PYREXIA OF UNKNOWN ORIGIN Dr. Alaa Jumaa PUO is A Common disease presenting ATYPICALLY.

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PYREXIA OF UNKNOWN ORIGIN Dr. Alaa Jumaa

Transcript of PYREXIA OF UNKNOWN ORIGIN Dr. Alaa Jumaa PUO is A Common disease presenting ATYPICALLY.

Page 1: PYREXIA OF UNKNOWN ORIGIN Dr. Alaa Jumaa PUO is A Common disease presenting ATYPICALLY.

PYREXIA OF UNKNOWN ORIGIN

Dr. Alaa Jumaa

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PUO is

A Common disease presenting ATYPICALLY

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Terminology

Old Definition: Petersdorf and Beeson (1961)

1. Fever higher than 38.3oC on several occasions.

2. Duration of fever – 3 weeks

3. Uncertain diagnosis after one week of study in hospital

New Definition: Eliminated the in-hospital evaluation

requirements → 3 outpatient visits, or 3 days in hospital. … Ambulatory as well as in hospital

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Categories of Illness Causing PUO

Infections 30 - 40 %

Malignancies 20 – 25 %

Collagen Vascular Disease 10 – 20 %

Miscellaneous 15 – 20 %

Undiagnosed 10 – 15 %

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Epidemiology and Etiology

1970 → up to date: Infection is the most frequent.

1930 → 70% undiagnosed PUO 2000 → 5-10% undiagnosed PUO

Diagnostic Advances:

Modify the spectrum of PUO causing diseases:1. Serology: HIV / Brucella / SLE

2. Imaging Tech: Abscesses/Solid Tumor

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Geography

Malaria Saudi (malaria area)/Africa/India

Brucella Saudi/Gulf Area

Kala-Azar Yemen/Sudan/India

Leprosy Yemen/Najran…

Typhoid India/Pakistan/Egypt/Indonesia

Histoplasmosis USA … (West Coast)

Tuberculosis

All over the world.Liver Abscess

AIDS

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Infect Neopl CVD Other Unknown

India UK

J Postgrad Med 2001; 47(2):104-107

Geography

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DIAGNOSIS AND TREATMENT

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Diagnostic Approach

Careful History Physical Examination (repeated) Diagnostic Testing

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History

Verify the presence of fever:Series of 347 patients → for prolonged fever

→ 35% were ultimately: a. No fever

b. Factitious Fever

Duration of Fever:The longer the duration → the less likely to

have infection and malignancy.

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History

A history of exposure to wild or domestic animals should be solicited (zoonotic disease )

Ingestion of dirt is a particularly important clue to infection with Toxoplasma gondii (toxoplasmosis).

Ancestry from the Mediterranean should suggest the possibility of familial Mediterranean fever (FMF).

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History

Travel: Travel to an area known to be endemic for certain disease:

Name of the area, duration of stay Onset of illness … (incubation period)

1 – 10 Days 10 – 21 Days Weeks - Months

Malaria Malaria Kala Azar

Plague Typhoid Amoebiasis

Dengue Brucella HIV

Salmonella Hepatitis A Hepatitis

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History

Drug and Toxin History:almost all drug can cause drug fever … Antihistaminebeta lactamanti-TB … Salicylates and other NSAID …eye drops, which may be associated with

atropine-induced fever.

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History

Localizing Symptoms: May Indicate the source of fever:

Bone ach osteomylitis

Bone Metastasis

Headache Chronic Meningitis

RUQ Pain Liver Abscess

LUQ Pain Splenic Abscess

Subtle changes in behavior Granulomatous Meningitis

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History

Family History:search for possible infectious or hereditary

disorders Tuberculosis FMF

Past Medical Condition:Lymphoma → may recurRheumatic Fever → may recur

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Physical Examination

Document the Fever: Significant and persistent for more than ONE occasion.

Analyzing the Pattern: Neither specific Nor sensitive enough to be considered

diagnostic … EXCEPT

Tertian & Quarter Pattern → MalariaPel-Ebstein Pattern → Lymphoma/TuberculosisPulse-Temp Dissociation → Typhoid/Brucellosis

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Pattern of Fever

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Physical Examination

Sweating in a febrile child should be noted familial dysautonomia, or exposure to atropine.

A careful ophthalmic examination is important Hyperemia of the pharynx, with or without

exudate, suggests infectious mononucleosis, CMV infection,

toxoplasmosis, salmonellosis ,Kawasaki disease. The muscles and bones should be palpated

carefully.

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Physical Examination

Examine for Lymphadenopathy

Cervical Area 1. Lymphoma(Localized) 2. Tuberculosis

3. Infectious Mononucleosis

4. Lymphadenitis (bacterial)

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Diagnostic Testing

1. CBC with a differential WBC count and a urinalysis should be part of the initial laboratory evaluation.

2. An erythrocyte sedimentation rate (ESR).

3. C-reactive protein is another acute-phase reactant that becomes elevated and returns to normal more rapidly than the ESR.

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Diagnostic Testing

serology1. Anti-nuclear Antibodies

2. Rheumatoid Factor

3. CMV Antibody … IgM

4. Heterophile Antibody Test in children and young adult

5. Tuberculin Skin Test … 5 unit ID

6. Thyroid Function Test

7. HIV Screening

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Diagnostic Testing

CulturesBlood

Obtain more than 3 blood cultures from separate venipunctures over 24 hr period if you are suspecting inf. Endocarditis prior antimicrobial use.

Incubate the blood for 4 weeks, to detect the presence of SBE & Brucellosis

Sputum: For TuberculosisAny normal sterile:

CSF/urine/pleural or peritoneal fluid Bone marrow aspirate → Tuberculosis/Brucellosis Lymph node Bx → TB

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Diagnostic Testing

Imaging Studies: … to localize abnormalities for definite tests or treatmentChest x-ray:

Atelectasis } 1. Liver

↑ Hemi diaphragm } Abscess 2. Spleen

Pleural Effusion } 3. Pancreatic

4. Subphrenic Mediastinal mass → Lymphoma/Tuberculosis/

Sarcoid If CXR is (N) → Repeat on weekly basis

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Diagnostic Testing

CT-Scan → CT scan chest Mediastinal mass → Tuberculosis/Lymphoma/

Sarcoidosis CT-Scan Abdomen → very effective to visualize

All types of abscesses Retroperitoneal tumor, lymph node or haematoma

MRI: spleen, lymph node and the brain Radionuclide scans

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The majority of disease remaining after an

initial NEGATIVE work-up are:

1. Neoplasm

2. Seronegative Collagen Vascular Disease

3. Increasing Tuberculosis

4. Increasing Drug Addition

5. Endocarditis

6. HIV with or without infection or malignancy

7. Implanted prosthetic devices

8. Travel … New Exposure

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Therapeutic Trials

Limitation and risk of empirical therapeutic trials:Rarely specificUnderlying disease may remit spontaneously

false impression of success.Disease may respond partially and this may

lead to delay in specific diagnosis.Side effect of the drugs can be misleading.

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Therapeutic Trials

To hold therapeutic trials in the early stage… except in:

Patient who is very sick to wait. All tests have failed to uncover the etiology. Tuberculosis Culture-negative endocarditis.

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