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517362
malignant disease in children
Descrição
Paediatrics (Malignancy) Mapa Mental sobre malignant disease in children, criado por v.djabatey em 31-01-2014.
Sem etiquetas
malignancy
paediatrics
paediatrics
malignancy
Mapa Mental por
v.djabatey
, atualizado more than 1 year ago
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Criado por
v.djabatey
quase 11 anos atrás
26
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Resumo de Recurso
malignant disease in children
not common
1 child in 500 develops Ca by 15 years old
120-140 new cases per 10^6 kids under 15 years in Western countries
types of disease seen
1. leukaemia
commonest
affects kids of all ages (but there's an early childhood peak)
2. brain & spinal tumours
3. neuroblastoma
almost always seen in 1st 6 years of life
4. soft tissue sarcomas
5. Wilms tumour
almost always seen in 1st 6 years of life
6. (Hodkin lymphoma &) bone tumours
peak incidence in teen & early adult life
7. retinoblastoma
still commonest disease causing death in childhood beyond neonatal period
5 year survival of kids w/ all forms of Ca
about 75%
but long term medical & psychosocial difficulties
aetiology
precise aetiology is unclear in most cases
likely to involve interaction btw env factors & host genetic susceptibility
few established env risk factors
in most cases a specific mutation isn't known
even though Ca occurs due to sporadic but possibly heritable mutations in cellular growth & controlling genes
bilat retinoblastoma
e.g. of inherited Ca
assoc w/ mutation within RB gene on chromosome 13
lots of syndromes assoc w/ increased risk of Ca in childhood
assoc btw Down syn & leukaemia
neurofibromatosis & glioma
clinical presentation
localised mass
conseqs of disseminated disease
bone marrow infiltration
causing systemic ill health
conseqs of Pa from a mass on local strucs or tissues
e.g. airway obstruction 2ndary to enlarged lymph nodes in the mediastinum
Ix
radiology
combo of US, plain X ray, CT & MRI
to locate solid tumours & ID & localise evidence of mets
nuclear medicine
e.g. radiolabelled technetium bone scan
ID bone or bone marrow disease
using special markers (MIBG)
localise tumours of neural crest origin e.g. neuroblastoma
tumour marker studies
increased urinary catecholamine excretion (e.g. vanillylmandelic acid)
useful to confirm diag of neuroblastoma
high alpha-fetoprotein
often seen in germ cell tumours & liver tumours
levels used to monitor Rx & response
pathology
all diags need histological confirmation
bone marrow aspiration
for leukaemia
biopsy
for most solid tumours
but not always possible for brain tumours
immunohistochemistry
to differentiate tumour types
molecular & genetic techniques
used to confirm diag
e.g. translocation of chromosomes 11 & 22 in Ewing sarcoma
used to predict diagnosis
e.g. amplification of N-myc oncogene assoc w/ poor prognosis in neuroblastoma
Mx
detailed ix to define extent of disease (staging) vital to Rx
kids treated as part of collaborative studies that are consistent in care & have helped improve outcomes
initial ix & Rx in specialist centres
w/ MDTs to give intensive medical & psychosocial support needed
subsequent mx shared btw specialist centre, referral hospital & local services in community
teens & young adults
have poorer survival outcomes than kids
related to specific types & biological behaviour of their tumours
are their own distinct population
related to the particular social/psychological needs
-> development of age-approp Rx protocols, facilities & support networks
Rx
chemotherapy
uses
as primary curative Rx e.g. in acute lymphoblastic leukaemia
to control primary or metastatic disease before local Rx w/ surgery &/or radiotherapy e.g. sarcoma or neuroblastoma
as adjuvant Rx to deal w/ residual disease & get rid of presumed micromets e.g. after initial local surgery in Wilms tumour
radiotherapy
still has role in Rx of some tumours
risk of damage to growth & function greater in kid than adult
need adeq protection of normal tissues & careful positioning & mobilisation of pt during Rx
can be hard in practice
surgery
initial surgery often restricted to biopsy to get diag
more extensive ops usually done to remove residual tumour after chemo &/or radiotherapy
high-dose therapy w/ bone marrow rescue
limitation of chemo & radiotherapy is risk of irreversible damage to normal tissues, esp bone marrow
bone marrow stem cell transplantation can be used to intensify Rx of pts w/ admin of potentially lethal doses of chemo &/or radiation
source of marrow stem cells
allogeneic
from a compatible donor
used in mx of high risk or relapsed leukaemia
autologous
from pt himself, harvested beforehand, while marrow uninvolved or in remission
Rx of solid tumours w/ poor prognosis using conventional chemo e.g. advanced neuroblastoma
supportive care & (short- term) S/Es of Rx
bone marrow suppression
anaemia
may need blood transfusions
thrombocytopenia & bleeding
blood product support needed
esp for kids
w/ leukaemia
undergoing intensive therapy needing bone marrow transplantation
under Rx with more intensive solid tumour protocols
neutropenia
-> infection
immunosuppression
infection
due to Rx & underlying disease kids w/ Ca are immunocompromised & @ risk of serious infection
kids w/ fever & neutropenia
admit promptly to hospital for cultures & broad spec Abx
opportunistic infections assoc w/ Ca
Pneumocystis jiroveci (carinii) pneumonia
esp in kids w/ leukaemia
disseminated fungal infection
aspergillosis
candidiasis
coag -ve staph infections of central venous catheters
viral
most no worse than in kids w/o Ca
attn to measles & chicken pox
atypical presentation & life-threatening
if non-immune, immunocomp kids @ risk from contact w/ these viruses
give Ig or zoster immune globulin promptly for some protection
Rx
aciclovir for established varicella infection
none available for measles
use of live vaccines
contraindicated during chemo & from 6 months-1 year afterward
after this re-immunisation against common childhood infections recommended
GI mucosal damage, nausea & vomiting, anorexia
->undernutrition
gut mucosal damage from chemo ->
diarrhoea
G-ve infection
mouth ulcers
oommon
painful
if severe, can stop child eating enough
many chemo agents nauseating & induce vomiting
partially prevented by routine use of antiemetic
drug-specific S/Es
doxorubicin
cardiotoxicity
cyclophosphamide
haemorrhagic cystitis
vincristine
neuropathy
extent of S/Es not always predictable
monitoring needed during & sometimes after Rx done
other supportive care issues
venous access
central venous catheters
avoid discomfort of multiple venepunctures
risk of infection
fertility preservation
risk of infertility due to Ca Rx in some pts
surgical removal of testis or ovary out of radiotherapy field
sperm banking
boys need to mature enough to achieve this
preservation of ovarian cortical tissue
uncertain long term efficiency
psychosocial support
counselling
practical support
transport
finances
accommodation
care of siblings
give detailed written material to parents
encourage return to normal life once Rx established
early return to school
severe stress-> marital probs & behavioural difficulties in child & siblings
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Saiba mais
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Semelhante
leukaemia
v.djabatey
lymphomas
v.djabatey
bone tumours
v.djabatey
palliative care
v.djabatey
brain tumours
v.djabatey
neuroblastoma
v.djabatey
soft tissue sarcomas
v.djabatey
Wilms tumour (nephroblastoma)
v.djabatey
retinoblastoma
v.djabatey
rare tumours
v.djabatey
Child development
as0180.2010
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