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Hello, baby!
Laura Bruno, M.D.
Milia
White papules
Sebaceous glands
Commonly on nose
Mongolian Spot
Gray-blue
Common in dark-skinned
and Asian infants
Buttocks, or back,
shoulders
Erythema
Toxicum
Maculopapular
Eosinophils
Benign
Small vesicles
Polymorphonuclear
leukocytes
Neonatal Acne
Fetal glandular
development
Hormonal stimulation
6 month resolution
Strawberry Hemangioma
30% newborns
Commonly on face
Cavernous Hemangioma
Subcutaneous
Usually do not
involute
May grow
Sturge-Weber
assoc.:ophthalmic division
of trigemminal n.
Usually benign
Associated with
neurocutaneous
syndromes: check #
and size (mm.)
Herpes Neonatorum
Vesicular
Caput Succedaneum
Prolonged labor
Serosanguinous fluid
Above periosteum
Newborn Hematomas
QuickTime and a
decompressor
are needed to see this picture.
Cephalohematoma
Subperiosteal
hemorrhage
Well demarcated
Resorb, calcify
Hyperbilirubinemia?
Red Reflex
Leukocoria
White reflex
Retinoblastoma: 30%
b/l
Retinal abnormalities
Subconjunctival Hemorrhage
Benign
Spontaneous
resolution in days
Conjunctivitis
Chemicalearly onset,
resolves 2-3 days,
esp.silver nitrate
Gonococcalonset at 2-3
days of life, intense
Chlamydialonset at 1-2
weeks of life, assoc.
pneumonia
Urogenital
malformations
Deafness
Preauricular Sinus
Failure of fusion of
hillocks arising from
branchial arches
Autosomal dominant
Recurrent infections
require antibiotics
Epsteins Pearls
White
Epithelialized
Gums = Epsteins,
may also be on roof of
mouth or soft palate
Cleft Lip
Incomplete embryonic
fusion of maxillary and
nasal processes
uni- or bi-lateral
Cleft Palate
Failure of fusion of
palatine plates
Variable severity
Concerns: cosmetic;
feeding: suck, milk
leaks into nasal cavity-infection: recurrent
otitis media, sinus
infections; t+a
hypertrophy; speech
Shoulder Dystocia
Torticollis
Erbs Palsy
Damage to 5th and 6th
cervical roots
Paralysis of shoulder
and arm
Internal rotation,
adduction, flexed
wrist=waiters tip
Neuro, PT
Polydactyly
Hereditary
Commonly lateral to
5th digit
Estrogenization
Breast engorgement
f/m
Swollen labia
Vaginal d/c
Swollen scrotum
Ligamentous laxity
Justa-ductal narrowing
Symptomatic with closure
of ductus arteriosus: heart
failure, esp.if complicated
Prompt diagnosis and
treatment: femoral pulses,
heart mm, 4-limb BPs
Associations: Turners
Syndrome, cardiac
anomalies (VSD)
Transposition of Great
Arteries
Congenital Diaphragmatic
Hernia
Umbilical Hernia
Common, ~70%
infants
Usually benign
Resolution by 2 years
Incarceration <1%
Omphalocele
Periumbilical defect,
umbilical cord involved
Variable contents: bowel,
liver, spleen
Covered by fetal sac
Prenatal diagnosis
Associations in 50-70%
cases:Trisomy, congenital
heart, GI
Gastroschisis
Inguinal Hernia
0.5-1% term
5-10% preterm
R>L
Soft, NT, reducible
Increases with pressure
Complications:
incarceration,
strangulation
Surgery
Hypospadias
Contraindication to
circumcision
Urological consult,
surgery
Sacral Dimple
Meningocele
Developmental Dysplasia of
the Hip
Club Foot
Talipes equinovarus
Abnormality of both foreand hindfoot and ankle
1-2/1000 live births
M>F
Hereditary
Early intervention:
manipulation and serial
casts vs. surgery
Breastfeeding Position
Observation
Infant parallel to
mothers body
Newborn Stool
Meconium
Breastfeeding stools
Variable frequency
Discharge Planning:
Bye-bye, baby!
Before Discharge