Evidence map›Paper›PMID 40759168›Full record

ArticleDeutsche medizinische Wochenschrift (1946)2025

[Retrospective analysis of a patient cohort with suspicion of systemic amyloidosis, finally not confirmed].

Philine Ritter, Stefan Schönland, Markus Weiler, Jörg Beimler, Fabian Aus dem Siepen, Carsten Müller-Tidow, Ute Hegenbart

Abstract readEnglish Abstract
In one paragraph

Article in Deutsche medizinische Wochenschrift (1946), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Philine RitterUniversitätsklinikum Heidelberg Amyloidose-Zentrum Medizinische Klinik V. (Hämatologie, Onkologie, Rheumatologie).ORCID 0009-0003-7829-5574
Stefan SchönlandUniversitätsklinikum Heidelberg Amyloidose-Zentrum Medizinische Klinik V. (Hämatologie, Onkologie, Rheumatologie).
Markus WeilerUniversitätsklinikum Heidelberg Klinik für Neurologie.
Jörg BeimlerUniversitätsklinikum Heidelberg Medizinische Klinik X. (Nephrologie).
Fabian Aus dem SiepenUniversitätsklinikum Heidelberg Medizinische Klinik III. (Kardiologie, Angiologie und Pneumologie).
Carsten Müller-TidowUniversitätsklinikum Heidelberg Medizinische Klinik V. (Hämatologie, Onkologie, Rheumatologie).
Ute HegenbartUniversitätsklinikum Heidelberg Amyloidose-Zentrum Medizinische Klinik V. (Hämatologie, Onkologie, Rheumatologie).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic amyloidoses present with non-specific symptoms which lead to a wide spectrum of possible differential diagnoses. In this retrospective study we analyzed a patient cohort that was referred to the amyloidosis center Heidelberg under the suspicion of amyloidosis but ultimately did not receive the diagnosis of amyloidosis after diagnostic work-up. The usefulness of differential diagnosis (DDX) generators in the diagnostic process of amyloidosis is unclear.Included in this retrospective analysis were the data of patients who were referred to the amyloidosis center between 2014 and 2020 and who did not receive the diagnosis of amyloidosis.In order to test the usefulness of the DDX-Generator, 90 patients without amyloidosis were selected from this cohort and compared to another cohort of 30 random patients with confirmed amyloidosis.The diagnosis of amyloidosis was ruled out in 351/2829 (12,4%) patients. The most frequent diagnoses were polyneuropathies (n=129/351, 36,7%) and cardiomyopathies (n=76/351, 21,7%). Plasma cell dyscrasia associated diseases were only present in 17/351 (4,8%) of patients. The cause of the disease remained unknown in 160/186 (86,0%) patients with a mean follow-up time of 34,5 months.In the non-amyloidosis cohort, the DDX generator listed amyloidosis as a possible differential diagnosis in the top 10 differential diagnoses in 25/90 (27,8%) cases.In the amyloidosis-cohort, amyloidosis was significantly more often present in the top 10 differential diagnoses (n=28/30, 93,3%,).Point of contact for patients with unknown or rare diseases are the centers for rare diseases. DDX-Generators could aid physicians to consider amyloidosis as a possible differential diagnosis.

Indexed as

AmyloidosisAgedAged, 80 and overCohort StudiesDiagnosis, DifferentialFemaleHumansMaleMiddle AgedRetrospective Studies

Identifiers

PMID40759168
PMCPMC12396889

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