OBJECTIVES DEFINITION CAUSES TYPES PATHOGENESIS GRANULOMATOUS...
-
Upload
grant-lyons -
Category
Documents
-
view
228 -
download
2
Transcript of OBJECTIVES DEFINITION CAUSES TYPES PATHOGENESIS GRANULOMATOUS...
Granulomatous diseases
OBJECTIVES DEFINITION CAUSES TYPES PATHOGENESIS GRANULOMATOUS
DISEASES:TB,LEPROSY,LEISHMANIA,SCHISTOSOMIASIS,SARCOIDOSIS,ACTINOMYCOSIS.
Definition:
Granulomatous inflammation is a distinctive pattern of chronic inflammatory reaction.
It is a protective response to chronic infection or foreign material, preventing dissemination and restricting inflammation.
Some autoimmune diseases such as rheumatoid arthritis and Crohns disease are also associated with granulomas.
Granulomas
the predominant cell type is an activated macrophage with a modified epithelial-like (epithelioid) appearance
Lymphocytes.
Occasional plasma cells.
A granuloma is a microscopic aggregation of macrophages that are transformed into epithelium-like cells surrounded by a collar of mononuclear leukocytes, principally lymphocytes and occasionally plasma cells.
Epithelioid cells fuse to form giant cells containing 20 or more nuclei.
The nuclei arranged either peripherally (Langhans-type giant cell) or
haphazardly (foreign body-type giant cell).
These giant cells can be found either at the periphery or the center of the granuloma.
Slide 3.41
Fibrous connective tissue often surrounds granulomas (remodeling of tissue)
Areas within the granuloma can undergo necrosis (prototype: caseous necrosis in tuberculosis). Necrosis can lead to calcification or liquefaction and formation of a cavern if
drained.
Infectious causes: Bacteria
Tuberculosis Leprosy
Parasites Schistosomiasis
Fungi Histoplasmosis Blastomycosis
Metal/Dust Berylliosis Silicosis
Foreign body Granulomas: endogenous ( keratin, necrotic bone or adipose tissue uric acid crystals)
Exogenous(wood, silica, asbestos, silicone,suture…)
Specific chemicals:
Beryllium
Sarcoidosis (unknown cause)
Type of granulomas:
1. Foreign body granulomas – form when material such as talc, sutures, or other fibers are large enough to preclude phagocytosis by a single macrophage.
Immune granulomas - caused by insoluble particles that are capable of inducing a cell-mediated response. This type of immune response produces granulomas when the inciting agent is poorly soluble or particulate. Macrophages engulf the foreign material and process and present some of it to appropriate T lymphocytes, causing them to become activated, responding T cells produce cytokines, such as IL-2 which activates other T cells and IFN- which is important in transforming macrophages into epithelioid cells and multinucleate giant cells.
Foreign body aspiration
Berrylliosis
caseation
The classic example for the immune granuloma is that caused by the bacillus of tuberculosis. In this disease, the granuloma is referred to as a tubercle and is classically characterized by the presence of central caseous necrosis. Caseating necrosis is rare in other granulomatous diseases.
There are many atypical presentations that it is always necessary to identify the specific etiologic agent by: special stains for organisms (acid-fast stains for tubercle bacilli), culture methods (tuberculosis, fungal disease), and serologic studies (syphilis). In sarcoidosis, the etiologic agent is unknown.
Granuloma: bacilli are inhaled by droplets
Bacteria are phagocytosed by alveolar macrophages
After amassing substances that they cannot digest, macrophages lose their motility, accumulate at the site of injury and transform themselves into nodular collections; the Granuloma
A localized inflammatory response recruits more mononuclear cells
The granuloma consists of a kernel of infected macrophages surrounded by foamy macrophages and a ring of lymphocytes and a fibrous cuff (containment phase)
Containment usually fails when the immune status of the patient changes; the granuloma caseates, ruptures and spills into the airway
Langhans Giant Cell
Caseous Necrosis
Epithelioid Macrophage
Lymphocytic Rim
Pathology of Pathology of TuberculosisTuberculosis
2-10micrometer in length. Struntrually gram positive but also
containslarge amount of lipids in the cell wall:making them acid fast.
No toxins No spores Obligate Aerobic
Elicit granulomatous inflammation.
M. tuberculosis hominis & M. bovis M. avium, M.intracellulare in AIDS -
Atypical TB
Infects one third of world population..! 3 million deaths due to TB every year Under privileged population -
Crowding, Poverty, malnutrition, economic burden.
Since 1985 incidence is increasing in westAIDS, Diabetes, Immunosuppressed
patients, Diabetes, Drug resistance.
Tuberculosis is a chronic communicable disease in which the lungs are the prime target,although any organ may be infected.
TUBERCULOSIS
Primary TB SecondaryTB Progressive pulmonary TB Miliary TB
PATHOGENESIS
The course of tuberculosis depends on age and immune competence AND total burden of the organisms
Tuberculous Infection: refers to growth of the organism in a person,whether there is symptomatic disease or not.
Active Tuberculosis; refers to infection manifested by tissue destruction-----symptomatic disease.
Primary tuberculosis is the form of disease that develops in a previously unexposed and unsensitized person.
Tuberculosis is a type of delayed tissue hypersensitivity to the tuberculous bacillus which elicit a cell-mediated immune response which will resists the growth and spread of the mycobacterium.
This hypersensitivity reaction produces the pathologic feature of tuberculosis in immunocompetent individuals, i.e. granulomas, caseation, cavity formation.
The sequence of events which occur after inhalation of infectious agent in a previously unexposed immunocompetent individual are:The mycobacterium will gain access to the
alveolar macrophage through receptors.
* Once the organisms are inside the cytoplasm of the macrophage it will inhibit the microbicidal response of the macrophage (ineffective phagolysosome).
Multiplication of the organism inside the alveolar macrophage
processing& presentation of the antigen on the surface
A clone of sensitized T-cells proliferate, produce gamma INT.
Activation of the macrophages(augmenting
their capacity to kill mycobacteria)
The lytic enzymes of the activated macrophages if released, also damaged host tissues.
This activation of macrophages and destruction of mycobacteria comprises the cell mediated immunity.
M. tuberculosisM. tuberculosis enters macrophages enters macrophages Once inside the macrophage, Once inside the macrophage, M. tuberculosisM. tuberculosis
replicates within the phagosome by blocking replicates within the phagosome by blocking fusion of the phagosome and lysosome. fusion of the phagosome and lysosome.
Thus the earliest stage of primary Thus the earliest stage of primary tuberculosis (<3 weeks) in the nonsensitized tuberculosis (<3 weeks) in the nonsensitized individual is characterized by proliferation of individual is characterized by proliferation of bacteria in the pulmonary alveolar bacteria in the pulmonary alveolar macrophages and airspaces, with resulting macrophages and airspaces, with resulting bacteremia and seeding of multiple sites. bacteremia and seeding of multiple sites.
About 3 weeks after infection, a TH1 About 3 weeks after infection, a TH1 response against response against M. tuberculosisM. tuberculosis is is mounted that activates macrophages to mounted that activates macrophages to become bactericidal.become bactericidal.
TH1 cells are stimulated by TH1 cells are stimulated by mycobacterial antigens drained to the mycobacterial antigens drained to the lymph node. lymph node.
About 3 weeks after infection, a TH1 About 3 weeks after infection, a TH1 response against response against M. tuberculosisM. tuberculosis is is mounted that activates macrophages to mounted that activates macrophages to become bactericidal.become bactericidal.
TH1 cells are stimulated by TH1 cells are stimulated by mycobacterial antigens drained to the mycobacterial antigens drained to the lymph node. lymph node.
Mature TH1 cells, both in lymph nodes Mature TH1 cells, both in lymph nodes and in the lung, produce IFN-γ. and in the lung, produce IFN-γ.
IFN-IFN-γ γ is the critical mediator which drives is the critical mediator which drives macrophages to become competent to macrophages to become competent to contain the M. tuberculosis infection.contain the M. tuberculosis infection.
IFN-γ stimulates formation of the IFN-γ stimulates formation of the phagolysosome in infected macrophages, phagolysosome in infected macrophages, exposing the bacteria to an inhospitable exposing the bacteria to an inhospitable acidic environment. acidic environment.
IFN-γ also stimulates expression of IFN-γ also stimulates expression of inducible inducible nitric oxide synthase (iNOS), synthase (iNOS), which produces which produces nitric oxide (NO). NO (NO). NO helps in the destruction of several helps in the destruction of several mycobacterial constituents, from cell wall mycobacterial constituents, from cell wall to DNA. to DNA.
In addition to stimulating macrophages to In addition to stimulating macrophages to kill mycobacteria, the TH1 response kill mycobacteria, the TH1 response orchestrates the formation of granulomas orchestrates the formation of granulomas and caseous necrosisand caseous necrosis. .
Activated macrophages, stimulated by Activated macrophages, stimulated by IFN-γ, produce TNF, which recruits IFN-γ, produce TNF, which recruits monocytes. monocytes.
These monocytes differentiate into the These monocytes differentiate into the "epithelioid histiocytes" that characterize "epithelioid histiocytes" that characterize the granulomatous responsethe granulomatous response
In immunocompromised persons granulomas are poorly formed or not formed at all and the infection progress at the primary site in the lung ,lymph nodes or in multiple sites---------progressive primary tuberculosis.
Is characterized by: Ghon Focus ----- lung lesion of primary
TB,involves upper segments of the lower lobes or lower seg.of the upper lobe.
Ghon complex----- combination of a peripheral ghon focus and involved mediastinal or hilar lymphnode.
Microscopically the classic lesion of TB is a caseous granuloma
Clinical and pathologic implications of primary tuberculosis
1] Development of resistance to the infection.
2] The foci of scarring may harbor viable bacilli for life and act as a nidus for
reactivation.3] The disease may develop into
progressive primary tuberculosis in immunocompro- mised patients such as AIDS patients, elderly, and malnourished children.
In patients with progressive primary tuberculosis, the tissue reaction is different.
No well-formed granulomatous reaction or caseation necrosis is seen in tissue affected.
Resembles acute bacterial pneumonia with lower and middle lobe consolidation, pleural effusion and hilar lymphadenopathy.
Cavitary lesions are rare. Disseminated disease with tuberculous
meningitis and miliary tuberculosis.
Is the pattern of disease that arises in a previously sensitized host.
Is usually a reactivation of dormant primary lesions when the host resistance is lowered.
Or exogenous reinfection by a high dose of virulent bacilli which occur more commonly in endemic areas.
Only 5% of patients with primary disease develop secondary tuberculosis.
Pathologic features of secondary tuberculosis:
In secondary pulmonary tuberculosis, the lesions involves the apices of both lungs and appear grossly as sharply circumscribed firm areas with central caseation and cavitation surrounded by fibrous wall.
It can heal by fibrosis leaving a residual apical scar.
Histologically, epithelioid granulomas with central caseation and Langhan’s type giant cells.
Other clinicopathologic forms of secondarytuberculosis depends on the organ involved
andIncludes
Cough,low grade fever wt.loss, anorxiaCavitaton may be accompanied by
haemoptysisChest radiographs show unilateral or
bilateral apical cavities.
Complications of secondary TBScarring &calcificationSpread to other areas
Pleural fibrosis&adhesionsRupture of caseous lesion
Implantation of bacteriain the larynx ---hoarseness
Miliary pulmonary diseaseMiliary pulmonary disease
Occurs when organisms drain through Occurs when organisms drain through lymphatics into the lymphatic ducts, lymphatics into the lymphatic ducts, which empty into the venous return to which empty into the venous return to the right side of the heart and thence into the right side of the heart and thence into the pulmonary arteries.the pulmonary arteries.
Individual lesions are either microscopic Individual lesions are either microscopic or small, visible (2-mm) foci of yellow-or small, visible (2-mm) foci of yellow-white consolidation scattered through the white consolidation scattered through the lung parenchyma. lung parenchyma.
Miliary lesions may expand and coalesce Miliary lesions may expand and coalesce to yield almost total consolidation of to yield almost total consolidation of large regions or even whole lobes of the large regions or even whole lobes of the lung.lung.
With progressive pulmonary tuberculosis, With progressive pulmonary tuberculosis, the pleural cavity is invariably involved, the pleural cavity is invariably involved, and serous and serous pleural effusions,pleural effusions, tuberculous empyematuberculous empyema, or , or obliterative obliterative fibrous pleuritisfibrous pleuritis may develop. may develop.
Miliary tuberculosis is most prominent in :Miliary tuberculosis is most prominent in : the liver,the liver, bone marrow,bone marrow, spleen, spleen, adrenals, adrenals, meninges, kidneys, fallopian tubes, and meninges, kidneys, fallopian tubes, and
epididymis. epididymis.
May appear in any of the organs or May appear in any of the organs or tissues seeded hematogenously and may tissues seeded hematogenously and may be the presenting manifestation of be the presenting manifestation of tuberculosistuberculosis
Isolated-organ tuberculosisIsolated-organ tuberculosis
Organs that are typically involved include Organs that are typically involved include the meninges (tuberculous meningitis), the meninges (tuberculous meningitis), kidneys (renal tuberculosis), adrenals kidneys (renal tuberculosis), adrenals (formerly an important cause of Addison (formerly an important cause of Addison disease), bones (osteomyelitis), and disease), bones (osteomyelitis), and fallopian tubes (salpingitis). fallopian tubes (salpingitis).
When the vertebrae are affected, the When the vertebrae are affected, the disease is referred to as Pott's disease.disease is referred to as Pott's disease.
Paraspinal "cold" abscesses in these Paraspinal "cold" abscesses in these patients may track along the tissue patients may track along the tissue planes to present as an abdominal or planes to present as an abdominal or pelvic masspelvic mass
LymphadenitisLymphadenitis is the most frequent form is the most frequent form of extrapulmonary tuberculosis, usually of extrapulmonary tuberculosis, usually occurring in the cervical region occurring in the cervical region ("scrofula"). ("scrofula").
Intestinal tuberculosisIntestinal tuberculosis contracted by contracted by the drinking of contaminated milk. the drinking of contaminated milk.
In developed countries today, intestinal In developed countries today, intestinal tuberculosis is more often a complication tuberculosis is more often a complication of protracted advanced secondary of protracted advanced secondary tuberculosis, secondary to the swallowing tuberculosis, secondary to the swallowing of coughed-up infective material. of coughed-up infective material.
Adrenal TB - Addison Disease
Spinal TB - Potts Disease
Diagnosis of TB
Clinical features are not confirmatory.Zeil Nielson Stain - 1x104/ml, 60% sensitivityRelease of acid-fast bacilli from cavities intermittent.3 negative smears to assure low infectivity*Culture most sensitive and specific test.
Conventional Lowenstein Jensen media 3-6 wks.Automated techniques within 9-16 days
PCR is available, but should only be performed by experienced laboratoriesPPD for clinical activity / exposure sometime in life.
AFB - Ziehl-Nielson stain
Colony Morphology – LJ Slant
BacterialTuberculosis (Mycobacterium tuberculosis)Leprosy (Mycobacterium leprae)Syphilitic gumma (Treponema pallidum)
ParasiticSchistosomiasis (Schistosoma mansoni, S. haematobium,S. japonicum)
FungalHistoplasma capsulatumBlastomycosisCryptococcus neoformansCoccidiodes immitis
Inorganic Metals or DustsSilicosisBerylliosis
Foreign BodySuture, breast prosthesis, vascular graft
UnknownSarcoidosis
Gram stain Most bacteriaAcid fast stain Mycobacteria, nocardiae
(modified)Silver stains Fungi, legionellae,
pneymocytosisPeriod acid-Schiff Fungi, amebaeMucicarmine CryptococciGiemsa Campylobacteria, leishmaniae, malaria,
parasitesAntibody probes Viruses, rickettsiaeCulture All classesDNA probes Viruses, bacteria, protozoa
Polarizingmicroscope Foreign body
Tuberculin TestTuberculin Test
It is a classic example of delayed It is a classic example of delayed hypersensitivity.hypersensitivity.
The The tuberculin reactiontuberculin reaction, is produced by , is produced by the intracutaneous injection of tuberculin, the intracutaneous injection of tuberculin, a protein-lipopolysaccharide component a protein-lipopolysaccharide component of the tubercle bacillus. of the tubercle bacillus.
In a previously sensitized individual, In a previously sensitized individual, reddening and induration of the site reddening and induration of the site appear in 8 to 12 hours, reach a peak in appear in 8 to 12 hours, reach a peak in 24 to 72 hours, and thereafter slowly 24 to 72 hours, and thereafter slowly subside. subside.
Morphologically, delayed type Morphologically, delayed type hypersensitivity is characterized by the hypersensitivity is characterized by the accumulation of mononuclear cells accumulation of mononuclear cells around small veins and venules, around small veins and venules, producing a perivascular "cuffing" .producing a perivascular "cuffing" .
Plasma proteins escape, giving rise to Plasma proteins escape, giving rise to dermal edema and deposition of fibrin in dermal edema and deposition of fibrin in the interstitium.the interstitium.
The latter appears to be the main cause The latter appears to be the main cause of induration, which is characteristic of of induration, which is characteristic of delayed hypersensitivity skin lesions.delayed hypersensitivity skin lesions.
In fully developed lesions, the In fully developed lesions, the lymphocyte-cuffed venules show marked lymphocyte-cuffed venules show marked endothelial hypertrophy and, in some endothelial hypertrophy and, in some cases, hyperplasia. cases, hyperplasia.
Leprosy/Hansen diseaseLeprosy/Hansen disease
M. lepraeM. leprae is an acid-fast obligate is an acid-fast obligate intracellular organism that grows very intracellular organism that grows very poorly in culture. poorly in culture.
It grows more slowly than other It grows more slowly than other mycobacteria and grows best at 32° to mycobacteria and grows best at 32° to 34°C, the temperature of the human skin34°C, the temperature of the human skin
PathogenesisPathogenesis
Is a slowly progressive infection caused Is a slowly progressive infection caused by by Mycobacterium lepraeMycobacterium leprae, affecting the , affecting the skin and peripheral nerves and resulting skin and peripheral nerves and resulting in disabling deformities.in disabling deformities.
M. lepraeM. leprae is likely to be transmitted from is likely to be transmitted from person to person through aerosols from person to person through aerosols from lesions in the upper respiratory tract. lesions in the upper respiratory tract.
Inhaled Inhaled M. lepraeM. leprae, like , like M. tuberculosisM. tuberculosis, is , is taken up by alveolar macrophages and taken up by alveolar macrophages and disseminates through the blood, but disseminates through the blood, but grows only in tissues of the skin and grows only in tissues of the skin and extremities. extremities.
leprosy remains endemic among an leprosy remains endemic among an estimated 10 to 15 million people living estimated 10 to 15 million people living in poor tropical countriesin poor tropical countries
Like Like M. tuberculosisM. tuberculosis, , M. lepraeM. leprae secretes secretes no toxins, and its virulence is based on no toxins, and its virulence is based on properties of its cell wall. properties of its cell wall.
The cell wall is similar enough to that of The cell wall is similar enough to that of M. tuberculosis.M. tuberculosis.
Cell-mediated immunity is reflected by Cell-mediated immunity is reflected by delayed type hypersensitivity reactions to delayed type hypersensitivity reactions to dermal injections of a bacterial extract dermal injections of a bacterial extract called called leprominlepromin
Leprosy has two strikingly different Leprosy has two strikingly different patterns of diseasepatterns of disease. .
1)1) Patients with the less severe form, Patients with the less severe form, tuberculoid leprosytuberculoid leprosy, have dry, scaly skin , have dry, scaly skin lesions that lack sensation. They often lesions that lack sensation. They often have large, asymmetric peripheral nerve have large, asymmetric peripheral nerve involvement. involvement.
The more severe form of leprosy, The more severe form of leprosy, lepromatous leprosylepromatous leprosy, includes symmetric , includes symmetric skin thickening and nodules. This is also skin thickening and nodules. This is also called called anergic leprosyanergic leprosy, because of the , because of the unresponsiveness (anergy) of the host unresponsiveness (anergy) of the host immune system. immune system.
In lepromatous leprosy, damage to the In lepromatous leprosy, damage to the nervous system comes from widespread nervous system comes from widespread invasion of the mycobacteria into invasion of the mycobacteria into Schwann cells and into endoneural and Schwann cells and into endoneural and perineural macrophages. perineural macrophages.
- In advanced cases of lepromatous leprosy, - In advanced cases of lepromatous leprosy, M. lepraeM. leprae is present in sputum and blood. is present in sputum and blood.
3- People can also have intermediate forms 3- People can also have intermediate forms of disease, called of disease, called borderline leprosyborderline leprosy. .
Begins with localized skin lesions that are Begins with localized skin lesions that are first flat and red but enlarge and develop first flat and red but enlarge and develop irregular shapes with indurated, elevated, irregular shapes with indurated, elevated, hyperpigmented margins and depressed hyperpigmented margins and depressed pale centers (central healing). pale centers (central healing).
Morphology of Tuberculoid Morphology of Tuberculoid leprosyleprosy
Neuronal involvement dominates Neuronal involvement dominates tuberculoid leprosy. tuberculoid leprosy.
Nerves become enclosed within Nerves become enclosed within granulomatous inflammatory reactions. granulomatous inflammatory reactions.
Nerve degeneration causes skin Nerve degeneration causes skin anesthesias and skin and muscle atrophy anesthesias and skin and muscle atrophy that render the patient liable to trauma of that render the patient liable to trauma of the affected parts, with the development the affected parts, with the development of indolent skin ulcers.of indolent skin ulcers.
Morphology of Tuberculoid Morphology of Tuberculoid leprosyleprosy
Tuberculoid leprosyTuberculoid leprosy
Contractures, paralyses, and Contractures, paralyses, and autoamputation of fingers or toes may autoamputation of fingers or toes may ensue. ensue.
Facial nerve involvement can lead to Facial nerve involvement can lead to paralysis of the eyelids, with keratitis and paralysis of the eyelids, with keratitis and corneal ulcerations. corneal ulcerations.
On microscopic examination, all sites of On microscopic examination, all sites of involvement disclose granulomatous involvement disclose granulomatous lesions closely resembling those found in lesions closely resembling those found in tuberculosis, and bacilli are almost never tuberculosis, and bacilli are almost never found. found.
The presence of granulomas and absence The presence of granulomas and absence of bacteria reflect strong T-cell immunity. of bacteria reflect strong T-cell immunity.