Lapkas Spon TB 26 Juli 2023
Lapkas Spon TB 26 Juli 2023
Lapkas Spon TB 26 Juli 2023
RESPIROLOGY DIVISION
Irfadah Dinar
C105192003
Supervisor :
DEPARTMENT OF PEDIATRICS
MAKASSAR
2023
1
TABLE OF CONTENT
A. INTRODUCTION………………..……………………………………………………3
B. CASE REPORT………………………………………………………………………..4
I. PATIEN IDENTITY....................................................................................................4
II. PARENT IDENTITY....................................................................................................4
III. ANAMNESIS (SUBJEKTIVE)...................................................................................4
1. Personal or social history of the patient…………………………………………..4
2. Family History and socio-economic background.....................................................5
IV. DATA OF PATIENT’S CASE....................................................................................7
1. Physical Examination (Objektive)..................................................................................7
2. Supporting Examination…………………………………………………………………….8
V. RESUME.......................................................................................................................15
VI. WORKING DIAGNOSIS..........................................................................................15
VII. MANAGEMENT PLAN (PLANNING)..................................................................16
VIII. FOLLOW UP HYSTORY DISEASE.....................................................................18
IX. PROGNOSIS................................................................................................................24
X. DICSUSSION.................................................................................................................25
1. Definition..........................................................................................................................28
2. Pathophysiology...............................................................................................................29
3. Clinical manifestations....................................................................................................30
4. Supporting Examinations...............................................................................................31
5.Treatment............................................................................................................................33
XI. SUMMARY.....................................................................................................................35
REFERRENCES………………………………………………………………………………….36
2
CASE REPORT
Respirology Division
A. INTRODUCTION
This paper reports a case of tuberculous spondylitis in a girl aged 16 years and 9 months.
3
B. CASE REPORT
I. PATIENT IDENTITY
Name : NH
Gender : Girl
Date of birth : 12 – 03 - 2006
Age at the time of case : 16 years 9 Months
Come to hospital : 1 Januari 2023
No. Medical Record : 1003xxx
Addres : Polman, Sulawesi Selatan
Start to be accepted as a case : 1 January 2023
4
Weakness on both lower limbs was experienced in the last 3 months and getting
worse in the last 1 month before admission. Initially, she felt numbness on both legs. The
weakness was symmetric on both lower limbs. She was still able to feel tactile sensation
on skin. There was a complain of backpain in the last 3 months before admission. The
pain was getting worse in the last 2 weeks before admission. The pain appeared when she
was standing and disappeared when she laid down. There was a history of fever in the
past 3 months. The fever was not continuous and improved with taking antipyretic
medication. There was no seizure, cough, and shortness of breath. There was no nausea
and vomiting. She had a decrease appetite. The urine was red-colored and the stool was
yellow.
There was history of hospitalization in W Hospital on 24 – 29 December 2022 with
spondylitis tuberculosis and treated with FDC antituberculosis drugs for intensive phase
1st month 4th day. There was history of Mantoux test (PM Hospital) and result was
positive (induration ≥ 10 cm). The patient had history of trauma (motorcycle accident),
but the exact incidence was unclear.
5
The patient received vitamin K1 injection. Hepatitis B vaccination was given on the
first day and oral polio on the next day after birth. There was no history of cyanosis,
pallor, jaundice, seizures or bleeding.
4) Nutrition History
The patient was breastfed from birth until 2 months of age, cow's milk was given
thereafter until 2 years of age. Complementary foods were first introduced at 6 months of
age in the form of milk porridge, followed by steamed rice at 9 months of age and family
meals from 1 year of age. About 2 weeks before admission, her appetite decreased and
she ate only two meals a day, with rice, meat/chicken, fish, eggs, vegetables, fruits and
biscuits.
The patient's primary caregiver was his mother. Regarding health care, the mother
seemed worried about her child's condition. The patient was brought to W Hospital due to
weakness of both limbs.
6
The family was able to provide adequate food, however the patient had a poor
appetite in the last 3 months. Clothing needs were also met. yang buruk dalam 3 bulan
terakhir. Kebutuhan sandang juga terpenuhi.
Care (pshycosocial)
The parent-child relationship appeared close and loving. Both mother and father loved
the patient very much. The mother was patient and tried to care more about her son's
illness..
The father is 43 years old, a Muslim, a junior high school graduate and works as a
self-employed person with a monthly income of approximately Rp 1,000,000. The mother
is 41 years old, a Muslim, a junior high school graduate, and a housewife. The patient
lives with her parents and 3 sisters in a permanent house measuring approximately 7 x 10
m2, consisting of 4 bedrooms, 1 living room, 1 kitchen, and 2 bathrooms..
The family's source of drinking water is from a well. Water for daily activities such as
washing and bathing comes from a well. The source of electricity comes from the State
Electricity Company (PLN). Ventilation and light in the house are sufficient. The closest
health facility to the patient's house is the Community Health Center (Puskesmas), which
is ± 1.5 km away. Hospital bills are covered by national health insurance.
Hone (stimuli)
Early stimulation was provided by both parents early on which included touching and
hugging, playing together and talking. He also likes to play with his brother.
a. Status present
- General condition : moderate illness
- Awareness : GCS 15 (E4M6V5)
- Heart rate : 98 x/minutes reguler, enough volume
- Breathing : 22 x/minutes, reguler, negative retraksi
- Blood pressure : 100/60 mmHg
- Temperature : 36.7°C
7
- Saturation : 99% with room air
- Pain scale : 3 NRS
b. Nutritional state and antropometri
- Actual Weight : 39 kg
- Height : 160 cm
- Actual BW : 39 kg
- Ideal BW : 49 kg
- Body Height : 160 cm
- Head circumference (HC) : 54 cm (-2 SD<HC<0 SD, Nellhaus curve)
(Appendix 1)
- Weight-for-Height : 79,6% (wasted, CDC NCHS 2000 chart)
(Appendix 2)
- Height-for-age (H/A) : 98,2% (Normal, CDC-NCHS 2000 chart)
(Appendix 2)
- Weight-for-age (W/A) : 73,6% (underweight, CDC-NCHS 2000 chart)
(Appendix 2)
- Height Age (HA) : 14 years old.
- RDA from HA : 60 Kkal/BW/day
- Father’s height : 170 cm
- Mother’s height : 160 cm
- Genetic potential height : 150–167 cm (P3 – P65, CDC-NCHS 2000 chart)
- Mid-parental height : 158.5 cmAssessment of nutritional status based on
the CDC 2000 curve, the patient was categorized as
underweight, thin and normal stature..
8
9
c. General State
System Description
Face No elderly face, no dysmorphic, no cranial nerve palsy, no erythema on the cheeks.
Chest Symmetrical shape and movement, no piano chest, no deformity, no chest retraction
Heart Ictus cordis is not visible and palpable, normal I-II heart sounds, no murmurs or
gallops.
Abdomen Flexible, normal bowel sounds, no palpable liver and spleen, no ascites.
10
Lymph No lymphadenopathy.
nodes
Spine There is a gibbus in the 11th thoracic region, accompanied by tenderness, without
scoliosis
Ekstremity No wasting, baggy pants, and edema. Extremities warm, capillary filling time less
than 2 seconds, no edema. BCG scar + 5 mm in the deltoid region of the right upper
arm.
Status neurologis
Nervus II : round pupil, diameter isochor 2,5 mm/ 2,5 mm, ligh reflex positive
Saraf III, IV, VI : movement of the eyein all directions within normal limits
Motoric
11
Tonus : Decrease in the lower extremities
Klonus : Positive
Score tuberkulosis: 10
Contact :3
Nutrition state :1
Fever :1
Cough :0
Lymphadenopathy :0
X Ray Thorax :1
Joint/bone :1
Tuberkulin test :3
12
Figure 1. Mantoux test result and Gibbus
2. Supporting Examination
HCT - 37-47%
13
Parameter Result Normal Value
Neut 52-75 %
14
Figure 3. CT scan non-kontras thoracolumbar in RS PM, 20 December 2022
15
V. RESUME
A 16-year-and-9-month-old girl was admitted to the Pediatric Emergency Department of
W Hospital due to chief complaint of weakness on both lower limbs experienced in the last 3
months and getting worse in the last 1 month before admission. Initially, she felt numbness
on both legs. The weakness was symmetric on both lower limbs. She was still able to feel
touch sensation on skin. There was a complain of backpain in the last 3 months before
admission. The pain was getting worse in the last 2 weeks before admission. There was
history of hospitalization in W Hospital in 24 – 29 December 2022 with diagnosed of
spondylitis tuberculosis and treated with FDC antituberculosis drugs for 4th day first month
of intensive phase.
The general condition of patient was moderate ill, with wasted, GCS 15, vital sign
within normal limit. There were BCG scar on right deltoid. There was gibbus in 11th thoracal
region, accompanied with tenderness, without any scoliosis. From neurologic status, nerve
cranial within normal. Motoric examination revealed the decreased of movement ability and
tone normal in both lower extremities, and increased of physiology and pathologic reflexes.
The clonus was positive. Laboratory test revealed microcytic hypochromia. Chest x-ray in
PM Hospital, December 20th 2022: Pneumonia suspects to specific type. Non-contrast CT
scan of thoracolumbar showed compression fracture in column vertebra thoracal XI.
Tuberculosis score was 10. Conclusion:
4. Wasted (E.44)
Spondylitis Tuberculosis
16
Therapy Anti-tuberculosis Drugs 2 (R/H/Z/E) + 10 (R/H) Intensive phase 1st month 5th
day (Fixed Dose Combination 4 regiments: 4 tablets/ 24 hours / oral)
Intensive phase of anti-tuberculosis drugs for 2 months with 4 regimens:
Isoniazid (dose: 10-15 mg/kg/day) 150 mg/24 hours/day
Rifampicin (dose: 10-20 mg/kg/day) 300 mg/24 hours/day
Pyrazynamide (dose: 30-40 mg/kg/day) 550 mg/24 hours/day
Ethambutol (dose: 15-25 mg/kg/day) 450 mg/24 hours/day
Followed by anti-tuberculosis drugs for 10 months with 2 regimens:
Isoniazid (dose: 10-15 mg/kg/day) 150 mg/24 hours/day
Rifampicin (dose: 10-20 mg/kg/day) 300 mg/24 hours/day
Therapy Anti-tuberculosis Drugs 2 (R/H/Z/E) + 10 (R/H) Intensive phase 1st month 5th
day (Fixed Dose Combination 4 regiments: 4 tablets/ 24 hours / oral)
Correction after 2 weeks – 1 month of Anti-tuberculosis drugs treatment at
intensive phase
Education Inform the parents about paraparesis inferior due to compression fracture of
vertebra thoracal XI
17
Need correction after 2 weeks – 1 month of Anti-tuberculosis drugs treatment at
intensive phase
Diagnostic Ferritin, reticulocytes, blood smear, complete blood count, MCV, MCH
Therapy Wait for further result to differentiate cause of anemia
Monitoring Vital sign
Pale
Signs of tissue anoxia
Laboratory results for anemia diagnostic
Education Inform the parents that their child’s hemoglobin level below standard from the age
of the child
Planned to differentiate the cause of anemia with several laboratory examination
Transfusion only needed if the patient gets tissue anoxia
Wasted
18
VIII. FOLLOW UP HISTORY OF DISEASE
There is jaundice
Lung :
No retraction
No ronkhi
No wheezing
Abdomen :
19
Peristaltic sounds are normal
Ekstremity
Sensorik ordinary
Laboratorium Examination
rifampisin sensitive
20
chronic anemia disease (D52.9), Moderate Malnutrition (E44.0)
Complication :Paraparesis inferior due to compression fracture of the
11th thoracic vertebrae (G82.22)
- Jaundice↓
Lung :
No retraction
21
No ronkhi
No wheezing
Abdomen :
Ekstremity
Sensorik ordinary
A 1. Tuberkulosis Spondilitis
2. Paraparesis inferior due to fracture compression TXI
3. Chronic anemia disease
4. Moderate malnutrition
P FDC Stop
Parasetamol 500mg/8 hrs/intravena
22
Acid ursodeoxyholic 250 mg/8 hrs/oral
Sensoric ordinary
Lung :
No retraction
23
Breath sound vesiculer
No ronkhi
No Wheezing
Heart:
Abdomen :
Laboratorium RSWS
Hb 9,0 g/dl, MCV 72,5 fl, MCV 20,3, SGPT 28 U/L SGOT 31 U/L
A Tuberkulosis Spondilitis
Paraparesis inferior due to fracture compression TXI
Chronic anemia disease
Moderate Malnutrition
24
Acid ursodeoxyholic 250 mg/8 hrs/oral
IX. PROGNOSIS
25
X. DISCUSSION
Case Analysis
26
by the bacterium Mycobacterium tuberculosis. As many as 50% of spondylitis tuberculosis
sufferers have lesions in the spine and 10-45% of them experience neurological decline. This
splitting of Mycobacterium tuberculosis bacterial infection in the spine will complicate
management and aggravate the clinical condition because of the potential for permanent
neurological deficits and deformities.6 The spread of tuberculosis infection will cause
inflammation of the paradiscus, there is hyperemia, edema spinal cord and osteoporosis.
Destruction of bone loss occurs progressively, due to lysis of bone tissue in part anterior, as
well as the presence of secondary ischemia, periarthritis and endarteritis, will cause the
collapse of the section. This will cause a loss of mechanical strength bones to hold weight so
then collapse of the vertebrae with the intervertebral joints with the posterior neural arch
remaining intact, so it will progressive kyphotic deformity develops (posterior angulation)
depending on the degree of damage, level the lesion and the number of vertebrae involved are
frequently referred to as gibbous. When this deformity arises, then it is a sign that this disease
has extends.3,4,5 Neurological deficits occur in 12–50 percent of sufferers. Possible deficits
include: paraplegia, paresis, hypesthesia, radicular pain and/or cauda equina syndrome.
Radicular pain indicates interference with the roots (radiculopathy). 3 To reduce pain, the
patient will be reluctant to move his back, so that it seems stiff. The patient will refuse if
ordered to bend down or lift objects from the floor. The pain will decrease if the patient rests.
Complaints of deformity of the spine (kyphosis) occur in 80% of cases accompanied by the
appearance of gibbus. Old disorders may be accompanied by paraplegia or without
paraplegia. Paraplegia in spondylitis tuberculosis patients with active disease or known as
Pott's paraplegia, there are 2 types of neurological deficits found in the early stages of the
disease which is known as early onset, and paraplegia in recovered patients which usually
develops several years after the primary disease is cured which is known with slow onset. 2
The children with spondylitis tuberculosis usually present with persistent localized back pain,
loss of appetite, weakness of both lower limb and inability to walk. The child is usually pale,
listless, and anemic. They also have a cautious gait and tend to walk keeping both hands at
thigh to support the trunk. If the cervical spine is involved, they walk supporting the head
with both hands.
This case, the diagnosis of spondylitis tuberculosis can be established by a complete
clinical examination including a history of close contact with tuberculosis patients,
epidemiology, clinical symptoms, and neurological examination. Modern imaging methods
such as X ray, CT scan, MRI from patient help establish the diagnosis of spondylitis
tuberculosis.2,8 Patient have positive Mantoux test. The gold standard for the traditional
27
diagnosis is the examination of clinical samples of the patients, namely a blood smear test for
Mycobacterium tuberculi, along with typical histological examinations and laboratory tests
including complete blood count, ESR and CRP, as well as further auxiliary examinations to
diagnose the corner curriculum. However, due to the growth requirements and slow growth
rate of TB bacilli, their culture is challenging. The TST is frequently performed, but its
sensitivity and specificity are limited, even in high-incidence areas of TB; even after in
individuals with repeated exposure to TB bacillus, a ~20% negative rate of the TST has been
estimated.14,15 Spondylitis tuberculosis in children is suspected clinically and the diagnosis
can be confidently made on plain X‐rays and magnetic resonance imaging (MRI)
observations supported by raised ESR and positive Mantoux test. When clinic-radiological
diagnoses are doubtful, the fine‐needle aspiration cytology/biopsy for a histopathological
diagnosis is indicated.
The goals of treatment in spinal TB are to eradicate the disease and to prevent and/or
correct spinal deformity and neurological deficits.1 TB of the spine is a medical disease;
surgical intervention is indicated for spinal deformity, neurological complications, instability,
large abscesses and to obtain tissue in a case of diagnostic dilemma and suspected MDR TB. 8
(Level of evidence 1A) The clinical appearance of kyphotic deformity has been classified as
knuckle (one vertebral involvement), gibbus (two vertebrae) and rounded kyphus (more than
three vertebrae). Patient has gibbus and paraperese inferior. This patient had 4 types of anti-
drugs tuberculosis (2RHZE/10RH). Multidrug antitubercular treatment (ATT) is the mainstay
of treatment in both complicated and uncomplicated TB.1(Level of evidence 1A) Treatment
INH and rifampicin should be administered during the entire treatment. A 4-drug regimen
usually includes INH, rifampicin, and pyrazinamide and ethambutol. Long treatment is still
controversial. Although some research says it requires medication only 6-9 months, routine
treatment is carried out for 9 months to 1 year. Treatment duration usually based on
improvement in clinical symptoms or clinical stability of the patient. 2,13,17 Drugs commonly
used for the treatment is as shown in Table 1. (Level of evidence 1A)
The patient treated with FDC antituberculosis drugs for first month of intensive phase.
But then, in 7th day of hospitalization instruction for the patients is stop antituberculosis drugs
because of icterus, elevated liver enzyme and cholestasis. Patient then have drug induced
liver injury (DILI). Based on DILI expert working group DILI is defined as an elevation in
the serum concentration of alanine aminotransferase (ALT) ≥ 3x ULN and total bilirubin >2x
ULN.15 The FDC ATT was stopped then she was given ursodeoxycholic acid.
Ursodeoxycholic acid in DILI was largely demonstrated by case reports and observational
28
studies, it appears to be safe and leads to a reduction in bilirubin. 18,19 Level of evidence 1A)
After the symptom’s improved ATT was reintroduce with separate regimen simultaneously.
A study in India revealed that there was no difference in the recurrence rate of hepatotoxicity
between reintroduction ATT simultaneously nor separatedly. 19 The patient has severe TB
such as spondylitis TB, thus the ATT cannot be stopped completely. Hepatotoxic ATT such
as INH, rifampicin and pyrazinamide were switched to less hepatotoxic ATT such as
levofloxacin and amikacin until hepatitis is resolved, while ethambutol was continued. 20,21
Once liver functions were normal the original drugs can be reintroduced sequentially in the
order: INH, rifampicin, and pyrazinamide with daily monitoring of her clinical condition and
liver function.13 The liver function and clinical condition were monitoring periodically. There
was no yellowish appearance, no icteric and liver functions within the normal limit during the
reintroduction of antituberculosis drugs.
The hypochromic microcytic anemia found in this case might still be caused by iron
deficiency anemia or chronic disease due to TB infection. Another possibility of anemia
experienced by patients is chronic disease due to TB infection. Examination of the iron
profile that has been done and ferritin was high. Patient was diagnosed anemia of chronic
disease.
The prognosis for spondylitis tuberculosis varies depending on the clinical
manifestations that occur. Poor prognosis associated with miliary tuberculosis and meningitis
tuberculosis, sequelae can occur including deafness, blindness, paraplegia, mental retardation,
movement disorders and others. Prognosis improves if treatment is carried out sooner. High
mortality occurs in children aged less than 5 years to 30%. 8 Prognosis in this patient was: 1)
quo ad vitam was ad bonam, since the manifestations during hospitalization this patient has a
significant improvement; 2) quo ad functionam was ad malam because the motoric
examination revealed the decreased of movement ability and tone in both lower extremities;
3) quo ad sanactionam was ad bonam, because the patient had improvement appetite and the
patient feel better.
Spondylitis Tuberculosis
1. Definition
29
infection in the spine will complicate management and aggravate the clinical condition due to
potential neurologic deficits and permanent deformities. The spine is the most frequent site of
bone tuberculosis infection, with approximately 50% of osteoarthritic tuberculosis cases. As
many as 50% of patients with TB spondylitis have spinal lesions and 10-45% of them have
neurologic deficits.5
If the Mycobacterium tuberculosis infection affects the vertebral corpus, the damage
causes spinal instability and disruption of surrounding structures. The patient may be
paralyzed due to compression of the spinal cord. Irreversible paralysis not only disturbs and
burdens the patient himself, but also his family and society.5 In this patient, neurological
deficits were found.
2. Pathophisiology
TB spondylitis can result from direct infection (primary), where the bacteria directly
infect the corpus, or indirect infection (secondary), where the bacteria spread hematogenously
or lymphogenously from the site of infection elsewhere to the spinal corpus. Most TB
spondylitis is a secondary infection of the lungs, but in some cases it is a primary infection.
Anatomically the intervertebral disc is an avascular structure and the paradiscus artery
divides on both sides of the disc and reaches the subchondral region of the upper and lower
endplate of each disc. This supply of vertebral arteries favors subchondral bone involvement
on both sides of the disc, paradiscal, which is the most common type encountered in
tuberculous spondylitis. TB causes granulomatous inflammation characterized by infiltration
of lymphocytes and epithelioid cells, which can combine to form classical Langhans-type
giant cells and end in caseous necrosis of the affected tissue forming an abscess. With
progressive destruction of the vertebral bodies, deformation of the spine leads to kyphosis. 6
The lungs are the port d'entree for more than 98% of TB infection cases, as the size of
the bacteria is very small at 1-5 μ, inhaled TB germs reach the alveolus and are immediately
overcome by nonspecific immunological mechanisms. Alveolus macrophages will
phagocytize TB germs and are able to destroy most TB germs. In a minority of cases,
macrophages are unable to destroy TB germs and the germs replicate in the macrophages.
The TB germs in the macrophage continue to multiply, eventually causing the macrophage to
lyse, and the TB germs form colonies at that site. The first location of a TB germ colony in
lung tissue is called the primary focus of Ghon.7
30
The most common form of hematogenous spread is occult hematogenic spread, where
TB germs spread sporadically and gradually, causing no clinical symptoms. TB germs will
then reach various organs throughout the body. The target organs are those that are well
vascularized, such as the brain, bones, kidneys, and the lungs themselves, especially the lung
apex or upper lobe of the lung. The part of the spine that is often attacked is the peridiscal,
which occurs in 33% of cases of TB spondylitis and starts from the metaphyseal part of the
bone, with spread through the longitudinal ligament. Anterior occurs in about 2.1% of cases
of TB spondylitis. Disease starts and spreads from the anterior longitudinal ligament.
Radiology shows scaling of the anterior vertebrae, central occurring in approximately 11.6%
of cases of TB spondylitis. Disease is confined to the center of a single vertebral body,
resulting in vertebral collapse and kyphosis deformity. At these various sites, TB germs will
replicate and form germ colonies before cellular immunity is established to limit growth. 4
3. Clinical manifestation
Like the clinical manifestations of TB patients in general, the patient experienced the
following conditions: weight loss for 3 consecutive months without apparent cause,
prolonged fever without apparent cause, enlarged superficial lymph nodes that did not hurt,
cough for more than 30 days, recurrent diarrhea that did not recover with diarrhea treatment
accompanied by lumps / masses in the abdomen and signs of fluid in the abdomen..5
Clinical manifestations of TB spondylitis only appear after the child has learned to walk
or jump. The first symptom is usually a lump on the spine accompanied by pain. To reduce
the pain, the patient will be reluctant to move their back, making it seem stiff. The patient
will refuse if ordered to bend over or lift things from the floor. The pain will decrease if the
31
patient rests. Complaints of deformity in the spine (kyphosis) occur in 80% of cases
accompanied by the onset of gibbus, which is a back that bends and forms an angle, is an
unstable lesion and can develop progressively. There are two clinical types of kyphosis:
mobile and rigid. In 80% of cases, kiposis occurs 20% of cases have more than 10 kiposis
and only 4% of cases more than 30%. Long-standing disorders may be accompanied by
paraplegia or without paraplegia. Abscesses may occur in the spine which may radiate to the
lower thoracic cavity or down the inguinal ligament.5
In this case, the clinical symptoms found were weakness in the lower limbs There was a
history of fever for the last 3 months. She had decreased appetite.
4. Supporting Examination
In some cases infection occurs in the anterior part of the vertebral body up to the
intervertebral disc characterized by the destruction of the end plate. Posterior elements are
usually also affected. Spread to the intervertebral discs occurs directly resulting in erosion of
the anterior vertebral bodies caused by soft tissue abscesses. The widespread availability of
computerized tomography scan (CT scan) and magnetic resonance scan (MR scan) has
increased their use in the management of spinal TB. CT scans are performed to elucidate
spinal sclerosis and destruction of the vertebral bodies so as to determine damage and
posterior extension of the inflamed tissue, bone material, and to diagnose posterior spinal
32
involvement as well as involvement of the sacroiliac join and sacrum. This can help guide
biopsy and surgical planning interventions. CT scan examination is indicated if the radiology
examination results are doubtful. CT scan images of TB spondylitis show calcifications in the
psoas accompanied by periperal calcifications. Magnetic resonance imaging (MRI) is
performed to detect tissue mass, appendicular TB, extent of disease, and subligamentous
spread of tuberculous debris. The gold standard for diagnosis of bone and joint tuberculosis is
mycobacterium culture of bone tissue or synovial fluid. Needle aspiration and biopsy (CT-
guided) are recommended for confirmation of TB spondylitis. Peripheral joint fluid analysis
is usually not helpful. Suspicion of TB infection is an indication for synovial biopsy.
Antimicrobial sensitivity testing of isolates is important.3
Bone biopsy can also be useful in difficult cases, but requires a high degree of skill and
experience as well as a good histology examination. Histologic examination will reveal
caseous necrosis and giant cell formations, while acid-resistant bacteria are not found and
cultures are often negative. There are no radiologic findings pathognomonic for bone and
joint TB. In early infection there may be soft tissue swelling, osteopenia and bone
destruction. In advanced infection there may be structural collapse, sclerotic changes and soft
tissue calcification. In TB spondylitis, pure osteolytic lesions without disc space involvement
may be seen and may be seen in multiple sites. Paravertebral abscesses may be seen on plain
photographs. In arthritic TB, Phemister's triad can be seen, namely juxtaposed-arthritic
osteopenia, peripheral bone erosion and gradual narrowing of the disc space. tuberculous
dactylitis of the hands or feet can show a balloon-like appearance in the phalanges. A thoracic
photograph can be done to determine former TB or pulmonary TB. MRI examination can
determine the extension of the infection to the soft tissues and structures around the bone
such as the spinal cord. 3In this case, the patient underwent a thoracic X-ray, thoracic MSCT
scan, and thoracic MRI.
33
from pyogenic infections clinically. TB spondylitis can also be differentiated from tumors,
which show nonspecific symptoms. 2
In this case, supporting examinations were performed to support the diagnosis, namely
there was a positive tuberculin test with an induration of > 10 mm (20 mm), on MRI
examination of the thorax obtained T10-T11 tuberculous spondylitis and severe slice
deformity.
5.Treatment
1. Rapid-onset paraplegia, is the active phase of vertebral disease beginning within the
first 2 years. The pathology that occurs is inflammatory edema, tubercle granulation
tissue, tubercle abscess, tubercle embryonic tissue or rarely found in ischemic spinal
cord lesion
2. Late-onset paraplegia, appearing more than 2 years after the disease is found in the
vertebral column. Neurologic complications may be related to disease or mechanical
compression of the spinal cord. Pathologies that may occur are adipose tissue,
tubercle debris, internal gibus, vertebral canal stenosis or severe deformity. The
severity of the neurological deficit depends on the degree of motor impairment.
In joint TB, early diagnosis and effective treatment are essential to save the joints, as
the findings early in the course of the disease are non-specific. Treatment uses standard OAT,
2 RHZE 10-16 RH, should be given 1 year to 18 months in some cases. It is recommended
34
for all patients to use traction, preferably skeletal traction. If necessary, traction on other
extremities can also be used to stabilize the pelvis..5
Drug administration when combined between INH and rifampicin, the dose of INH
should not be more than 10 mg / kgBB / hr and the dose of rifampicin should not be more
than 15 mg / kgBB / hr and in compounding should not be compounded in one puffer but
when taking the drug can be together. As an additional therapy, non-steroidal anti-
inflammatory drugs may be used early in diseases with non-specific superficial membrane
to providing medication, immobilization of the spinal region must be carried out. There are at
least 3 thoughts on the treatment of Potts paraplegia. According to Boswots Compos (cited in
10) the most important treatment is immobilization and early posterior arthrodesis. It is said
that 80% of patients who are detected early will be detected early; will recover after
arthrodesis. In his opinion, anterior decompression is indicated only in those few patients
who do not recover after arthrodesis. If this treatment does not provide improvement and
35
Non-operative treatment of early-stage paraplegia will show improved outcomes in
half of patients and late-stage in a quarter of patients. If Pott's paraplegia occurs then surgery
A. Absolut Indication
Paraplegia with onset during conservative treatment, paraplegia worsening or
persisting after conservative treatment, complete loss of motor strength for 1 month after
conservative treatment, paraplegia with uncontrolled spasticity due to a malignancy and
immobilization is impossible or there is a risk of necrosis due to pressure on the skin, severe
paraplegia with rapid onset, may indicate severe pressure due to mechanical accident or
abscess may also be the result of vascular thrombosis but this cannot be diagnosed, other
severe paraplegia, flaccid paraplegia, paraplegia in flexion, complete sensory loss or impaired
motor strength for more than 6 months. 4
B. Relative Indication
Recurrent paraplegia which is often accompanied by paralysis so that the initial attack
is often not recognized, paraplegia in old age, paraplegia accompanied by pain caused by
spasm or nerve root compression and complications such as stones or urinary tract infections.
Surgical procedures performed for TB spondylitis with paraplegia are costrotransversectomy,
anterolateral decompression and laminectomy. A complication that can occur is severe
kyposis. This occurs because the bone damage is so great that the bone that undergoes
destruction is very large. This will also facilitate the occurrence of paraplegia in the inferior
extremities known as Pott's paraplegia. The prognosis of TB spondylitis varies depending on
the clinical manifestations. A poor prognosis is associated with miliary TB and TB
meningitis, with sequelae including deafness, blindness, paraplegia, mental retardation and
movement disorders. The prognosis improves with earlier treatment. Mortality is high in
In this case, the patient was given Anti-Tuberculosis Drug therapy 2 (R/H/Z/E) + 10
(R/H), Intensive phase month 1 day 5 (Fixed Dose Combination of 4 regimens: 4 tablets/24
hours/orally).
XI. SUMMARY
36
A case of tuberculous spondylitis in a 16-year-old girl was reported. The diagnosis was based
on history taking, physical examination, laboratory and imaging. The management of this
patient was the administration of anti-tuberculosis drugs and clinical observation. The
patient's prognosis was good.
REFERENCES
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