being the most common subtype. iNHL are characterized by repeated relapses. Among available treatment lines, autologous (auto) and allogeneic (allo) HCT are the only curative options for relapsed disease. Nevertheless, the roles of both forms of HCT are evolving and are currently being challenged as T-cell engaging therapies emerge. The indications for auto-HCT and allo-HCT in 2023 are reviewed in this chapter.
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Carvajal-Cuenca, Alejandra, Stefano A. Pileri, and Elias Campo. "The World Health Organization Classification of Lymphoid Neoplasms." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_1.

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Schmidt, Christian, and Martin H. Dreyling. "Mantle Cell Lymphoma." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_10.

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Jardin, Fabrice, and Hervé Tilly. "Diffuse Large B-Cell Lymphoma." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_11.

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Dunleavy, Kieron, Cliona Grant, and Wyndham H. Wilson. "Primary Mediastinal B-Cell Lymphoma." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_12.

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William, Basem M., and Julie M. Vose. "T-Cell Lymphomas." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_13.

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Hoelzer, Dieter, and Thomas Burmeister. "Burkitt Lymphoma." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_14.

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Borthakur, Gautam, and Susan M. O’Brien. "Lymphoblastic Lymphoma." In Lymphoma. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-408-1_15.

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Conference papers on the topic "Lymphoma"

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Habijan, Marija, and Irena Galić. "Ensemble Transfer Learning for Lymphoma Classification." In 2024 31st International Conference on Systems, Signals and Image Processing (IWSSIP). IEEE, 2024. http://dx.doi.org/10.1109/iwssip62407.2024.10634025.

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Belluco, Rosana Zabulon Feijó, Carolina Gaze Gonçalves Fontenele Gomes, Camila Pires Marinho, et al. "Diffuse B-cell lymphoma in the male breast: A rare case report." In Brazilian Breast Cancer Symposium 2023. Mastology, 2023. http://dx.doi.org/10.29289/259453942023v33s1052.

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Introduction: Lymphomas are a heterogeneous group of cancers derived from the immune system, characterized by increased proliferation of lymph nodes or secondary lymphatic tissue. Breast involvement by lymphoma is uncommon, representing only 0.1% of malignant breast lesions. Clinical similarities with breast cancer make preoperative diagnosis of breast lymphoma difficult. Histologically, most primary breast lymphomas (PML) are of the B-cell type. The treatment of PML is based on the recommendations for the treatment of lymphomas of other locations according to the histological type, staging, a
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Giulino-Roth, Lisa G. "Abstract IA09: Genomics of common AYA lymphomas: Hodgkin lymphoma and primary mediastinal B-cell lymphoma." In Abstracts: AACR Virtual Meeting: Advances in Malignant Lymphoma; August 17-19, 2020. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/2643-3249.lymphoma20-ia09.

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Lima, Rodrigo Quevedo de, Eimi Nascimento Pacheco, Luiz Henrique Santana de Araujo, Cassio Fernando Paganini, and Katsuki Arima Tiscoski. "PLASMOBLASTIC LYMPHOMA WITH MAMMARY MANIFESTATION: A CASE REPORT." In Scientifc papers of XXIII Brazilian Breast Congress - 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s1085.

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Introduction: Plasmoblastic lymphoma (PBL) is a rare entity of non-Hodking lymphoma that usually occurs in the oral cavity in immunosuppressed patients. The involvement of other organs has rarely been reported. The breast can be the site of the initial manifestation of many diseases and in cases like this report, lymphomas should be considered as differential diagnoses. Case report: D.S., female, 28 years old, quality reviewer, married, two children. Carrier of human immunodeficiency virus (HIV) with recent treatment. Intern for investigation of liver, duodenal and breast abnormalities. She ha
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Gopalakrishnan, A., T. Olanipekun, D. Thomas, M. Mosunjac, and E. Flenaugh. "Incidental Primary Pulmonary Mucosa-Associated Lymphoid Tissue Lymphoma." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a3927.

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Goi, Mariana Copetti, Ana Paula Santana de z. Abreu, Sheila Cristina Lordelo Wludarski, Joaquim Teodoro de Araújo Neto, and Edison Mantovani Barbosa. "Primary breast lymphoma associated with invasive breast carcinoma: a case report." In XXVI Brazilian Mastology Congress. Mastology, 2024. https://doi.org/10.29289/259453942024v34s2039.

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Introduction: This case report describes a 54-year-old patient who developed invasive breast carcinoma in her left breast without further specifications, of the luminal B molecular subtype, concurrently with a primary breast lymphoma (diffuse large B-cell lymphoma with the germinal center B-cell subtype), which was definitively diagnosed only after surgical intervention. Synchronous occurrence of breast cancer and non-Hodgkin lymphoma (NHL) is an uncommon situation, with only 38 cases reported in the literature. It is extremely rare for both tumors to present as a collision tumor within the sa
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Rana, Seema, and Rajiv Tangri. "Anaplastic large cell lymphoma ALK negative vs. peripheral T cell lymphoma (NOS) - diagnostic dilemma." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685354.

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Middle aged female presented with generalised lymphadenopathy and fever for last one month. Peripheral blood findings were within normal limits. There was no extra nodal involvement. FNAC performed initially from a cervical node suggested possibility of Hodgkin’s lymphoma and a whole node biopsy was performed. Histopathogical examination revealed effaced nodal architecture and a polymorphous population of lymphocytes, plasma cells, neutrophils and scattered large mononuclear cells with prominent nucleolus. An initial panel of CD3, CD20, LCA, CD15, CD30 and PAX5 was performed. The large atypica
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Jabri, A., J. Alzubi, A. H. Ababneh, E. Verghese, B. Abuhalimeh, and H. A. Hussein. "Bronchus-Associated Lymphoid Tissue (BALT) Lymphoma Presenting as Pneumonia." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a2334.

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Pompermaier, Carolina, Willian Ely Pin, Mateus Xavier Schenato, Tales Antunes Franzini, and Guilherme Roloff Cardoso. "BREAST IMPLANT-ASSOCIATED ANAPLASTIC LARGE CELL LYMPHOMA: A LITERATURE REVIEW." In XXIV Congresso Brasileiro de Mastologia. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s1012.

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Objective: This review aims to bring updates about the relationship between the silicone implant and the breast implantassociated anaplastic large cell lymphoma (BIA-LCL), in order to have a better knowledge about this disease. Despite the low risk of its development, a better understanding of BIA-ALCL is of interest to women, oncologists, breast specialists, plastic surgeons, regulatory agencies, and the general public, as the number of women with breast implants is increasing worldwide. Methods: This article is based on a review of publications on the topic. A search for articles was carried
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Nandu, N. S., and H. Mangat. "An Incidental Lymphoma." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a4948.

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Reports on the topic "Lymphoma"

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Huang, James. The Correlation between Lymphoma Cell Size and PET–CT Metabolic Activity in Follicular Lymphomas. Science Repository OÜ, 2019. http://dx.doi.org/10.31487/j.rco.2018.01.006.

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Kwak, Larry W. Second-Generation Therapeutic DNA Lymphoma Vaccines. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada485134.

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Kwak, Larry W. Second Generation Therapeutic DNA Lymphoma Vaccines. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada540718.

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Kwak, Larry W. Second-Generation Therapeutic DNA Lymphoma Vaccines. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada504992.

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Rossari, Federico. Role of Circulating DNA in the Precocious Diagnosis of Lymphoma: an example in a Transplant-Related Aggressive Lymphoma. Science Repository OU, 2019. http://dx.doi.org/10.31487/j.cor.2019.02.02.

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Lin, Zhijuan, Xing Chen, Long Liu, Zhifeng Li, and Bing Xu. Chemo-Free Treatments in Relapsed and/or Refractory Follicular Lymphoma: A Network Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2021. http://dx.doi.org/10.37766/inplasy2021.11.0111.

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Abstract:
Review question / Objective: FL is the most common indolent B cell lymphoma worldwide and patients with FL always have long term survival. However, advanced FL remains incurable and there is no universal agreement on optimal regimen to manage relapsed FL. Condition being studied: The efficacy of chemo-free regimens, including CD20 antibodies and targeted agents, in relapsed and/or refractory Follicular lymphoma. Information sources: We used the MEDLINE, Embase, and Cochrane Library databases to search the RCTs met our selection criteria. We also searched clinicalTrials.gov and the internationa
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Tuscano, Joseph M. Targeted Lymphoma Cell Death by Novel Signal Transduction Modifications. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada503123.

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Tuscano, Joseph M. Targeted Lymphoma Cell Death by Novel Signal Transduction Modifications. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada525894.

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Tuscano, Joseph M. Targeted Lymphoma Cell Death by Novel Signal Transduction Modifications. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada538568.

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Tuscano, Joseph. Targeted Lymphoma Cell Death by Novel Signal Transduction Modifications. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada566413.

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