CLINICOPATHOLOGICAL CONFERENCE PEDIATRICS
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Transcript CLINICOPATHOLOGICAL CONFERENCE PEDIATRICS
CLINICOPATHOLOGICAL
CONFERENCE PEDIATRICS
Durante, Esperon, Espino, Fernando, Figuracion, Flores, Fong, Francisco,
Francisco, Garcia, Garcia, Garcia, Garcia, Garcia, Garimbao
SUBJECTIVE
10-year-old
intermittent headache of 1 year duration
vague
frontal headaches
occur twice a week, usually in the late afternoons
diagnosed to have Iron Deficiency Anemia
prescribed with oral Iron preparation
SUBJECTIVE
projectile vomiting
non-villous,
non-bloody
amounting to half a cup
occurs 2-3 times a day
did not experience tinnitus, gait disturbance,
gastrointestinal, and urinary problems
SUBJECTIVE
allergic to shrimp
diagnosed with asthma last 2007
family history of diabetes mellitus and hypertension
OBJECTIVE
slightly pale conjunctivae
+ horizontal nystagmus
GCS 15 (E4V5M6)
positive for Romberg’s sign
no motor or sensory deficit
negative for Babinski sign, ankle clonus, nuchal
rigidity, Kernig’s sign, and Brudzinski sign
COURSE IN THE WARDS
Admission
given Omeprazole 40 mg IV OD
Ist HOSPITAL DAY
given Dexamethasone 2.5mg q6h
for the treatment of vasogenic edema associated with brain
tumors
given Mannitol at 100 cc q6h
to prevent irritation of the esophageal mucosa due to multiple
bouts of vomiting
to decrease intracranial volume
Imaging studies were also done
COURSE IN THE WARDS
CSF analysis from ventricular drainage
5
cc of clear, colorless fluid
pH of 7.5
specific gravity of 1.010
RBC 514 x 106
WBC 1 x 106, 100% lymphocytes
glucose of 4.7 mmol/L
protein 0.11 g/L
(-) Pandy’s
COURSE IN THE WARDS
4TH HOSPITAL DAY
the
patient underwent an operation
Ceftriaxone 750 mg IV was started and other
medications were continued
6th HOSPITAL DAY
Limited
lateral eye movements on the left
COURSE IN THE WARDS
7TH HOSPITAL DAY
Omeprazole IV and Dexamethasone IV were
shifted to oral preparation
no
episodes of vomiting were noted
MRI of the whole spine and liver function test
to
evaluate for possible metastasis
LABORATORIES
Result
Interpretation
Calcium
Magnesium
Creatinine
2.62
1.0
61
Normal
Normal
Normal
Uric Acid
Sodium
Potassium
Chloride
281
143
3.7
105
Normal
Normal
Normal
Normal
LABORATORIES
4/4/09
4/9/09
Interpretation
HGB
141
128
Normal
HCT
0.42
0.38
Normal
PC
260
Normal
WBC
10.9
Normal
Neutrophils
0.66
Normal
Lymphocytes
0.24
Normal
Eosinophils
0.05
Normal
Stabs
0.01
Normal
ESR
21
Increased
Basophils
Blood Type: B+
LABORATORIES
Result
Interpretation
Color
colorless
Normal
Transparency
clear
Normal
pH
7.5
Normal
Specific Gravity
1.010
Normal
RBC
514
Increased
WBC
1(100% lymphocytes)
Normal
Total Protein
0.11
Slightly decreased
Glucose
4.7
Normal
Pandy’s Test
negative
Normal
POST OP EVALUATION
MRI of the spine
Normal
Audiometry
Normal
cervical, lumbar and thoracic spine
hearing acuity
CT scan
Heterogenous
hyperdense lesion in the cerebellar
vermis with perilesional edema and mass effect
Moderate extraventricular obstructive hydrocephalus
PRIMARY IMPRESSION:
MEDULLOBLASTOMA
Primarily considered due to:
Results of the patient’s CT scan (hyperdense lesion in
the cerebellar vermis)
most
common malignant hyperdense brain tumor arising
in the cerebellar vermis
The patient’s age (10 y/o)
usually
seen in 0-14 years of age
PRIMARY IMPRESSION:
MEDULLOBLASTOMA
Presenting signs and symptoms
vague
headache
vomiting
(+) Romberg sign
cranial nerve deficits
PRIMARY IMPRESSION:
MEDULLOBLASTOMA
Incidence
accounts
for 90% of embryonal tumors
2% of all primary brain tumors
18% of all pediatric brain tumors
predominately in males
majority occur in the midline cerebellar vermis
PRIMARY IMPRESSION:
MEDULLOBLASTOMA
Signs and Symptoms
signs
and symptoms of increased intracranial pressure
and;
headache,
nausea, vomiting, mental status changes, and
hypertension
cerebellar
ataxia,
dysfunction
poor balance, dysmetria
PRIMARY IMPRESSION:
MEDULLOBLASTOMA
Etiology and Pathogenesis
occur
in the posterior fossa
30–40% = chromosome 17p deletions
10–20% = genetic loses on chromosomes 1q and 10p
10% = abnormalities of chromosome 9p
arises from cerebellar stem cells
perivascular
formation
pseudorosette and Homer-Wright rosette
DIFFERENTIAL DIAGNOSIS:
EPENDYMOMAS
RULED IN due to:
-Age and the gender of the
patient
-Headache
-Projectile vomiting
-Presence of some cerebellar
signs
RULED OUT due to:
-Absence of lower CN
affectations
-Timing of the headache in
this illness gradually
decrease during the day and
relieved by vomiting
-In CT scan this will show
heterogenous hyperdense
lesion
DIFFERENTIAL DIAGNOSIS:
HEMANGIOBLASTOMA
RULED IN due to:
-Long history of headache (1
year)
-Vomiting
-Predominant in males
-presence of some cerebellar
signs
RULED OUT due to:
- low incidence in the
pediatric age group
-seen as a hypodense mass
with associated
hydrocephalus
DIFFERENTIAL DIAGNOSIS:
CRYPTOCOCCOMA
RULED IN due to:
-Intermittent headache
-projectile vomiting
-CSF analysis of the patient
which revealed 100%
lymphocytes
-hyperdense lesion on CT
scan
RULED OUT due to:
-CSF analysis was
unremarkable for a
cryptococcal etiology
-improvement with this
disease is noted with
administration of IV
Amphotericin B which was not
given to the patient
PLAN:
Diagnostic Procedures
Laboratory studies
Imaging studies
CBC, lectrolytes and liver and renal function tests
CT scan, MRI, and bone scan
Other procedures
audiography or brainstem auditory-evoked response,
lumbar Puncture
bone marrow aspirate
biopsy and histologic study of the specimen
PLAN:
Treatment
Surgery
to
relieve cerebrospinal fluid buildup
to confirm the diagnosis by obtaining a tissue sample
to remove as much tumor as possible
Glucocorticoid treatment
to
decrease the volume of edema surrounding brain
tumors
PLAN:
Treatment
ventriculostomy
to
divert excess cerebrospinal fluid from the brain
radiation therapy
to
reduce the number of left-over cells