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Relevant bibliographies by topics / Bicytopenia

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Academic literature on the topic 'Bicytopenia'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Bicytopenia"

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Sonu, Kumar, and Karan Ankit. "Clinical and Etiological Characteristics of Patients with Bicytopenia." International Journal of Pharmaceutical and Clinical Research 15, no. 4 (2023): 961–69. https://doi.org/10.5281/zenodo.12677596.

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<strong>Background: </strong>Erythrocytes, leukocytes, or platelets are only a few of the two types of blood cells that are reduced in bicytopenia. There are numerous studies on pancytopenia, however, there are very few that examine the range of etiologies for bicytopenia. The objective was to examine the clinical-hematological characteristics of patients with bicytopenia and to look into the various causes of bicytopenia. <strong>Method: </strong>200 patients with bicytopenia were selected for the study using systematic random sampling from those admitted to Indira Gandhi Insti

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Khalid, Nida, Hajra Azhar, Javeria Afzal, Zeneara Saqib, Sundus Durrani, and Muhammad Irfan. "Prevalence of Pancytopenia/ Bicytopenia in Pediatric Population and its Association with Etiology Based on Bone Marrow Findings." Pakistan Journal of Medical and Health Sciences 17, no. 5 (2023): 77–80. http://dx.doi.org/10.53350/pjmhs202317577.

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Background: An important clinico-haematological condition known as pancytopenia or bicytopenia is brought on by a multitude of disease processes that either directly or indirectly affect the bone marrow. Aim: To ascertain the prevalence of cytopenias in the pediatric population presenting to a tertiary care hospital in Rawalpindi and its correlation with age and gender distribution, clinical presentation, and aetiology. Study Design: Descriptive cross-sectional study. Methodology: It was a descriptive cross-sectional study carried out at Holy Family Hospital in Rawalpindi's hematology division

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Rampal, Raajit, Michael Marrone, Lisa Morere, et al. "Real-Word Effectiveness of Pacritinib in Patients with Myelofibrosis Who Have Thrombocytopenia and Anemia." Blood 144, Supplement 1 (2024): 6649. https://doi.org/10.1182/blood-2024-210274.

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Background: The co-occurrence of thrombocytopenia and anemia (bicytopenia) in patients with myelofibrosis (MF) is a therapeutic challenge because of treatment-related myelosuppression from JAK1/2 inhibitors. Pacritinib (PAC) is a JAK1-sparing inhibitor of JAK2/IRAK1/ACVR1 that can be administered at full dose, yielding consistent efficacy, regardless of baseline platelet count (PLT) or hemoglobin levels (Hb) (Gagelmann N. Clin Lymphoma Myeloma Leuk. 2024; S2152-2650(24)00246-5). Recent post-hoc data from the phase 3 PERSIST-2 study have shown that PAC is associated with spleen volume reduction

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Bahal, Neelima, Avneesh Malviya, and Sana Ahuja. "Clinicohaematological & Aetiological Profile of Bicytopenic / Pancytopenic Children in Dehradun, India - A 5-Year Study." Journal of Evolution of Medical and Dental Sciences 10, no. 18 (2021): 1347–52. http://dx.doi.org/10.14260/jemds/2021/284.

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BACKGROUND Cytopenia (bicytopenia / pancytopenia) in paediatric age group patients presents with variable clinical features from pallor, fever to organomegaly. Causes vary from megaloblastic anaemia to fatal leukaemias. The purpose of the study was to evaluate the etiological and clinico-haematological profile in children with bicytopenia and pancytopenia. METHODS The present retrospective study was carried out in the section of haematology, Department of Pathology of Shri Guru Ram Rai Institute of Health and Medical Sciences, Dehradun. All paediatric cases (up to 18 yrs.) with bone marrow exa

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Vijay Anand M, Logeshwaran K, Srenivas A, and Sathiya Suresh R. "Children with bicytopenia and pancytopenia – clinical picture, etiological spectrum, and outcome." Asian Journal of Medical Sciences 15, no. 6 (2024): 113–18. https://doi.org/10.71152/ajms.v15i6.3624.

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Background: Children who develop cytopenias present with several etiological causes, posing diagnosis, and management difficulties for both physicians and pathologists. With these in mind, we assessed the clinical profile and etiology of children who attended a healthcare facility in South India with bicytopenia or pancytopenia. Aims and Objectives: (1) The primary objective of this study was to find out the clinical and etiological spectrum in children with bicytopenia and pancytopenia who were admitted to the Institute of Child Health and Research Center, Government Rajaji Hospital, Madurai.

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Vijay Anand M, Logeshwaran K, Srenivas A, and Sathiya Suresh R. "Children with bicytopenia and pancytopenia – clinical picture, etiological spectrum, and outcome." Asian Journal of Medical Sciences 15, no. 6 (2024): 113–18. http://dx.doi.org/10.3126/ajms.v15i6.63565.

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Background: Children who develop cytopenias present with several etiological causes, posing diagnosis, and management difficulties for both physicians and pathologists. With these in mind, we assessed the clinical profile and etiology of children who attended a healthcare facility in South India with bicytopenia or pancytopenia. Aims and Objectives: (1) The primary objective of this study was to find out the clinical and etiological spectrum in children with bicytopenia and pancytopenia who were admitted to the Institute of Child Health and Research Center, Government Rajaji Hospital, Madurai.

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Pathak, Deepankar Raj, Ashish Kumar Chaurasiya, Rasish Subedi, Prabin Khatri, and Pooja Shah. "Primary Sjogren’s Syndrome with Bicytopenia: A Case Report." Journal of Nepal Medical Association 62, no. 269 (2024): 49–51. http://dx.doi.org/10.31729/jnma.8406.

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Sjogren’s syndrome is a chronic multisystem autoimmune disease presenting a wide variety of clinical manifestations ranging from mild sicca symptoms to severe systemic symptoms involving pulmonary, renal, musculoskeletal, cutaneous, and haematological diseases. These symptomatic diversities can delay the correct diagnosis of Sjogren’s Syndrome for a long time. Here, we report the case of a 59-year-old woman with fatigue and weakness in whom bicytopenia was documented. A thorough bicytopenia workup brought us to the final diagnosis of Sjogren’s syndrome. Hydroxychloroquine was started which nor

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Khush Bakht, Raza Muhammad Khan, and Shahtaj Khan. "Frequency of Bicytopenia in Slide-Positive Malaria Patients." Indus Journal of Bioscience Research 3, no. 2 (2025): 7–12. https://doi.org/10.70749/ijbr.v3i2.585.

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Background: Malaria is a life-threatening parasitic disease that remains a significant global health concern, particularly in endemic regions. Haematological abnormalities such as bicytopenia, characterised by the reduction of two blood cell lines (red blood cells, white blood cells, or platelets), are commonly observed in malaria patients. Methodology: A cross-sectional study was conducted over six months at the Department of Hematology, Hayatabad Medical Complex, Peshawar. A total of 138 patients, aged 16–60 years, with confirmed Plasmodium falciparum or Plasmodium vivax malaria, were includ

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Kim, Tong-Yoon, Gi-June Min, Young-Woo Jeon, et al. "Inferior Outcomes of Fludarabine–Cyclophosphamide–Rituximab Chemotherapy in Korean Chronic Lymphocytic Leukemia Patients with Concurrent Thrombocytopenia and Anemia." Biomedicines 13, no. 1 (2025): 194. https://doi.org/10.3390/biomedicines13010194.

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Background/Objectives: Anti-CD20 monoclonal antibodies combined with alkylator-based chemotherapy enhance survival in chronic lymphocytic leukemia (CLL). However, the risks of infection and bone marrow suppression may mean that new, targeted therapies are more appropriate for some patients than fludarabine–cyclophosphamide–rituximab (FCR). In the Republic of Korea, where insurance limits coverage to novel agents, FCR therapy should be carefully considered for patients with CLL. Methods: Using clinical data from 144 FCR-treated patients with CLL, we retrospectively analyzed clinical characteris

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Khattak, Imran Qadir, Mustaqeem Shah, Muhammed Irfan, Rizwan Ullah Khan, Mubashir Qadir Khattak, and Fida Muhammad Khan. "FREQUENCY OF BICYTOPENIA IN CHRONIC HCV PRE TREATMENT CASES." Khyber Journal of Medical Sciences 17, no. 1 (2024): 43–47. https://doi.org/10.70520/kjms.v17i1.530.

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Background: Platelets are blood cells that participate in wound healing and blood clotting. When their number decreases below 150,000/?L, this is known as thrombocytopenia. Thrombocytopenia may have no risk at all or it may lead to the risk of bleeding and thrombosis. To the best of our knowledge, no study has been undertaken on the frequency of bicytopenia in chronic HCV pretreatment cases in our local population.Objective: The objective is to investigate the occurrence rate of bicytopenia among chronic Hepatitis C Virus patients prior to treatment within our community.Methodology: A cross-se

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Book chapters on the topic "Bicytopenia"

1

Beck, Norman. "Pancytopenia and Bicytopenia." In Diagnostic Hematology. Springer London, 2009. http://dx.doi.org/10.1007/978-1-84800-295-1_13.

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Katoch, Pankaj, Vipin Roach, and Surinder Singh. "Clinico Haematological Profile in Paediatric Patients with Bicytopenia and Pancytopenia in a Tertiary Care Referral Centre of North India: A Prospective Observational Study." In Current Aspects in Pharmaceutical Research and Development Vol. 7. Book Publisher International (a part of SCIENCEDOMAIN International), 2022. http://dx.doi.org/10.9734/bpi/caprd/v7/15164d.

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de Oliveira Filho, Cezar Arruda, Isabela Pimenta Pelucio, Carolina Bertini Bonini, et al. "Bacterial meningitis secondary to otomastoiditis by Providencia Rettgeri in private of liberty." In Uniting Knowledge Integrated Scientific Research For Global Development V.2. Seven Editora, 2024. http://dx.doi.org/10.56238/sevened2024.018-026.

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Introduction: This case report describes a rare occurrence of meningitis caused by Providencia rettgeri in an inmate patient. Providencia rettgeri is a gram-negative bacterium that rarely causes meningitis, and is most commonly associated with urinary tract infections and septicemia in immunocompromised patients. (1) Case Presentation: Man, 29 years old, deprived of liberty, without comorbidities. Onset of otalgia, fever and otorrhea for 21 days, with previous use of Ceftriaxone + Oxacillin, without improvement. Admitted due to prostration for 02 days, mental confusion and lowering of the leve

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Conference papers on the topic "Bicytopenia"

1

Genz, Isabel Cristina Hilgert, Tiago Luan Branchi, Larissa Felcar Hill, et al. "BICYTOPENIA, FEVER AND MYALGIA IN BAGGIO-YOSHINARI SYNDROME (LYME-LIKE DISEASE)." In XL Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2023. http://dx.doi.org/10.47660/cbr.2023.1902.

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