Related Experiment Video
Updated: Oct 1, 2025

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
A case of medical liability involving an unexpected systemic amyloidosis
Nicola Galante1, Barbara Ciprandi1, Lorenzo Franceschetti1
1Sezione di Medicina Legale e delle Assicurazioni-Dipartimento di Scienze Biomediche per la Salute, Università degli Studi di Milano, Milano, Italy.
Insights
Autopsy revealed fatal amyloid cardiomyopathy, a rare condition missed during a patient's cardiac ablation. This case highlights the importance of autopsy in diagnosing occult systemic amyloidosis (AL-type).
Area of Science:
- Cardiology
- Pathology
- Medical Malpractice
Background:
- A 57-year-old man underwent transcatheter radiofrequency ablation for persistent atrial fibrillation and atrial flutter.
- Post-procedure, he experienced ventricular fibrillation and later died of nosocomial pneumonia.
Observation:
- A judicial autopsy was ordered due to alleged medical malpractice.
- Autopsy revealed occult restrictive cardiomyopathy with diffuse myocardial amyloid deposits.
- Amyloid deposits were found in multiple organs, positive for light chains, confirming AL-type systemic amyloidosis.
Findings:
- Histopathology confirmed diffuse amyloid deposition in the myocardium.
- Immunohistochemistry identified light chain positivity, indicative of AL-type amyloidosis.
- The autopsy was crucial for diagnosing the underlying systemic amyloidosis.
Implications:
- Undiagnosed systemic amyloidosis can present unusually, potentially leading to misinterpretations of medical events.
- This case underscores the diagnostic value of autopsy in complex medical scenarios.
- It highlights the need to consider rare conditions like amyloidosis in differential diagnoses, especially when clinical presentation is atypical.
Abstract:
The authors present a case of fatal amyloid cardiomyopathy, which was diagnosed only upon autopsy. A 57-year-old man was admitted to the hospital for scheduled percutaneous cardiac procedure of transcatheter radiofrequency ablation due to persistent atrial fibrillation and atrial flutter. Ventricular fibrillation was recorded in the monitor 2 h after the surgical procedure. Therefore, he was defibrillated and intubated, but he died for nosocomial pneumonia 26 days after being admitted. A judicial autopsy was ordered by the prosecutor due to an alleged medical malpractice. The autopsy confirmed the cause of death being pneumonia, but also revealed an occult restrictive cardiomyopathy with a thick and firm myocardium. Viscera samples were then collected for microscopic examination. Histopathologic analysis showed diffuse amyloid deposits in the myocardium, especially in the perivascular and subendocardial spaces. Amyloid deposits were also detected in all the other organs, except for the brain. Furthermore, immunohistochemistry for light chains was performed on the heart tissue sample, resulting to be positive. In the case presented herein, autopsy and histopathologic examination were crucial to diagnose an occult systemic amyloidosis (AL-type). In fact, it has been observed that the rarity of systematic amyloidosis and its unusual clinical onset were at first mistakenly perceived as a medical malpractice due to a technical error within the catheter ablation for atrial fibrillation. As a consequence, upon discussing the clinical and medicolegal implications concerning the case, the focus was placed on the undiagnosed systemic amyloidosis and on the causality between surgical procedure and the patient's death.
More Related Videos
10:04Imaging Amyloid Tissues Stained with Luminescent Conjugated Oligothiophenes by Hyperspectral Confocal Microscopy and Fluorescence Lifetime Imaging
Published on: October 20, 2017
15:04Interactions with and Membrane Permeabilization of Brain Mitochondria by Amyloid Fibrils
Published on: September 28, 2019