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Aplastic Anemia
Name-Sharma Anuj
Group-55
General information of disease
Aplastic anemia is a serious condition in which the bone marrow
does not produce enough new blood cells .
It may be passed down from the parents or develop sometime
during childhood .
Some symptoms include tiredness,paleness,frequent
infections,and easy bruising and bleeding !.
Name- Priya
Age-4 years old
A mother came with 4 years old female child with symptoms of fever
from past 2 weeks,has become more and more pale and
weak,complained of pain in the abdomen .measles at 2 years of
age ,no complications.
Child has no history of tuberculosis or syphilis ,no members of the
family have had any disease of the blood ! or the blood forming
organs .
Objective examination
Fever " more than 38.9* c
Skin pigmentation
Short stature
Microcephaly
Hypogonadism
Mental retardation
Skeletal anomalies
Primary diagnosis
Aplastic anemia
No lymphadenopathy
No murmur
No marked enlargement
Lungs # -Negative
Liver and spleen - normal
Laboratory $ diagnosis
Panytopenia
Bone marrow histology and cytology
-decreased marrow cellularity(<25%)
-increased fat cells component
No extensive fibrosis
-no malignancy or storage disease
-Dry T
ap(little materials)
Differential Diagnosis
Fanconi Anemia
Dyskeratosis Congenita
Acute Myelogenous leukemia
Anemia
Hairy cell leukemia
Paroxysmal nocturnal hemoglobinuria
T
reatment
Supportive care
Severe anemia-Packed Red cells
Severe thrombocytopenia-Platelet T
ransfusion
Infection-Antibiotics
Definitive therapy-Hematopoietic stem cell T
ransplant(HRCT)
THANKYOU %

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Aplastic Anemia ANUJ 55.pdf

  • 2. General information of disease Aplastic anemia is a serious condition in which the bone marrow does not produce enough new blood cells . It may be passed down from the parents or develop sometime during childhood . Some symptoms include tiredness,paleness,frequent infections,and easy bruising and bleeding !.
  • 3. Name- Priya Age-4 years old A mother came with 4 years old female child with symptoms of fever from past 2 weeks,has become more and more pale and weak,complained of pain in the abdomen .measles at 2 years of age ,no complications. Child has no history of tuberculosis or syphilis ,no members of the family have had any disease of the blood ! or the blood forming organs .
  • 4. Objective examination Fever " more than 38.9* c Skin pigmentation Short stature Microcephaly Hypogonadism Mental retardation Skeletal anomalies
  • 5. Primary diagnosis Aplastic anemia No lymphadenopathy No murmur No marked enlargement Lungs # -Negative Liver and spleen - normal
  • 6. Laboratory $ diagnosis Panytopenia Bone marrow histology and cytology -decreased marrow cellularity(<25%) -increased fat cells component No extensive fibrosis -no malignancy or storage disease -Dry T ap(little materials)
  • 7. Differential Diagnosis Fanconi Anemia Dyskeratosis Congenita Acute Myelogenous leukemia Anemia Hairy cell leukemia Paroxysmal nocturnal hemoglobinuria
  • 8. T reatment Supportive care Severe anemia-Packed Red cells Severe thrombocytopenia-Platelet T ransfusion Infection-Antibiotics Definitive therapy-Hematopoietic stem cell T ransplant(HRCT)