Hema Flashcards

1
Q

Physiologic anemia of infancy usualy lasts for how many weeks?

A

8-12

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2
Q

Physiologic anemia of prematurity has hemoglobin levels of

A

7-9 g/dl

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3
Q

Does physiologic anemia of prematurity require treatment?

A

Yes EPO or transfusion

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4
Q

Most important sign of iron deficiency anemia

A

Pallor

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5
Q

Expected rise in hemoglobin per day after iron treatment

A

0.1-0.4 g/dl

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6
Q

Treatment for IDA

A

Elemental iron

3-6mg/kg/day

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7
Q

After treatment of IDA, Repeat CBC should be done after

A

4 weeks

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8
Q

Target cells
Heinz bodies
Decreased retic count
Normal RDW

A

Thalassemia

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9
Q

Definitive diagnosis of thalassemia can be done through

A

Hb electrophoresis

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10
Q

This infection should be watched out for in thalassemia because it eats up the free iron

A

Yersinia enterocolitica

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11
Q

Tachycardia and splenomegaly

Increased reticulocyte and MCHC normal platelet count

A

Spherocytosis

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12
Q

Defect in spectrin or ankyrin
Osmotic fragility test
Increased MCHC, retic count
Normal MCV

A

Spherocytosis

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13
Q

Vasoocclusive crisis
Autosomal recessive
Crew cut or hair on end appearance of skull in xray
Howell Jolly bodies

A

Sickle cell anemia

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14
Q

Treatment for sickle cell

A

Hydration and analgesia for acute crises

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15
Q

Most common hereditary bleeding disorder

A

vWD

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16
Q

Most common and most serious congenital coagulation factor deficiency?

A

Hemophilia A

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17
Q

Most common hereditary hypercoagulable disorder?

A

Factor V Leiden

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18
Q

Hallmark of hemophilia

A

Prolonged bleeding

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19
Q

Earliest joint hemorrhage in children

A

Ankles

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20
Q

Treatment for mild von willebrand disease type 1

A

Desmopressin

21
Q

Laboratory finding in hemophilia

A

Increased PTT

22
Q

Laboratory finding in vWD

A

Increased PTT and bleeding time

23
Q

Laboratory finding in ITP

A

Increased bleeding time

Decreased platelet

24
Q

Laboratory finding in vitamin K deficiency

A

Increased PT

25
Laboratory finding in DIC
Decreased platelet count | Increased PT PTT bleeding time
26
What type of leukemia in childhood will have the best response to chemotherapy?
ALL
27
Site of relapse of ALL
bone marrow CNS Testes
28
Site of spread of ALL
Liver Spleen Lymph nodes
29
``` <2 years >10 years old Male WBC >100,000 on presentation CNS involvement Mediastinal mass ``` Poor prognostic factors of what disease
ALL
30
Renal tumor of embryonal origin
Wilms tumor
31
Painless abdominal enlargement with flank mass that DOES NOT cross the midline
Wilms
32
Drug of choice for PCP prophylaxis in children with ALL undergoing chemotherapy is
Co-trimoxazole
33
Embryonic tumor of neural crest origin
Neuroblastoma
34
Most common site where neuroblasts migrate
Sympathetic ganglia and adrenals
35
Differential diagnosis of small, round, blue cell tumors WARMER PN
``` Wilms Acute leukemia Rhabdomyosarcoma Mesothelioma/medulloblastoma Ewing sarcoma Retinoblastoma Primitive neuroectodermal tumor (PNET) Neuroblastoma ```
36
Associated with: Neurofibromatosis Beckwith- Weidemann syndrome WAGR syndrome
Wilms tumor
37
``` Associated with: N-myc oncogene Neurofibromatosis Hirschprung Tuberous sclerosis Pheochromocytoma ```
Neuroblastoma
38
``` Horner syndrome Abdominal mass that MAY cross the midline Cord compression Racoon eyes Dancing eyes and feet ```
Neuroblastoma
39
Diagnosis for neuroblastoma
Urine VMA and HVA Abdominal CT Bone marrow aspirate
40
``` Long bones and skull BM Liver LN Skin ``` Most common metastatic sites of
Neuroblastoma
41
What are the B symptoms of | Lymphoma?
High grade fever Weight loss Night sweats
42
``` Regional lymphadenopathy Chemotherapy Bimodal age distribution EBV, CMV, HHV 6 Reed Sternberg cells Contiguous LN spread ```
Hodgkin lymphoma
43
Hodgkin lymphoma type that has the Best prognosis
Mixed cellularity lymphocyte predominant
44
``` Systemic adenopathy Radiation for CNS involvement Chemotherapy 60% of lymphomas in chidren and adolescent EBV- Burkitt Non contiguous LN spread ```
Non-Hodgkin
45
Results from failure or autoimmune destruction of myeloid stem cells
Aplastic anemia
46
Most likely cause of aplastic anemia
Idiopathic
47
Typical PBS finding in aplastic anemia
Hypocellularity and pancytopenia
48
Aplastic anemia with microcephaly, microphthalmia, hearing loss and limb anomalies
Fanconi anemia