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AZERBAIJAN 1

MEDICAL
UNIVERSITY

 NAME: ZAKARYA KAMAL SATTOUF


 GROUP: 180B
 SUBJECT: MILIARY TUBERCULOSIS
 DATE; 12/7/2019
 INTRODUCTION

 Definition 2
 History
 Risk factors
 Types and forms
 Pathophysiology of miliary TB
 Clinical findings
 Diagnosis
 Differentiation
 Treatment
 Complication
 prevention
 References
 DEFINITION

 Miliary TB is an a form of disseminated TB 3


or Extra pulmonary TB that is caused by
sudden diffuse dissemination of tubercli
bacili through the bloodstream
( hematogenous spread of TB )
 The foci are possible caseous - necrotic
changes. Focal changes develop in the
interstitial tissues

 In miliary TB foci formed small ( 1-2 mm )


with productive tissue reaction

 Small foci look like millet grains


 Miliary Tuberculosis: mainly occurs in
children and young adults but may also
occur in older people and it is insidious in
onset in this older age group

 Miliary TB : is can be difficult to diagnose


especially in older age group in which case
it is known as Cryptic Tuberculosis (because
of its insidious onset
 HISTORY

 Miliary TB got its name in 1700 from John Jacob


Manget based on how it appears on autopsy
findings.
 The bodies would have a lot of very small spots
similar to hundreds of tiny seeds about
 2 millimeters long scatted in various tissues.

 Since a millet seed is about that size,


 the condition became known as miliary TB
 Small foci like millet seed which is
scatted in various tissues
 RISK FACTORS
4
• Age – Child & Elderly
• Immunosuppression
• Cancer
• Transplantation
• HIV
• Malnutrition
• Diabetes
• Silicosis
• End-stage renal disease
 TYPES

The miliary TB can be develop in the

1. Miliary pulmonary tuberculosis: occurs when the


organisms draining through the lymphatic and
pulmonary arterioles and enter to the venous blood
and circulate back to the lung
2. Systemic miliary tuberculosis ; occurs when bacteria
disseminate through the systemic arterial system.
 THE MAIN CLINICAL FORMS
OF MILIARY TB

SEPSIS

POLMONARY MILIARY TB TYPHOIDAL

MENINGITIC
 PATHOPHYSIOLOGY OF
MILIARY TB 5
• Tuberculosis infection in the lungs results in
erosion of the epithelial layer of alveolar cells
and the spread of infection into a pulmonary vein

• Bacteria reach the left side of the heart and


enter the systemic circulation, they may multiply
and infect extra pulmonary organs

• Once infected, the cell mediated immune


response is activated. The infected sites become
surrounded by macrophages which form
granuloma, giving the typical appearance of
miliary tuberculosis
 CLINICAL FINDINGS
6
• Patients may not be acutely ill
• Symptoms include
• Weakness and fatigue (90%)
• Fever and weight loss (80%)
• Chills, night sweats are common
• Cough,
• Hemoptysis
• Anorexia
• Hepatomegaly and lymphadenopathy are
common
 DIAGNOSIS

• CBC
7
- Leukopenia/leukocytosis
• ESR - elevated in approximately 50% of
patients
• Lumbar puncture - strongly considered
 Lymphocytic predominance (70%)
 Elevated protein levels (90%)
 Low glucose levels (90%)
 Acid-fast bacilli (≥40%)
• Cultures for mycobacteria
• PCR
 CHEST X-RAY
8
• Typical appearance only in 50% of cases
• Bilateral pleural effusions indicate
dissemination. This may be a useful clue.

• Nodules characteristic of miliary TB may


be better visualized on lateral chest
radiography (especially in the retro cardiac
space).

• Nodules are the size of millet seeds


(1-5mm, mean=2mm)
 CT SCAN
9
 MILIARY  ABDOMINAL
TUBERCULOSIS TYPHUS

• Breathlessness • The typhus begins with


• Cyanosis gradually developing of
• Tachycardia weakness and increase of
• irregular type fever temperature
• absence of dyspeptic • Bradycardia
disturbances  leucopenia
 leucocytes within the limits of  lymphocytosis
norm or leucocytosis up to • Widal’s reaction can be
15 000-18 000 positive just in typhus
  lymphopenia
 Monocytosis
• Roentgenograms confirm
suspicions on miliary lung
tuberculosis
 TREATMENT
10
• Four-drug regimen to start
 Isoniazid
 Rifampin
 Pyrazinamide
 Ethambutol or streptomycin
• Treatment may continue for 6-9 months
• 9-12 months with meningeal involvement
COMPLICATIONS
11
• Dissemination via bloodstream to
I. Prostate
II. Seminal vesicles
III. Epididymis
IV. Fallopian tubes
V. Endometrium
VI. Meninges
VII.Lymph nodes
VIII.Liver
IX. Spleen
X. Skeleton
XI. Kidneys
XII.Adrenals
 PREVENTION

BCG vaccination
 Effective in reducing the incidence of miliary
tuberculosis Not effective in individuals who are
already infected
 Should not be administered to
immunosuppressed hosts

 Targeted tuberculin testing


 Treatment of latent tuberculosis infection
REFERENCES:
12
https://www.slideshare.net/chaudharymahesh/miliary-tuberculos
is-dr-mahesh
http://tuberkulez-forever.com/tuberkulez-likbez/eng
https://
www.slideshare.net/DeepakKumarGupta2/granulomatous-infla
mmation-tuberculosis-syphillis
https://
www.slideshare.net/ghalan/pulmonary-tuberculosis-2941528
https://slideplayer.com/slide/10787857/
https://en.wikipedia.org/wiki/Jean-Jacques_Manget
https://
www.slideshare.net/chaudharymahesh/miliary-tuberculosis-dr-
mahesh
https://www.youtube.com/watch?v=9HUmsnp-nYg
https://www.healthline.com/health/miliary-tuberculosis

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