Documente Academic
Documente Profesional
Documente Cultură
FACULTY OF CLINICAL
SCIENCES
COLLEGE OF HEALTH SCIENCES
UNIVERSITY OF ILORIN, ILORIN
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TABLE OF CONTENTS
Title page
Table of contents
Outline of Case reports
Case report 1
Case report 2
Case report 3
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CASE REPORT 1
nd
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INTERVENTIONS AT PRESENTATION
RBS= 2.5mmol/l. RDT= +ve. PCV= 38%.
ASSESSMENT
Cerebral Malaria (RDT +ve, hyperpyrexia, Shock, multiple convulsions within
a 24 hours period)
Plan: IVF Normal saline 20mls/kg over 30 mins. IV 10% Dextrose water
2ml/kg stat. IV artesunate 2.4mg/kg at 0, 12, 24, 48 hr.
Difficulties in securing IV access. Had an interosseous line set for that purpose.
Samples for FBC, E,U and Cr, Blood culture, urinalysis to be taken. IV access
was later gained, IV Rocephin 100mg/kg daily was later added to the
intervention. BP, SP02 was monitored at intervals. Input-output chart was made.
Urinalysis result: Blood 4+ Ketone 2+, Protein 1+, pH= 5, Leucocyte= 2+, SG=
1.020
On examination after 30 mins, pupils are dilated and reactive, generalized
hypertonia.
DAY 2 (23/6/2015)
Child has improved, now conscious but drowsy. Last episode of convulsion was
14 hours ago.
I V artesunate, IV ceftriaxone continued. Child was rehydrate at 5% deficit and
maintenance.
DAY 4 (25/6/2015)
Child was conscious, afebrile (37.2oc) but pale. Liver was 8cm below the right
costal margin, mid-clavicular line, soft, smooth and non-tender. Spleen was
enlarged, 3cm from LCM, mid-clavicular line.
On CNS: Neck stiffness, cortical blindness and generalized hypertonia.
Not had any episode of convulsion in the last 48 hours. Still on IV fluid, IV
ceftriaxone and artesunate. IV gentamicin added. TPR showed intermittent
fever with a downward trend. CSF not suggestive of meningitis.
Photostimulation started, phenytoin also initiated.
E,U and Cr Na= 122mmol/l (reduced), K= 2.8mmol/l (reduced), Urea=
5.4mmol/l
DAY 5 (26/6/2015)
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Child is mildly pale, afebrile(37.0oc), not dehydrated. Liver and spleen still
enlarged. Cortical blindness still present, normal pupil reaction to light, global
hypertonia. IV artesunate discontinued, oral coartem initiated. IVfluid continued
at maintenance, IV ceftriaxone continued. Biophin initiated.
DAY 8 (29/6/2015)
Was transfused on account of falling PCV (33% to 21%). This is her 7th day on
ceftriaxone. Initial cortical blindness resolving. Paucity of movement on the left
upper limb. Other limbs moving adequately.
Plan: To commence physiotherapy, discontinue ceftriaxone, discharge patient
and counsel parents.
DAY 10 (30/6/2015)
Patient discharged. To see at the clinic.
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CASE REPORT 2
DATE: 07/06/15
NAME
AGE
SEX
HOSP. NO
TRIBE
RELIGION
INFORMANT
NURUDEEN Taiye
3 years
Male
596689
Yoruba
Muslim
Mother
PRESENTING COMPLAINTS
Abdominal swelling of 2 month
Weight loss of 1 month
HISTORY OF PRESENTING COMPLAINTS
Patient was in his usual state of health until 2 months ago when mother noticed
swelling of the abdomen. Swelling was described as diffuse, hard and
progressive. No selling in other parts of the body. No history of constipation,
vomiting, diarrhea.
Weight loss started about a month ago, noticed by mother, it was rapidly
progressive evidence by the appearance of bony prominences and looseness of
previously fitting cloths.
There was history of bone pain and itching. No change in the frequency, colour
and output of urine.
Illness did not initially interfere with routine activities.
Has presented at a peripheral hospital (Child specialist hospital, center Igboro)
from where he was referred here based X-ray findings for expertise management.
SUMMARY: I have presented a 3 years old boy who presented at the Emergency
Paediatrics Unit on account of progressive diffuse abdominal swelling with
associated weight loss, pruritus of about 2 months duration.
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GENERAL EXAMINATION
Child is a toddler who is conscious, acute-on-chronically Ill-looking, mildly pale,
anicteric, afebrile (36.7oC), not cyanosed, well hydrated, no pedal oedema.
Presence of left supraclavicular lymph node.
ANTHOPOMETRY
Weight 9 Kg (small for age)
OFC 51 cm (appropriate for age)
Length 90cm
Mid Upper Arm Circumference: 12cm at 6cm from the acromium
SYSTEMIC EXAMINATION
Abdominal system
Abdomen was grossly distended, clean and dry dressing over the Right Upper
Quadrant. Mild generalized tenderness. Multiple Intra abdominal masses.
Normoactive bowel sound
Cardiovascular system
Pulse Rate was 122 beats per minute, pulse is regular and of full volume. Blood
pressures was 100/70 mmHg. Heart sounds were S1, S2 only.
Respiratory System
Respiratory rate was 44 cycles per minute. Chest wall is symmetrical, no
scarification. Equal chest expansion, resonant percussion. Vesicular breath sound
with good air entry. No added sounds.
Central Nervous System
Child is conscious but lethargic. No signs of meningeal irritation. Pupils were
reactive to light, active movements of all limbs, anterior and posterior
frontanelles are closed. Tones and reflexes are normal.
ASSESEMENT (07/06/15)
A 3 years old child with multiple intra-abdominal masses. ? Burkitt lymphoma
Differentials: Nephroblastoma, Neuroblastoma
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PLAN
Admit patient
PCV 25%
Full blood count plus differentials, genotype, blood culture, urinalysis,E U & Cr
RDT for malaria - negative
RBS 4.3 mmol/l
IVF 4.3% dextrose saline = D10 in 1250 mls over 24 hours
Ultrasound guided Biopsy for histology
Ultrasound scan
Monitor vital signs
Apply penile conduit and monitor urine output.
Counsel and inform mother about childs condition.
FOLLOW UP
DAY 3 (09/06/15)
3 years old boy with multiple intra-abdominal masses ?Burkitt lymphoma.
Histology result shows small round blue cell. No new complaint.
TPR chart was normal
O/E Child is a toddler who is conscious, acute-on-chronically Ill-looking, mildly
pale, anicteric, afebrile (36.7oC), not cyanosed, well hydrated, no pedal oedema.
Presence of left supraclavicular lymph node.
Assessment: Burkitt lymphoma
Plan:
IVF 4.3% dextrose saline = D10 in 1250 mls over 24 hours
Tab Allopurinol 100mg b.d
IM Pentazocin 10mg 8 hrly
Allow oral intake if tolerated
Tab Captopril 12.5mg b.d
Monitor Blood Pressure and other vitals
IV Cefuroximme 375mg 12 hrly
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DAY 7 (13/6/15)
Continue previous management
Give IV Ondasetron 2mg stat
Commence IVF hyperhydration at 3 litres/m2/day
Commence cytotoxics (Cyclophosphamide, Vincristine and Methotrexate)
DAY 10 (16/06/15)
Continue previous management
Discontinue Pentazocine
IVF 4.3% D/S at 2 litres/day
Patient developed multiple mouth ulcers after chemotherapy
DAY 11 (17/06/15)
Continue Antibiotics
Continue Allopurinol
Continue Captopril
Complete 10 days of Cefuroxime
Transfer to ward
DAY 13 (19/06/15)
Child was said to be passing loose stool and had 6 episodes in the last 24 hours
Continue IV fluid at 2 litres/day at 28 drops per minute
Continue Allopurionol
Complete 10 days of Cefuroxime (indicated because child had mucositis after
chemotherapy)
DAY 14 (20/06/15)
Discontinue IV fluid
Liberal oral fluid intake
Discontinue Cefuroxime
Monitor vital signs
DAY 15 (21/06/15)
Update, FBC, Blood culture, ESR
PCV- 26%
Vital signs: BP-120/70 mmHg, HR-128 beats per minute
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DAY 17 (23/06/15)
Child has mucositis and tongue ulcerations which have worsened. There was
facial puffiness. TPR showed Intermittent fever
IV fluid 4.3% D/S at 1250 ml dly
Discontinue Septrin
Continue Captopril, Cefuroxime
DAY 24 (30/06/15)
Hb-10g/dl, MCHC-30g/dl, PCV-32%, RBC-4.08x106/microliter, WBC-2.5x103/
microliter, MCV-78fl, MCH-24pg, Platelet-126x103/microliter, neutrophil-35%,
Lymphocyte-60%, others-5%
DAY 25 (01/07/15)
Continue Cephalexin
Continue hyperhydration
Discharge home, 2nd course of chemotherapy scheduled for 06/07/15
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CASE REPORT 3
DATE: 12/06/15
NAME:
AGE:
SEX:
HOSPITAL NUMBER:
ADDRESS:
TRIBE:
RELIGION:
INFORMANT:
ASHRAFF Muhammed
23 months
Male
381001
Sango, Ilorin
Nupe
Muslim
Mother
PRESENTING COMPLAINTS
Refusal of feed of 2 days duration
Fever of 2 day duration
Vomiting of 1 day duration
HISTORY OF PRESENTING COMPLAINTS
Patient was in his usual state of health until 2 days prior to presentation when
the child started refusing feeds with associated passage of loose stool. Passage
of loose stool started few hours prior to presentation and experienced about 12
episodes, stool was brownish in colour, mucoid but non-bloody, each bout was
about 120mls. However, patient was on haematinics prescribed at a peripheral
center.
Fever started the same day as the refusal of feeds, fever was of sudden onset,
high, continuous relieved transiently by Paracetamol and tepid sponging. There
was no associated convulsion, no discharge from any craniofacial orifices.
Vomiting started few hours to presentation. It started at night, patient had 6
episodes of projectile, non-billous vomiting and contains recently ingested
drugs and feeds. Vomitus does not contain blood.
Prior to presentation at the Emergency Paediatric Unit, Patient had presented at
a private hospital where he was given antibiotics, antimalarial, Oral Rehydration
Salt and Paracetamol. His condion however did not improve to mothers
expectation warranting a self-referral here.
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NUTRITIONAL HISTORY
Child was exclusively breastfed for about six months before complimentary
feeds was commenced. Child is currently on the familys diet.
IMMUNIZATION HISTORY
Child has been completely immunized according to the National programme on
immunization schedule.
DEVELOPMENTAL HISTORY
Gross motor, fine motor and speech development has been progressive and not
adversely eventful. Child gained head control at two months, sit at five months
and stand without support at twelve months. Child is ambulatory.
FAMILY AND SOCIAL HISTORY
Patient is the second child in a monogamous family with two children, resides
with his parent in a flat apartment. Uses mosquito treated net. Mother has a
Bachelor-in-Science degree and works at the state ministry while the father has
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ANTHROPOMETRY
Weight 9Kg (appropriate for age)
OFC 47 cm (appropriate for age)
Length 80cm
Mid Upper Arm Circumference: 16cm at 6cm from the acromium
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SYSTEMIC EXAMINATION
Central nervous system
Child is conscious and irritable. Neck is supple, no signs of meningeal irritation.
Pupils were reactive to light, active movements of all limbs, anterior and
posterior frontanelles are closed. Tones and reflexes are normal.
Cardiovascular System
Pulse rate is 110 beats per minute. No precordial hyperactivity, apex beat at the
fourth left intercostal space mid clavicular line. First and second heart sounds
only were heard. Blood Pressure is 80/50 mmHg
Respiratory System
Respiratory rate is 17 breaths per minute. Chest wall is symmetrical, no
scarification. Equal chest expansion, resonant percussion. Vesicular breath
sound with good air entry. No added sounds.
Abdominal
Abdomen is full, moves with respiration, no scar or scarifications. Soft with no
area of tenderness, liver is 4cm below the Right Costal Margin, it is smooth,
non-tender and soft. Spleen are not enlarged and the kidneys are not ballotable.
Percussion note tympanitic, bowel sound normoactive.
ASSESEMENT
23 months old known HbSS with Sepsis with evidence of mild dehydration
(5%)
PLAN
Admit patient
PCV 25%
Full blood count plus differentials, genotype, blood culture, urinalysis,E U & Cr
RDT for malaria - negative
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FOLLOW UP
DAY2 (13/06/15)
23 months old known HbSS boy being managed as a case of Sepsis with mild
dehydration. Stool colour is normal and volume of urine output has increased.
No new complaint.
TPR chart was normal
O/E child is conscious and alert, afebrile, not pale, anicteric, not dehydrated,
acyanosed, not in any obvious respiratory distress, no peripheral
lymphadenopathy, no pedal edema, no finger clubbing.
Assessment: Resolving sepsis, resolved dehydration
Plan: Continue present management
DAY 3 (14/06/15)
23 months old known HbSS boy being managed as a case of resolving Sepsis.
No new complaint.
TPR chart was normal
O/E child is conscious and alert, afebrile, not pale, anicteric, not dehydrated,
acyanosed, not in any obvious respiratory distress, no peripheral
lymphadenopathy, no pedal edema, no finger clubbing.
Assessment: Resolving sepsis
Plan: remove penile conduit
Change parenteral antibiotics to oral
Fluid intake orally
Counsel mother on need to present child regularly at the sickle cell clinic
Discharge to clinic
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