3D Printed Right Lung Miliary Tuberculosis

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  • 3D Printed Right Lung Miliary Tuberculosis
  • 3D Printed Right Lung Miliary Tuberculosis
  • 3D Printed Right Lung Miliary Tuberculosis
  • 3D Printed Right Lung Miliary Tuberculosis
Retail Price $895.00
Today's Price $815.00
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Developed from real patient case study specimens, the 3D printed anatomy model pathology series introduces an unmatched level of realism in human anatomy models. Each 3D printed anatomy model is a high-fidelity replica of a human cadaveric specimen, focusing on the key morbidity presentations that led to the deceasement of the patient. With advances in 3D printing materials and techniques, these stories can come to life in an ethical, consistently reproduceable, and easy to handle format. Ideal for the most advanced anatomical and pathological study, and backed by authentic case study details, students, instructors, and experts alike will discover a new level of anatomical study with the 3D printed anatomy model pathology series.

Clinical History

A 74-year old male presented with increasing shortness of breath and hemoptysis. Further history reveals 20kg weight loss in 6 months, night sweats and a chronic cough. He has recently moved from a country where TB is endemic. On examination, he has hypoxic and tachypnoea and has bilateral crepitations throughout his lung fields and a dull left lung base on percussion. His quantiferon gold blood test is positive. His chest x-ray showed bilateral small nodular deposits and a left basal pneumonia. He died from respiratory failure soon after admission.


The right lung has been sliced longitudinally and mounted to display the cut surface. The bronchi and bronchioles are mildly ectatic. Scattered throughout the entire lung parenchyma are large numbers of small, pale yellows nodules less than 1 mm in diameter. Similar tiny subpleural nodules are seen on the surface of the visceral pleura. The nodules are tubercles. This is miliary tuberculosis, so-called due to the resemblance of the nodules to millet seeds.

Further Information

Tuberculosis (TB) is a chronic pulmonary and systemic infectious disease caused by Mycobacterium tuberculosis. Transmission most commonly occurs via inhalation of aerosolized droplets of this pathogenic bacteria, first described by Robert Koch (1882). Risk factors for contracting TB include being an inhabitant of a developing country where the disease is endemic, immunosuppression (e.g. HIV, steroid use, anti-TNF use and diabetes), chronic lung disease (e.g. silicosis), alcoholism and malnutrition.

After initial pulmonary infection of M. tuberculosis clinical manifestation varies. In 90% of individuals with an intact immune system they enter an asymptomatic latent infection phase. This latent TB may reactivate at any time in the patient's life. In the other 10% of patients, especially in the immunocompromised, they develop primary disease which is immediate active TB infection. Manifestations of primary TB include pulmonary infection symptoms (e.g. consolidation, effusion and hilar adenopathy) and extra pulmonary symptoms including lymphadenopathy, meningitis and disseminated miliary TB.

Secondary tuberculosis occurs when there is reactivation of previous latent TB infection. Around 10% of latent TB will reactivate usually during periods of weakened host immunity. Typical symptoms of reactivation are cough, hemoptysis, low grade fever, night sweats and weight loss.

Miliary TB occurs when the mycobacterium erodes into a pulmonary vein and seeds elsewhere. The organism can circulate back to the lung and disseminate thought the lung parenchyma as in this case. Systemic miliary tuberculosis can occur when the mycobacterium is disseminated through the arterial system. The TB can then deposit in any organ but most commonly in the liver, bone marrow, spleen and adrenal glands.

The immune response against TB is mediated via TH1 cells stimulate alveolar macrophages to attack the mycobacteria. These macrophages surround the infection forming a granuloma surrounding a central area of caseous (white cheese-like) necrosis. Secondary pulmonary TB may heal with fibrosis or progress as in this case. Progressive pulmonary TB sees erosion and expansion of the infectious lesion into adjacent lung parenchyma. This leads to evacuation of the caseous center leading to fibrous cavitation. Erosion of blood vessels can occur causing hemoptysis. Post treatment of TB the tissue heals by fibrosis but does not recover the pulmonary architecture.

TB diagnosis is usually made with a clinical history and chest x-ray and multiple sputum cultures. Mantoux skin tuberculin test and serum interferon gamma release assay may also be used to help screen for infection. Biopsies may be taken of suspected infection site for culture to assist diagnosis. Treatment involves prolonged courses of multiple antibiotics, which depend on the antibiotic resistance of the infecting mycobacterium.

Advantages of 3D Printed Anatomical Models

  • 3D printed anatomical models are the most anatomically accurate examples of human anatomy because they are based on real human specimens.
  • Avoid the ethical complications and complex handling, storage, and documentation requirements with 3D printed models when compared to human cadaveric specimens.
  • 3D printed anatomy models are far less expensive than real human cadaveric specimens.
  • Reproducibility and consistency allow for standardization of education and faster availability of models when you need them.
  • Customization options are available for specific applications or educational needs. Enlargement, highlighting of specific anatomical structures, cutaway views, and more are just some of the customizations available.

Disadvantages of Human Cadavers

  • Access to cadavers can be problematic and ethical complications are hard to avoid. Many countries cannot access cadavers for cultural and religious reasons.
  • Human cadavers are costly to procure and require expensive storage facilities and dedicated staff to maintain them. Maintenance of the facility alone is costly.
  • The cost to develop a cadaver lab or plastination technique is extremely high. Those funds could purchase hundreds of easy to handle, realistic 3D printed anatomical replicas.
  • Wet specimens cannot be used in uncertified labs. Certification is expensive and time-consuming.
  • Exposure to preservation fluids and chemicals is known to cause long-term health problems for lab workers and students. 3D printed anatomical replicas are safe to handle without any special equipment.
  • Lack of reuse and reproducibility. If a dissection mistake is made, a new specimen has to be used and students have to start all over again.

Disadvantages of Plastinated Specimens

  • Like real human cadaveric specimens, plastinated models are extremely expensive.
  • Plastinated specimens still require real human samples and pose the same ethical issues as real human cadavers.
  • The plastination process is extensive and takes months or longer to complete. 3D printed human anatomical models are available in a fraction of the time.
  • Plastinated models, like human cadavers, are one of a kind and can only showcase one presentation of human anatomy.

Advanced 3D Printing Techniques for Superior Results

  • Vibrant color offering with 10 million colors
  • UV-curable inkjet printing
  • High quality 3D printing that can create products that are delicate, extremely precise, and incredibly realistic
  • To improve durability of fragile, thin, and delicate arteries, veins or vessels, a clear support material is printed in key areas. This makes the models robust so they can be handled by students easily.
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Warranty Information

5 Year Warranty
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