9:00 G6PD deficit patient have firstly in the hemolytic attak a macrocytosis due to reticulcytosis Nb:The most common cause of macrocytosis is reticulocytosis 16:37 RDW normal or slightly increased in thalassemia RDW increased ~20 in IDA,vitamine B12 RDW 30~40 in sideroblastic anemia 28:00 patient with acute hemolysis ال Hb يبدأ يتحسن لكن reticulocytes تفضل عالية هنا ممكن تلخبطنا وتطرح السؤال هل hemolysis مازال شغال الجواب لأ هو فقط bone marrow خذ وقت حتى. Compensate 28:45 megacaryocytic element 38:35 iron profile: ferritinemia, transferritine saturation Acute phase rectants:crp, pct , ESR 38:37 myelocytic element 40:00 LAD =leucocyte addision deffect : severe neutrophilia with Profond immune deficiency 40:13 lymphocytes absolute count different according the age 43:55 blood film examination and others 46:50 clinical cases 49:00 1/3 of IDA have splenomegaly Case 1 IDA Follow up : cbc and hemoglobine electrophoresis to search thalasemia Nb: thalasemia and IDA may be associated Case 2 thalasemia with possible infection regarding thrombocytosis Nb: Investigation: iron profile,Hemoglobine electrophoresis Because some types of thalasemia the Hemoglobine electrophoresis is not accruate there is only high Hb A2 IDA have Hb A2 is low Nb: Patient with thalasemia3 may be masked by IDA so advise don't interpret or demand hemoglobine electrophoresis in presence of IDA 52:40 Case 3 homocystinuria: pancytopenia with congenital anomalies Case 4 sideroblastic anemia Case 5 sphercytosis with aplastic crisis due to barbovirus infection barbovirus infection regarding slawed cheeck appearance Pallor,splenomegalie due to aplastic crisis not hemolytic crisis Jandice because the patient is gilbert Case 6 LAD =leucocyte addision deffect : severe neutrophilia with Profond immune deficiency Case 7 fanconi anemia Case 8 inhereted macrothrombocytopenia with dohle bodies suggestive of "MHB..." Case 9 berner solier sdr
Thanks so much , I had already uploaded a lecture titled *coagulation profile interpretation and approach to a bleeding child*....and Iam going to upload more pediatric hematology lectures soon
If any question, just post it and I would be happy to answer
9:00 G6PD deficit patient have firstly in the hemolytic attak a macrocytosis due to reticulcytosis
Nb:The most common cause of macrocytosis is reticulocytosis
16:37 RDW normal or slightly increased in thalassemia
RDW increased ~20 in IDA,vitamine B12
RDW 30~40 in sideroblastic anemia
28:00 patient with acute hemolysis
ال Hb يبدأ يتحسن لكن reticulocytes تفضل عالية هنا ممكن تلخبطنا وتطرح السؤال هل hemolysis مازال شغال
الجواب لأ هو فقط bone marrow خذ وقت حتى. Compensate
28:45 megacaryocytic element
38:35 iron profile: ferritinemia, transferritine saturation
Acute phase rectants:crp, pct , ESR
38:37 myelocytic element
40:00 LAD =leucocyte addision deffect : severe neutrophilia with Profond immune deficiency
40:13 lymphocytes absolute count different according the age
43:55 blood film examination and others
46:50 clinical cases
49:00 1/3 of IDA have splenomegaly
Case 1 IDA
Follow up : cbc and hemoglobine electrophoresis to search thalasemia
Nb: thalasemia and IDA may be associated
Case 2 thalasemia with possible infection regarding thrombocytosis
Nb: Investigation: iron profile,Hemoglobine electrophoresis
Because some types of thalasemia the Hemoglobine electrophoresis is not accruate there is only high Hb A2
IDA have Hb A2 is low
Nb: Patient with thalasemia3 may be masked by IDA so advise don't interpret or demand hemoglobine electrophoresis in presence of IDA
52:40 Case 3 homocystinuria: pancytopenia with congenital anomalies
Case 4 sideroblastic anemia
Case 5 sphercytosis with aplastic crisis due to barbovirus infection
barbovirus infection regarding slawed cheeck appearance
Pallor,splenomegalie due to aplastic crisis not hemolytic crisis
Jandice because the patient is gilbert
Case 6 LAD =leucocyte addision deffect : severe neutrophilia with Profond immune deficiency
Case 7 fanconi anemia
Case 8 inhereted macrothrombocytopenia with dohle bodies suggestive of "MHB..."
Case 9 berner solier sdr
جزاكم الله خيرا د.عمرو
جزاكم الله عنا خير الجزاء ورزقكم من الطيبات ونفع بكم وسدد خطاكم الي ما فيه صلاحكم واتم نعمه عليكم ظاهرة وباطنه انه سبحانه سميع قريب مجيب الدعوات
شكرا د عمرو بالتوفيق دائما يارب
Excellent and very informative
جزاكم الله كل خير
دكاترة جامعتنا ❤❤❤❤
محاضرة اكتر من رائعة ما شاء الله
شكرا جزيلا وجزاكم الله خيرا كثيرا🌷🌷
Many thanks for this amazing lecture
جزاك الله خيرا
و اياكم يا فندم
It is a great lecture, i really enjoyed it. Waiting for the rest of the haematology series. May Allah bless you
Thanks so much , I had already uploaded a lecture titled *coagulation profile interpretation and approach to a bleeding child*....and Iam going to upload more pediatric hematology lectures soon
I have seen the coagulation profile, it is a wonderfull lecture, Thanks alot. Keep the good work dear doctor, May Allah bless you.
الف شكر علي الشرح الرائع يا د عمرو ياريت حضرتك تكمل interpretation on leukocytosis and leukopenia
There will be a separate lecture for Neutropenia soon
جزاكم الله خيراً
Thank you 😊 💓
Very good and informative lecture
جزاكم الله خيرا
حضريك معلقتش علي بس علي ال band ratio في ال infection
Clarify please dr Ahmed
What are factors affect CBC
هل ممكن fasting cause he consent ration وبالتالى HB يطلع طبيعى بالرغم من ان الطفل anemic
Many thanks Dr Amr