I hope everyone enjoy and get benefit from my questions big thanx for the knight , mobic , and a very big one for ali al kafaji[COLOR=green]
mobic777- 12-13-2007
HII
A PREVIOUSLY healthy 3 year old boy is brought to the emergency department by his mother because of 2-day hx of ahigh fever ,rash and red eyes, his temperture is 39.5C physical exam shows bilateral conjuctival injection ,an enlarged left sided cervical lymphnode(1.7)cm ,fissured lips, ared tongue with red papillae , pharyngeal hyperemia , erythematous palms and soles , and aconfluent ,blanching erythematous rash on the trunk LAB FINDING :ESR 28mm/h platelet count 490,000/mm
DUE TO THIS CONDITION , THE P IS AT INCREASED RISK FOR WHICH OF THE FOLLOWING COMLICATION ?
A-BLINDNESS
B-CORONARY ANEURYSM
C-GLOMERULONEPHRITIS
D-HEPATITIS
E-SPLENIC RUPTURE
GOOD LUCK
hammodi- 12-13-2007
i know this is scarlet fever but i don't know the complication.
mobic777- 12-13-2007
NO ITS NOT , ITS MUCH COMLICATED
THINK AGAIN
The Knight- 12-13-2007
Blindness
bloodstone- 12-13-2007
Glonerulonephritis??
sarmad- 12-13-2007
i think Coronary aneurysm (as the Dx is Kawasaki dis-MucoCutaneousLymphnode synd-)
hammodi- 12-13-2007
i thought of scarlet fever coz of the red tongue and blanching rash on trunk, anyway, let us know what is this.
ali al-kafaji- 12-13-2007
hmmm i have no idea........
mobic777- 12-14-2007
HII THE ANSWER IS B- CORONARY ANEURYSM THE DISEASE IS CALLED KAWASAKI(MUCOCUTANEOUS LYMPHNODE SYNDROM): IT OCCURE IN INFFANTS AND YOUNG CHILDREN (LESS THAN 4 Y) clinical features include: acute febrile illness,conjuctivitis,generalised maculopapular rash , lyphadenopathy this disease affect the medium and large size arteries but the coronary artery is the most affected ( 70%)
well done DR. SARMAD
GOOD LUCK
Dr.Leo1984- 12-14-2007
But the clinical features resemble the scarlet fever , mo?
what's the characteristics features of kawasaki in your example????
mobic777- 12-14-2007
HII
Kawasaki disease is a systemic vasculitis predominantly affecting children under the age of 5 years. It has a number of classic clinical features required for diagnosis.
In 1990 the American Heart Association committee on rheumatic fever, endocarditis, and Kawasaki disease2 gave the case definition that has been generally accepted—ie, a febrile illness of at least five days with at least four of the five following signs and no other reasonable cause for the findings:
Bilateral conjunctival injection – (there is no corneal ulceration but there may be a concomitant anterior uveitis on slit lamp examination)
Oral changes (erythema of lips or oropharynx, strawberry tongue due to prominent papillae, or fissuring of the lips) Peripheral extremity changes (oedema, erythema, or generalised or periungal desquamation); erythema is seen in the first week whereas desquamation begins about 14–21 days after the onset of the illness
Rash – this starts in the first few days; it is often diffuse and polymorphic and lasts a week before fading. Vesicles are rarely seen; however, the rash can appear macular, maculopapular, urticarial, scarlettina or even morbilliform Cervical lymphadenopathy is found in about 50% of cases; most often there is a painful solitary enlarged lymph gland, > 1.5 cm in diameter
AS FOR THE DIFFERENCE BETWEEN IT AND SCARLET FEVER: 1- IN KAWASAKI THE LYMPHADENOPATHY IS MORE EXTENSIVE 2- IN SCARLET FEVER YOU DONT SEE CONJUCTIVITES, ALSO THERE IS RAPID RESPONSE TO ANTIBIOTIC
mobic777- 12-17-2007
hii
A 77-year-old man has developed increasing dyspnea for the past 3 years. On physical examination he has a diastolic murmur. A chest radiograph shows an enlarged heart and prominent aorta. He dies from complications of pneumonia. At autopsy, the thoracic aorta is aneurysmally dilated. A microscopic section of the aorta shows chronic inflammation and luminal narrowing of vasa vasora. There is disruption of the aortic medial elastic fibers. Which of the following conditions is most likely to cause these findings?
A Hypercholesterolemia
B Marfan syndrome
C Polyarteritis nodosa
D Takayasu arteritis
E Tertiary syphilis
F Wegener granulomatosis
good luck
smile- 12-18-2007
i think the answe is tertiary syphlis
sufyan- 12-18-2007
either polyarteritis nodosa or tertiary syphilis
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