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  • 1
    In: Journal of Hematology and Allied Sciences, Scientific Scholar, Vol. 1 ( 2021-05-31), p. 33-37
    Abstract: To describe the case series of patients with myeloid sarcoma with their clinicopathological characteristics, cytogenetics, molecular markers, prognosis, and outcome. Material and Methods: Retrospective retrieval of data of myeloid sarcoma cases in acute myeloid leukemia was done from the electronic health records of our hospital and this case series includes the data of three years starting from January 2018 and the follow-up information was assimilated until December 2020. Results: We present twelve patients in this case series with myeloid sarcoma and all these patients had bone marrow involvement at presentation. Most of the cases were less than 20 years of age and orbit (66.7%) was the commonest site of presentation in this series. Aberrant CD 19 expression on immunophenotyping was a common associate (66.9%) and t(8;21) was the commonest cytogenetic abnormality reported in our case series. Despite of high dose intensive therapy with daunorubicin and cytarabine followed by high-dose cytarabine (HiDAC) consolidation, patients had a median relapse-free survival and median overall survival of 160 days and 299.5 days respectively. Local radiotherapy for consolidation in two of our patients had no additional benefit. Conclusion: Myeloid sarcoma is extramedullary collection of myeloid blasts with or without bone marrow involvement. They were commonly seen in young patients and t(8;21) being a common cytogenetic abnormality associated with it. The treatment outcome of patients with myeloid sarcoma seems dismal and systemic therapy remains the modality of choice.
    Type of Medium: Online Resource
    ISSN: 2768-6825 , 2833-4248
    Language: English
    Publisher: Scientific Scholar
    Publication Date: 2021
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  • 2
    Online Resource
    Online Resource
    Scientific Scholar ; 2021
    In:  Journal of Hematology and Allied Sciences Vol. 1 ( 2021-12-07), p. 69-74
    In: Journal of Hematology and Allied Sciences, Scientific Scholar, Vol. 1 ( 2021-12-07), p. 69-74
    Abstract: Myelodysplastic syndrome (MDS) is a group of myeloid neoplasms. The clinical manifestations and treatments vary depending on the subtype and risk stratification of the disease. There is a paucity of data on Indian patients with MDS. This study was undertaken to understand MDS with regard to their clinical presentation, pathological, cytogenetic profiles and also to assess their therapeutic outcomes and prognosis from our center in Eastern India. Materials and Methods: This is a prospective observational study conducted in the department of hematology at a tertiary care teaching hospital from eastern part of India. The diagnosis of MDS was made from the peripheral blood examination, bone marrow aspirate examination, cytogenetics, and Fluorescence in situ hybridization results, according to the WHO guidelines. Patients were risk stratified using Revised International Prognostic Scoring System (R-IPSS) and subsequent therapeutic planning was done, with either supportive therapy in the form of recombinant human erythropoiesis stimulating agents, colony stimulating factors, packed red blood cell support as needed for low risk MDS patients. High risk patients were treated with hypomethylating agents such as Azacytidine, Decitabine, or Lenalidomide. Results: The mean duration of follow-up of patients with MDS from the point of diagnosis was 1.8 years (range 4 months–6 years). The median OS was 1.33 years. The median OS in the analysis of our patient cohort with low, intermediate, high, and very high R-IPSS was 1.67 years, 1.33 years, 1.67 years, and 1.67 years, respectively. No patients of very low risk group were identified in our study. Conclusion: Our findings reflect that MDS-MLD with low or intermediate R-IPSS risk groups is the most common types of MDS. Although supportive therapy was used to treat patients irrespective of other therapy given (depending on the risk group of the patient), it was used alone even in higher risk groups due to logistic reasons in some cases. Those patients who received supportive care alone also had a good survival duration. However, a longer follow-up duration is required to firmly establish this outcome. The median age of patients (55 years) was also lower than established studies with a median overall survival of 1.67 years.
    Type of Medium: Online Resource
    ISSN: 2768-6825 , 2833-4248
    Language: English
    Publisher: Scientific Scholar
    Publication Date: 2021
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    Scientific Scholar ; 2005
    In:  Indian Journal of Dermatology, Venereology and Leprology Vol. 71, No. 4 ( 2005), p. 246-
    In: Indian Journal of Dermatology, Venereology and Leprology, Scientific Scholar, Vol. 71, No. 4 ( 2005), p. 246-
    Type of Medium: Online Resource
    ISSN: 0378-6323
    Language: English
    Publisher: Scientific Scholar
    Publication Date: 2005
    detail.hit.zdb_id: 2129139-1
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