Cgi: Difference between revisions

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{{PAGENAME}} - short region of dna in which the frequency of the cg sequence is higher than in other regions.
{{DISPLAYTITLE:Chronic Granulomatous Inflammation}}
{{med-stub}}
{{Infobox medical condition
{{dictionary-stub2}}
| name = Chronic Granulomatous Inflammation
{{short-articles-ni}}
| image =
| caption =
| field = [[Immunology]]
| symptoms = Persistent inflammation, tissue damage
| complications = Fibrosis, organ dysfunction
| onset = Variable
| duration = Chronic
| causes = Infectious agents, autoimmune diseases, foreign bodies
| risks = Genetic predisposition, environmental factors
| diagnosis = Biopsy, imaging studies
| treatment = Corticosteroids, immunosuppressants, surgery
| prognosis = Variable
}}
 
'''Chronic Granulomatous Inflammation''' (CGI) is a type of [[chronic inflammation]] characterized by the formation of [[granulomas]], which are small aggregates of [[macrophages]] that have transformed into [[epithelioid cells]]. This condition can occur in response to a variety of stimuli, including persistent infectious agents, foreign bodies, and certain autoimmune diseases.
 
==Pathophysiology==
Chronic granulomatous inflammation is a complex immune response that occurs when the immune system attempts to isolate substances it perceives as foreign but is unable to eliminate. The formation of granulomas is a hallmark of this type of inflammation. Granulomas are composed of macrophages, which transform into epithelioid cells and often fuse to form [[multinucleated giant cells]]. These structures are surrounded by a collar of [[lymphocytes]] and sometimes [[fibroblasts]].
 
The process begins with the activation of macrophages by [[T-helper cells]], particularly the Th1 subset, which secrete [[cytokines]] such as [[interferon-gamma]] (IFN-γ). This cytokine milieu promotes the transformation of macrophages into epithelioid cells and the formation of multinucleated giant cells. The persistent presence of the inciting agent leads to chronic inflammation and tissue damage.
 
==Causes==
Chronic granulomatous inflammation can be caused by a variety of factors, including:
 
* '''Infectious agents''': Certain bacteria, fungi, and parasites can cause granulomatous inflammation. Notable examples include [[Mycobacterium tuberculosis]], which causes [[tuberculosis]], and [[Histoplasma capsulatum]], which causes [[histoplasmosis]].
 
* '''Autoimmune diseases''': Conditions such as [[sarcoidosis]] and [[Crohn's disease]] are associated with granuloma formation.
 
* '''Foreign bodies''': The presence of foreign materials, such as [[sutures]] or [[silica]], can lead to granuloma formation as the body attempts to wall off the foreign substance.
 
==Clinical Presentation==
The clinical presentation of chronic granulomatous inflammation varies depending on the underlying cause and the organs involved. Common symptoms include:
 
* Persistent [[fever]]
* [[Fatigue]]
* [[Weight loss]]
* Localized pain or discomfort
* Organ-specific symptoms, such as cough and dyspnea in pulmonary involvement or abdominal pain in gastrointestinal involvement
 
==Diagnosis==
The diagnosis of chronic granulomatous inflammation typically involves a combination of clinical evaluation, imaging studies, and histopathological examination. A [[biopsy]] of the affected tissue is often necessary to confirm the presence of granulomas. Imaging studies, such as [[X-rays]], [[CT scans]], or [[MRI]], may be used to assess the extent of organ involvement.
 
==Treatment==
The treatment of chronic granulomatous inflammation depends on the underlying cause. General approaches include:
 
* '''Corticosteroids''': These are often used to reduce inflammation and suppress the immune response.
 
* '''Immunosuppressants''': Drugs such as [[methotrexate]] or [[azathioprine]] may be used in autoimmune conditions.
 
* '''Antimicrobial therapy''': In cases of infectious granulomatous inflammation, appropriate antibiotics or antifungal medications are used.
 
* '''Surgical intervention''': In some cases, surgical removal of the granulomatous tissue may be necessary.
 
==Prognosis==
The prognosis of chronic granulomatous inflammation varies widely depending on the cause and the organs involved. Some conditions, such as sarcoidosis, may resolve spontaneously, while others, like tuberculosis, require prolonged treatment. Chronic inflammation can lead to complications such as fibrosis and organ dysfunction.
 
==See Also==
* [[Granuloma]]
* [[Chronic inflammation]]
* [[Immune system]]
 
==External Links==
* [Link to relevant medical resources]
 
{{Medical conditions}}
[[Category:Inflammatory diseases]]
[[Category:Immunology]]
[[Category:Pathology]]

Latest revision as of 16:59, 1 January 2025


Chronic Granulomatous Inflammation
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Persistent inflammation, tissue damage
Complications Fibrosis, organ dysfunction
Onset Variable
Duration Chronic
Types N/A
Causes Infectious agents, autoimmune diseases, foreign bodies
Risks Genetic predisposition, environmental factors
Diagnosis Biopsy, imaging studies
Differential diagnosis N/A
Prevention N/A
Treatment Corticosteroids, immunosuppressants, surgery
Medication N/A
Prognosis Variable
Frequency N/A
Deaths N/A


Chronic Granulomatous Inflammation (CGI) is a type of chronic inflammation characterized by the formation of granulomas, which are small aggregates of macrophages that have transformed into epithelioid cells. This condition can occur in response to a variety of stimuli, including persistent infectious agents, foreign bodies, and certain autoimmune diseases.

Pathophysiology[edit]

Chronic granulomatous inflammation is a complex immune response that occurs when the immune system attempts to isolate substances it perceives as foreign but is unable to eliminate. The formation of granulomas is a hallmark of this type of inflammation. Granulomas are composed of macrophages, which transform into epithelioid cells and often fuse to form multinucleated giant cells. These structures are surrounded by a collar of lymphocytes and sometimes fibroblasts.

The process begins with the activation of macrophages by T-helper cells, particularly the Th1 subset, which secrete cytokines such as interferon-gamma (IFN-γ). This cytokine milieu promotes the transformation of macrophages into epithelioid cells and the formation of multinucleated giant cells. The persistent presence of the inciting agent leads to chronic inflammation and tissue damage.

Causes[edit]

Chronic granulomatous inflammation can be caused by a variety of factors, including:

  • Foreign bodies: The presence of foreign materials, such as sutures or silica, can lead to granuloma formation as the body attempts to wall off the foreign substance.

Clinical Presentation[edit]

The clinical presentation of chronic granulomatous inflammation varies depending on the underlying cause and the organs involved. Common symptoms include:

  • Persistent fever
  • Fatigue
  • Weight loss
  • Localized pain or discomfort
  • Organ-specific symptoms, such as cough and dyspnea in pulmonary involvement or abdominal pain in gastrointestinal involvement

Diagnosis[edit]

The diagnosis of chronic granulomatous inflammation typically involves a combination of clinical evaluation, imaging studies, and histopathological examination. A biopsy of the affected tissue is often necessary to confirm the presence of granulomas. Imaging studies, such as X-rays, CT scans, or MRI, may be used to assess the extent of organ involvement.

Treatment[edit]

The treatment of chronic granulomatous inflammation depends on the underlying cause. General approaches include:

  • Corticosteroids: These are often used to reduce inflammation and suppress the immune response.
  • Antimicrobial therapy: In cases of infectious granulomatous inflammation, appropriate antibiotics or antifungal medications are used.
  • Surgical intervention: In some cases, surgical removal of the granulomatous tissue may be necessary.

Prognosis[edit]

The prognosis of chronic granulomatous inflammation varies widely depending on the cause and the organs involved. Some conditions, such as sarcoidosis, may resolve spontaneously, while others, like tuberculosis, require prolonged treatment. Chronic inflammation can lead to complications such as fibrosis and organ dysfunction.

See Also[edit]

External Links[edit]

  • [Link to relevant medical resources]