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14 Cards in this Set

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Acquired Neutropenia: Hematological Disorders 
- Low levels of circulating neutrophils
-NEUTROPENIA = <1500mm3
- Drug induced, Chemotherapy, Infections, Autoimmune disorders,Genetic
- Systemic: onset usually accompanied by fever, malaise, general ...

Acquired Neutropenia: Hematological Disorders


- Low levels of circulating neutrophils


-NEUTROPENIA = <1500mm3


- Drug induced, Chemotherapy, Infections, Autoimmune disorders,Genetic


- Systemic: onset usually accompanied by fever, malaise, general weakness & sore throat


- Oral: ulceration of oral cavity, oropharynx & throat Isolated necrotic patches in the mucosaAbsence of inflammation due to low numbers of granulocytes


- Hemorrhage, necrosis, increased salivation & fetid odor Occurrence of rapidly destructive periodontitis

Leukemia (Acute and Subacute): Hematological Disorders


-abnormal numbers and forms of immature white blood cells in the circulating blood


- widespread infiltrates in the liver, spleen, lymph nodes and other body sites


- Gingiva a peculiar bluish red, spongelike, friable and bleeds persistently on the slightest provocation


- Gingival hemorrhage due to thrombocytopenia


- In acute leukemia = acute necrotizing ulcerative gingivitis

Anemia: Hematological Disorders


- gingival pallor


- tongue (red, shiny and smooth dorsal surface)


- atrophy of papillae

Thrombocytopenia: Hematological Disorders


- decrease platelets


- spontaneous bleeding, spontaneous gingival haemorrhage


- mucosal surface purpura (petechiae, ecchymoses, vesicles and hematomas)

Down Syndrome: Genetic Disorders


- Increased numbers of Prevotella intermedia


- deep pockets, substantial plaque & moderate gingivitis, usually generalized, more severe in lower anteriors, marked recession, progress rapid, acute necrotizing lesions frequently found


- Explanation of Prevalence:


1.) Reduced resistance to infections due to poor circulation


2.) Defect in T-Cell maturation and in PMN chemotaxis

Papillon-Lefevre Syndrome: Genetic Disorders
- Hyperkeratotic skin lesions 
- Severe destruction of periodontium 
-  usually occur before age 4 
- Hyperkeratosis of palms, soles, knees and elbows
-Signs
> Primary teeth lost by 5 or 6 yrs 
> Perman...

Papillon-Lefevre Syndrome: Genetic Disorders


- Hyperkeratotic skin lesions


- Severe destruction of periodontium


- usually occur before age 4


- Hyperkeratosis of palms, soles, knees and elbows


-Signs


> Primary teeth lost by 5 or 6 yrs


> Permanent teeth lost by 15 yrs


> Extremely thin cementum


> No significant alterations in peripheral blood lymphocytes & PMN’s


> Predominantly plasma cell infiltrate


> Considerable osteoclastic activity


> Lack of osteoblastic activity


> Bacterial microbiota similar to adult periodontitis

Diabetes: Not Otherwise Specified


- both IDDM & NIDDM = risk factors


- Increased susceptibility to infection and host response have been identified as likely factors


- Signs


> Severe Gingival Inflammation


> Acute Gingival or Periodontal Abscesses


> Rapidly Advancing Periodontal Disease


> Increased attachment Loss and bone Loss


- Those who are well-controlled and who maintain excellent oral hygiene are at no greater risk than non-diabetics


- Well-controlled diabetics respond as well to periodontal therapy as non-diabetics


- Therapy improves not only their periodontal condition but may also improve metabolic control of the disease

Agranulocytosis: Hematological Disorders

- severe form of neutropenia


- low levels of circulating neutrophils(< 500 mm3)


- generalized painful stomatitis


- spontaneous bleeding, and necrotic tissues

Lazy Leucocyte Syndrome: Hematological Disorders

- rare


- qualitative and quantitative neutrophil defects


- recurrent infectionsoral manifestations (gingivitis, oral ulcerations, rapidly progressive bone loss).

Leukocyte Adhesion Deficiency: Genetic Disorders

- Deficiency in cell surface integrins


- Onset: during or immediately following eruption of primary teeth


- Signs


> Extreme acute inflammation


> Proliferation of gingival tissues


> Rapid bone destruction


> Profound defects in neutrophils & monocytes > Absence of neutrophils in gingival tissues


> Frequent respiratory tract infections & sometimes otitis media (inflammation of ear)


> All primary teeth affected but permanent teeth variably affected

Chediak-Higashi Syndrome: Genetic Disorders

- Affects organelle production in most cells


- Mainly affects melanocytes, platelets & phagocytes


- Functional neutrophil defects include: decreased chemotaxis, degranulation, microbiocidal activity


- Manifested by recurrent bacterial infections


- Also produces partial albanism & mild bleeding disorders


- Includes rapidly destructive periodontitis and oral ulcerations

Hypophosphatasia: Genetic Disorders

- characteristics: rickets, poor cranial bone formation, craniostenosis & premature loss of primary teeth (particularly incisors)


- Low serum alkaline phosphatase


-Teeth lost with no clinical evidence of inflammation


- Low cementum formation



HIV: Not Otherwise Specified


- 5% Of HIV patients develop NUP


- PMN activity in HIV clients is hindered


- This allows Candida albicans to colonize subgingivally increasing the risk for periodontitis


- Results: T-cell counts of less than 200, combined with age >35 = increased the risk for > 3mm clinical attachment loss by more than 600%


- Signs:


> Linear Gingival erythema


> NUP


> Advanced Periodontitis with severe bone loss > Candidiasis


> Large Intraoral Herpetic Lesions


> Hairy Leukoplakia


> Kaposi’s Sarcoma

Familial and Cyclic Neutropenia: Genetic Disorders

- Low levels of circulating neutrophils


- <1500mm3


- caused by genetics