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Rima Hemangioma
Rima Hemangioma
*Rima Asmarani
ABSTRACT
CEREBELLUM CAVERNOUS HEMANGIOMA
Rima Asmarani* Soetedjo**
ABSTRACT
Background
Hemangiomasare benign tumorsorhamartomasthatoccurdue to interferenceon the
developmentandformation ofblood vessels and canoccurin allorganssuch as the liver,
spleen, brain, bone, andskin. The prevalence ofthe most commonin newbornswitha
percentageof 5-10% in childrenaged lessthanoneyear. Nevertheless, it is possible in
adults. The prognosis dependson thelocation, size, complication and management of
the tumor
Case Report
Reported man aged 25, a labour, came with 3 months of having a chronic
progressive head pain accompanied by projectile vomiting, and imbalance. Brain
MSCT scan imaging shows a hipodens and isodens mass in the cerebellum, after
contrast injection shows enhancement at isodens lesion, tend to be a cerebellum
astrocytoma. This patient treated with dexamethasone and tumor surgical
evacuation. The result of the anatomic pathology is cavernous hemangioma.
Conclusion
Cavernous Hemangioma is a benign neoplasma because of the disturbance of
angiogenes . Diagnosis is based on history, physical examination and imaging.
Definitive diagnosis established by anatomical pathology. The Prognosis of this tumor
depend on location, size, complication, and good management.
Cerebellum Anatomy
LCS Flow
Disturbance of LCS flow
hidrocephalus
peningkatan TIK
Cerebellum Disorder
HHipotonus
AAtaksia
NNistagmus
DDismetri
Intentional Tremor
HEMANGIOMA DEFINITION
EPIDEMIOLOGY
The prevalence of hemangiomas 1-3% in
neonates and 10% in infants up to 1 year of
age.
the most common sites of hemangioma is at the
head and neck (60%)
In areas of the oral cavity is often found on the
lips, tongue and buccal mucosa.
Approximately 80% of cases is single lesions, and
the of this lesions were multiple.
ETIOLOGY
&PATHOMECHANISME
The occurrence of hemangiomas is still unknown
(presumably from interruption angiogenesis
process with the mechanisme of increasing levels
of angiogenesis factor or reduced angiogenesis
inhibitors)
The cause is related with blood vessel growth
control mechanisms.
Hemangioma Classification
Capillary Hemangioma
Strawberry hemangioma
(hemangioma simplek)
Granuloma piogenik
Cavernosum hemangioma
Mix Hemangioma
The others....
1.
2.
3.
4.
5.
6.
7.
Intramuscular hemangioma
Synovial hemangioma
Osseus hemangioma
Choroidal hemangioma
Spindle cell hemangioma
Gorham disease
Kassabach-Merritt syndrome
DIAGNOSIS
Head CT Scan
MRI
MRI is very important and sensitive in detecting tumors in the posterior fossa.
Biopsy
MANAGEMENT
The management of hemangiomas :
Conservative
Active
Active Management of hemangioma:
A. Surgery
B. Radiotheraphy
C.Corticosteroid
D Sclerotic agent
E. Electrocoagulation
F. freezing
G. Antibiotic
PROGNOSIS
In general, the prognosis depends on the
location of the tumor, complications and
good management
small or superficial hemangiomas may
disappear completely by itself. Large
cavernous hemangioma should be
evaluated and receive the proper
management.
CASE REPORT
Patient Identity
Name : Mr. W
Age : 25 years old
Sex : Laki-laki
Marriage status: unmarried
Last Education : SeniorHigh School
Occupation : labour
Address : Mawar Indah Purwodadi
Date of admission : 21 April 2015
Medical record : C526746
Anamnesis
Recent History
Chief complaint: headache
Onset
: 3 months ago, getting
worse
Quality
: throbbing pain
Quantity
: ADL helped by family
Chronology
3 months before hospital admission the patient complained
of throbbing pain in head, intermittently, especially when
straining to defecate, so patients are afraid to defecate.
Patient also complained of vomiting 5 times / day, nausea
(-). Patient's family brought him to the clinic and treated for
three days, given a pain-reducing medication then patient
getting better.
2 months before hospital admission headache was getting
worse. not relieved by taking medication, nausea (-), vomiting
(+), and the patient's gait was unsteady. Patients also felt
dizzy, continuously, and not influenced by the movement of
the head, aggravated when the patient opened his eyes and
walks, tinnitus (-), hearing loss (-). The patient felt weak and
had to be assisted when stand up. Seizures (-), loss of
consciousness (-), bowel and bladder no complaints.
The patient's family brought him to hospital in Purwodadi and
got a head scan. The Doctor said that there was a brain
tumor, then the patient was referred to Kariadi hospital
Aggravating factor
: Attenuating factor
: Concomittant symptom : vomit,
dizziness
CLINICAL FINDINGS
Status Presens
Level of Conscioussness : Compos mentis
: GCS : E4M6V5 = 15
Blood Pressure
: 130 / 80 mmHg
Heart Rate
: 84 x/ mnt
Respiratory Rate
: 20 x/ mnt
T
: 36,7 o C
VAS
:5
Height
: 166 cm,
Weight
: 50 kg
BMI
: 23,44 (normoweight)
Status Internus
Head
Eye
(-/-)
Neck
not
Thorax
Cor
: mesosefal, simetric
: conjungtiva anemis (-/-), ikterik sclera
: simetric, freely, enlargement of nnll(-), JVP
increase
: normal heart sound, murmur (-),gallop (-)
Paru
: normal breathing, Rh-/-, Wh -/- Abdomen
: supel, peristaltic (+) normal,
unpalpable liver
and spleen, ascites (-)
Neurologic State
Level of conscioussness : GCS E4 M6 V5 = 15
Head
: mesocephal, simetris
Eye
Neck
Cranial Nerves
: normal
Coordination Tests
Past pointing test : Right dismetri
(+), Intensional Tremor(-)
Finger to nose test : Right dismetri
(+), Intensional Tremor (-)(-)
Rebound Phenomenon (-)
Right Disdiadokokinesia (+)
Gait Ataksia (+)
Laboratory
Examination
Result
Normal point
Hematologi
Hemoglobin
15,4
gr%
12.00-15.00
Hematrokrin
44.8
35-47.0
Eritrosit
4.92
million/mmk
3.90-5.60
MCH
31.4
Pg
27.00-32.00
MCV
91.2
Fl
76.00-96.00
MCHC
34.5
g/dl
29.00-36.00
Lekosit
11.0
thousand/mmk
4.00-10.60
Trombosit
256
thousand/mmk
150.0-400.0
RDW
13.1
11.60-14.80
MPV
4.72
Fl
4.00-11.00
Kimia Klinik
GDS
112
mg/dL
74-106
Ureum
19
mg/dL
15-39
Creatinin
0.79
mg/dL
0.60
Natrium
135
mmol/L
136-145
Kalium
4.2
mmol/L
3.5-5.1
Chlorida
105
mmol/L
98-107
Magnesium
0.99
mmol/L
0.74-0.99
Calcium
2.43
mmol/L
2.12-2.52
PPT
10.4
Detik
9.4-11.3
control
10.7
Detik
APTT
30.4
Detik
control
29.9
Detik
Elektrolit
Coagulation
23.4-36.8
Thorax X Ray
Impression: in normal state
theres no sign of
metastasis
Head CT Scan
non contrast
contrast
Neurologic Formulation
Patient, Mr. W,25 years old man, Javannesse, a labour, right
handed, unmarried, came with chief complaint a chronic
progressive headache, with vomiting, and impaired balance
since 3 months. The patient has no significant past medical
history.
On physical examination found vital signs, BP: 140/80, HR:
84x/mnt, RR;20x/mnt, t: 36,7. The neurological examination
level of conscioussness composmentis (GCS:E4M6V5),
headachache,with VAS=5, signs of the cerebellar syndrome (+).
On contrast head CT scan appeared SOL in Cerebellum and
Hydrocephalus. A collection of signs and symptoms consistent
leading to increased Intracranial Pressure due to Cerebellum
SOL.
The most likely diagnosis in this patient is Cerebellar
Astrocytoma
Diagnosis
Clinical Diagnosis:
- Chronic progressive headache, vomitus (signs of
ICP increasing)
- Ataksia,
- Right Dismetria,
- Right Disdiadokokinesia
- Hipotonus
- Central Vertigo
Topical Diagnosis : Cerebellum
Etiology : Hidrosephallus et causa Cerebellum SOL
dd/ Astrocytoma
Px : Consult to ophtalmologist,
&neurosurgeon
Tx : - IVFD RL 20 dpm
- Inj Dexametason 10mg/6jam
(intravena)
- Inj Ranitidin 50mg/12jam (intravena)
- Na. Diclofenac 500mg/8jam (orally)
- Acetazolamide 500 mg/ 8 jam (orally)
Mx : Vital signs, GCS, and neurologic
deficits
PROGRESS NOTE
HARI
24-04-2015
(day hospital treatment:4)
25-4-2014
(day hospital treatment:5)
29-4-2014
( day hospital treatment:8)
O GCS
BP
HR
RR
t
PE
E4 M6 V5, VAS: 4
130/80mmHg
80x/mnt
20x/mnt
36,1C
No changes
E4 M6 V5,VAS:4
120/80mmHg
100x/mnt
24x/mnt
36,8C
No changes
E4 M6 V5 , VAS :4
110/70mmHg
86x/mnt
20x/mnt
36,2C
No changes
Lab
A
P
Dx
Tx
-IVFD RL 20 dpm
-Inj Dexametason 10mg/6jam
(intravena) day 4
-Inj Ranitidin 50mg/12jam
(intravena)
-Na. Diclofenac 500mg/8jam orally
-Acetazolamide 500mg/8jam orally
-IVFD RL 20 dpm
-Inj Dexametason 10mg/6jam
(intravena) day 5
-Inj Ranitidin 50mg/12jam
(intravena)
-Na. Diclofenac 500mg/8jam
orally
-Acetazolamide 500mg/8jam
orally
- IVFD RL 20 dpm
-Inj Dexametason 10mg/8 jam
(intravena) day 8 , tapp off day2
-Inj Ranitidin 50mg/12jam
(intravena)
-Na. Diclofenac 500mg/8jam orally
-Acetazolamide 500mg/8jam orally
-Craniotomy
Mx
Ex
No changes
No changes
No changes
Surgery report
1. Informed consent & profilactic antibiotic
2. The position of the patient is sleeping face down
3. Disinfection & cover with sterile doek
4. linea mediana posterior incission
5. Incission deepen to the periosteum
6. Set aside to lateral & plug retraktors
7. Burr hole 2 & craniotomy from inion to magnum foramen
8. Open duramater
9. Obtained redness and partially cystic mass, cystic pungtion
10.Separate the mass from the cerebellum
11.Feeding artery from the cerebellum
12.
Draining artery from the cerebellum
13. Lift tumor and manage bleeding
14.
Sewing duramater & manage bleeding
15.
Cut duramater & plug the drain
HARI
30-04-2015
(day hospital treatment:9,
Day 1 post craniotomy in ICU)
Surgical wound pain
01-5-2015
(day hospital
treatment:10,day 2 post
craniotomy in ward)
02-5-2015
day hospital treatment:11,
day 3 post craniotomy)
E4 M6 V5,VAS:4
E4 M6 V5 , VAS:3
130/70mmHg
100x/mnt
24x/mnt
39,3C
No changes, drain:100cc
130/70mmHg
86x/mnt
20x/mnt
39C
No changes, drain:80 cc
Lab
Con sult
Cerebellum SOL dd/
astrocytoma, 1st day Post
craniotomy
Dx
Tx
septic
HARI
03-05-2015
(day hospital treatment:-12,
day 4 post craniotomy)
04-5-2015
(day hospital treatment:13,
day 5 post craniotomy)
05-5-2015
(day hospital treatment:14, day
6 post craniotomy)
O GCS
BP
HR
RR
t
PF
E4 M6 V5, VAS: 3
130/70mmHg
80x/mnt
20x/mnt
36,5C
Gait ataksia (-), others No changes,
drain:70cc
E4 M6 V5,VAS:2
130/70mmHg
100x/mnt
24x/mnt
36,3C
No changes, drain:60 cc
E4 M6 V5, VAS:2
130/70mmHg
86x/mni
20x/mnt
36C
No changes, drain:25 cc
Lab
Con sult
Cerebellum SOL dd/
astrocytoma, 4th day Post
craniotomy
Septic
Dx
Tx
- IVFD RL 30 dpm
- Inj. Tramadol 100mg/8jam
(intravena)
- Inj. Omeprazol 40mg/12jam
(intravena)
- Vit B1,B6,B12 1tab/8jam (orally)
-Miring kanan-kiri /2jam
-Inj. Ceftriakson 2 grm/ 24 jam iv
day 2
-Inj. Paracetamol 1 grm/ 8 jam iv
- IVFD RL 30 dpm
- Inj. Tramadol 100mg/8jam
(intravena)
- Inj. Omeprazol 40mg/12jam
(intravena)
- Vit B1,B6,B12 1tab/8jam (orally)
-Miring kanan-kiri /2jam
-Inj. Ceftriakson 2 grm/ 24 jam iv
day 3
-Paracetamol 500 mgrm/ 8 jam
orally, if t>37.5
HARI
06-05-2015
(day hospital treatment:15,
day 7 post craniotomy)
07-5-2015
(day hospital treatment:16,
day 8 post craniotomy)
08-5-2015
(day hospital treatment:17,
day 9 post craniotomy)
O GCS
BP
HR
RR
t
PE
E4 M6 V5, VAS: 2
120/80mmHg
80x/mnt
20x/mnt
36,5C
No changes, drain:25cc
E4 M6 V5,VAS:2
120/70mmHg
80x/mnt
20x/mnt
36,3C
No changes, drain:-
E4 M6 V5, VAS:1-2
120/70mmHg
86x/mnt
20x/mnt
36C
No changes
Lab
Con sult
Cerebellum SOL dd/
astrocytoma, 7th day Post
craniotomy
Dx
Tx
- IVFD RL 30 dpm
Mx
Wait PA result
-IVFD RL 30 dpm
wait PA resullt
IVFD RL 30 dpm
- Vit B1,B6,B12 1tab/8jam (orally)
-Miring kanan-kiri /2jam
-Inj. Ceftriakson 2 grm/ 24 jam iv stop
- Paracetamol 500m grm/ 8 jam orally
HARI
09-05-2015
(day hospital treatment:18,
day 10 post craniotomy)
Surgical wound pain (reduced)
120/80mmHg
80x/mnt
20x/mnt
36,5C
No changes
10-5-2015
(day hospital treatment:19,
day 11 post craniotomy)
11-5-2015
(day hospital treatment:20,
day 12 post craniotomy)
E4 M6 V5,
E4 M6 V5, VAS:1-2
120/70mmHg
80x/mnt
20x/mnt
36,3C
No changes
120/70mmHg
86x/mnt
20x/mnt
36C
No changes
Lab
Con sult
Dx
Tx
- IVFD RL 30 dpm
Mx
Ex
No changes
No changes
Outpatient
Patologi Anatomi
DECISION MAKING
NO
Active Problem
Date
NO
Inactive
problem
1.
Chronic Progressive
21/04/2015
headache)since 3
months7
2.
Vomitus7
21/04/2015
3.
Hipotonus7
21/04/2015
4.
Dismetri7
21/04/2015
5.
Disdiadokokinesia7
21/04/2015
6.
Hidrocephalus7
21/04/2015
7.
Hemangioma cavernosum
21/04/2015
cerebellum
Date