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Brucellosis
‫دهنده‬ ‫ترتیب‬
:
‫دوکتور‬
‫عبدالقهار‬
«
‫مومن‬
‫زاده‬
»
‫نظر‬ ‫تحت‬
:
‫فیضی‬ ‫هللا‬ ‫ذبیح‬ ‫دوکتور‬ ‫پوهنوال‬
‫الرحیم‬ ‫الرحمن‬ ‫هللا‬ ‫بسم‬
CONTENTS
1. Introduction
2. Etiology
3. Epidemiology
4. Pathogenesis
5. Clinical features
6. Organ systems involvement (complications)
7. Diagnosis
8. Differential diagnosis
9. Treatment
10. Prognosis
11. prevention
INTRODUCTION
Genus brucella
Alpha-2 subgroup of protobacteria
Chronic granulomatous infection
 Zoonotic disease
ETIOLOGY
 Brucella abortus (cattle)
 Brucella melitensis ( goat and sheep )
 Brucella suis ( Swine )
 Brucella canis ( Dog )
gram ( - )
Aerobic
None spore forming
None motile
ETIOLOGY…
B.ovis
B.neotomae
B.ceti
B.pinnipedialis
B.microti
B.inopinata
EPIDEMIOLOGY
Brucella exist world wide ( rare in industrialized countries)
Mediterranean , India , Mexico , central and south America
Risk factor :
1. exposure to infected animals and animal’s product
2. Inhalation of infected aerosols
PATHOGENESIS
Rout of infection:
1. Skin ( cut and abrasions )
2. Inhalation ( infected aerosol )
3. Ingestion ( meat and dairy products )
4. Inoculation ( conjunctival sac of the eye )
PATHOGENESIS……..
Risk for infection depend on:
1. Nutritional status
2. Immune status
More virulent species
1. Brucella melitensis
2. Brucella suis
Smooth lipopolysaccharide
of cell wall
PATHOGENESIS……
This organism is Facultative intracellular and can:
1. Survive and replicate in monocyte and macrophage
2. Ingested by macrophage and localize within RES
3. Granuloma formation
PATHOGENESIS…..
The major factor in recovery:
1. Antibody against lipopolysaccharide and cell wall
2. Cell mediated response (macrophage activation enhance
intracellular killing)
3. Sensitized T lymphocyte (interferon gamma ,TNF alpha)
CLINICAL FEATURES
Brucellosis is a systemic illness and can be:
1. Acute ( < 2months )
2. Subacute ( 2 – 12 months )
3. Chronic ( > 1 years )
Incubation period : 7days – 3months
Symptoms generally beginning 2-4 weeks after exposure
CLINICAL FEATURES…..
Most patient have classic triad:
1. fever ( FUO ) : continues or intermittent and persist for several months.
2. arthralgia / arthritis: particularly knee , hip , ankle (child) sacroiliac ( adult )
3. hepatosplenomegaly
 Less common lymphadenopathy
CLINICAL FEATURES….
Other symptoms include:
1. Refuse to bear weight on an extremity + fever = typical presentation
2. Headache
3. Pharyngitis
4. Cough
5. vomiting
6. Abdominal pain
7. Diarrhea
8. Rashes
9. Night sweats
10. Weakness
CLINICAL FEATURES….
Invasion of nervous system can cause: 1%
1. Headache
2. Mental change
3. Depression
4. Symptom of meningitis
CLINICAL FEATURES….
Neonatal and congenital infection resulting from :
1. Transplacentally
2. Breast milk
3. Blood transfusion
ORGAN SYSTEMS OF
INVOLVEMENT
Skeletal system :
1. Arthritis
2. Movement limitation , swelling and tenderness of affected joint
3. Disclosing hip
4. Vertebral involvement
1. MRI
2. Radionuclide bone
scan
3. ultrasound
CENTRAL NERVOUS SYSTEM
1. Meningitis
2. encephalitis
3. Myelitis
4. Neuritis
5. Mycotic aneurysm
6. Brain abscess
ALIMENTARY TRACT
1. Nausea
2. Vomiting
3. Anorexia
4. Weight loss
5. Abdominal discomfort
Rare case of:
1. Cholecystitis
2. Ileitis
3. Colitis
4. pancreatitis
RETICULOENDOTHELIAL
SYSTEM
 Liver ( elevated liver enzyme or normal )
1. B.Abortus (noncaseating granuloma)
2. B.suis (suppurative abscess)
3. B.melitensis (hepatic lesion and nonspecific reactive hepatitis)
4. Rarely chronic hepatospleenic abscess (surgery)
CARDIOVASCULAR SYSTEM
1. Endocarditis (common)
2. Arterial and venous thrombosis
3. Cutaneous Vasculitis
4. Endarteritis
5. Myocarditis
6. Pericarditis
Peripheral and
cerebrovascular aneurysm
GENITOURINARY TRACT
1. Orchitis and epididymitis (adult)
2. Nephritis
3. Glomerulonephritis
RESPIRATORY TRACT
1. Cough ( common)
2. Respiratory tract lesion <5%
3. pneumonia
4. Pulmonary nodule
5. Empyema
HEMATOLOGIC SYSTEM
Mild hematologic abnormalities are
1. Anemia
2. Lymphocytosis
3. Thrombocytopenia
Rare life threatening complications are:
1. Pancytopenia
2. Thrombocytopenic purpura
3. Mucosal bleeding
DIAGNOSIS
1. History of exposure
2. Laboratory findings :
•Blood culture (gold standard) : prior to antibiotic therapy
•Bone marrow culture when organism is in RES (even after antibiotic)
•Serum agglutination test ( =>1:160 or =>1:320 ) except of B.canis
•ELISA (IgG and IgM)
DIAGNOSIS….
• Enzyme immunoassay indication:
1. Complicated cases
2. Suspected chronic brucellosis
3. Reinfection
DIFFERENTIAL DIAGNOSIS
1) Tularemia
2) Cat scratch disease
3) Typhoid fever
4) Chronic malaria
5) HIV
6) Sarcoidosis
7) Histoplasmosis
8) Blastomycosis
9) M.Tuberculosis infection
10) Atypical mycobacteria infection
11) Rickettsia infection
12) Yersinia infection
TREATMENT
1. Doxycycline
2. Aminoglycosides
3. Cephalosporin ( ceftriaxone )
4. Rifampicin
5. Streptomycin
TREATMENT
PROGNOSIS
 With specific antimicrobial therapy ( good outcome )
 Most of deaths are result of organ system involvement
PREVENTION
1. Prevent from exposure to infected animals
2. Use Pasteurized milk and dairy product
3. No vaccine currently exist
REFERENCES ….
GHAI 8th
Nelson
Pediatrics infectious disease 5th
‫جهان‬ ‫یک‬ ‫تان‬ ‫توجه‬ ‫از‬
‫سپاس‬
brucelosis.Dr.Abdulqahar Mominzada

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brucelosis.Dr.Abdulqahar Mominzada