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DISEASES INVOLVING
BLOOD PLATELETS-II
INDIAN DENTAL ACADEMY
Leader in continuing Dental Education
www.indiandentalacademy.com
LEARNING OBJECTIVES
• At the end of the lecture student should be able to
• Describe etiology, clinical features &
histopathological features of thrombocytasthenia
• Describe etiology, clinical features &
histopathological features of thrombocytopenic
purpura
www.indiandentalacademy.com
• THROMBOCYTASTHENIA
•It is characterized by qualitative defect in the blood
platelet.
•FAMILIAL THROMBASTHENIA (Glanzman
thrombasthenia)-hereditary,chronic hemorrhagic disease
transmitted as an autosomal recessive trait.
•C/F -Excessive bleeding following minor trauma.
www.indiandentalacademy.com
• Purpuric hemorrhages of skin are common.
• Epistaxis and GIT bleeding.
• O/F-
• Spontaneous gingival bleeding.
• Palatal petechiae.
• L/F-Bleeding time prolonged
• Clot retraction is impaired .
• Number of platelet normal.
• Amount of certain membrane glycoprotein on the
surface of the platelet is reduced.www.indiandentalacademy.com
THROMBOCYTOPATHIC
PURPURA
•A group of rare disorders of unknown etiology in
which the patients manifest a bleeding tendency due to
qualitative defects in blood platelets.
•Severe bleeding tendency and bruise easily even after
minor trauma.
•Menstrual bleeding so severe as to require blood
transfusion.
O/M : Gingival bleeding
www.indiandentalacademy.com
•Excessive and prolonged bleeding from dental
extractions may be a serious management problem.
L/F
•Platelate count – Normal
•Bleeding time prolonged or normal
•Storage pool disease – Deficiency in nonmetabolic
storage pool of the platelet adenine nucleotides.
•Portsmouth syndrome: Abnormal or absent collagen
induced platelet aggregation.
•Bernard soulier syndrome – abnormal platelet
response to fibrinogen
Treatment :Conventional haemostatic agent and blood
transfusion.
www.indiandentalacademy.com
THROMBOCYTHEMIA
(THROMBOCYTOSIS)
•It is characterized by increase in number of platelets.
•Types – Primary  unknown
Secondary  after injury, inflammation,
surgical procedures or parturition.
•In association with anemia, myeloid leukemia,
tuberculosis,polycythemia.
•Secondary thrombocytosis may be due to over
production of cytokines – IL-1, IL,-6, IL-11www.indiandentalacademy.com
C/F
• Bleeding tendency inspite of elevated platelet
count.
• Epistaxis and bleeding into GIT
O/M
• Spontaneous gingival bleeding
• Excessive and prolonged bleeding after dental
extraction.
L/F- Platelete count increase 14 lacs per cubic
milimeter.
• Clotting time, prothombin time, clot retraction
and tourniquet test  normal
www.indiandentalacademy.com
SUMMARY
• Etiology, clinical features & histopathological
features of thrombocytasthenia.
• Etiology, clinical features & histopathological
features of thrombocytopenic purpura
www.indiandentalacademy.com
BIBLIOGRAPHY
• Shafer’s-6th edition- Oral Pathology
• Sembulingam- Physiology
www.indiandentalacademy.com
THANK YOU!
www.indiandentalacademy.com

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Diseases of platelets 2/endodontic courses

  • 1. DISEASES INVOLVING BLOOD PLATELETS-II INDIAN DENTAL ACADEMY Leader in continuing Dental Education www.indiandentalacademy.com
  • 2. LEARNING OBJECTIVES • At the end of the lecture student should be able to • Describe etiology, clinical features & histopathological features of thrombocytasthenia • Describe etiology, clinical features & histopathological features of thrombocytopenic purpura www.indiandentalacademy.com
  • 3. • THROMBOCYTASTHENIA •It is characterized by qualitative defect in the blood platelet. •FAMILIAL THROMBASTHENIA (Glanzman thrombasthenia)-hereditary,chronic hemorrhagic disease transmitted as an autosomal recessive trait. •C/F -Excessive bleeding following minor trauma. www.indiandentalacademy.com
  • 4. • Purpuric hemorrhages of skin are common. • Epistaxis and GIT bleeding. • O/F- • Spontaneous gingival bleeding. • Palatal petechiae. • L/F-Bleeding time prolonged • Clot retraction is impaired . • Number of platelet normal. • Amount of certain membrane glycoprotein on the surface of the platelet is reduced.www.indiandentalacademy.com
  • 5. THROMBOCYTOPATHIC PURPURA •A group of rare disorders of unknown etiology in which the patients manifest a bleeding tendency due to qualitative defects in blood platelets. •Severe bleeding tendency and bruise easily even after minor trauma. •Menstrual bleeding so severe as to require blood transfusion. O/M : Gingival bleeding www.indiandentalacademy.com
  • 6. •Excessive and prolonged bleeding from dental extractions may be a serious management problem. L/F •Platelate count – Normal •Bleeding time prolonged or normal •Storage pool disease – Deficiency in nonmetabolic storage pool of the platelet adenine nucleotides. •Portsmouth syndrome: Abnormal or absent collagen induced platelet aggregation. •Bernard soulier syndrome – abnormal platelet response to fibrinogen Treatment :Conventional haemostatic agent and blood transfusion. www.indiandentalacademy.com
  • 7. THROMBOCYTHEMIA (THROMBOCYTOSIS) •It is characterized by increase in number of platelets. •Types – Primary  unknown Secondary  after injury, inflammation, surgical procedures or parturition. •In association with anemia, myeloid leukemia, tuberculosis,polycythemia. •Secondary thrombocytosis may be due to over production of cytokines – IL-1, IL,-6, IL-11www.indiandentalacademy.com
  • 8. C/F • Bleeding tendency inspite of elevated platelet count. • Epistaxis and bleeding into GIT O/M • Spontaneous gingival bleeding • Excessive and prolonged bleeding after dental extraction. L/F- Platelete count increase 14 lacs per cubic milimeter. • Clotting time, prothombin time, clot retraction and tourniquet test  normal www.indiandentalacademy.com
  • 9. SUMMARY • Etiology, clinical features & histopathological features of thrombocytasthenia. • Etiology, clinical features & histopathological features of thrombocytopenic purpura www.indiandentalacademy.com
  • 10. BIBLIOGRAPHY • Shafer’s-6th edition- Oral Pathology • Sembulingam- Physiology www.indiandentalacademy.com