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CASE
PRESENTATION
By Dr. Saifullah Chang
House Officer
Pediatric department GMMMC
HISTORY:
 21 days Abdul Kabeer S/O Shahnawaz
Muhammad Naveed R/O Sukkur ,
vaccinated according to EPI schedule;
presented to us with complain of
 Fits
 Fever 5th
day of life
HOPI:
 Fits were sudden in onset just after birth,
generalized tonic clonic in nature with up rolling of
eyes , continued for 6 hours in duration, multiple
attacks with interval of 15 minutes apart
 Baby taken to private hospital , went under
treatment and discharged on tab. Pheno
 Then developed fits and fever at 5th
DOL
 Fits were of same nature
 Fever was sudden in onset, high grade ,not
associated with rigors and chills or respiratory
distress , relieved by injectable medications given
at peads emergency
BIRTH HISTORY
ANTENATAL:
 Mother was young aged approx. 18 years with good
nutritional status and healthy background
 No any history of chronic maternal illness
 Booked case
 Vaccinated for tetanus
 Multivitamin supplements during pregnancy
 5 U/S were done at 3rd
6th
7th
9th
months respectively
all were normal showing single intrauterine fetus
with adequate growth , cardiac activity and liquor
 No history of leaking and P/V bleeding
 No any adverse previous obstetric outcome
NATAL:
 History of prolonged labour one hour in duration
 Trial taken by dia at home
 Emergency cesarean section was done at local
private setup
POST NATAL:
 History of delayed cry, after one hour of birth
 Suctioning and tactile stimulation was done
 Resuscitation was done in OT
 Baby developed fits after then
 Incubated for 4 days at private setup
 No history of jaundice and skin rash
FEEDING HISTORY:
 Breastfed at 5th
D.O.L
 No any history of early introduction of enteral feed
FAMILY HISTORY:
 First baby
 no previous issue
 History of child with cerebral palsy in
paternal side of family
ON EXAMINATION:
An ill pale looking
lethargic baby, on
oxygen support through
nasal cannula ,
cannulated on left foot ,
lying on bed poorly
responsive to tactile
stimulation , not crying
well
Vitals
 HR:128 B/P/M
 RR:46 B/min
 Temp:99.8F
 FOC:38 cm
 Anterior fontanel: bulging
and tense
 Weight: 2.5 KG
 Sub vitals
 A+ J- C- D+ E-
SYSTEMIC EXAMINATION:
CNS:
 Poor primitive reflexes
 Poor Moro, poor sucking, rooting, grasping
 Tone was increased
CHEST EXAMINATION:
On inspection: normal chest movements with
respiration
On palpation: no tenderness, mass, crepitus
On percussion: resonant note
On auscultation: B/L clear, N/V/B
ABDOMINAL EXAMINATION:
On inspection: normal symmetry normal
movement with respiration
On palpation: no tenderness, rebound
tenderness ,mass , no viceromegaly
On percussion: tympanic note
On auscultation: bowel sounds were audible
CARDIOVASCULAR
EXAMINATION:
 Normal 1st
and 2nd
heart sounds
 Apex beat palpable at 5th
intercostal space
 No any added sounds
ON INVESTIGATIONS:
CBC showed
 Hb: 9.6 mg/dl
 WBC: 11500 mg/dl
 Plt: 210,000 mg/dl
SERUM U/C/E SHOWED
 Urea: 52 mg/dl
 Creatinine: 0.3 mg/dl
 Sodium: 122.5 mg/dl
 Potassium:5.9 mg/dl
 Chloride: 85.1 mg/dl
 Calcium: 9.7 mg/dl
IMAGING:
U/S showed
 Moderately dilated all four ventricles
 Intraventricular septation
 Edema of brain parenchyma
DIFFERENTIA
L DIAGNOSIS
?
DIFFERENTIAL DIAGNOSIS:
 Hydrocephalus
 Meningitis
 Encephalitis
 Chronic haemolytic anemia(thalasemia)
 Rickets
 Osteogenesis imperfecta
 Epiphyseal dysplasia
HYDROCEPHALUS
 Defined as, congenital or Acquired disorder in
which there is excessive Accumulation of CSF
within cerebral ventricles.
 There are two main types of hydrocephalus
I. Communicating (Non obstructive)
II. Non communicating ( Obstructive)
CAse presentation on pediatric hydrocephalus
CAse presentation on pediatric hydrocephalus
ETIOLOGY
Congenital
 Congenital aqueductal stenosis
 Dandy walker malformation: Massive Dilation of
fourth ventricle which obstructs Csf flow & there
is hypoplasia of cerebellar vermis
 Arnold chiari malformation type II: The
cerebellar tonsils are displaced downward and
obstructs the Csf flow .
 Archnoid cyst or congenital tumours
 Intrauterine infections like CMV, Syphillis ,
toxoplasmosis
ACQUIRED HYDROCEPHALUS
 Secondary to infections of nervous systems e:g
Bacterial meningitis

 Brain tumours
 Archnoiditis secondary to bleeding into
subarchnoid space from a ateriovenous
malformation , aneurysm or trauma.
 IntraventriculAr haemorrhage in preterm
infants.
PHYSIOLOGY
CAUSES
 Increased production of CSF
 A block in CSF flow
 Impaired absorption of CSF

 Most common mechanism for producing
hydrocephalus is impaired absorption of Csf due
to obstruction of flow or dysfunction of absorptive
mechanisms.
SIGNS & SYMPTOMS
 There are signs & symptoms of primary process
I,e Infection , trauma,bleeding
 May be sign & symptoms of raised intracranial
pressure secondary to normal pressure
hydrocephalus.
 NonSpecific symptoms
 Headache, vomiting personality & behaviour
changes ( irritable lethargy drowsiness)
 Nonspecific signs
 3rd
and 6th
cranial nerve defecit, paresis of
extraocular muscles leading to diplopia , there
may be papilledema.
 Sunset Sign:produced by paralysis of upward gaze &
results in sclera being visible above the iris
 In an infant accelerated rate of enlargement of head is
prominent sign.
 Spasticity first develops in lower than upper in
ascending pattern due to stretching of motor nerve
fibers around lateral ventricles.
 There may be bibniskis sign , brisk tendon reflexes &
clonus.
 Cracked pot or Macewen Sign
INVESTIGATIONS
 X-ray
 CT scan
 MRI
ON CT
NON COMMUNICATING
HYDROCEPHALUS
TREATMENT
 Includes specific therapy for any undertling
disease ie(meningitis ,brain abcess, tumour)
 Medical therapy to decrease Csf production in
slowly progresssive hydrocephalus includes
Acetazolamide,foursemide & glycerol.
 A ventriculo peitoneal shunt is created between
ventricles and peritoneal cavity is the most
effective surgical method of treating
hydrocephalus
 Complications of shunt are mechanical
obstruction of shunt are mechanical obstruction
of shunt are meningitis or ventriculitis . Common
organism is staph Epidermidis
CAse presentation on pediatric hydrocephalus

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CAse presentation on pediatric hydrocephalus

  • 1. CASE PRESENTATION By Dr. Saifullah Chang House Officer Pediatric department GMMMC
  • 2. HISTORY: 21 days Abdul Kabeer S/O Shahnawaz Muhammad Naveed R/O Sukkur , vaccinated according to EPI schedule; presented to us with complain of Fits Fever 5th day of life
  • 3. HOPI: Fits were sudden in onset just after birth, generalized tonic clonic in nature with up rolling of eyes , continued for 6 hours in duration, multiple attacks with interval of 15 minutes apart Baby taken to private hospital , went under treatment and discharged on tab. Pheno Then developed fits and fever at 5th DOL Fits were of same nature Fever was sudden in onset, high grade ,not associated with rigors and chills or respiratory distress , relieved by injectable medications given at peads emergency
  • 5. ANTENATAL: Mother was young aged approx. 18 years with good nutritional status and healthy background No any history of chronic maternal illness Booked case Vaccinated for tetanus Multivitamin supplements during pregnancy 5 U/S were done at 3rd 6th 7th 9th months respectively all were normal showing single intrauterine fetus with adequate growth , cardiac activity and liquor No history of leaking and P/V bleeding No any adverse previous obstetric outcome
  • 6. NATAL: History of prolonged labour one hour in duration Trial taken by dia at home Emergency cesarean section was done at local private setup
  • 7. POST NATAL: History of delayed cry, after one hour of birth Suctioning and tactile stimulation was done Resuscitation was done in OT Baby developed fits after then Incubated for 4 days at private setup No history of jaundice and skin rash
  • 8. FEEDING HISTORY: Breastfed at 5th D.O.L No any history of early introduction of enteral feed
  • 9. FAMILY HISTORY: First baby no previous issue History of child with cerebral palsy in paternal side of family
  • 10. ON EXAMINATION: An ill pale looking lethargic baby, on oxygen support through nasal cannula , cannulated on left foot , lying on bed poorly responsive to tactile stimulation , not crying well Vitals HR:128 B/P/M RR:46 B/min Temp:99.8F FOC:38 cm Anterior fontanel: bulging and tense Weight: 2.5 KG Sub vitals A+ J- C- D+ E-
  • 11. SYSTEMIC EXAMINATION: CNS: Poor primitive reflexes Poor Moro, poor sucking, rooting, grasping Tone was increased
  • 12. CHEST EXAMINATION: On inspection: normal chest movements with respiration On palpation: no tenderness, mass, crepitus On percussion: resonant note On auscultation: B/L clear, N/V/B
  • 13. ABDOMINAL EXAMINATION: On inspection: normal symmetry normal movement with respiration On palpation: no tenderness, rebound tenderness ,mass , no viceromegaly On percussion: tympanic note On auscultation: bowel sounds were audible
  • 14. CARDIOVASCULAR EXAMINATION: Normal 1st and 2nd heart sounds Apex beat palpable at 5th intercostal space No any added sounds
  • 15. ON INVESTIGATIONS: CBC showed Hb: 9.6 mg/dl WBC: 11500 mg/dl Plt: 210,000 mg/dl
  • 16. SERUM U/C/E SHOWED Urea: 52 mg/dl Creatinine: 0.3 mg/dl Sodium: 122.5 mg/dl Potassium:5.9 mg/dl Chloride: 85.1 mg/dl Calcium: 9.7 mg/dl
  • 17. IMAGING: U/S showed Moderately dilated all four ventricles Intraventricular septation Edema of brain parenchyma
  • 19. DIFFERENTIAL DIAGNOSIS: Hydrocephalus Meningitis Encephalitis Chronic haemolytic anemia(thalasemia) Rickets Osteogenesis imperfecta Epiphyseal dysplasia
  • 20. HYDROCEPHALUS Defined as, congenital or Acquired disorder in which there is excessive Accumulation of CSF within cerebral ventricles. There are two main types of hydrocephalus I. Communicating (Non obstructive) II. Non communicating ( Obstructive)
  • 23. ETIOLOGY Congenital Congenital aqueductal stenosis Dandy walker malformation: Massive Dilation of fourth ventricle which obstructs Csf flow & there is hypoplasia of cerebellar vermis Arnold chiari malformation type II: The cerebellar tonsils are displaced downward and obstructs the Csf flow . Archnoid cyst or congenital tumours Intrauterine infections like CMV, Syphillis , toxoplasmosis
  • 24. ACQUIRED HYDROCEPHALUS Secondary to infections of nervous systems e:g Bacterial meningitis Brain tumours Archnoiditis secondary to bleeding into subarchnoid space from a ateriovenous malformation , aneurysm or trauma. IntraventriculAr haemorrhage in preterm infants.
  • 26. CAUSES Increased production of CSF A block in CSF flow Impaired absorption of CSF Most common mechanism for producing hydrocephalus is impaired absorption of Csf due to obstruction of flow or dysfunction of absorptive mechanisms.
  • 27. SIGNS & SYMPTOMS There are signs & symptoms of primary process I,e Infection , trauma,bleeding May be sign & symptoms of raised intracranial pressure secondary to normal pressure hydrocephalus. NonSpecific symptoms Headache, vomiting personality & behaviour changes ( irritable lethargy drowsiness) Nonspecific signs 3rd and 6th cranial nerve defecit, paresis of extraocular muscles leading to diplopia , there may be papilledema.
  • 28. Sunset Sign:produced by paralysis of upward gaze & results in sclera being visible above the iris In an infant accelerated rate of enlargement of head is prominent sign. Spasticity first develops in lower than upper in ascending pattern due to stretching of motor nerve fibers around lateral ventricles. There may be bibniskis sign , brisk tendon reflexes & clonus. Cracked pot or Macewen Sign
  • 30. ON CT
  • 32. TREATMENT Includes specific therapy for any undertling disease ie(meningitis ,brain abcess, tumour) Medical therapy to decrease Csf production in slowly progresssive hydrocephalus includes Acetazolamide,foursemide & glycerol.
  • 33. A ventriculo peitoneal shunt is created between ventricles and peritoneal cavity is the most effective surgical method of treating hydrocephalus Complications of shunt are mechanical obstruction of shunt are mechanical obstruction of shunt are meningitis or ventriculitis . Common organism is staph Epidermidis