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ORAL MANIFESTATIONS
OF BLOOD DISORDERS
Arsalan Wahid Malik
‫يم‬ ِ‫ح‬َّ‫ر‬‫ال‬ ِ‫من‬ْ‫ح‬َّ‫ر‬‫ال‬ ِ‫هللا‬ ِ‫م‬ْ‫س‬ِ‫ب‬
DISORDERS OF RBC
Iron-deficiency Anemia
Megaloblastic Anemia
Pernicious Anemia
Aplastic Anemia
Haemolytic Anemia
Sickle-cell Anemia
DISORDERS OF WBC
Leukaemia
Leukopenia
ANEMIA
 Level of Hb in blood is low
 Decreased number of red cells
1.Due to blood loss
 Acute
 Chronic
2.Due to inadequate production of cells
 Iron deficiency anemia
 Megaloblastic anemia
 Pernicious anemia
 Aplastic anemia
3.Due to excessive red cells destruction
 Hemolytic anemia
 Sickle cell anemia
Microcytosis:
 Average size of red cell is reduced
 e.g. Iron-deficiency anemia
Hypochromia:
 When there is less than the normal amount of Hb in cells
 e.g. iron deficiency anemia
Macrocytosis:
 Average size of cell is greater than normal
 e.g. megaloblastic anemia
Anisocytosis:
 Inequality in size of cells
 e.g. megaloblastic anemia
IRON-DEFICIENCY ANEMIA:
Inadequate intake of iron
Excessive blood loss
Diagnosis:
 Hb level is low
 Microcytic erythrocytes
 Hypochromic erythrocytes
 The number of red cells per unit volume does not
vary
MEGALOBLASTIC ANEMIA:
Vitamin B12 deficiency
Folic acid deficiency
Macrocytosis
Anisocytosis
PERNICIOUS ANEMIA:
 Autoimmune condition causing atrophy of gastric
mucosa with failure to secrete intrinsic factor due to
anti-intrinsic factor antibody
Diagnosis:
 Antibodies to intrinsic factor can be detected in
blood
APLASTIC ANEMIA:
 Disease of stem cell producing hypoplasia of bone
marrow elements
 Failure of production of all bone marrow cells
(pancytopenia)
 Suppression of bone marrow
Etiology:
 Autoimmune disease
 Cytotoxic drugs/chemotherapeutic agents
 Chloramphenicol/sulphonamides
 Benzene/toluene
 Radiation
HAEMOLYTIC ANEMIA:
 Excessive destruction of RBC
 Shortened life span and require more rapid
replacement
 Increase in unconjucated bilirubin in blood with mild
jaundice
Cause:
Autoimmune
Infections
Abnormal Hb and erythrocytes
SICKLE-CELL ANEMIA:
 Red cell contain abnormal HbS
 When HbS is deoxygenated it causes distortion and
produces a sickle shaped cells
Clinical Features:
 Jaundice
 Growth retardation
 Skeletal abnormalities
 Bone pain
Oral Manifestations:
 Delayed eruption
 Hypoplasia of teeth
 Radiolucencies in jaw
 Osteomyelitis
CLINICAL FEATURES OF ANEMIA
Pallor
Fatigue/weakness
Breathlessness
Tachycardia
Palpitations
Jaundice
Increased susceptibility to infections
Purpura
Constipation/diarrhea
ORAL MANIFESTATION OF ANEMIA:
 Generalized stomatitis
 Mucosal pallor
 Atrophy of filiform papillae of tongue
 Glossitis
 Disturbed taste sensations
 Angular cheilitis
 Gingivitis
 RAS
 Susceptibility to infections
 Candidial infections
 Plummer-Vinson syndrome
Plummer-Vinson syndrome
Iron-deficiency anemia
Glossitis and stomatitis
Angular cheilitis
 Pharyngo-esophageal ulcers
 Dysphagia
 Cracking/splitting of nails
Tongue is red, smooth, depapillated with angular cheilitis due to Candida
infections
Iron-deficiency Anemia
Bilateral angular cheilitis with stomatitis
LEUKAEMIA
 Overproduction of white cells which suppresses
other cells of marrow
Acute leukemia
 Immature cells
 Sudden onset
 Affects children
3-5 yrs of age
Chronic leukemia
 Abnormal cells
 Slow progressing
disease of adults
 Asymptomatic
ETIOLOGY OF LEUKEMIA:
 Radiation
 Viruses
 Chemical agents
 Drugs
 Phenylbutazone
 Chloramphenicol
 Cotrimoxazole
 Carbamazepine
 Thiouracil
 Cytotoxic drugs
SIGNS/SYMPTOMS
 Splenomegaly
 Hepatomegaly
 Lymphadenopathy
 Anemia
 Infections
 Purpura
 Fever
 Weight loss
 Bone pains
 Weakness
 Fever
 Weight loss
 Anorexia
 Bleeding
 Infections
 Anemia
 Thrombocytopenia
 Splenomegaly
 Hepatomegaly
 Lymphadenopathy
Acute Leukemia Chronic Leukemia
ORAL MANIFESTATIONS:
 Gingival swelling
 Gingival bleeding
 Mucosal swelling with loosening and exfoliation of
teeth
 Mucosal ulcerations
 Oral infections-candidal
 Leukemia deposits
 Purpura and petechiae
 Anemia
 Cervical lymph node enlargement
 Leukemic infiltration of salivary and lacrimal glands
leukemia
Ulcerated tumor mass formed by emigration
of leukaemic cells
Leukemia-gingiva are swollen and purplish with ulceration along the
palatal aspect of anterior teeth due to increased susceptibility to
infections
LEUKOPENIA:
Deficiency of white cells <than 5000/L
Cause:
 Leukemia
 Aplastic anemia
 Autoimmune disorders
 HIV and EBV infections
 Drugs
 Carbamazepine
 Phenylbutazone
 Chloramphenicol
 Sulphonamides
 Cotrimoxazole
 Thiouracil
 Cytotoxic drugs
CLINICAL FEATURES:
 Fever
 Weakness
 Sore throat
 Increased susceptibility to infections of oral cavity
 Ulcerations of gingiva, mucosa and pharynx
Management:
 Stop the drug
 Antibiotics
 Blood transfusion if necessary
 Improve oral hygiene
 Avoid extractions

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Oral manifestations of blood disorders

  • 1. ORAL MANIFESTATIONS OF BLOOD DISORDERS Arsalan Wahid Malik ‫يم‬ ِ‫ح‬َّ‫ر‬‫ال‬ ِ‫من‬ْ‫ح‬َّ‫ر‬‫ال‬ ِ‫هللا‬ ِ‫م‬ْ‫س‬ِ‫ب‬
  • 2. DISORDERS OF RBC Iron-deficiency Anemia Megaloblastic Anemia Pernicious Anemia Aplastic Anemia Haemolytic Anemia Sickle-cell Anemia
  • 4. ANEMIA  Level of Hb in blood is low  Decreased number of red cells 1.Due to blood loss  Acute  Chronic 2.Due to inadequate production of cells  Iron deficiency anemia  Megaloblastic anemia  Pernicious anemia  Aplastic anemia 3.Due to excessive red cells destruction  Hemolytic anemia  Sickle cell anemia
  • 5. Microcytosis:  Average size of red cell is reduced  e.g. Iron-deficiency anemia Hypochromia:  When there is less than the normal amount of Hb in cells  e.g. iron deficiency anemia Macrocytosis:  Average size of cell is greater than normal  e.g. megaloblastic anemia Anisocytosis:  Inequality in size of cells  e.g. megaloblastic anemia
  • 6. IRON-DEFICIENCY ANEMIA: Inadequate intake of iron Excessive blood loss Diagnosis:  Hb level is low  Microcytic erythrocytes  Hypochromic erythrocytes  The number of red cells per unit volume does not vary
  • 7. MEGALOBLASTIC ANEMIA: Vitamin B12 deficiency Folic acid deficiency Macrocytosis Anisocytosis
  • 8. PERNICIOUS ANEMIA:  Autoimmune condition causing atrophy of gastric mucosa with failure to secrete intrinsic factor due to anti-intrinsic factor antibody Diagnosis:  Antibodies to intrinsic factor can be detected in blood
  • 9. APLASTIC ANEMIA:  Disease of stem cell producing hypoplasia of bone marrow elements  Failure of production of all bone marrow cells (pancytopenia)  Suppression of bone marrow Etiology:  Autoimmune disease  Cytotoxic drugs/chemotherapeutic agents  Chloramphenicol/sulphonamides  Benzene/toluene  Radiation
  • 10. HAEMOLYTIC ANEMIA:  Excessive destruction of RBC  Shortened life span and require more rapid replacement  Increase in unconjucated bilirubin in blood with mild jaundice Cause: Autoimmune Infections Abnormal Hb and erythrocytes
  • 11. SICKLE-CELL ANEMIA:  Red cell contain abnormal HbS  When HbS is deoxygenated it causes distortion and produces a sickle shaped cells Clinical Features:  Jaundice  Growth retardation  Skeletal abnormalities  Bone pain Oral Manifestations:  Delayed eruption  Hypoplasia of teeth  Radiolucencies in jaw  Osteomyelitis
  • 12. CLINICAL FEATURES OF ANEMIA Pallor Fatigue/weakness Breathlessness Tachycardia Palpitations Jaundice Increased susceptibility to infections Purpura Constipation/diarrhea
  • 13. ORAL MANIFESTATION OF ANEMIA:  Generalized stomatitis  Mucosal pallor  Atrophy of filiform papillae of tongue  Glossitis  Disturbed taste sensations  Angular cheilitis  Gingivitis  RAS  Susceptibility to infections  Candidial infections  Plummer-Vinson syndrome
  • 14. Plummer-Vinson syndrome Iron-deficiency anemia Glossitis and stomatitis Angular cheilitis  Pharyngo-esophageal ulcers  Dysphagia  Cracking/splitting of nails
  • 15. Tongue is red, smooth, depapillated with angular cheilitis due to Candida infections Iron-deficiency Anemia
  • 16. Bilateral angular cheilitis with stomatitis
  • 17. LEUKAEMIA  Overproduction of white cells which suppresses other cells of marrow Acute leukemia  Immature cells  Sudden onset  Affects children 3-5 yrs of age Chronic leukemia  Abnormal cells  Slow progressing disease of adults  Asymptomatic
  • 18. ETIOLOGY OF LEUKEMIA:  Radiation  Viruses  Chemical agents  Drugs  Phenylbutazone  Chloramphenicol  Cotrimoxazole  Carbamazepine  Thiouracil  Cytotoxic drugs
  • 19. SIGNS/SYMPTOMS  Splenomegaly  Hepatomegaly  Lymphadenopathy  Anemia  Infections  Purpura  Fever  Weight loss  Bone pains  Weakness  Fever  Weight loss  Anorexia  Bleeding  Infections  Anemia  Thrombocytopenia  Splenomegaly  Hepatomegaly  Lymphadenopathy Acute Leukemia Chronic Leukemia
  • 20. ORAL MANIFESTATIONS:  Gingival swelling  Gingival bleeding  Mucosal swelling with loosening and exfoliation of teeth  Mucosal ulcerations  Oral infections-candidal  Leukemia deposits  Purpura and petechiae  Anemia  Cervical lymph node enlargement  Leukemic infiltration of salivary and lacrimal glands
  • 21. leukemia Ulcerated tumor mass formed by emigration of leukaemic cells
  • 22. Leukemia-gingiva are swollen and purplish with ulceration along the palatal aspect of anterior teeth due to increased susceptibility to infections
  • 23. LEUKOPENIA: Deficiency of white cells <than 5000/L Cause:  Leukemia  Aplastic anemia  Autoimmune disorders  HIV and EBV infections  Drugs  Carbamazepine  Phenylbutazone  Chloramphenicol  Sulphonamides  Cotrimoxazole  Thiouracil  Cytotoxic drugs
  • 24. CLINICAL FEATURES:  Fever  Weakness  Sore throat  Increased susceptibility to infections of oral cavity  Ulcerations of gingiva, mucosa and pharynx Management:  Stop the drug  Antibiotics  Blood transfusion if necessary  Improve oral hygiene  Avoid extractions