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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/28552
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dc.contributor.authorPîrlii Iulius-
dc.date.accessioned2024-10-28T12:50:28Z-
dc.date.accessioned2024-11-18T14:28:47Z-
dc.date.available2024-10-28T12:50:28Z-
dc.date.available2024-11-18T14:28:47Z-
dc.date.issued2024-
dc.identifier.citationPîrlii Iulius. Clinical and hematological features and diagnostic options in extranodal aggressive non-Hodgkin's lymphomas. In: Abstract Book. MedEspera 2024. The 10th International Medical Congress for Students and Young Doctors. 24-27 April 2024, Chișinău, Republic of Moldova, p. 130. ISBN 978-9975-3544-2-4.en_US
dc.identifier.isbn978-9975-3544-2-4-
dc.identifier.urihttps://ibn.idsi.md/collection_view/3104-
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/28552-
dc.descriptionUniversitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, Chişinău, Republica Moldovaen_US
dc.description.abstractIntroduction. Lymphomas can be simply defined as malignant neoplasms of lymphocytes and their precursor cells. Common sites of extranodal manifestations are the gastrointestinal tract, especially the ventricle, pharynx, thyroid gland and skin. In the head and neck region, the most common site is Waldeyer's ring. Aim of study. To identify and evaluate the clinical-evolutionary, hematological features and diagnostic options in aggressive extranodal non-Hodgkin's lymphomas. Methods and materials. We studied the ambulatory cards and medical records of 80 patients with morphologically confirmed diagnoses of non-Hodgkin's lymphoma, who had at least one extranodal presentation. Results. Among studied patients, all had at least one extranodal involvement, in 43% of cases the nasopharynx was affected, 38% the liver, 25% the spleen, 14% the spinal cord. Most patients spend 4 months -1 year to establish a concrete diagnosis. Sometimes this was due to the patient's own fault, postponing the visit to the doctor until the last moment or atypical symptoms making the diagnosis more difficult to establish. The presence of B symptoms was recorded in 42% of patients, and 76% had stage IV at diagnosis. The anemic syndrome was present in 14% of cases, with specific changes in the differential blood count. The final diagnosis was proved on the basis of morphology and immunohistochemical examination of the biopsied lymph nodes or tissue. The immunohistochemistry panel used was: CD20, CD3, CD5, CD10, CD45, BCL2, BCL6, Ki-67, IRF4/MUM1, and MYC which confirmed the diagnosis of lymphoma with the specification of the immunohistochemical type. Complete staging and monitoring of the disease evolution was possible due to high-precision MRI, CT PET-CT investigations. Patients received treatment courses of RCHOP, RCOP, BR with 80% of cases achieving clinic-morphological remission. Conclusion. A surgically excised tissue with immunohistochemical examination is widely accepted as the gold standard for lymphoma diagnosis based on current international guidelines. It should be evaluated by immunocytochemistry, flow cytometry (if received unfixed), FISH studies, DNA and RNA extraction for molecular diagnosis. their precursor cells. Common sites of extranodal manif estations are the gastrointestinal tract, especially the ventricle, pharynx, thyroid gland and skin. In the head and neck region, the most common site is Waldeyer's ring. Aim of study. To identify and evaluate the clinical-evolutionary, hema tological features and diagnostic options in aggressive extranodal non-Hodgkin's lymp homas. Methods and materials. We studied the ambulatory cards and medical records of 80 pa tients with morphologically confirmed diagnoses of non-Hodgkin's lymphom a, who had at least one extranodal presentation. Results. Among studied patients, all had at least one extranodal invo lvement, in 43% of cases the nasopharynx was affected, 38% the liver, 25% the spleen, 14% t he spinal cord. Most patients spend 4 months -1 year to establish a concrete diagnosis. Someti mes this was due to the patient's own fault, postponing the visit to the doctor until the last mom ent or atypical symptoms making the diagnosis more difficult to establish. The presence of B symptoms was recorded in 42% of patients, and 76% had stage IV at diagnosis. The anemic syndrome was pres ent in 14% of cases, with specific changes in the differential blood count. The fina l diagnosis was proved on the basis of morphology and immunohistochemical examination of the bio psied lymph nodes or tissue. The immunohistochemistry panel used was: CD20, CD3, CD5, CD10, CD45, BCL2, BC L6, Ki-67, IRF4/MUM1, and MYC which confirmed the diagnosis of lymphoma with the specification of the immunohistochemical type. Complete staging and monitoring o f the disease evolution was possible due to high-precision MRI, CT PET-CT investigations . Patients received treatment courses of RCHOP, RCOP, BR with 80% of cases achieving clinic- morphological remission. Conclusion. A surgically excised tissue with immunohistochemical exami nation is widely accepted as the gold standard for lymphoma diagnosis based o n current international guidelines. It should be evaluated by immunocytochemistry, flow cytometry (if received unfixed), FISH studies, DNA and RNA extraction for molecular diagnosis.en_US
dc.publisherInstituţia Publică Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” din Republica Moldovaen_US
dc.relation.ispartofMedEspera 2024en_US
dc.titleClinical and hematological features and diagnostic options in extranodal aggressive non-Hodgkin's lymphomasen_US
dc.typeOtheren_US
Appears in Collections:MedEspera 2024

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