3D Printed Tertiary Syphilis

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  • 3D Printed Tertiary Syphilis
  • 3D Printed Tertiary Syphilis
  • 3D Printed Tertiary Syphilis
  • 3D Printed Tertiary Syphilis
  • 3D Printed Tertiary Syphilis
  • 3D Printed Tertiary Syphilis
Retail Price $1,710.00
Today's Price $1,555.00
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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 66-year old male presents with postprandial epigastric pain. Of note, he is deaf and non-verbal. On examination, he has a tender epigastrium and several nodular tender lesions over his forehead and scalp. Blood tests show a low hemoglobin, impaired hepatic function and are positive for anti-treponemal antibodies. After admission, he has a large gastrointestinal bleed, and dies despite intervention.


This specimen is the vault of the patient's skull. On the external surface, there are multiple circumscribed necrotic lesions in the parasagittal area to the left of the midline. The lesions are brown in color and measure up to 3-4 cm in maximum diameter. The lesions have eroded the outer table of the skull and the adjacent periosteum is thickened with a fibrinous inflammation. These lesions are chronic syphilitic lesions or gumma of the skull, which are characteristic of benign tertiary syphilis.

Further Information

Syphilis is a chronic infection caused by the spirochete bacterium Treponema pallidum. Sexually transmitted infection is most common, but it may also be congenitally-acquired by transplacental transmission of the bacteria. Those who have the higher risk of infection, include those of a sexually active age, intravenous drug users, HIV-infected patients and homosexual males. Syphilis infection rates decreased significantly with the introduction of penicillin in 1943, which remains the main treatment today. However, the infection rate has been increasing since the early 2000’s.

Syphilis is divided into three stages with distinct clinical and pathological features with characteristic proliferative endarteritis affecting small vessels. Primary syphilis occurs usually 3 weeks after initial infection. This manifests typically as a single, painless and erythematous lesion called a chancre at the site of inoculation. The syphilis spreads throughout the body from this chancre, which then heals spontaneously after 3 to 6 weeks.

Secondary syphilis occurs weeks to a few months after the primary chancre resolves in 75% of untreated patients. During this stage patients commonly have generalized symptoms, such as malaise, lymphadenopathy and skin rashes. Palmar/plantar rashes are the most frequent site but rashes can also be diffuse. These rashes can be maculopapular, scaly or pustular. Condylomata lata are elevated gray plaques that arise on the moist mucous membranes, such as oral or genital regions. Other less common manifestations include hepatitis, gastrointestinal invasion or ulceration and neurosyphilis - discussed below.

Tertiary syphilis has three main characteristics: cardiovascular syphilis, neurosyphilis and gummatous syphilis. These occur after a latent period of 5 years or more in one third of untreated patients.

Cardiovascular syphilis involves an aortitis for which the exact pathophysiology is unclear. The vasculitis involves the ascending thoracic aorta leading to progressive dilation of the aortic root which can cause aortic valve insufficiency and aneurysms. Clinical manifestation usually happens 15-30 years post initial infection.

Neurosyphilis can be symptomatic or asymptomatic. It occurs in 10% of untreated patients. Early clinical manifestations include headaches, meningitis, hearing loss and ocular involvement, most commonly uveitis, causing vision loss. Late manifestations can occur up to 25 years post initial infection. Main features are meningovascular neurosyphilis, paretic neurosyphilis and tabes dorsalis. Meningovascular involvement involves chronic meningitis and endarteritis which can lead to

strokes. Tabes dorsalis is caused from degeneration of the posterior columns within the spinal cord. This causes loss of proprioception, ataxia, loss of pain sensation, and loss of reflexes. Paretic neurosyphilis is caused by invasion and damage of the brain parenchyma, most commonly the frontal lobes. This leads to progressive cognitive impairment and mood disturbance.

Gummatous syphilis is characterized by the formation of nodular lesions most commonly bone, skin and mucosa of the upper airway and mouth called gummas. Gummas can occur anywhere including viscera. The formation of gummas is rare but occurs more frequently in HIV-infected patients. Skeletal involvement causes pain and pathological fractures.

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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