The Discovery And Historical Background Of Banti’s Syndrome
Published on: November 11, 2024
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Innocensia Kambewe

Master's degree, Public Health (Social Behavioral Change Communication), University of the Witwatersrand

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Jhernel Rhudd

Bachelor of Science in Medical Biochemistry

The discovery of Banti’s Syndrome revolutionized the way doctors understand the spleen and its functions. This breakthrough completely transformed the way hypertension and liver health is looked at. When doctors, nurses and other healthcare professionals understand how portal hypertension, splenomegaly, and hemolytic anemia are interconnected, they are able to create principles and guidelines that help when evaluating and diagnosing these symptoms for eons to come.   

For this piece we will dive into Banti’s syndrome’s history, using evidence-based data to paint a holistic picture of how the disease was discovered, how these findings were brought into the world, and by whom. 

Guido Banti: The founding father of Banti’s Syndrome

Guido Banti was the first person to discover this syndrome in the late 1900s. Banti began exploring and figuring out similarities in some symptoms that his patients exhibited. They all presented with an enlarged spleen, anemia, and clinical evidence of high blood pressure within the vein that takes blood to the liver. What he found most intriguing was how these patients did not have any symptoms of liver disease, a factor that prompted more research.

Born the 8th of June, 1852, in a small town in Tuscany. Banti always had a keen interest in hematology (the study of blood) and pathology (the study of diseases). The work he did that focused on understanding diseases of the spleen and blood was what led him to this discovery. With time and after gaining a solid foundation in medical science at the University of Pisa he focused on delving into deeply understanding pathology and hematology.1

Understanding Banti’s Syndrome

Banti’s syndrome is known differently in different regions of the world. In India they call it non-cirrhotic fibrosis3, In the United States of America it is called hepatoportal sclerosis and in Japan they named it idiopathic portal hypertension (IPH).4

This shows us how different this disease is seen by different cultures and medical professionals from vast parts of the world. Proving that understanding the historical context of Banti’s syndrome will aid in understanding the disease itself at a profoundly deeper level. 

Getting a more contextual view of Banti’s Syndrome is what helps the advancement in medical diagnoses and treatments. This knowledge creates the best and most holistic look at how the disease has evolved while providing a foundation for research and guiding scientists and doctors in their studies and practice.

The Discovery Stage

Banti’s early research on the syndrome started in the year 1900 to 1910 in Italy. This syndrome was then discovered in the late 19th century. 

He began this process by looking into patients with significant spleen enlargement and blood cell abnormalities. The symptoms that come hand in hand with these issues such as abdominal swelling, unusual bleeding and uncontrollable bruising, symptoms that were common among these patients were recorded to be used for future analysis.

After conducting comprehensive physical examinations and autopsies on the spleen, liver and abdomen. He went on to look into blood samples from his patients so he could determine the extent of the anaemia and how low the levels of blood cells had gotten in the liver. Banti chose to focus on any changes he found in these organs following the symptoms he initially identified. This process of cross-referencing aided him in creating the link between the symptoms and spleen dysfunction.1

The Elimination Stage

Banti’s syndrome can only be diagnosed after all diseases pertaining to the liver or spleen have been ruled out. Because of this Banti needed to rule out any other illnesses that could cause spleen enlargement, anaemia, and hypertension in the portal vein. He performed several additional tests to ensure that any liver diseases, infections, and tumours or malignancies did not have similar symptoms or affected the body in similar ways.

To do this, he employed the use of ultrasounds, laboratory tests and CT scans to have a concentrated and evident view of liver functions and bone marrow in his patients,2

The Hypothesis Stage

After he examined and re-examined the symptoms and correlated them to the symptoms he initially identified. He was able to exclude other potential diagnoses and confirm that his findings and observations did not align with other known conditions. This allowed him to create a hypothesis based on the consistent pattern of symptoms that were aligned with the Banti’s Syndrome.

Through engaging with other medical personnel and researchers in a similar field, he was able to build and test his hypothesis on the existence of Banti’s Syndrome. Working with other professionals aided in increasing the reliability and validity of his research.

So, what is Banti's Syndrome?

Initially, this condition starts with congestion in the spleen. This is when the spleen becomes very large due to high blood pressure in the vessels feeding blood into the organ, causing it to trap and destroy more blood cells than normal (white and red blood cells and platelets). This all happens without any effect on the liver. This enlargement of the spleen is scientifically called Splenomegaly.

This is then followed by the introduction of several symptoms because the spleen is breaking down more red blood cells than the body can produce. Hence leading the body to experience Hemolytic anaemia.

As the spleen breaks down more and more red blood cells, the exertion causes the reduction of white blood cells and platelets in the spleen and liver. Leaving the body defenceless and more susceptible to all kinds of infections while increasing the risk of bleeding and bruising in the body. This right here is referred to as Pancytopenia.

With the congestion in the spleen comes increased pressure in the vein that transports blood to the liver. The high blood pressure in the portal vein leads to the development of enlarged veins in the oesophagus and stomach. Increasing susceptibility to bleeding in the stomach due to  Portal hypertension.2

Simply, Banti’s syndrome can be identified through the following symptoms:

  • Fatigue
  • Weakness
  • Easy bruising
  • Frequent infections in the body
  • Stomach aches
  • Gastrointestinal bleeding, which can cause hematemesis and melena

It is vital to keep in mind that a person is only diagnosed with Banti's syndrome when the doctors have ruled out all other possible reasons someone could have an enlarged spleen, a shortage of blood cells, and high blood pressure in the veins that lead to the liver.2 Only after other diseases are excluded can a condition be identified as Banti's syndrome.

Impact on Modern Medicine

This discovery had a monumental impact on modern medicine. This impact was multifaceted in the way that it aided in the advancement of hematology and hepatology fields worldwide. In turn leading to the improvement of diagnostic techniques, treatment strategies and clinical practices.5

In spite of the positives, any discovery must come with some challenges. For Guido’s discovery, there are still a lot of difficulties when it comes to diagnosis leading to a vast number of misdiagnosed patients. This clearly highlights the need for more research and creating innovative methods to understand and work with spleen related illnesses, especially at the primary healthcare level like doctors, nurses and many others.5

Conclusion

Through Banti’s research, a new perspective and framework for understanding and diagnosing conditions of the spleen and blood was created. His work created a platform and foundation for more research and advancements in the study of the liver also known as “hematology and hepatology”.

Summary

Banti’s syndrome was discovered in the early th century by Gaudi Banti. As a pathologist his journey to this discovery was paved through his knowledge and his curious mind. Always wanting to be at the forefront of his industry and a constant thirst for learning new things. Banti’s syndrome is a very rare disease and only diagnosed after all possible diagnostics do not align with the patient’s syndrome. This disease affects the spleen without hurting the liver in any way, one of the reasons Banti was incredibly fascinated by this disease. Knowing and understanding the historical background of Banti’s Syndrome will aid in creating the best foundations for disease diagnosis and employing innovative methods to work on diseases of the spleen. 

References

  1. Nesi G, Santi R. Banti, Guido (1852–1925). Encyclopedia of pathology (Internet). 2017 Jan 1 (cited 2024 Jul 29);55–6. Available from: https://link.springer.com/referenceworkentry/10.1007/978-3-319-41995-4_497
  2. Khan AR, Muhammad Hayyan Wazir, Salma Waqar, Ullah R, Gul A. Banti’s Syndrome in an Adult Male: A Case Report. Curēus (Internet). 2022 May 31 (cited 2024 Jul 23); Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246469/
  3. Eapen C, Goel A, Ramakrishna B, Zachariah U, KG Sajith, DeepakK Burad, et al. What makes non-cirrhotic portal hypertension a common disease in India? Analysis for environmental factors. The Indian Journal of Medical Research (Internet). 2019 Jan 1 (cited 2024 Jul 29);149(4):468–8. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676844/
  4. Mustafa Serdar Cantez, Nelgin Gerenli, Vildan Ertekin, Mine Güllüoğlu, Özlem Durmaz. Hepatoportal Sclerosis in Childhood: Descriptive Analysis of 12 Patients. Journal of Korean Medical Science (Internet). 2013 Jan 1 (cited 2024 Jul 29);28(10):1507–7. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792606/
  5. Gupta J, Fulare S, Deshmukh S. Surgical approach towards management of Banti’s syndrome: A rare disorder. ~ 14 ~ International Journal of Case Reports in Surgery (Internet). 2020;2(1):14–6. Available from: https://www.casereportsofsurgery.com/article/15/2-1-8-651.pdf
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Innocensia Kambewe

Master's degree, Public Health (Social Behavioral Change Communication), University of the Witwatersrand

Innocensia is a Public Health, Social Behavioural Communications (SBCC) expert with a strong background in qualitative research. She has a neverending passion for health information dissemination, always ensuring that what she writes is accessible and easy to understand for everyone.

Innocensia’s work includes co-authoring peer-reviewed research and designing evidence-based educational modules for professional development. With a strong commitment to ethical research practices, she excels in disseminating complex data through accessible and impactful reports. She is also passionate about advancing public health initiatives, particularly in mental health and social behavior change.

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