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Acute Leukemia of Ambiguous Lineage with a Rare Abnormality Del17p by FISH Analysis


Article Information

Title: Acute Leukemia of Ambiguous Lineage with a Rare Abnormality Del17p by FISH Analysis

Authors: Naeem Abbas, Samra Waheed, Aisha Jamal, Ali Saleem, Tahir Sultan Shamsi

Journal: National Journal of Health Sciences

HEC Recognition History
Category From To
Y 2024-10-01 2025-12-31
Y 2023-07-01 2024-09-30
Y 2022-07-01 2023-06-30

Publisher: National Institute of Blood Disease Welfare Society

Country: Pakistan

Year: 2020

Volume: 5

Issue: 2

Language: en

Keywords: FlowcytometryAcute undifferentiated leukemiaDeletion 17pFlourescnece in situ hybridizationAllogeneic haematopoetic stem cell transplantation

Categories

Abstract

Abstract: The World Health Organization (WHO) has categorized acute undifferentiated leukemia (AUL) as a rare subtype of acute leukemia of ambiguous lineage (ALAL). The prognosis of AUL is considered poor and it expresses no known lineage-specific markers. In majority of the cases, AUL has been associated with karyotypic abnormalities, most commonly deletion 5q and complex karyotype. Deletion 17p correlation with acute myeloid leukemia and myelodysplastic syndome has been previously established and is associated with poorer outcomes. Herein we are reporting a case of forty years old male who was referred to National institute of blood diseases and bone marrow transplantation with complains of fever, multiple neck swellings, and early satiety and was diagnosed as Acute Undifferentiated Leukemia along with deletion 17p. This is a rare entity and can aid in further diagnostic and therapeutic approaches.


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