Amyloidosis treatment

The treatment of amyloidosis differs considerably depending on the type of protein.

Treatment of AL amyloidosis

AL-type amyloidosis is caused by the deposition of subunits of defense proteins, the so-called immunoglobulin light chains. These light chains are formed by pathologically altered immune cells in the bone marrow or the lymph glands (plasma cells/lymph cells). AL amyloidosis is closely related to the development of tumorous diseases of the bone marrow and lymph glands, such as multiple myeloma and non-Hodgkin’s lymphoma. As with these diseases, treatment therefore also consists of systemic immuno-chemotherapy. This is intended to prevent the further production of light chains and the further formation of AL amyloid. The intensity of this chemotherapy depends on the patient’s resilience and general health. The organs most frequently affected are the heart, kidneys, nerves and intestines.

Treatment of hereditary and genetic amyloidosis

Hereditary amyloidosis is rare. However, there is an accumulation of patients in different regions of the world. Switzerland is not specifically affected. The cause of the disease is usually the faulty production of a protein that is formed in the liver. This transport protein is called transthyretin and the disease transthyretin (ATTR) amyloidosis. The main areas affected by the deposits are the nerves, the heart, the intestines and the eyes. Since transthyretin is produced in the liver and treatment is intended to prevent further production of this protein, liver transplantation is an important treatment option. Transthyretin amyloidosis can also occur as a new genetic change without being inherited from a parent. In addition to ATTR amyloidosis, there are other genetic amyloidoses. However, these are even rarer.

Treatment of AA amyloidosis

Type AA amyloidosis can occur in any chronic inflammation that lasts for years. Typical causes are chronic infections of the lungs or skin, chronic inflammatory rheumatic diseases, chronic inflammatory bowel diseases and, more rarely, hereditary febrile illnesses. Therapeutically, the focus is always on treating the underlying disease. The organs most frequently affected by AA aymloidosis are the kidneys and the intestines.

We offer all established treatment options for patients with amyloidosis

  • Supportive therapy incl. Physiotherapy, occupational therapy, psycho-oncology, counseling services, etc.
  • Heart failure treatment
  • Pacemaker implantation
  • Renal replacement procedure
  • Anti-inflammatory therapy
  • Outpatient and inpatient immuno-chemotherapy
  • Autologous and allogeneic stem cell transplantation
  • Organ transplants (liver, kidney, heart)
  • TTR amyoid-directed therapies, if available in Switzerland

Amyloidosis network

The amyloidosis network at the University Hospital Zurich was founded in 2013 by our interdisciplinary team of specialists from the Departments of Gastroenterology, Hematology, Cardiology, Nephrology, Neurology, Neuropathology, Pathology and Rheumatology, the Institute of Medical Genetics at the University of Zurich and the Cantonal Hospital of Graubünden. Our aim is to extend and improve the lifespan and quality of life of affected people. Patients are cared for in close cooperation with the referring doctors.

Responsible professionals

Rahel Schwotzer, Dr. med.

Senior Physician, Department of Medical Oncology and Hematology

Tel. +41 44 255 81 39
Specialties: Systemic amyloidosis, General Hematology

Andreas Flammer, Prof. Dr. med.

Senior Physician, Department of Cardiology

Tel. +41 43 253 83 08
Specialties: Head of heart failure and heart transplantation, Head of Assist-Devices Consultation, Co-Head of the Amyloidosis Network Zurich

Markus Manz, Prof. Dr. med.

Director of Department, Department of Medical Oncology and Hematology

Tel. +41 44 255 38 99
Specialties: Leukemias, Lymphomas, Plasma cell diseases

Frank Ruschitzka, Prof. Dr. med.

Director of Department, Department of Cardiology

Tel. +41 44 255 21 21
Specialties: Heart failure, Heart transplantation

Heiko Pohl, MHD, PD Dr. med.

Attending Physician, Department of Neurology

Tel. +41 44 255 55 11

Hans Heinrich Jung, Prof. Dr. med.

Senior Physician, Department of Neurology

Tel. +41 44 255 55 20
Specialties: Neuromuscular diseases, Dementia / Memory Clinic, Neurogenetic diseases / neurological rare diseases

Luc Biedermann, Prof. Dr. med.

Senior Physician, Department of Gastroenterology and Hepatology

Tel. +41 44 255 85 48
Specialties: Chronic inflammatory bowel disease (IBD), Eosinophilic esophagitis (EoE) and eosinophilic gastrointestinal diseases (EGID), Celiac disease

Beat Müllhaupt, Prof. Dr. med.

Senior Physician, Department of Gastroenterology and Hepatology

Tel. +41 44 255 85 48
Specialties: Acute and chronic liver diseases, Acute liver failure, Transplant hepatology

Robert Manka, MSc, Prof. Dr. med.

Senior Physician, Institute for Diagnostic and Interventional Radiology
Senior Physician, Department of Cardiology

Tel. +41 44 255 12 51
Specialties: Cardiac imaging (heart MRI & heart CT), Interventional cardiology, Consultation hours for complex coronary interventions

Aju Pazhenkottil, Executive MBA HSG, Prof. Dr. med.

Senior Attending Physician, Department of Nuclear Medicine
Attending Physician, Department of Consultation-Liaison Psychiatry and Psychosomatic Medicine

Tel. +41 44 255 39 50
Specialties: Specialist in multimodal non-invasive cardiac imaging (cardiac CT, MRI, PET, SPECT, echocardiography), Specialist in cardiology FMH, Focus on psychocardiology

Felix Tanner, Prof. Dr. med.

Senior Physician, Vice Director of Department, Department of Cardiology

Tel. +41 43 253 79 40

For patients

As a patient, you cannot register directly for a consultation. Please get a referral from your primary care physician, specialist. For questions please use our contact form.

Contact form

For referrering physicians

University Hospital Zurich
Department of Medical Oncology and Hematology
Raemistrasse 100
8091 Zurich

Tel. +41 44 255 38 99
Patient registration form

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