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An example for the foreign body-induced pathogenesis is inhaled silica (mostly quartz) particles that are strongly
irritating and cytotoxic to macrophages that engulf them.
The pathology of the mature granuloma is caused by several factors: 1) It is a space-occupying lesion that
physically impinges on the neighboring tissue. 2) Leakage from activated macrophages of cytokines (TNFα),
oxygen (H2O2, O2, OH•, O2•) and nitrogen (NO) derivatives and proteolytic enzymes that damage the
neighboring tissue. 3) Caseous necrosis. In some, especially the M. tuberculosis-induced granulomas the
centrally located macrophages die by a variety of causes which comprise the toxic effect of M.
tuberculosis products, loss of vascularization, lack of oxygen, the CD8+ T cell-mediated lysis of bacilli-laden
macrophages and TNFα-induced apoptosis (programmed cell death) (15,49). The necrotic center is devoid of M.
tuberculosis. Apparently the vigorous macrophage activity achieved its goal (56). Such necrosis is never observed
in the sarcoid lesions. If the outer wall of the granuloma is well-vascularized the lesion involutes. In contrast low
vascularization promotes cavity formation and severe tissue pathology (56). 4) In progressive disease the
caseous necrosis of the M. tuberculosis granuloma proceeds due to proteolytic activity to liquefactive necrosis,
the surrounding lung tissue lyzes and cavities form. Further erosion of the neighboring blood vessels and airways
facilitates the spread of the bacilli. Cavitary tuberculosis is dangerous, it abrogates the protective function of the
granuloma, the bacilli spread within the host and by cough and droplet infection disseminate to the outside
environment (15). 5) As a consequence of intragranulomatous cytokine (TGF-β, TNFα, for Th1 lesions, IL-4, IL-13
for Th2 lesions) activity fibroblasts or myofibroblasts get activated and lay down collagen fibers which coalesce to
a dense fibrotic tissue. With the elimination of the pathogen or the antigenic stimulus most granulomas burn out
by fibrosis. When the healing process is normal minimal residual scarring is left behind. Locally secreted TGF-β
also induces in macrophages or fibroblasts the production of TIMPs (tissue inhibitors of metalloproteases) that
block the degradation of the deposited collagen fibers (7). The burnt-out foci of the M. tuberculosis tubercle then
undergo calcification which can be observed in chest x rays. Unlike the TB granulomas, the sarcoid or
schistosome worm egg-induced granulomas never calcify (Table 2). Overt fibrosis that occurs in the
granulomatous lungs or livers then derange organ function. Excessive tissue fibrosis can cause pulmonary or
portal hypertension and death in sarcoidosis, or schistosomiasis respectively. Suppuration at the center of the
granulomas also occurs in deep fungal infections (blastomycosis,coccidioidomycosis) and lymphogranuloma
venereum. Granuloma annulare a benign dermal inflammation shows necrobiotic degeneration of dermal
collagen, surrounded by palissading inflammatory cells (35,55). In humans the schistosome egg induced
immunopathology is manifested by postgranulomatous liver and intestinal fibrosis (14,41). Here the balance
between the Th1-Th2 responses comes into play. Most infected individuals suffer from a milder intestinal form of
the disease. However about 5-10 percent of the patients develop the hepatosplenic manifestations with severe
hepatic (Symmers’) fibrosis, portal hypertension, ascites fluid formation, gastrointestinal bleedings and occasional
death. In several studies the complexity of various contributory factors to immunopathology emerged.
Hepatosplenic disease in Kenya was associated with high IFN-γ, TNF-α and low IL-5 cytokine production. Such
profile is observed in the Th1 type TB granuloma. Thus results indicated that inability of a patient to develop a
strong Th2 response leads to disease (43).Further research revealed that periportal fibrosis is age and gender
dependent and induced by high TNF-α production (8). This conclusion remains controversial because a recent
Brazilian study found that hepatic fibrosis at the early hepatosplenic stage is associated with high Th2 type
cytokine chiefly IL-5, IL-10 and IL-13 production (14). This latter observation is in accordance with murine
experiments that clearly showed impaired granuloma formation and liver fibrosis in mice defective in type 2 IL-4,
IL-13 cytokine production. Thus in the clear cut murine system the Th2 response appears to dampen the early
tissue-destructive IFN-γ mediated inflammation (54), yet it contributes to the pathology by IL-4, IL-13 cytokine-
mediated liver fibrosis (60).
DIFFERENTIAL DIAGNOSIS
Granulomas are caused by an extremely broad range of disease processes. These can be conveniently divided
into infectious and non-infectious causes. One of the difficulties in arriving at a diagnosis is that many etiologies
have similar clinical syndromes. However, specific tests may help in distinguishing the two types of granulomas.
Infectious Causes
Although many infections are associated with granuloma formation, relatively few microorganisms cause the
majority of cases. Mycobacteria and fungi are commonly associated with granulomatous infection, and in
particular,tuberculosis is the most common cause of granulomas worldwide. However, all mycobacteria can be
associated with granulomas. Most clinically important fungi are also associated with granuloma formation,
including Aspergillus, Cryptococcus,Candida, and Histoplasma to name a few. Other important causes of
granulomas are parasitic infections (schistosomiasis, leishmaniasis, dirofilariasis, etc.) and rarely, viral infections
caused by cytomegalovirus, Epstein-Barr virus and measles(Table 1-4). Relatively few bacterial infections
typically cause granulomas during infection, including brucellosis, Q-fever, cat-scratch disease (33)
(Bartonella), melioidosis, Whipple’s disease (20), nocardiosis and actinomycosis. Tuberculosis can often be
distinguished by its tendency to produce caseation necrosis within granulomas, though the other infectious
etiologies are almost impossible to differentiate from each other based solely on histologic appearance (Table 3).
One common thread among these disparate infectious syndromes is their general chronicity, many typically
associated with weeks, even months of clinical symptoms before diagnosis is made. In addition, therapy is usually
prolonged, for months to years before clinical resolution.
Non-Infectious Causes
Whereas infections can often be confirmed with bacterial cultures of affected tissues, non-infectious causes of
granulomas may be difficult to diagnose, and often remain a diagnosis of exclusion. Berylliosis is a T lymphocyte-
mediated non-necrotizing granulomatous disorder that develops in beryllium metal-exposed workers(39).
Sarcoidosis is one of the most common non-infectious granulomatous diseases, characterized by non-necrotizing
epithelioid granulomas with giant cells in multiple organ systems, primarily the lungs(4,18,30). Over the years
mycobacterial and propionibacterial organisms have been proposed as etiological agents of the disease. A
recent study detected M. tuberculosis catalase-peroxidase protein within sarcoidosis tissues providing further
indication for the infectious etiology of the disease (42). Crohn’s disease is characterized by non-caseating ileal
and colonic granulomas (Table 3). Mucosal permeability to luminal pathogens among them M.
paratuberculosis have been proposed as pathogenic factors(48,59). Another group of diseases are the vasculitis
syndromes (46), which include Wegener’s granulomatosis, Churg-Strauss disease, and Takayasu’s arteritis to
name a few. These usually cause necrotizing granulomas (18).Rheumatoid pulmonary nodules are often
associated with granulomas. In the liver, autoimmune diseases such as hepatitis and primary biliary cirrhosis are
often characterized by granulomatous pathology (17).
Foreign bodies such as talc, silicone, surgical sutures may also elicit granulomatous reactions with less complex
histological appearance. Often the clinical presentation is organ specific such as renal granulomas caused by
antibiotics, anti-inflammatory agents,diuretics(31).In the lung, aspiration of vegetable matter that remains under-
graded can evoke granulomatous response.
LABORATORY DIAGNOSIS
Laboratory diagnosis is an indispensable aid in the diagnosis of the granuloma etiology. Presently, a wide range
of laboratory methodologies is available for the correct diagnosis of the granulomatous condition. This includes
the histopathological examination of the granulomatous tissue, intragranulomatous localization and identification
by staining, immunohistochemistry, immunofluoroscence of the putative pathogen and its in vitro cultivation.
Recent advances in molecular biology, proteomics (42) provided further sensitive and rapid tests for the correct
diagnosis. The immune etiology of the granulomatous diseases can now be confirmed by testing patient’s serum
or T lymphocyte responses to the suspected granulomagenic organisms. The novel methodologies require
expensive diagnostics, reagents, sophisticated instrumentation and expertise. In the following sections the
methodologies will be described (Table 4).
Cultures
To establish the infectious etiology of the granuloma, cultures are prepared from homogenized biopsied
tissues.Care must be exercised to rigorously exclude an accidental contaminant in the sample. Growth of the
pathogens(bacteria, fungi) on selective and/or differential solid medium provides information on the Gram
staining properties: purple for Gram+,pink for Gram- of the pathogenic bacteria, as well as the morphology ,color
of the colonies, biochemical activity and antibiotic resistance of the organisms. Final identification of the
pathogens taken from the isolated colonies can be made by specific antibodies. Using enriched media: sheep
blood agar, chocolate agar, brain heart infusion agar many organisms can be grown overnight. However several
classical granulomagenic organisms such as Mycobacteria, Brucella, Listeria or Histoplasma grow slowly and
final diagnosis may be made only after 7-30 days. This is a disadvantage when there is an urgency for a quick
diagnosis. The actual choice of the biopsied tissue taken is also decisive for success. The highest percentage
of M. tuberculosis positive cultures was obtained from samples with necrotic granuloma centers, whereas poorly
formed granulomas yielded much lower positive cultures. Burnt-ot fibrotic lesions were usually culture negative.
Culture of Brucella
Brucella is a Gram-coccobacillus. Isolation from blood or tissues is done on bacterial media under aerobic or
anaerobic condition. The organism is fastidious, grows on enriched media such as trypticase soy agar
supplemented with 5 percent sheep blood, brain heart infusion agar or chocolate agar under 8-10 percent
CO2.Growth is slow may take 7 or more days, but it is recommended to hold cultures for 3 weeks. Additional
flora is sometimes suppressed by added bacitracin,polymyxin inhibitors. On positive plates small non-hemolytic
colonies appear. Biochemical activity such as catalase, urease, oxidase, H2S production and sensitivity to basic
fuchsin aid in the correct identification (37).
Culture of Listeria
Listeria is a Gram+ coccobacillus. It can be grown on sheep blood agar where it shows β hemolytic action, and
brain heart infusion agar with added glucose. It can break down esculin by its β glucosidase enzyme and exhibits
phospholipase activity as virulence factor. Those properties are utilized in a selective chromogenic medium
where glucosidase activity on a chromogenic substrate is observed. Within 24-48 hr blue turquoise colonies
appear and phospholipase action generates a white precipitate around the colonies (37).
Culture of Fungi
Most clinically important fungi can be isolated on Sabouraud’s dextrose agar with specific modifications
(Emmons) that favor growth of common clinical species. Cultures are usually positive within 3-7 days, though
certain fungi may take weeks to grow. Such is Histoplasma capsulatum a fastidious dimorphic fungus that grows
in the yeast form in the lungs. Granulomas can be isolated by bronchoscopic biopsy. The fungus can be grown on
brain heart infusion agar with added gentamicin, vancomycin chloramphenicol antibiotics to prevent the growth of
contaminating bacteria. At 30-37oC it grows slowly (2-4 wks) as budding yeasts. Nocardia and Actinomyces will
grow on routine media taking up to 2 weeks to yield a positive culture.
Stains
Multiple differential stains are available to the pathologist for identification of potential infectious causes of
granuloma. The tissue sample has to be properly fixed to preserve the cellular and acellular elements of the
biopsied material. The paraffin-embedded tissue is sliced to 5-6µm thick sections and stained by a variety of
stains that reveal the various cellular and tissue elements.
Haematoxylin-Eosin (H&E) is the most widely used stain for the microscopic diagnosis of granuloma etiology. The
lesions are usually well-delineated from the surrounding tissue. The stained slide will show cellular nuclei stained
purple and cytoplasm stained light rose or red. Such stain can distinguish by morphology lymphocytes,
macrophages, epithelioid cells, granulocytes and fibroblasts. Within the granuloma the characteristic palissading
arrangement of the epithelioid cells interspersed with lymphocytes or the peripheral lymphoid cells is seen.
Central caseous necrosis, giant cells with numerous nuclei provide clues for the architecture and /or the etiology
of the lesion. Eosinophils and mast cells present in helminthic granulomas may be degranulated and need special
tissue stains for identification (16).Some microorganisms can be seen and identified within the granuloma by the
H&E stain.
Dominici stain is used for the identification of tissue eosinophils which stains the granules bright red. A more
specific identification uses immunofluorescence microscopy. A primary antibody prepared against the cationic
major basic protein (MBP) within the eosinophilic granules binds to the protein. Then a fluoresceinated secondary
antibody that recognizes the primary antibody is applied. After the proper washes and controls the preparation is
identified under the microscope where the granules show bright green fluorescence.
Acidified Toluidin blue stain is used for the identification of tissue mast cells. The sulfated acid
mucopolysaccharides within the granules stain red to purple. A more specific immunohistochemistry method uses
a specific antibody prepared to the tryptase enzyme within the granules of the mast cells. The bound primary
antibody couples with the secondary antibody-biotin-streptavidin-horseradish peroxidase complex which stains
the granules reddish brown. Non-specific esterase stain is used for the detection of tissue macrophages. The
substrates used are naphtyl acetate or butyrate. The cytoplasmic enzyme stains red.
Immunohistochemistry, Immunofluorescence
Advances in the identification of specific surface markers of T and B lymphocyte and the different T lymphocyte
phenotypes made the preparation of specific antibodies possible. Presently an array of commercially available
antibodies can identify T lymphocytes (anti- CD3 marker), T helper lymphocytes (anti-CD4 marker), cytotoxic T
cells (anti-CD8 marker), B lymphocytes (anti-CD20 marker), and macrophages(anti-CD68 marker). Application of
such antisera to the granuloma tissue with the avidin-biotin-horseradish peroxidase complex can reveal the exact
identity and location of the granuloma cells.An elegant refinement uses double immunofluoresence for further
analysis of the T helper lymphocyte subset. The first antibody tagged with one fluorochrome will identify the CD4+
T cell while a second antibody specific for a certain cytokine(IFNγ,IL-4,IL-10 etc) with a different fluorochrome tag
penetrates the cell membrane rendered permeable by a chemical and will stain the intracellular cytokine. The
intracellular cytokine content either IFNγ or IL-4 will identify the T helper1 (Th1)or T helper 2 (Th2) phenotypes
respectively of the CD4+ T cell,which in turn characterizes the granuloma and predicts its efficacy in the
elimination of an intracellular invader such as M. tuberculosis.
Application to the granuloma of a specific stain for the identification of an invader can provide the final evidence
for the etiology of the lesion. This sometimes is fraught with difficulties. A very efficient granuloma should show a
paucity of the invader having had eliminated the majority of it by cellular mirobiocidal activity. In fact scrutiny of the
biopsied material from patients with confirmed clinical TB reveals only a low percentage of acid fast bacilli (AFB)
positive lesions. Nevertheless the gold standard for the diagnosis of TB is the presence of AFB in the granuloma
tissue. The standard stain is the Ziehl-Neelsen acid fast stain. An alternative stain for M. tuberculosis detection is
the auramine-rhodamine fluorescent stain that has affinity for the mycolic acid cell wall component of the bacilli.
In a dark field bacilli are bright yellow. Such stain enhances the sensitivity of detection(11).However the presence
of AFB within the granulomas does not prove that the pathogen is M. tuberculosis, because acid-fast M. avium or
other mycobacteria may also be present.
Treponema pallidum is also difficult to detect by regular stains. Needle-aspirated regional lymph node tissue can
be stained with fluorescein tagged anti-treponema antibody and under dark field the stained bacilli fluoresce bright
green.
Localization by immunohistochemistry within sarcoid-like granuloma macrophages of inhaled pigeon antigen
helps to confirm the diagnosis of hypersensitivity pneumonitis. Fungi are detected in tissues with Gomori’s
methenamine silver stain that stains the cell wall brown to black. The procedure may generate artifacts, therefore
the morphology of the fungus has to be ascertained. The periodic acid Schiff (PAS) reagent stains red the cell
wall of Candida. The Calcofluor white (fluorescent) staining may also be used to stain fungi. Specialized stains
such as the Fontana-Masson to detect melanin in fungi and the mucicarmine stain for cryptococcal cell-wall
polysaccharide may further assist in determining the fungal etiology. Despite the use of specific stains, in many
instances organisms due to their paucity in the histopathologic specimen can not be demonstrated and cultures
are needed for identification.
The periodic acid Schiff (PAS) reagent stains glycogen as well as mucopolysaccharides in the tissues.
Molecular Methods
Staining of tissue sections and culture of viable pathogens can provide the most definitive diagnosis for the
etiology of the granuloma. As mentioned in the previous sections the paucity of the pathogen such as AFB and
low sensitivity of the staining method can prevent the correct diagnosis. Though by means of laser capture
microdissection granulomas can be obtained free from the surrounding tissue (53) growth of pathogens (M.
tuberculosis, fungi) may take weeks, delaying diagnosis. The advent of molecular methods especially the
polymerase chain reaction (PCR) as a diagnostic tool made the detection of uncultivable organisms possible. The
standard, nested, or real time (RT) PCR enjoy wide-spread use because the laboratory can utilize for the assay
the formalin-fixed, paraffin-embedded histological sections. The sensitivity and speed of detecting a specific
message for a pathogen may surpass that of a culture because result is obtained within 24 hr. However, some of
these assays are not standardized and caution must be used in the interpretation because false-positive results
may occur.(13,27,38,44,48,53). Currently commercial kits with primer probes specific for pathogen DNA are
available which greatly amplify the sensitivity of the detection. For M. tuberculosis diagnosis the insertion
sequence (IS) 6110 is routinely used with great success. Compared with the efficacy of the Ziehl-Neelsen staining
or culture, laboratories report double or triple sensitivity and specificity in detection. Another commercial kit
(Genprobe) for Mycobacterium tuberculosis detection targets the 16S rRNA genes with sensitivity and specificity
of >95% in smear positive cases. The usefulness of the assay in extra-pulmonary TB is unclear, particularly
when histopathologic stains are negative. The great advantage of the PCR assay is its applicability to detecting
the DNA of any bacilli or fungi. However it is labor-intensive because for each pathogen a specific probe has to
be prepared or obtained. A more sophisticated assay uses the DNA microarray method in which multiple DNA
probes with known identities are fixed on a glass surface and molecular hybridization is carried out with the
pathogen DNA (36,45).This assay can simultaneously detect hundreds or thousands of genes. Such approach is
very helpful in the differential diagnosis when more than one pathogen has to be considered. Low density
microarray can simultaneously detect Mycobacterium spp, Yersinia spp, Bartonella and other
pathogens(45).Microarray has also been applied to the simultaneous differentiation of Mycobacteria species.
Using the DNA gyrase B subunit (gyrB) genes as a probeMycobacterium tuberculosis, Mycobacterium avium,
Mycobacterium intracellulare and other species could be identified (23).
Histopathology
The histologic appearance in stained sections of a particular granulomatous lesion may provide information as to
its etiology. The morphology (compact organized, diffuse, encased in fibrous capsule) and the cellular
composition of the lesion are helpful guidelines(18).First,the immune or foreign body characteristics have to be
established. The latter can be diagnosed with some assurance because the irritant (talc, quartz, silicon, graphite,
suture) is present within the granuloma. As mentioned in previous sections neither the presence of epithelioid nor
the type of giant cells can differentiate between the two types of granulomas. The presence within the granulomas
of CD4+ or CD8+ T lymphocytes is indicative of an immune etiology. This is the case in sarcoidosis(4) or Crohn’s
disease(25,59).
Histopathological differentiation of the various granulomatous diseases is a challenging task because often
neither the morphology nor the cellular composition can furnish a clue. The M. tuberculosis induced tubercle, the
beryllium metal-induced pulmonary granuloma (39,58) or the sarcoid lesion (4,18,30) all contain epitheliod cells
and T lymphocytes. The central caseating necrosis associated with granulomas is characteristic of tuberculous,
but not the beryllium-induced, sarcoid or Crohn’s disease lesions (Table 3). An additional difficulty for the
pathologist is the morphological spectrum seen in TB or leprosy (2). In TB tissue responses range from sheets of
foamy macrophages packed with acid fast-staining bacilli to hematogeneously spread 1-3 mm size miliary
granulomas in immunocompromised humans, to caseting or non-caseating organized epithelioid garnulomas (51).
Necrotizing granulomas are often indicative of vasculitic lesions. In the necrobiotic (collagenolytic) granulomas the
cellular infiltrate contains also neutrophils and eosinophils (35,55). The presence of associated pathologic findings
can also be useful, such as the eosinophilic infiltrate and/or eosinophil cationic protein in the serum in Churg-
Strauss disease. Examination of stained slides does not only aid in the correct diagnosis of the disease, but can
be a valuable tool in retrospective analyses of archival material. Detection in hundreds of slides of AFB of proven
TB cases can establish a correlation between the presence of AFB and active or dormant infection. A multivariate
analysis of the presence of epithelioid granulomas with subsequent surgical bowel resection revealed that in
Crohn’s disease the frequency of granuloma presence may indicate a more aggressive disease process (25).
The usual dilemma, however, is what to make of granulomatous inflammation when none of the above clues is
present, and repeat biopsies and cultures may be necessary to arrive at a final diagnosis.
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