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Artículos de revistas sobre el tema "Lymphoma/pathology"

Autor: Grafiati
Publicado: 2 de junio de 2025
Última modificación: 31 de julio de 2025

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1

Takata, Katsuyoshi, Tomoko Miyata-Takata, Yasuharu Sato, and Tadashi Yoshino. "Pathology of Follicular Lymphoma." Journal of Clinical and Experimental Hematopathology 54, no. 1 (2014): 3–9. http://dx.doi.org/10.3960/jslrt.54.3.

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2

Norton, A. J. "The pathology of lymphoma." Imaging 11, no. 4 (1999): 201–13. http://dx.doi.org/10.1259/img.11.4.110201.

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3

Muller-Hermelink, H. K., A. Zettl, W. Pfeifer, and G. Ott. "Pathology of lymphoma progression." Histopathology 38, no. 4 (2001): 285–306. http://dx.doi.org/10.1046/j.1365-2559.2001.01120.x.

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4

Coupland, S. E. "Molecular pathology of lymphoma." Eye 27, no. 2 (2012): 180–89. http://dx.doi.org/10.1038/eye.2012.247.

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5

Heckendorn, Emily, and Aaron Auerbach. "Pathology of Extranodal Lymphoma." Radiologic Clinics of North America 54, no. 4 (2016): 639–48. http://dx.doi.org/10.1016/j.rcl.2016.03.001.

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6

Mathas, Stephan, Sylvia Hartmann, and Ralf Küppers. "Hodgkin lymphoma: Pathology and biology." Seminars in Hematology 53, no. 3 (2016): 139–47. http://dx.doi.org/10.1053/j.seminhematol.2016.05.007.

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7

Micaily, Bizhan. "Pathology and Management of Lymphoma." American Journal of Clinical Oncology 8, no. 3 (1985): 270. http://dx.doi.org/10.1097/00000421-198506000-00015.

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8

Cesarman, Ethel. "Pathology of lymphoma in HIV." Current Opinion in Oncology 25, no. 5 (2013): 487–94. http://dx.doi.org/10.1097/01.cco.0000432525.70099.a4.

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9

Mann, Karen P. "Molecular Pathology of Malignant Lymphoma." Surgical Pathology Clinics 5, no. 4 (2012): 879–902. http://dx.doi.org/10.1016/j.path.2012.08.005.

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10

Goldschmidt, H., M. Wallmeier, U. Hegenbart, and R. Haas. "Malignant lymphoma. Pathology, diagnosis, therapy." Der Radiologe 37, no. 1 (1997): 1–9. http://dx.doi.org/10.1007/s001170050171.

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11

Blewitt, R. W. "Update on lymphoma pathology III: lymphoma classification and nodal lymphomas." Morecambe Bay Medical Journal 3, no. 4 (1999): 122–28. http://dx.doi.org/10.48037/mbmj.v3i4.561.

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Lymphoma classification has for years been confusing and at times exasperating, based solely on haematoxylin-and eosin-stained histological sections. Several major advances have allowed a new and less subjective classification to be developed:
 • use of immunostains
 • recognition that extranodal lymphomas are special
 • discovery of specific cytogenetic abnormalities in lymphomas
 • better understanding of lymphocyte physiology
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12

Powell, Roger. "Clinical pathology updates: Lymphoma - misunderstood disease?" Companion Animal 12, no. 6 (2007): 84–86. http://dx.doi.org/10.1111/j.2044-3862.2007.tb00192.x.

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13

Burg, Gunter, Reinhard Dummer, Stefan Dommann, Frank Nestle, and Brian Nickoloff. "Pathology of Cutaneous T-cell Lymphoma." Hematology/Oncology Clinics of North America 9, no. 5 (1995): 961–95. http://dx.doi.org/10.1016/s0889-8588(18)30053-4.

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14

Tanpitukpongse, Teerath P., Shahmir Kamalian, Michael Punsoni, Mala Gupta, and Douglas S. Katz. "Radiology–pathology conference: primary adrenal lymphoma." Clinical Imaging 36, no. 2 (2012): 156–59. http://dx.doi.org/10.1016/j.clinimag.2011.08.022.

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15

Chan, C. C. "Molecular pathology of primary intraocular lymphoma." American Journal of Ophthalmology 137, no. 5 (2004): 975. http://dx.doi.org/10.1016/j.ajo.2004.02.095.

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16

Bezerra, Alanna Mara Pinheiro Sobreira, Denise da Cunha Pasqualin, João Carlos de Campos Guerra, et al. "Correlation between flow cytometry and histologic findings: ten year experience in the investigation of lymphoproliferative diseases." Einstein (São Paulo) 9, no. 2 (2011): 151–59. http://dx.doi.org/10.1590/s1679-45082011ao2027.

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Objective: To demonstrate the advantages of correlating flow cytometry immunophenotyping with the pathology/ immunohistochemistry of lymph nodes or nodules in the diagnosis of lymphoproliferative diseases. Methods: A retrospective study was carried out of 157 biopsy or fine-needle aspiration lymph nodes/ nodule specimens taken from 142 patients, from 1999 and 2009. The specimens were simultaneously studied with fow cytometry and pathology at Hospital Israelita Albert Einstein. The specimens were prepared in hematoxylin/eosin, Giemsa, or monoclonal antibody stained slides for detecting specific
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17

Commins, Deborah L. "Pathology of primary central nervous system lymphoma." Neurosurgical Focus 21, no. 5 (2006): 1–10. http://dx.doi.org/10.3171/foc.2006.21.5.3.

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✓ The understanding of primary central nervous system lymphoma (PCNSL) has lagged behind that of the much more common systemic, nodal lymphomas. Reasons for this include the relative rarity of PCNSL and the fact that these lesions differ in some ways from their histologically similar systemic counterparts. The purpose of this paper is twofold: first, the author provides concise descriptions of the pathological features of both common and uncommon types of PCNSL while discussing issues such as the confusion surrounding histological classification of PCNSLs, problems related to intraoperative di
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18

Blewitt, RW. "Update on lymphoma pathology IV: Extranodal lymphomas." Morecambe Bay Medical Journal 3, no. 5 (1999): 177–80. http://dx.doi.org/10.48037/mbmj.v3i5.586.

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19

Vega, Francisco. "Pathology and Pathogenesis of T-Cell Lymphoma." Clinical Lymphoma Myeloma and Leukemia 20 (September 2020): S89—S93. http://dx.doi.org/10.1016/s2152-2650(20)30474-2.

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20

Tomoka, Tamiwe, Nathan D. Montgomery, Eric Powers, et al. "Lymphoma and Pathology in Sub-Saharan Africa." Clinics in Laboratory Medicine 38, no. 1 (2018): 91–100. http://dx.doi.org/10.1016/j.cll.2017.10.007.

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21

Dalla-Favera, R. "6 Molecular pathology of B cell lymphoma." European Journal of Cancer Supplements 8, no. 4 (2010): 4–5. http://dx.doi.org/10.1016/s1359-6349(10)70677-7.

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22

Mandal, Prakas Kumar, Supriyo Sarkar, Malay Kumar Ghosh, and Maitreyee Bhattacharyya. "Simultaneous dual pathology in lymph node." Mediterranean Journal of Hematology and Infectious Diseases 6, no. 1 (2014): e2014036. http://dx.doi.org/10.4084/mjhid.2014.036.

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[Abstract]Tubercuous lymphadenitis and Non Hodgkins’ Lymphoma are common in India. As both diseases can occur in elderly persons there is a definite chance of co-existence of both diseases; but that coexistence has not been reported. Here we present a unique case in an elderly woman who had synchronous double pathology of tuberculosis (TB) and Diffuse Large B cell Lymphoma (DLBCL) of the lymph nodes. Key words:- lymph nodes, tuberculosis (TB), Diffuse Large B cell Lymphoma (DLBCL).
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23

Jordan, Jacob, Jordan S. Goldstein, David L. Jaye, Metin Gurcan, Christopher R. Flowers, and Lee A. D. Cooper. "Informatics Approaches to Address New Challenges in the Classification of Lymphoid Malignancies." JCO Clinical Cancer Informatics, no. 2 (December 2018): 1–9. http://dx.doi.org/10.1200/cci.17.00039.

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Purpose Lymphoid malignancies are remarkably heterogeneous, with variations in outcomes and clinical, biologic, and histologic presentation complicating classification according to the World Health Organization guidelines. Incorrect classification of lymphoid neoplasms can result in suboptimal therapeutic strategies for individual patients and confound the interpretation of clinical trials involving personalized, class-based treatments. This review discusses the potential role of pathology informatics in improving the classification accuracy and objectivity for lymphoid malignancies. Design We
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24

Kukreti, Vishal, Bruce Patterson, Jeannie Callum, Ed Etchells, and Michael Crump. "Pathology the Gold Standard – A Retrospective Analysis of Discordant “Second-Opinion” Lymphoma Pathology and Its Impact on Patient Care." Blood 108, no. 11 (2006): 348. http://dx.doi.org/10.1182/blood.v108.11.348.348.

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Abstract A change in diagnosis on review of pathology, “second-opinion pathology”, is not uncommon for hematological malignancies with a range of between 11–20%. Hence, there is a significant potential for incurring a diagnostic error with implications during the clinical management of patients. We conducted a retrospective review to evaluate both potential and actual medical error noted in the management of lymphoma patients treated at Princess Margaret Hospital (PMH), by evaluating results of pathological review and identifying patients with a change in diagnosis between the initial referrin
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25

Tanking, Chonthicha, and Supawat Ratanapo. "Diagnostic challenge in primary cardiac lymphoma: a case report." European Heart Journal - Case Reports 4, no. 5 (2020): 1–5. http://dx.doi.org/10.1093/ehjcr/ytaa160.

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Abstract Background Primary cardiac lymphoma is an extra-nodal non-Hodgkin’s lymphoma, which usually responds well to chemotherapy. The disease has high mortality rate unless it is recognized and treated in time. Tissue pathology is crucially the diagnosis gold standard for treatment plan. This is a case report of an elderly female who presented with a huge right-sided cardiac tumour obstructing tricuspid flow. Case summary An 81-year-old Asian female presented with clinical right-sided heart failure. Echocardiogram showed a large mass compressing and obliterating the right atrium. Trans-jugul
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26

Ohshima, Koichi. "Molecular Pathology of Adult T-Cell Leukemia/Lymphoma." Oncology 89, no. 1 (2015): 7–15. http://dx.doi.org/10.1159/000431058.

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27

Nishizijka, Yasuaki. "Experimental Studies on Pathology of Lymphoma in Mice**." Pathology International 9 (December 12, 2008): 669–83. http://dx.doi.org/10.1111/j.1440-1827.1959.tb02960.x.

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28

Kobayashi, Kazutoyo, Makoto Igarashi, Raymond A. McBride, Ryusuke Saito, and Akikatsu Kataura. "Temporal Bone Pathology of Metastatic T-Cell Lymphoma." Acta Oto-Laryngologica 105, sup447 (1988): 113–19. http://dx.doi.org/10.3109/00016488809102866.

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29

Leventaki, Vasiliki, Siddharth Bhattacharyya, and Megan S. Lim. "Pathology and genetics of anaplastic large cell lymphoma." Seminars in Diagnostic Pathology 37, no. 1 (2020): 57–71. http://dx.doi.org/10.1053/j.semdp.2019.12.002.

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30

Kwong, Y. L., Alexander C. L. Chan, and Raymond H. S. Liang. "Natural killer cell lymphoma/leukemia: pathology and treatment." Hematological Oncology 15, no. 2 (1997): 71–79. http://dx.doi.org/10.1002/(sici)1099-1069(199705)15:2<71::aid-hon601>3.0.co;2-u.

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31

Travaglino, Antonio, Mirella Pace, Silvia Varricchio, et al. "Hashimoto Thyroiditis in Primary Thyroid Non-Hodgkin Lymphoma." American Journal of Clinical Pathology 153, no. 2 (2019): 156–64. http://dx.doi.org/10.1093/ajcp/aqz145.

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Abstract Objectives To assess the prevalence of Hashimoto thyroiditis (HT) in primary thyroid lymphoma (PTL) and whether it differs between mucosa-associated lymphoid tissue (MALT) lymphoma and diffuse large B-cell lymphoma (DLBCL). Methods Electronic databases were searched for studies assessing HT prevalence in PTL, based on antithyroid antibodies, clinical history, or pathology. Pooled prevalence of HT and its association with histotype (MALT or DLBCL) were calculated. Results Thirty-eight studies with 1,346 PTLs were included. Pooled prevalence results were 78.9% (any HT evidence), 65.3% (
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32

Von Ende, Elizabeth, Travis Kauffman, Philip A. Munoz, and Santiago Martinez-Jiménez. "Primary Pulmonary Anaplastic Large Cell Lymphoma: A Rare Malignancy and Rare Cause of the Luftsichel Sign." Case Reports in Radiology 2018 (2018): 1–5. http://dx.doi.org/10.1155/2018/8574642.

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Primary pulmonary lymphomas are rare with primary pulmonary non-Hodgkin lymphoma accounting for only 0.3% of primary lung neoplasms. Of these, the large majority are made up of marginal zone B-cell lymphoma and diffuse large B-cell lymphoma. We present a case of a very rare primary pulmonary anaplastic large cell lymphoma presenting as the luftsichel sign on chest radiograph. Pertinent imaging and pathology findings are discussed.
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33

Tsuyama, Naoko, Kana Sakamoto, Seiji Sakata, Akito Dobashi, and Kengo Takeuchi. "Anaplastic large cell lymphoma: pathology, genetics, and clinical aspects." Journal of Clinical and Experimental Hematopathology 57, no. 3 (2017): 120–42. http://dx.doi.org/10.3960/jslrt.17023.

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34

МУСАКУЛОВА, А. М., А. В. БАЛМУХАНОВА, А. С. АУБАКИРОВА, Г. С. ЖУНУСОВА, А. М. БАЛМУХАНОВА, and А. Х. ИБРАЕВА. "EXOPHTHALMOS IN LYMPHOMA AND ENDOCRINE PATHOLOGY OF THE ORBIT." Farmaciâ Kazahstana, no. 2 (June 14, 2022): 73–82. http://dx.doi.org/10.53511/pharmkaz.2022.70.33.011.

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Экзофтальм может быть как одно -, так и двусторонним процессом, который является частым и важным симптомом при различных патологиях орбиты. Широкий спектр всех заболеваний орбиты показывает, что клиника этих нозологий очень схожа. Соответственно, экзофтальм может сопровождаться разнообразными симптомами, от нейрогенных или миогенных до изменений роговицы. Симптомы при появлении зависят от основного заболевания и могут проявляться системно. Ткани орбиты могут поражаться различными заболеваниями, которые в некоторых случаях могут маскировать. Целью данного исследования является определение диффе
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35

Davey, Frederick R., and Robert E. Hutchison. "Pathology and immunology of adult T-cell leukemia/lymphoma." Current Opinion in Oncology 3, no. 1 (1991): 13–20. http://dx.doi.org/10.1097/00001622-199102000-00003.

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36

Randall, Cara, and Yuri Fedoriw. "Pathology and diagnosis of follicular lymphoma and related entities." Pathology 52, no. 1 (2020): 30–39. http://dx.doi.org/10.1016/j.pathol.2019.09.010.

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37

Kim, Wook Youn, Matthew Pugh, Stefan Dojcinov, and Leticia Quintanilla-Martinez. "‘Grey zones’ in the differential diagnosis of lymphoma pathology." Diagnostic Histopathology 25, no. 6 (2019): 191–216. http://dx.doi.org/10.1016/j.mpdhp.2019.04.006.

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38

Hsi, Eric D. "Update in large cell lymphoma: understanding the pathology report." Hematology 2015, no. 1 (2015): 605–17. http://dx.doi.org/10.1182/asheducation-2015.1.605.

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Abstract The diffuse aggressive large B-cell lymphomas are a heterogeneous group of B-cell malignancies. Although many are readily recognized due to characteristic clinical and pathologic features, several problematic areas still exist in diagnosis of these lymphomas due to a variety of reasons that include imprecise or difficult-to-apply diagnostic criteria, gaps in our understanding of lymphoma biology, and limitations in technologies available in the clinical laboratory compared to the research laboratory. This may result in some degree of confusion in the pathology report, particularly if
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39

Violeta Filip, Petruta, Denisa Cuciureanu, Laura Sorina Diaconu, Ana Maria Vladareanu, and Corina Silvia Pop. "MALT lymphoma: epidemiology, clinical diagnosis and treatment." Journal of Medicine and Life 11, no. 3 (2018): 187–93. http://dx.doi.org/10.25122/jml-2018-0035.

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Primary gastric lymphoma (PGL) represents a rare pathology, which can be easily misdiagnosed because of unspecific symptoms of the digestive tract. Histologically, PGL can vary from indolent marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT) to aggressive diffuse large B-cell lymphoma (DLBCL). During the years, clinical trials revealed the important role of Helicobacter pylori (H. pylori) in the pathogenesis of gastric MALT lymphoma. Infection with Helicobacter pylori is an influential promoter of gastric lymphomagenesis initiation. Long-term studies revealed that er
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40

Kaushik, Chhavi, Nitin Relia, Kedar Jambhekar, and Tarun Pandey. "Unusual CT and MR Imaging Characteristics of Splenic Lymphoma." Case Reports in Oncological Medicine 2011 (2011): 1–3. http://dx.doi.org/10.1155/2011/298357.

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Lymphoma is the most common malignancy of the spleen. The imaging features of splenic lymphoma are nonspecific and mostly lymphomas present as a diffusely enlarged spleen. Focal lesions are described but remain of low density or intensity on CT or MRI, respectively. We describe a histologically proven case of splenic lymphoma that showed an atypical hyperdense/hyperenhancing appearance on imaging suspicious for a vascular pathology. To the best of our knowledge and based on review of English literature, such an appearance of splenic lymphoma is extremely unusual and rare.
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41

Anžej Doma, Saša, and Andrej Doma. "Lymphoplasmacytic lymphoma relapse presenting as isolated multifocal subcutaneous adipose tissue infiltrates on 18F-FDG PET/CT." Acta Radiologica Open 12, no. 5 (2023): 205846012311730. http://dx.doi.org/10.1177/20584601231173052.

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Lymphoplasmacytic lymphoma (LPL)/Waldenström macroglobulinemia (WM) is an uncommon mature B cell lymphoma usually involving the bone marrow and, less commonly, the spleen and/or lymph nodes. This case presents a pathology-confirmed isolated extramedullary relapse of LPL, located in subcutaneous adipose tissue, 5 years after successful treatment of WM.
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42

Tang, Ranbie, Xi Chen, Mengna Liu, Qiaoqiao Shu, and Liang Cai. "MALT Lymphoma in Histologic Transformation." Clinical Nuclear Medicine 49, no. 3 (2024): 276–77. http://dx.doi.org/10.1097/rlu.0000000000005057.

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Abstract An 81-year-old woman experienced compression symptoms due to diffuse enlargement of the thyroid gland. The cytopathological results of thyroid fine-needle suggested malignancy. Therefore, she underwent bilateral thyroidectomy. Postoperative pathology indicated mucosa-associated lymphoid tissue (MALT) lymphoma. Three months later, she found a progressively enlarged mass in her neck. The biopsy showed MALT lymphoma with highly aggressive B-cell lymphoma transformation. 18F-FDG PET/CT showed increased metabolism in multiple lymph nodes. However, some of these lymph nodes were negative in
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43

Gurando, A. V., O. V. Shuliga-Nedayhlebova, V. V. Telniy, and D. V. Pominchuk. "Secondary breast lymphoma. A case report." HEALTH OF WOMAN, no. 3(129) (April 30, 2018): 54–57. http://dx.doi.org/10.15574/hw.2018.129.54.

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In this article, in a specific clinical case, the features of the image of secondary lymphoma of the breast with the use of a multimodal clinical-radiological approach were determined and the main literature sources for increasing awareness of this rare but very important pathology are given. Radiologic features of breast lymphomas are non-pathognomonic and may mimic different forms of invasive breast cancer. However, radiologists and clinicians should be aware of this rare pathology to avoid a misinterpretation. The multimodal clinical and radiological approach can be as close as possible to
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44

Hasan, Shaakir, and Aruna Turaka. "Primary mucosa-associated lymphoid tissue lymphoma of the thyroid with concomitant papillary carcinoma." Journal of Radiotherapy in Practice 13, no. 4 (2014): 490–92. http://dx.doi.org/10.1017/s1460396914000090.

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AbstractObjectivePapillary thyroid carcinoma combined with thyroid mucosa-associated lymphoid tissue (MALT) lymphoma is exceedingly rare and there is no standard management.Case reportWe report a rare association of MALT lymphoma of thyroid in a 60-year-old woman with Hashimoto's thyroiditis along with an incidental focus of papillary carcinoma.ConclusionPatients with Hashimoto's thyroiditis are prone to develop other thyroid pathology, including rare tumours such as MALT lymphoma. The differential diagnosis for a neoplasm in such patients should be wide.
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45

Al-Taher, Raed, Abdallah Alabadla, Salameh Al-Halaseh, and Ghasaq Saleh. "Intussusception in a 4-Year-Old Male Due to Burkitt Lymphoma." Case Reports in Pediatrics 2023 (March 27, 2023): 1–4. http://dx.doi.org/10.1155/2023/3535164.

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Intussusception is the invagination of a proximal bowel segment into a distal segment causing bowel obstruction, especially in children. In some cases, it can be caused by a pathological lead point, such as Burkitt lymphoma. Burkitt lymphoma has several patterns of clinical presentations, such as jaw or facial bone tumor in the endemic form, in contrast to an abdominal presentation most often with massive disease and ascites. We describe a case of a 4-year-old male who presented bowel obstruction. Using X-ray and ultrasound findings, ileocecal intussusception was then diagnosed. Resection and
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46

Hafi, Zakaria El, Mohamed Salem Ould Moctar, Razika Bencheikh, Mohamed Anass Benbouzid, Adelilah Oujilal, and Leila Essakalli. "Laryngeal Lymphoma: A Case Report." Scholars Journal of Medical Case Reports 12, no. 01 (2024): 35–38. http://dx.doi.org/10.36347/sjmcr.2024.v12i01.009.

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Primary laryngeal lymphoma is a rare entity, accounting for less than 1% of all primary laryngeal neoplasms. It is mainly primary non-Hodgkin's malignant lymphoma (NHLM). We report a new case in a 56-year-old woman who presented with progressive onset dysphonia [1]. Laryngoscopy revealed a budding lesion of the glotto-supglottic level (vocal cords, arytenoids, ventricular bands, epiglottis). Histology showed a peripheral T-cell lymphoma, CD3 and Ki67 positive, this pathology is difficult to diagnose, requires particular vigilance and should be managed according to current treatment trends for
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47

Tanaka, Hiroaki, Chihiro Kuwabara, Yusuke Isshiki, and Yoshio Suzuki. "Multiple cystic lung lesions and autoimmune thrombocytopaenia developing after chemotherapy for pulmonary indolent B-cell lymphoma with plasmacytic differentiation." BMJ Case Reports 11, no. 1 (2018): e227548. http://dx.doi.org/10.1136/bcr-2018-227548.

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Among lung malignancies, primary pulmonary lymphoma is rare and many of them are indolent B-cell lymphomas. We describe a case of primary pulmonary indolent B-cell lymphoma with plasmacytic differentiation, which exacerbated with the manifestation of macroglobulinaemia and was successfully treated using chemotherapy. The patient subsequently developed pulmonary cysts and thrombocytopaenia due to autoimmune pathology and was successfully treated using prednisolone. This case suggests that in indolent B-cell lymphoma with plasmacytic differentiation, immunoglobulin M level should be carefully fo
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48

Al-Sheneber, Ibrahim, and Henry R. Shibata. "Primary Gastric Lymphoma." Cancer Control 4, no. 3 (1997): 245–52. http://dx.doi.org/10.1177/107327489700400306.

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Background Gastric lymphoma is a common presentation of non-Hodgkin's lymphoma. Controversy reigns about many aspects of its classification and management, especially regarding roles for surgical resection. Methods The authors review the clinical features, staging, pathology, prognosis, and management issues with an emphasis on the role of surgical resection. Results Staging usually can be completed using noninvasive techniques. Those with a low-grade B-cell MALT type lymphoma with Helicobacter pylori infection may be treated with antibiotics and close follow-up. Patients with stage I or II di
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49

Mugabe Byiringiro, Fiacre, Felix Manirakiza, Déogratias Ruhangaza, Thierry Zawadi Muvunyi, and Belson Rugwizangoga. "Pathology Characteristics of Lymphomas in Rwanda: A Retrospective Study." East African Health Research Journal 5, no. 2 (2021): 170–73. http://dx.doi.org/10.24248/eahrj.v5i2.669.

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Background: Lymphomas have been a global challenge for many decades and despite measures for prevention and management, the incidence continues to increase. There are two main categories, which are Non-Hodgkin’s Lymphomas and Hodgkin’s Lymphomas and most common etiologies are environmental, genetic alteration, radiation and some viruses. Objective: To describe pathology characteristics of lymphomas in Rwanda based on Hematoxylin and Eosin stained glass slides and immuno histo chemistry, and classify them according to clinical aggressiveness. Patients and Methods: We conducted a retrospective o
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Poddubnaya, Irina V., Elena A. Baryakh, Vladimir I. Vorobyev, et al. "Therapy of Hodgkin lymphoma in Russia during the COVID-19 pandemic." Journal of Modern Oncology 22, no. 2 (2020): 52–55. http://dx.doi.org/10.26442/18151434.2020.2.200206.

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Relevance. COVID-19 pandemic currently has a significant negative impact on the treatment of patients with oncological pathology, including patients with classic Hodgkin lymphoma. Generalized data on publications on the impact of concomitant pathology on the severity of infection show a significant increase in the risk of death from infection in male patients, aged 60 years, with the presence of 3 concomitant diseases, among which particularly negative role is played by diseases of the cardiovascular system, diabetes, oncology, chronic lung disease, immunodeficiency conditions. Particularly da
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