Hemato-onco Flashcards

(27 cards)

1
Q

factori de risc pentru boala hemolitica a nou-nascutului

A

hemoragie materno-fetala: avort, amniocenteza, sangerare de trimestru 3

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2
Q

cand trebuie administrata imunoglobulina Rho D dupa nastere la mame Rh (-)

A

daca mama are fat Rh + in primele 72 de ore

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3
Q

ce cauzeaza incompatibilitatea Rh mama-fat?

A

hemoliza severe si cel mai probabil deces fetal

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4
Q

Anemia Fanconi: transmitere genetica

A

autosomal recesiva

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5
Q

Anemia Fanconi: ce da boala?

A

insuficienta medulara
pancitopenie
risc de leucemie

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6
Q

Anemia Fanconi: clinica 6

A

oboseala, dispnee de efort
infectii frecvente
statura mica
pigmentari tegumentare (cafe au lait / zone hipopigmentare)
rinichi in potcoava
anomalii ale degetelor

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7
Q

Anemia Fanconi: marker serici, biopsie medulara si analiza cromozomiala

A

alfa-fetoproteina crescuta
hipocelularitate
multiple rupturi ale benzilor

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8
Q

Anemia Fanconi: tratament

A

antibiotice
transfuzii
transplant medular / celule stem hematopoietice
factori de crestere hematopoietici
androgeni / corticosteroizi cresc activitatea medulara

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9
Q

Anemia Fanconi: evolutie

A

deces in copilarie frecvent

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10
Q

Anemia Diamod-Blackfan: ce reprezinta?

A

anemie congenitala pura, cel mai probabil defect in celulele eritroide progenitoare

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11
Q

Anemia Diamod-Blackfan: clinica 6

A

oboseala, dispnee
cianoza si paloare precoce
anomalii cranio-faciale / degete
sufluri cardiace
dizabilitate intelectuala
hipogonadism

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12
Q

Anemia Diamod-Blackfan: VEM si reticulocitele?

A

VEM crescut, reticulocite scazute

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13
Q

Anemia Diamod-Blackfan: biopsia medulara

A

activitate scazuta dar multa eritropoietina

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14
Q

Anemia Diamod-Blackfan: tratament

A

transfuzii
corticosteroizi
transplant medular

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15
Q

Neuroblastomul: ce reprezinta?

A

tumora cu originea in creasta neurala care apare inÖ
suprarenala sau in ganglionii simpatici

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16
Q

Neuroblastomul: facori de risc

A

neurofibromatoza
scleroza tuberoasa
feocromocitomul
sindrom Beckwith-Wiederman (crestere anormala)
sindromul Turner (monosomie X)
consum matern scazut de folat

17
Q

Neuroblastomul: clinica 13

A

distensie si durere abdominala
masa abdominala
diaree
hepatomegalie
scadere ponderala
stare generala alterata
febra
durere osoasa
HTA
sindrom Horner
proptoza (Exoftalmie)
echimoza periorbitala
tulburari de miscare

18
Q

Neuroblastomul: ce investigatie de laborator faci?

A

urina pe 24 de ore, posibil acid vanilmandelic si homovanilic crescute

19
Q

Neuroblastomul: ce investigatie imagistica faci?

A

CT-abdominal pt localizarea tumorii

20
Q

Neuroblastomul: tratament

A

rezectie chirurgicala
chimioterapie
radioterapie

21
Q

Neuroblastomul: prognostic

A

sub un 1 prognostic prost, peste prognostic bun

22
Q

Neuroblastomul: metastaze?

23
Q

Care este cel mai frecvent sarcom de tesuturi moi la copii?

A

Rabdomiosarcomul

24
Q

Rabdomiosarcomul: prezentare clinica

A

masa dureroasa de tesuturi moi cu edem, frecvent efect de masa

25
Rabdomiosarcomul: cum stabilesti diagnosticul?
prin biopsie
26
Rabdomiosarcomul: imagistica?
CT sau RMN pt stabilire extensie
27
Rabdomiosarcomul: tratament
rezectie chirurgicala radioterapie chimioterapie