MindMap Gallery tuberculosis
This is a mind map about tuberculosis, a chronic respiratory infectious disease caused by Mycobacterium tuberculosis that invades the human lungs.
Edited at 2024-03-13 10:55:35This is a mind map about bacteria, and its main contents include: overview, morphology, types, structure, reproduction, distribution, application, and expansion. The summary is comprehensive and meticulous, suitable as review materials.
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This is a mind map about the reproductive development of animals, and its main contents include: insects, frogs, birds, sexual reproduction, and asexual reproduction. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about bacteria, and its main contents include: overview, morphology, types, structure, reproduction, distribution, application, and expansion. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about plant asexual reproduction, and its main contents include: concept, spore reproduction, vegetative reproduction, tissue culture, and buds. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about the reproductive development of animals, and its main contents include: insects, frogs, birds, sexual reproduction, and asexual reproduction. The summary is comprehensive and meticulous, suitable as review materials.
tuberculosis
Tuberculosis spreads among people
Mainly spread by droplets
Source of infection → tuberculosis patient → positive sputum smear
★Tuberculosis is acid-resistant Mycobacterium
The occurrence and development of tuberculosis in the human body
primary infection
primary tuberculosis
First inhalation of aerosol (Mycobacterium tuberculosis vs alveolar macrophages)
(Primary focus) → Mycobacterium tuberculosis survives and grows and reproduces inside and outside alveolar macrophages.
Inflammatory lesions in lung tissue
primary syndrome
Mycobacterium tuberculosis in the primary lesion follows the lymphatic drainage in the lungs → hilar lymph nodes → lymph node enlargement
★↑The combination of primary lesion and enlarged tracheobronchial lymph nodes
★↑The primary lesion continues to expand to other organs (tuberculosis)
secondary tuberculosis
Mycobacterium tuberculosis enters the human body and reproduces for the first time → the human body develops specific immunity to the bacilli
Reduce the size of primary lesions/hilar lymph nodes/calcify/stop reproduction
There are still a small number of tuberculosis that have not been eliminated, and long-term dormancy has become a source of secondary tuberculosis.
Tuberculosis Immunity and Delayed Allergy
The main immune mechanism of tuberculosis is cellular immunity
koch phenomenon
primary allergic reaction
secondary immune response
secondary tuberculosis
Secondary tuberculosis has obvious clinical symptoms (prone to cavities and excretion of bacteria) → is contagious
two ways
Tuberculosis caused by the reactivation of latent Mycobacterium tuberculosis bacteria left over from the primary tuberculosis infection period (endogenous infection)
Relapse of Mycobacterium tuberculosis infection (exogenous infection)
pathology
Classification
inflammatory exudation
hyperplasia
Degenerative lesions → Caseous necrosis
Basic pathological changes
Destruction and repair at the same time
Mainly hyperplasia manifestation → tuberculosis miliary nodules
Caseous necrosis → mostly occurs when Mycobacterium tuberculosis is highly virulent/low body resistance
Pathological changes and outcomes
Indicates worsening of the disease course → acute chestnut tuberculosis (spread through blood and lymphatic channels)
Become an endogenous source of infection → Lesion latent secondary tuberculosis
heal
clinical manifestations
symptom
respiratory symptoms
Cough/phlegm for more than two weeks/blood in the phlegm
phlegm
Cavities are formed → there is more phlegm
Combined with other bacterial infections → there may be thick sputum
Most patients have a small amount of hemoptysis (about 3/1 of the population)
Caused by telangiectasia
Very few cases of massive hemoptysis
Caused by rupture of bronchial artery/aneurysm
Difficulty breathing is seen in
caseous pneumonia
Massive pleural effusion
Tuberculosis lesions spread to the pleura → chest pain
Hemoptysis
Classification
Most patients have a small amount of hemoptysis (about 3/1 of the population)
Caused by telangiectasia
Very few cases of massive hemoptysis
Caused by rupture of bronchial artery/aneurysm
Fever after hemoptysis
Low fever (blood clot absorption)
High fever (infection)
systemic symptoms
Afternoon hot flashes/night sweats/fatigue
★★Special symptoms
A few patients may have rheumatic fever-like symptoms → nodular rheumatism
Nodular/annular erythema may be seen near affected joints
Tuberculosis diagnosis
imaging diagnosis
Chest X-ray examination (anterior/lateral chest radiography) (preferred conventional method)
Classification
Secondary
Posterior apical segment of upper lobe/dorsal segment of lower lobe/posterior basal segment
primary
Lower part of upper leaf/upper part of lower leaf
★Memory
The tuberculosis bacilli infected the person for the first time and was not sensible, so he was lazy and stayed near the bronchus, feeling that there was enough oxygen, that is to say, the lower section of the upper lobe and the upper section of the lower lobe. Later, he was cured; the second time he infected the person, he learned Be smart, go to the place farthest from the bronchus, where there is also enough oxygen, that is, where the posterior segment of the upper leaf tip is hidden.
Infiltration/proliferation/calcification can coexist → easy to form cavities
★★Confirmed
Sputum culture
Sputum Mycobacterium tuberculosis test
Sputum tuberculosis bacilli examination (whether the bacterium is excreted) → Infectious
Tuberculin/PPD/antibody test → determine whether you have been infected in the past
Erythrocyte sedimentation rate → Whether it is the active phase
Tuberculosis bacteria found in sputum (reliable basis for diagnosing pulmonary tuberculosis)
tuberculin test
Negative
4-8 weeks before tuberculosis infection (die)
Malnutrition/HIV infection/severe illness
Miliary tuberculosis (this type of tuberculosis is more serious)
★Allergy can only be established 4-8 weeks after Mycobacterium tuberculosis infection
Masculine meaning
Vaccination with BCG vaccine
Have not been vaccinated with BCG but are positive
ever infected
Infants and young children → not vaccinated → positive (most valuable for diagnosing active tuberculosis)
active tuberculosis
Negative → positive or less than 10mm → greater than 10mm
There is a new infection
Is there any mobility?
X-image performance
Have mobility
Patchy shadows with blurred edges (central dissolution, cavities, disseminated lesions)
No mobility
Calcification, induration, fibrosis, high density of lesions/clear boundaries
Tuberculosis classification
primary tuberculosis
dumbbell shadow
blood group disseminated pulmonary tuberculosis
acute miliary tuberculosis
Performance
Acute onset and persistent high fever
systemic toxaemic inflammation
Chest X-ray size/density/distribution are uniform
secondary tuberculosis
Infiltrative pulmonary tuberculosis (spotted shadow) (cloudy shadow)
Tuberculosis (calcification focus)
Caseous pneumonia (ground glass) → later cavity (worm-eaten cavity) appears
Chills and high fever/sudden onset
Frequent elimination of bacteria
Fibrous cavitary tuberculosis (the most contagious) (thick-walled cavities/lung textures like weeping willows)
Long course of disease/repeated progression and deterioration/prolonged recovery
Severe damage to lung tissue
Severely impaired lung function
★The hilum moves upward (pulled by fibers)
★Source
Primary tuberculosis bacteria have not been completely eliminated
tuberculous pleurisy
Various tuberculosis imaging diagnoses
primary tuberculosis
hilar lymphadenopathy
infiltrative pulmonary tuberculosis
Commonly seen at the apex of the upper lobe/dorsal and posterior base of the lower lobe
Blood type disseminated type (chestnut type pulmonary tuberculosis)
Uniform size/density/distribution
chronic fibrocavitary tuberculosis
Identification of various holes
thin wall cavity
cavitary tuberculosis
thick wall cavity
fiber cavity type
Cavity with liquid level
lung abscess
treat
Mycobacterium tuberculosis is divided into ABCD based on metabolic status
A bacterial group → reproduces rapidly, is large in number, and is the main part
Isoniazid
B flora → semi-quiescent
pyrazinamide
C flora → semi-quiescent
rifampicin
D flora → completely dormant
Memory:un (I) believable
in principle
Early/Regular/Full Process/Moderate/Combined
Reinforcement stage (bad guys doing evil) (HRZE)
Isoniazid Rifampicin Pyrazinamide Ethambutol
Consolidation Phase (Only Bad Guys) (HR)
Isoniazid Rifampicin
treat
drug
All bactericides
Isoniazid
rifampicin
semi-bactericidal medicine
Streptomycin
pyrazinamide
plan
consolidation therapy
prevention
Isoniazid (orally for 6 months)
Asymptomatic
Isoniazid Rifampicin
Consolidate curative effect and prevent recurrence
Symptomatic
Isoniazid Rifampin Streptomycin/Pyrazinamide
strengthen
Involves the brain
Isoniazid Rifampicin Pyrazinamide Streptomycin
Rapid sterilization
abbreviation
Rifampicin R(RFP)
Isoniazid H(INH)
Pyrazinamide Z (PZA)
Ethambutol E
Replenish
1 medicine for prevention
Asymptomatic 2 medicines
3 medicines for symptoms
4 drugs that seriously affect the brain
Replenish
Most common
infiltrative pulmonary tuberculosis
The most contagious
chronic fibrocavitary type
The sickest
caseous tuberculosis
allergy supplements
Type I allergic reaction (immediate type→anaphylaxis→IgE mediated)
Allergy/Shock/Asthma
Type 2 allergy (cytotoxicity→IgG mediated)
Rheumatism/blood-related diseases (blood transfusion, hemolysis, vascular damage)
Type III allergy (immune complex type → vasculitis type)
Rheumatoid/Hepatitis/Serum Sickness
Type IV allergic reaction (delayed type→T cell mediated)
Tuberculosis/contact dermatitis
Replenish
Thin-walled cavity Fluid level Neutrophils↑
lung abscess
Thin-walled cavity No fluid level Neutrophils—
tuberculosis