Senin, 31 Oktober 2011

Behçet’s disease-Short note

Behçet’s disease
  • Idiopathic multisystem disease 
  • More common in men
  • Occurs in 3rd - 4th decade
  • Highest incidence in Mediterranean region and Japan
  • Associated with HLA-B5

: Unknown
Various bacteria and viruses suggested
No good evidence to suggest any of them
Perpetuated by autoimmune response and CD4 + T-cells
Tumour necrosis factor (TNF) thought to be important

Oral aphthous ulceration – 100%

Genital ulceration – 90%

Skin lesions – 80%
Erythema Nodosum
  • Acneiform
  • Uveitis 70% (inflam. of iris, ciliary body or choroid)

CNS involvement – strokes, fits

Major vessels eg superior Vena cava obstruction
Increased skin response to trauma eg blood taking

Ocular Features

Acute iritis
  • Pain, redness & ¯VA
  • Flare (PTN exudation)
  • Inflammatory cells in anterior chamber
  • KPs (Inflammatory cells at posterior surface of cornea)
Recurrent hypopyon
  • (Fluid level of WBC)
  • The red or white eye

Marked inflammation of the eye
Retinal vasculitis and haemorrhage (inflam. of retinal vessels)
Occlusive periphlebitis (venous sheathing &  occlusion)
Retinal microinfarcts
Very damaging to vision: retinal damage and optic nerve atrophy
Cataract or glaucoma


  • Systemic Steroids
  • Systemic immunosuppressive agents
  • Interferon-alpha may have immunodulating effects
  • Anti-TNF monoclonal antibodies may be of help

Mucocele, Ranula and Dermoid cyst-Short note

Mucocele of lower lip

Mucocele of Tongue

Definition Mucoceles, or mucous cysts, are a common phenomenon or lesion of the oral mucosa, originating from minor salivary glands and their ducts.

Etiology Local minor trauma and duct rupture or ductal obstruction, probably due to a mucous plug.

Clinical features Two main types of mucocele are recognized, according to their pathogenesis: extravasation mucocele (common), which results from duct rupture due to trauma and spillage of mucin into the surrounding soft tissues; and mucous retention cyst (uncommon), which usually results fromductal dilation due to ductal obstruction. 

Clinically, mucocele presents as a painless, dome-shaped, solitary, bluish or translucent, fluctuant swelling that ranges in size from a few millimeters to several centimeters in diameter. A common finding is that the cyst partially empties and then re-forms due to the accumulation of new fluid. The lower lip is the most common site of involvement, usually laterally, at the level of the bicuspids. Less common sites are the buccal mucosa, tongue, floor of the mouth, and soft palate. Extravasation mucoceles display a peak incidence during the second and third decades, while the mucous retention types are more common in older age groups.

Laboratory tests Histopathological examination.

Differential diagnosis Lymphangioma, hemangioma, lipoma, mucoepidermoid carcinoma, Sjögren syndrome, lymphoepithelial cyst.

Treatment Surgical excision or cryosurgery.


Definition Ranula is a formof mucocele that occurs exclusively on the floor of the mouth.

Etiology Trauma or ductal obstruction.

Clinical features It presents as a smooth, fluctuant, painless swelling on the floor of the mouth, lateral to the midline. The color ranges fromnorm al to a translucent bluish, and the size is usually in the range of 1–3 cm, or larger. The diagnosis is usually based on clinical  criteria.

Laboratory tests Histopathological examination.

Differential diagnosis Dermoid cyst, abscess, hemangioma, lymphangioma, lymphoepithelial cyst.

Treatment Surgical removal or marsupialization.

Dermoid Cyst
Dermoid cyst

Definition and etiology Dermoid cyst is an uncommon developmental cystic lesion arising from embryonic epithelial remnants.

Clinical features It presents as a slow-growing, painless swelling with a normal or yellowish-red color and a characteristic soft dough like consistency on palpation. The size varies from a few millimeters to 10 cm in diameter, and the lesion usually occurs in the midline of the floor of the mouth. If the cyst is located above the geniohyoid muscle, it can displace the tongue upward and create difficulty in mastication, speech, and swallowing. When the cyst occurs below the geniohyoid muscle, it may protrude submentally. Rarely, dermoid or epidermoid cysts may develop in the lips. The cyst frequently appears in early adulthood.

Laboratory tests Histopathological examination.

Differential diagnosis Ranula, abscess, lymphoepithelial cyst, cystic hygroma.

Treatment Surgical removal.

Jumat, 28 Oktober 2011

Examination of Eye-Video

Systematic way of Examining the Eye-Video
  • Brief introductionBrief introduction
  • USE the alcohol cleansing gel BEFORE you touch the patient
  • Ask ––‘‘May I examine you?’’
  • Ask ––‘‘Is your ear/nose/neck tender?’

Neck Examination Video

Systematic way of Examining the of Neck-Video

  • Brief introductionBrief introduction
  • USE the alcohol cleansing gel BEFORE you touch the patientyou patient
  • Ask ––‘‘May I examine you?you?’’
  • Ask ––‘‘Is your ear/nose/neck tender?tender?’

Regeneration healing (repair)-General Pathology Lecture note

Objectives of this Post
  • Review the normal physiology and concepts of cell proliferation, cell growth, cell “cycle”, and cell differentiation
  • Understand the basic factors of tissue regeneration
  • Understand the relationships between cells and their extracellular matrix (eECM)
  • Understand the roles of the major players of healing---angiogenesis, growth factors (GFS), and fibrosis
  • Differentiate 1st & 2nd intention healing
Regeneration: growth of cells to replace lost tissues
Healing: a reparative tissue response to a wound, inflammation or necrosis, often leads to fibrosis 
Granulation tissue 
“Organizing” inflamation

  • Replacement of lost structures
  • Is dependent on the type of normal turnover the original tissue has
  • Can be differentiated from “compensatory” growth

Healing (repair)
  • Needs a wound, inflammatory process, or necrosis
  • Many disease appearances anatomically are the result of “healing” such as atherosclerosis
  • Often ends with a scar
  • Fibrosis, as one of the 3 possible outcomes of inflammation, follows “healing”
  • Requires a connective tissue “scaffold”
  • Fibrosis occurs in proportion to the damage of the ECM
Cell population fates
  • Hormonal, especially steroid hormones
  • Eg., EPO, CSF
  • Unidirectional, gain and loss

*One of the most key concepts in neoplasia
  • Ectoderm
  • Mesoderm
  • Entoderm

Cell cycle

Quiescent (not a very long or dominent phase)

Pre-synthetic, but cell growth taking place

  • Cells which have continuous “turnover” have longer, or larger s-phases, i.e., dna synthesis
  • S-phase of tumor cells can be prognostic

M (mitotic:, P,M,A,T cytokinesis)

Cell types
Labile: eg. marrow, GI
Quiescent: liver, kidney
Non-mitotic: neuron, striated muscle

Stem cells (totipotential*)
  1. Embryonic
  2. Adult
Embryonic stem cells
  • Differentiation
  • Knockout mice (mice raised with specific gene defects)
  • Repopulation of damaged tissues, in research
Adult Stem cells

Marrow (hemocytoblast)
(hematopoetic stem cells)

Non-marrow (reserve)

Marrow stromal cell

Adult tissue differentiation and regeneration parallels embryonic development

Growth factors (GFS)
  • Locomotion
  • Contractility
  • Differentiation
  • Angiogenesis
Growth factors (GFS)
Transforming (alpha, beta)
Vascular endothelial
Platelet derived
Cytokines (TNF, IL-1, interferons)

Cell players (source and targets)
  • Lymphocytes, especially t-cells
  • Macrophages
  • Platelets
  • Endothelial cells
  • Fibroblasts
  • Keratinocytes
  • “mesenchymal” cells
  • Smooth muscle cells
E(epidermal) GF
  • Made in platelets, macrophages
  • Present in saliva, milk, urine, plasma
  • Acts on keratinocytes to migrate, divide
  • Acts on fibroblasts to produce “granulation” tissue
T(transforming) GF-alpha
  • Made in macrophages, t-cells, keratinocytes
  • Similar to egf, also effect on hepatocytes
H(hepatocyte) GF
  • Made in “mesenchymal” cells
  • Proliferation of epithelium, endothelium, hepatocytes
  • Effect on cell “motility”
Ve(vascular endothelial) GF
  • Made in mesenchymal cells
  • Triggered by hypoxia
  • Increases vascular permeability
  • Mitogenic for endothelial cells
  • Key substance in promoting “granulation” tissue
Pd(platelet derived) GF
  • Made in platelets, but also many other cell types
  • Chemotactic for many cells
  • Mitogen for fibroblasts
  • Angiogenesis
  • Another key player in granulation tissue
F(fibroblast) GF
  • Made in many cells
  • Chemotactic and mitogenic, for fibroblasts and keratinocytes
  • Re-epithelialization
  • Angiogenesis, wound contraction
  • Hematopoesis
  • Cardiac/skeletal (striated) muscle
T(transforming) GF-beta
  • Made in many cells
  • Chemotactic for PMNS and many other types of cells
  • Inhibits epithelial cells
  • Fibrogenic
  • Anti-inflammatory
K(keratinocyte) GF

  • Made in fibroblasts
  • Stimulates keratinocytes:
    • Migration
    • Proliferation
    • Differentiation
I (insulin-like) GF-1
  • Made in macrophages, fibroblasts
  • Stimulates:
    • Sulfated proteoglycans
    • Collagen
    • Keratinocyte migration
    • Fibroblast proliferation
  • Action similar to gh (pituitary growth hormone)
TNF (tumor necrosis factor)
  • Made in macrophages, mast cells, t-cells
  • Activates macrophages
  • Key influence on other cytokines
  • Made in macrophages, mast cells, t-cells, but also many other cells
  • Many functions:
  • Chemotaxis
  • Angiogenesis
  • Regulation of other cytokines

  • Made by lymphocytes, fibroblasts
  • Activates macrophages
  • Inhibits fibroblasts
  • Regulates other cytokines
  • Autocrine (same cell)
  • Paracrine (next door neighbor) (many gfs)
  • Endocrine (far away, delivered by blood, steroid hormones)

Transcription factors
  • TNF
  • IL-6
  • HGF

Extracellular matrix (ECM)
  • Collagen(s) I-xviii
  • Elastin
  • Fibrillin
  • Cams (cell adhesion molecules)
    • Immunoglobulins, cadherins, integrins, selectins
  • Proteoglycans
  • Hyaluronic acid
  • Maintain cell differentiation
  • “scaffolding”
  • Establish microenvironment
  • Storage of GF’s
  1. Collagen one - bone (main component of bone)
  2. Collagen two - cartwolage (main component of cartilage)
  3. Collagen three - rethreeculate (main component of reticular fibers)
  4. Collagen four - floor - forms the basement membrane
Genetic collagen disorders
  • I                               osteogenesis imperfecta, e-d
  • Ii                              achondrogenesis type ii               
  • Iii                             vascular ehlers-danlos
  • V                             classical  e-d
  • Ix                            stickler syndrome
  • Iv                            alport syndrome
  • Vi                            bethlem myopathy
  • Vii                           dystrophic epidermolysis bullos.
  • Ix                            epiphyseal dysplasias
  • Xvii         gen. Epidermolysys bullosa
  • Xv, xviii knobloch syndrome

Regeneration: growth of cells to replace lost tissues
Healing: a reparative tissue response to a wound, inflammation or necrosis

  • Follows inflammation
  • Proliferation and migration of connective tissue cells
  • Angiogenesis (neovascularization)
  • Collagen, other ecm protein synthesis
  • Tissue remodeling
  • Wound contraction
  • Increase in wound strength (scar = fibrosis)
Angiogenesis (neovascularization)
  • From endothelial precursor cells
  • From pre-existing vessels
  • Stimulated/regulated by gf’s, especially VEGF
  • Also regulated by ECM proteins
  • AKA, “granulation”, “granulation tissue”, “organization”, “organizing inflammation”

Wound healing
1 intention
Edges lined up
2 intention
Edges not lined up
More granulation
More epithelialization
More fibrosis

“Healthy” granulation tissue

  • Deposition of collagen by fibroblasts
  • With time (weeks, months, years?) The collagen becomes more dense, ergo, the tissue becomes “stronger”
Wound retarding factors (local)
  • Decreased blood supply
  • Denervation
  • Local infection
  • FB
  • Hematoma
  • Mechanical stress
  • Necrotic tissue
Wound retarding factors (systemic)
  • Decreased blood supply
  • Age
  • Anemia
  • Malignancy
  • Malnutrition
  • Obesity
  • Infection
  • Organ failure

Kamis, 27 Oktober 2011

Maxillary Sinus in Health and Disease-Oral Surgery Lecture

Anatomical facts and location:
√ The largest para-nasal sinuses.
√ Situated in the maxilla.
√ Has pyramidal shape.
√ Lateral nasal bone forms its base.
√ Apex headed towards the zygomatic bone.
√ Canine fossa, orbital floor and hard palate form the pyramidal walls.
√ Communicates with nasal cavity through maxillary ostium, in the posterior end of hitus simlunaris of middle meatus.

Anatomical morphology:
√  Size varies from one person to another.
√  Asymmetry existed in the same individual.
√  Small in children and grows up with aging.
√  Average height is about 3.5 cm, depth 3.2 cm and width 2.5 cm.
√  Capacity of about 15 cc.
√  Divided into several compartments by bony septa (underwood’s septa).
√  Lined with pseduo-stratified columnar ciliary epithelium (schneiderian membrane).

Relation with other structures:
√ Alveolar bone and dentition.
√ Nasal cavity and nasopharynex.
√ Orbital cavity and its contents.
√ Hard palate and oral cavity proper.
√ Pterygomaxillary fissure and its contents.
√ Neurovascular structures including infraorbital and superior alveolar nerve.

√  Develops from invagination of the mucous membrane of middle meatus of the nasal cavity at about the 3rd month of intrauterine life.
√  Fully development reaches with the age of 16 years.
√  Loss of permanent teeth and alveolar bone may make the sinus to appear huge in size.

Blood supply:
Blood supply from facial, maxillary, infraorbital, greater and lesser palatine arteries and lateral and posterior nasal branches of sphenopalatine artery.
Venous drainage to the anterior facial vein, sphenopalatine vein and pterygopaltine plexus.

Nerve supply:
√  Infraorbital nerve.
√  Posterior, middle and anterior superior alveolar nerves.
√  Greater and lesser palatine nerves.

Lymphatic drain:
The lymphatic drain of the sinus is through the nose or the submandibular lymph nodes.

Unknown but the following functions have been proposed:
√  Speech and voice resonance.
√  Reduce weight of skull.
√  Warmth inspired air.
√  Filtration of inspired air.
√  Immunologic barrier ( body defense).

  1. Congenital anomalies.
  2. Inflammatory diseases.
  3. Cysts and odontogenic infection.
  4. Bone metaplasia and benign tumors.
  5. Neoplasia.
  6. Trauma.

Congenital anomalies:
√  Cleft palate.
√  Facial fistula and cleft.
 √ Cystic formation.
√  Atresia.

Inflammatory diseases:
√  Bacterial infection.
√  Bacterial infection secondary to viral infection.
√  Fungal infection.


Acute sinusitis:
Suppurative or non suppurative inflammation of the mucosal lining of the sinus. It involves one or both sinuses.

√  Secondary to hay fever and allergic rhinitis.
√  Secondary to acute rhinitis (common cold) and URT infection.
√  Bacterial infection due to: dental sepsis, swimming and diving, trauma and foreign body dislodgment.

Sings and symptoms:
√  Headache.
√  Pain and tenderness.
√  Nasal obstruction.
√  Nasal discharge.
√  Toxic manifestations.
√  Heavy filling with bending.
√  Nasal congestion.
√  X-ray and transillumination findings.

√  Rest and fluid and mouth hygiene.
√  Antibiotics (C&S); pneumococci and streptococci are the most causative organisms.
√  Analgesics and antihistamines.
√  Local treatment (decongestant and steam inhalation).
Chronic sinusitis:
It is a chronic type of infection affected the mucosal lining of one  or both sinuses, resulted in mucopus or pus collection. A polypoidal type of inflammation can lead to formation of multiple or single mucosal polyps. 

√  As a consequence of non resolved acute sinusitis.
√  Dental abscesses.
√  Virulent organism with low resistance.
√  Foreign body dislodgement or trauma

Signs and symptoms:
√  Headache.
√  Nasal obstruction
√  Nasal discharge.
√  Fatigue.
√  Hyposmia/ cacosmia.
√  Transllumination findings.
√  Proof puncture.

√  Antibiotics.
√  Systemic decongestants.
√  Sinus wash-out.

Mycotic infection:
Opportunistic infection caused by maxillary sinus flora fungi environment in susceptible individual, leads to obliteration of the sinus space and erosion of its bony components.

Complications of sinusitis:
  • Orbital abscess and orbital cellulites.
  • Intracranial abscesses.
  • Meningitis.
  • Cavernous sinus thrombosis.
  • Spread of infection to neighboring sinuses, structures and organs.
  • Osteomyelitis.
  • Gastrointestinal disturbances.

Cysts and odontogenic tumors:

Odontogenic cysts:
√ radicular cysts.
√ residual cysts.
√ dentigerous cysts.
√ premordial cysts.

Non-odontogenic cysts.
Mucocele and retention cysts.

Odontogenic tumors:
√ ameloblastoma.
√  Myxoma.

Bone metaplasia and benign tumors:
√  Fibrous dysplasia.
√  Ossifying fibroma.
√  Transitional papilloma.
√  Osteoma.
√  Giant cell lesions.

√  Squamous cell carcinoma.
√  Adenocarcinoma.
√  Sarcoma (osteosarcoma).
√  Ewing’s sarcoma.

√  Tuberosity fracture.
√  Dentoalveolar fracture.
√  LeFort’s fractures.
√  Zygomatic complex fracture.
√  Pure and impure orbital floor fractures.
√  Establishment of oro-antral fistula.

Clinical examination:

√ Assess asymmetry.
√ Color of overlaying skin.

√  Tenderness.
√  Swelling and expansion.
√  Depression.

Examination of nasal passage
√ Nasal patency.
√ Pus discharge.
√ Nasal polyps.
√ Erythema, redness, change in the color of nasal mucosa.

Diagnostic sinus lavage
√ sinus rinsing through the canine fosaa.
√ Nasal antrostomy.

Radiographical examination:
Routine radiographical examination
√ Orthopantomogram (OPG)
√ Occipitomental (water’s view), with lateral tilt.


Special investigation and radiographical examination
  • Sinuscopy
  • Sinogram
  • CT scan
  • MRI
  • Microbiology and histological examination:
  • Culture and sensitivity and biopsy.