Showing posts with label Oral Medicine. Show all posts
Showing posts with label Oral Medicine. Show all posts

Thursday, August 21, 2014

Best of fives for dentistry- Sjögren's syndrome mcq review

                                                           Sjögren's syndrome




What is CREST?
CREST is a form of Systemic Sclerosis (scleroderma) which is characterized by Calcinosis (calcium deposits), usually in the fingers; Raynaud's;loss of muscle control of the Esophagus, which can cause difficulty swallowing; Sclerodactyly, a tapering deformity of the bones of the fingers; and Telangiectasia, small red spots on the skin of the fingers, face, or inside of the mouth. (Also see: What is Scleroderma?, Types of Scleroderma and Systemic Symptoms)
Calcinosis            Raynaud's              Esophagus            Sclerodactyly            Telangiectasia
It takes only two of the five CREST symptoms for a diagnosis of  CREST (either "pure" or "plus") to be made. For example, a patient with Calcinosis and Raynaud's would have CREST (which for precision may also be written as CRest, but it is CREST nonetheless.)

CALCINOSIS
The systemic forms of scleroderma can cause small white calcium lumps to form under the skin on fingers or other areas of the body.
This is called calcinosis . The lumps may break through the skin and leak a chalky white liquid.
These most commonly occur on the hands, or near joints such as elbows or knees, although they may appear anywhere.

Raynaud's
Raynaud's is a vascular disorder commonly found in sclerodema. It is an extreme spasm of blood vessels in response to cold or stress. The fingers and/or toes become white and/or blue, and may become red on re-warming.

sclerodactyly
When the skin on the fingers become tight, stretched, wax-like, and hardened it is called sclerodactyly. Sclerodactyly is commonly associated with atrophy of the underlying soft tissues.

Telangiectasia are dilated superficial blood vessels

Sunday, August 17, 2014

Candidosis mcq review


ANTIFUNGAL AGENTS


ANTIFUNGAL  AGENTS

Most fungal infections in the oral cavity are due to Candida species,
most commonly Candida albicans.
Where candidosis is related to dentures, denture hygiene  instruction should be stressed. Non-metal dentures should be soaked regularly overnight in sodium hypochlorite 1% (Milton’s solution) and metal-containing dentures similarly in chlorhexidine 0.2% solution.
Nystatin and amphotericin (polyenes)
These agents attach to the fungal cell membrane and disrupt fluid and electrolyte permeability. They are not absorbed from the GI tract and hence act locally .
        Dosage regimens for nystatin and amphotericin
Nystatin
Pastilles 100 000 units
Oral suspension 100 000 units/ml
Ointment/cream 100 000 units/g
Amphotericin
Lozenges 10mg
Oral suspension 100 mg/ml
Miconazole (an imidazole)
Similar action to the polyenes. Effective against some Gram-positive
bacteria such as Staph. aureus. More effective than polyenes in angular cheilitis due to possible mixed fungal/bacterial infection.
Available as oral gel, cream and in combination with hydrocortisone.
Oral gel (25 mg/ml) 5–10 ml held over area affected (after food) or applied to fitting surface of upper denture for the treatment of denture stomatitis (chronic erythematous candidosis).
Cream (2%) Apply to angles of lips 2–3 times daily. Cream or ointment (2%) with hydrocortisone (1%) Apply to angles of lips 2–3 times daily. May be useful for clearing long-standing angular cheilitis but should not be used for longer than 10 days.
Fluconazole (a triazole)
This systemically acting agent inhibits fungal enzymes concerned
with ergosterol synthesis. It appears to have low systemic toxicity.
Form Capsules (50 mg) and oral suspension (50 mg/5 ml). Dose 50 mg daily for 7–14 days. Higher doses will be required in immune compromised patients.
Cautions Avoid in renal disease, pregnancy and lactation, children.
Side effects Nausea, diarrhea and allergic manifestations are the most serious effects.
Main interactions are with antihistamines, oral hypoglycaemic agents and warfarin.
Itraconazole is another potent triazole antifungal agent.

Sunday, February 16, 2014

A NOTE ON ANATOMY OF PAROTID GLAND

Parotid gland


The parotid gland is the largest of the salivary glands.

The parotid, a serous compound tubulo-alveolar gland, is yellowish, lobulated, and irregular in shape.

It occupies the interval between the sternomastoid muscle and the mandible.

Average Wt - 25gm (varies in weight from 14 to 28 gm)



Surface anatomy

The parotid gland lies inferior to the zygomatic arch, anteroinferior to the external acoustic meatus, anterior to the mastoid process, and posterior to the ramus of the mandible.


Relations





The parotid gland is enclosed in a sheath (parotid fascia) and is shaped roughly like an inverted pyramid, with three (or four) sides (fig A).

It has a base (from which the superficial temporal vessels and auriculotemporal nerve emerge),apex (which descends inferior and posterior to the angle of the mandible),and lateral, anterior, and posterior (or posterior and medial) surfaces.
The lateral surface is superficial and contains lymph nodes.

The anterior surface is grooved by the ramus of the mandible and masseter (fig.B), producing a medial lip (from which the maxillary artery emerges) and a lateral lip, under cover of which the parotid duct, branches of the facial nerve, and the transverse facial artery emerge (see fig. C).

The posterior surface is grooved by  the mastoid process and the sternomastoid and digastric muscles and  more medially by the styloid process and its attached muscles.

Medially, the superior part of the gland is pierced by the facial nerve and the inferior part by the external carotid artery.

The following structures lie partly within the parotid gland, from superficial to deep:


1. The facial nerve forms the parotid plexus within the gland and separates the glandular tissue partially into superficial and deep layers ("lobes"). In surgical excision of the parotid gland (e.g., for a tumor), damage to the facial nerve is a possibility.

2. The superficial temporal and maxillary veins unite in the gland to form the retromandibular vein, which contributes in a variable manner to the formation of the external jugular vein (see fig. D).

3. The external carotid artery divides within the parotid gland into the superficial temporal and maxillary arteries.


Parotid duct

The parotid duct is about 7 cm long

The parotid duct, emerging under cover of the lateral surface, runs anteriorward on the masseter and turns medially to pierce the buccinator.

The branching of the duct can be examined radiographically after injection of a radio-opaque medium. 

The parotid duct, which is palpable, opens into the oral cavity on the parotid papilla opposite the upper second molar tooth.

Innervation of parotid gland ( fig. E)




Preganglionic parasympathetic secretomotor fibers (from the glossopharyngeal, tympanic, and lesser petrosal nerves) synapse in the otic ganglion.

Postganglionic fibers travel with the auriculotemporal nerve and so reach the gland.

Cranial nerves VII and IX communicate, so that secretory fibers to each of the three major salivary glands may travel in both the facial and glossopharyngeal nerves.

The sympathetic supply to the salivary glands includes vasomotor fibers.

Blood supply


The arteries supplying the parotid gland are derived from the external carotid, and from the branches given off by that vessel in or near its substance. The veins empty themselves into the external jugular, through some of its tributaries.

Lymphatics


The lymphatics end in the superficial and deep cervical lymph glands, passing in their course through two or three glands, placed on the surface and in the substance of the parotid.




Sunday, November 13, 2011

A Note on Bone Swellings in Jaw Bones


Bone Swellings

Bone swellings are lesions that characteristically present as asymptomatic hard lumps, covered by normal epithelium. Developmental disorders, benign and malignant tumors are included in this group of lesions.
  •        Torus mandibularis
  •        Torus palatinus
  •        Multiple exostoses
  •        Osteoma
  •        Osteosarcoma
  •         Chondrosarcoma
  •         Burkitt lymphoma
  •         Multiple myeloma
  •         Paget disease
  •       Odontogenic tumors

Torus Mandibularis
Definition and etiology Torus mandibularis is a developmental malformation of unknown etiology.
Clinical features It presents as an asymptomatic bony swelling, covered by normal mucosa. The lesion displays slow growth during the second and third decades of life. Characteristically, the lesions appear bilaterally on the lingual surface of the mandible, usually in the area adjacent to the bicuspids. The diagnosis is based on clinical criteria.
Torus mandibularis
Treatment Unnecessary unless full denture construction is required.

Torus Palatinus
Torus palatinus at the midline of the hard palate
Definition and etiology Torus palatinus is a developmental malformation of unknown etiology.
Clinical features It presents as a slow-growing, nodular, lobular or spindled, asymptomatic bony swelling covered by normal mucosa. Characteristically, the lesion appears along the midline of the hard palate.It occurs more often in women, and usually appears during the third decade of life. The diagnosis is based on the clinical findings.
Treatment Unnecessary unless full denture construction is required.

Multiple Exostoses
Multiple exostoses may occur on the buccal surface of the maxilla, and rarely on the mandible. Clinically, the lesions appear as multiple asymptomatic bony swellings. The diagnosis is based on the clinical findings.
Multiple exostoses on the maxilla.
Treatment Unnecessary unless full denture preparation is required.

Osteoma
Definition Osteoma is a benign neoplasm that consists of mature compact or cancellous bone.
Etiology Unknown.
Clinical features
It presents as an asymptomatic, slow-growing bony swelling of the jaws. The size ranges from a few millimeters to several centimeters. Multiple jaw osteomas are a common feature of Gardner syndrome.
Gardner syndrome: osteoma of the mandible.
Laboratory tests Histopathological examination, radiography.
Differential diagnosis Exostoses, osteosarcoma.
Treatment Surgical excision.

Osteosarcoma
Definition Osteosarcoma is the most common primary malignant neoplasm of bone.
Etiology Unknown.
Clinical features
The jaws are affected in 6–7% of cases, and usually during the third decade of life. Both jaws are affected equally and it is more common in men. Clinically, the lesion presents as a rapidly growing hard swelling that progressively produces facial deformity. Pain, paresthesia, tooth loosening, and nasal obstruction may also occur.
Osteosarcoma of the upper jaw, presenting as a hard swelling.
Laboratory tests Histopathological examination, radiography, CT scans.
Differential diagnosis Chondrosarcoma, Ewing sarcoma, metastatic tumors, odontogenic tumors and cysts, giant-cell tumor.
Treatment Surgical excision and supplementary radiotherapy and chemotherapy.

Chondrosarcoma
Chondrosarcoma  is more common in men than in women, between 30 and 60 years of age. Clinically, it appears as a painless hard swelling that progressively enlarges, causing extensive bone destruction with pain and loosening of the teeth.

Burkitt Lymphoma
Definition Burkitt lymphoma is a high-grade malignant B-lymphocyte lymphoma.
Etiology Epstein–Barr virus is closely associated.
Clinical features
The malignancy is prevalent in central Africa (the endemic form), and usually affects children 2–12 years of age. Cases have also been observed in other countries (the nonendemic form), and recently in patients with AIDS. The jaws are the most common site of lymphoma (60–70%). Clinically, it presents as a rapidly growing hard swelling that causes bone destruction, tooth loss, and facial deformity.Pain, paresthesia and large ulcerating or nonulcerating masses may also be seen.
Burkitt lymphoma, facial deformity.
Burkitt lymphoma, gingival mass
Burkitt lymphoma on the gingiva in a young patient with AIDS
Laboratory tests Histopathological examination, radiography.
Differential diagnosis Central giant-cell granuloma, ossifying fibroma, other non-Hodgkin lymphomas, and odontogenic tumors.
Treatment Chemotherapy, radiotherapy.

Multiple Myeloma
Definition Multiplemyeloma is a relatively rare malignant plasma-cell disorder.
Etiology Unknown.
Clinical features The malignancy is more common in men over 50 years of age, and the jaws are affected in about 30% of cases. Clinically, it presents with bone swelling, tooth mobility, pain, and paresthesia. A painless soft swelling, usually on the alveolar mucosa and gingiva, may develop as part of the overall disease spectrum.
Multiple myeloma, swelling on the gingiva
Laboratory tests Bone-marrow biopsy, radiography, serum and urine protein electrophoresis.
Differential diagnosis Plasmacytoma, non-Hodgkin lymphoma, Ewing sarcoma, leukemia, Langerhans cell histiocytosis.
Treatment Chemotherapy, radiotherapy.

Paget Disease
Definition Paget disease, or osteitis deformans, is a chronic, relatively common disorder characterized by uncoordinated bone resorption and deposition.
Etiology Unknown.
Clinical features Clinically, the signs and symptoms develop gradually and are characterized by bone pain, headache, deafness, visual disorders, dizziness, and progressive bone enlargement. Progressive expansion of the maxilla and the mandible lead to symmetrical thickening of the alveolar ridges.
Paget disease, enlarged maxilla
Edentulous patients may complain that their dentures do not fit due to alveolar enlargement.
Paget disease, alveolar enlargement
Delayed wound healing, bleeding, and osteomyelitis after tooth extraction may occur. The maxilla is more frequently affected than the mandible. Malesare more often affected than females. Two major forms of the disease are recognized: (a) the monostotic, and (b) the polyostotic. The clinical diagnosis should be confirmed by a histopathological and radiographic examination. Elevations of serum alkaline phosphatase and urinary hydroxyproline levels are common findings.
Differential diagnosis Fibrous dysplasia, osteosarcoma, multiple exostoses, fibro-osseous lesions.
Treatment Most cases require no treatment. Calcitonin and bisphosphonates may slow the pathological process.

Odontogenic Tumors
Definition Odontogenic tumors are a group of lesions that originate from odontogenic epithelium and ectomesenchyme.
Etiology Unknown. Some are neoplasms and others hamartomas.
Classification On the basis of the tissue of origin, three major varieties are recognized: (a) tumors of odontogenic epithelium, (b) tumors of odontogenic ectomesenchyme, and (c) mixedod ontogenic tumors.
Clinical features Most odontogenic tumors are usually asymptomatic for long time and are discovered only during a routine radiographic examination. However, with time they may form a usually painless slow-growing swelling or expansion of the mandible or the maxilla.
Odontogenic myxoma, expansion of the retromolar area
Extraosseous calcifying epithelial odontogenic tumor presenting as a gingival mass
The clinical signs and symptoms are not diagnostic and the final diagnosis should be made by radiographic and histopathological examinations.
Differential diagnosis Different varieties of odontogenic tumors, odontogenic cysts, osteosarcomas, chondrosarcomas, multiplemyeloma.
Treatment Surgical excision.

Friday, October 28, 2011

Oral manifestations of systemic diseases


GIT diseases
Crohn disease
diffuse labial, gingival or mucosal swelling
cobblestoning of buccal mucosa and gingiva
aphtous ulcers
mucosal tags
angular cheilitis
oral granulomas
Crohn disease
Ulcerative colitis
oral signs are present in periods of exacerbation of disease
aphtous ulceration or superficial hemorrhagic ulcers
angular stomatitis
pyostomatitis vegetans, pyostomatitis gangrenosum
pyostomatitis vegetans
Gastroesophageal reflux
reduction of the pH of the oral cavity below 5,5 – enamel damage
damage of the dentin – higher sensitivity (to temperature..), caries
enamel damage and
damage of the dentin
Chronic liver diseases
jaundice
petechiae or gingival bleeding (hemostasis disorder)

Hematologic diseases
Anemias
folate and vit. B12 deficiency or iron deficiency
glossitis
red colour
atrophic papilae
recurrent aphthae
candidal infection
angular stomatitis
oral pain

Leukemia
gingival hypertrophy
petechiae
mucosal ulcers
                  hemorrhage
            Treatment of leukemia
reactivation of herpes simplex virus – oral mucosistis
gingival hypertrophy in leukemia
Summary of oral manifestations of gastrointestinal and hematologic diseases
Labial swelling
Crohn's disease

Glossitis
   Crohn's disease
   Iron-deficiency anemia
   Pernicious anemia
   Ulcerative colitis

Erosion of enamel and dentin
Anorexia nervosa/bulimia
        Gastroesophageal reflux
Ulcerations and erosions
   Crohn's disease
   Iron-deficiency anemia
   Pernicious anemia
   Pyostomatitis vegetans
   Ulcerative colitis

Gingivitis
Anorexia nervosa/bullimia
Crohn's disease
Scurvy

Hemorrhage
Pyostomatitis vegetans
Scurvy
        Ulcerative colitis
Angular cheilitis
Iron-deficiency anemia

Aphthous ulcers
Crohn's disease
Pernicious anemia
Ulcerative colitis

Intraoral burning
   Iron-deficiency anemia
   Pernicious anemia

Candidiasis
   Crohn's disease (steriod therapy)
   Iron-deficiency anemia
   Pyostomatitis vegetans (steriod therapy)
   Ulcerative colitis (steroid therapy


Connective-tissue diseases
Sjögren syndrome
autoimmune disease
men : women - 1 : 9
50 years and older
     Main signs
sicca syndrome
keratoconjuctivitis sicca
xerostomia
     Oral signs
decrease in saliva
xerostomia
dry, red, wrinkled mucosa
difficulty in swalloving and eating
disturbance in taste and speech
increased dental caries
infections
atrophy of the papilae
candidiasis

Kawasaki disease
vasculitis of medium and large arteries
    Oral signs
swelling of papilae on the surface of the tongue (strawbery tongue)
intense erythema of the mucosal surfaces
cracked, cherry red, swolen and hemorrhagic lips

Scleroderma
diffuse sclerosis of the skin, GIT, heart muscle, lungs, kidney
    Oral signs
pursed lips – dificult to open the mouth
esophageal sclerosis ® gastroesophageal reflux – damage of enamel
pale, rigid mucosa
teleangiectasias
decreased mobility of tongue
salivary hypofunction

Lupus erythematosus
autoimmune disease
        Oral signs
ulcerations
similar tooral lesions of lichen planus – painful
petechiae
damage of salivary glands - xerostomia

Pulmonary diseases
Cystic fibrosis
    Oral signs
disorder of salivary glands
swelling lips
gingivitis
dryness

Sarcoidosis
    Oral signs
multiple, nodular, painles ulcerations of the gingiva, bucal mucosa, labial mucosa and palate
tumorlike swelling  of salivary glans
swelling of the tongue
xerostomia
                      facial nerve palsy
Cutaneous diseases
Psoriasis
    Oral signs
fissured tongue
small white papules
red and white plagues
bright red patches

Acantosis nigricans
hyperpigmentation, papillomatosis
    Oral signs
gingival hyperplasia
gingiva, tongue, lips – papilomas

Endocrine diseases
Diabetes mellitus
    Oral signs
xerostomia caused decreased salivation and increased glucosa level in saliva
gingivitis
oral infections
candidiasis
higher incidence of caries
bilateral enlargement of parotid glands
altered taste
burning mouth syndrome

Hypoparathyroidism
    Oral signs
candidiasis
upper lip twitching

Hyperparathyroidism
    Oral signs
loss of the lamina dura surrounding the roots of the teeth
decrease of trabecular density
osseous lesions „brown tumor“

Cushing´s syndrome
    Oral signs
fatty tissue deposition – „moon face“
osteoporosis ® pathological fractures of the mandible, maxilla or alveolar bone
delayed healing of fractures and also sof tissue injuries
moon face
Addison´s disease
Oral signs
„bronzing“ hyperpigmentation of the skin
oral mucosal melanosis – buccal mucosa, tongue
hyperpigmentation
Renal diseases
Uremic stomatitis
rare
in undiagnosed and untreated chronic renal failure
irritation and chemical injury of mucosa by ammonia or ammonium compounds
              Signs
painful plagues and crusts – bucal mucosa, the floor or dosrum of the tongue, floor of the mouth
Type I
generalized or localized erythema
exudate
pain, burning, xerostomia, halitosis, gingival bleeding, candidiosis
Type II
ulceration
secondary infection
anemia
painful plagues and crusts – bucal mucosa, the floor or dosrum of the tongue, floor of the mouth

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