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Hematology Theory Questions of DNB
Hematology & Oncology
These are Questions on Hematology asked in DNB Theory Exams. They are arranged topic wise till 2011.
| 1 | discuss the etiology and management of autoimmune hemolytic anemia. | Anemia | hematolgy | 2009 | |
| 2 | Classify causes of acquired pancytopenia. Write briefly about the mangement of acquired aplastic anemia. | Anemia | hematolgy | 2009 | |
| 3 | SN diagnosis and mangement of congenital heriditory spherocytosis. | Anemia | hematology | 1997 | |
| 4 | SN severe anemia in first year of life | Anemia | hematology | 2002 | |
| 5 | Diagrammatically outline the normal coagulation cascade. Outline diagnosis and management of DIC | Coagulation | hematolgy | 2009 | |
| 6 | SN antenatal diagnosis and carrier detection in hemophilia | Coagulation | hematology | 1998 | |
| 7 | SN Von Willebrand disease | Coagulation | hematology | 2001 | |
| 8 | Discuss the various aspects of management of a child with hemophillia A | Coagulation | hematology | 2007 | |
| 9 | SN DIC | DIC | hematology | 1996 | |
| 10 | Discuss the pathogenesis of DIC and relate it to the laboratory abnormalities observed in this entity. | DIC | hematology | 2008 | |
| 11 | SN G6PD deficiency | Hemolytic | hematology | 1999 | |
| 12 | SN pathogenesis of anemia in G6PD deficiency. | Hemolytic | hematology | 1999 | |
| 13 | List the common causes of macrocytic anemia. Describe the lag diagnosis of meglaoblastic anemia and treatment of juvenile pernicious anemia. | Hemolytic | hematology | 2004 | |
| 14 | clinicohematological profile of megaloblastic anemia | Hemolytic | hematology | 2006 | |
| 15 | heridatory spherocytosis | Hemolytic | hematology | 2006 | |
| 16 | Discuss causes, clinical manifestations laboratory findings and treatment of folate deficiency anemia in children | Hemolytic | hematology | 2007 | |
| 17 | Briefly outline normal erythropoiesis, Describe the diagnosis & management of G6PD deficiency. | Hemolytic | hematology | 2007 | |
| 18 | SN prevention of iron deficiency anemia in children | IDA | hematology | 1995 | |
| 19 | SN treatment of iron deficiency anemia | IDA | hematology | 1998 | |
| 20 | SN biochemical markers for diagnosis of iron deficiency anemia and response to treatment. | IDA | hematology | 2001 | |
| 21 | Enlist the causes and outline the D/D and management of Iron deficiency Anemia. | IDA | hematology | 2005 | |
| 22 | List the causes of microcytic hypochromic anemia. How will you differentiate between iron deficiency anemia and thallesemia? Discuss briefly the oral iron chelators. | IDA | hematology | 2008 | |
| 23 | Define febrile neutropenia & describe the treatment and care of a child with febrile neutropenia | Leukemia | infectious diseases | 2008 | |
| 24 | SN management of CNS leukemia | Leukemia | hematology | 1996 | |
| 25 | SN treatment and prognosis of ALL | Leukemia | hematology | 1997 | |
| 26 | SN Current therapy of ALL | Leukemia | hematology | 2005 | |
| 27 | Bone marrow transplantation in children | Leukemia | hematology | 2006 | |
| 28 | Management of a child with acute leukemia | Leukemia | hematology | 2006 | |
| 29 | prognostic indictors in acute leukemia | Leukemia | hematology | 2007 | |
| 30 | Define tumor lysis syndrome. Enlist its important constituents. Outline its etiology and describe the management. | Leukemia | hematology | 2008 | |
| 31 | SN utilty of peripheral blood smear examination in children | Misc | hematology | 1997 | |
| 32 | SN GVHD | Misc | hematology | 1999 | |
| 33 | Discuss the sequence of development of various hemoglobins during fetal life and outline the clinical relevance of their persistance after birth. | Misc | hematology | 2001 | |
| 34 | SN diagnosis and management of a 2 year old child with petechial skin rash | Platelets | hematology | 1998 | |
| 35 | SN management of neonatal thrombocytopenic purpura. | Platelets | hematology | 2000 | |
| 36 | Write differential diagnosis of a 5 year old child with petechial rash with fever. How will you manage a child with idiopathic thrombocytopoenic purpura | Platelets | hematology | 2004 | |
| 37 | various treatment modalities of acute ITP | Platelets | hematology | 2006 | |
| 38 | Alpha thalassemia. | Thal | hematolgy | 2007 | |
| 39 | SN current management of Thallesemia major | Thal | hematology | 1996 | |
| 40 | SN recent concepts in the treatment of Thalassemias in children | Thal | hematology | 1996 | |
| 41 | New modalities in the management of Beta thalassemia major | Thal | hematology | 1999 | |
| 42 | SN antenatal diagnosis of thalassemia | Thal | hematology | 1999 | |
| 43 | SN iron chelation therapy | Thal | hematology | 2000 | |
| 44 | SN Recent advances in the management of thalassemia. | Thal | hematology | 2001 | |
| 45 | SN Genetic basis of thalassemia syndrome | Thal | hematology | 2002 | |
| 46 | Ouline the antenatal management of a mother with an earlier child with thalassemia major. | Thal | hematology | 2007 | |
| 47 | Discuss the inherent hazards of blood transfusion in children and the necessary measures to avoid and minimize them. | Transfusion | hematolgy | 2007 | |
| 48 | List the causes of microcytic hypochromic anaemia .Provide differentiating features between iron deficiency anaemia & beta thalassemia trait. Describe the management of thalassemia major. | Thal | June.11 | 3+3+4 | |
| 49 | How will you classify childhood histiocytosis? Describe the diagnostic criteria, clinical manifestation & treatment for hemophagocytic lymphohistiocytosis. What are the infections associated with it? | onco | Dec.11 | 2+2+2+2+2 | |
| 50 | Define tumour lysis syndrome. Describe the pathophysiology of tumour lysis syndrome. How will you prevent occurrence of tumour lysis syndrome? | Onco | Dec.11 | 2+4+4 | |
| 51 | Classify childhood histiocytosis. Describe the clinical manifestations, diagnosis & treatment of Langerhans’s cell histiocytosis. | Onco | June.10 | 3+3+2+2 | |
| 52 | Clinical features, investigations & treatment of pheochromocytoma. | Onco | June.10 | 3+3+4 | |
| 53 | Outline the essential components & pathophysiology of tumor lysis syndrome. Describe its management. | Onco | June.11 | 2+4+4 | |
| 54 | Utility of immunophenotyping in the diagnosis of leukaemia in children. Outline the treatment of acute lymphoblastic leukaemia | ALL | Dec.2009 | 4+6 | |
| 55 | Enlist the common causes of macrocytic anaemia. Describe the laboratory diagnosis and treatment of megalobastic anaemia | anaemia | Dec.2009 | 2+3+5 | |
| 56 | Define pancytopenia. Enumerate common causes in children. How will you assess severity of acquired aplastic anemia in children? | Anemia | Dec.11 | 2+3+5 | |
| 57 | Discuss the etiology, pathogenesis & diagnostic workup of acute autoimmune haemolytic anaemia. | Haemolytic | Dec.10 | 3+3+4 | |
| 58 | Outline the method of extracting various blood components . What are the indications of usage of Fresh Frozen Plasma (FFP) & cryoprecipitate? | hemat | Dec.2009 | 5+5 | |
| 59 | Define pancytopenia. Enlist the causes & assessment of severity of aplastic anaemia in children. | Hemat | June.10 | 2+4+4 | |
| 60 | Describe the function of spleen. Describe clinical manifestations & management of asplenia/polysplenia. | hemat | June.10 | 4+3+3 | |
| 61 | Enlist the red blood cell metabolic enzyme pathways & the enzymes responsible for haemolysis. Discuss the pathogenesis involved in these haemolytic anemias. | Hemolysis | June.11 | 3+7 | |
| 62 | A 10 year old boy with hemophilia A, weighing 30 kg has come with bleeding in both knee joints. Discuss briefly the specific, supportive & prophylactic management of this child. | hemophilia | June.11 | 4+3+3 | |
| 63 | Write in brief regarding the etiology & management of idiopathic thrombocytopenic purpura. (ITP) | ITP | June.11 | 4+6 |