Evidence map›Paper›PMID 41095829›Full record

ArticleJournal of clinical medicine2025

A Rare Case of Systemic Amyloidosis Involving the Thyroid in a Young Patient.

Oliwia Julia Kasprzak, Kamila Stępińska, Kaja Kiedrowska, Tomasz Błaszkowski, Aleksandra Kudrymska, Sylwia Sikora, Maciej Miernik, Maciej Romanowski

Abstract readCase Reports
In one paragraph

Article in Journal of clinical medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Oliwia Julia KasprzakSurgical Scientific Society at the Department of General and Oncological Surgery, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Kamila StępińskaSurgical Scientific Society at the Department of General and Oncological Surgery, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Kaja KiedrowskaSurgical Scientific Society at the Department of General and Oncological Surgery, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Tomasz BłaszkowskiSurgical Scientific Society at the Department of General and Oncological Surgery, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Aleksandra KudrymskaDepartment of Pathomorphology, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Sylwia SikoraDepartment of Pathomorphology, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Maciej MiernikDepartment of General and Oncological Surgery, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.
Maciej RomanowskiSurgical Scientific Society at the Department of General and Oncological Surgery, Pomeranian Medical University in Szczecin, 71-252 Szczecin, Poland.ORCID 0000-0002-7401-9877

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thyroid amyloidosis is a rare condition associated with thyroid pathologies such as medullary carcinoma, papillary carcinoma, amyloid goitre, and benign lesions, with a clinically palpable goitre being exceptionally uncommon. As a result, many cases of benign thyroid enlargement caused by amyloid deposits remain undiagnosed. A 28-year-old male patient noticed progressive neck circumference enlargement, voice alteration, decreased appetite, weight loss, dysphagia, fever, and night sweats. Fine-needle aspiration biopsy of the thyroid gland did not reveal the cause of the goitre. A total thyroidectomy was performed. Histopathological examination confirmed advanced thyroid amyloidosis.

Indexed as

amyloidosisgoitrethyroid amyloidosisthyroid imagingthyroid surgery

Identifiers

PMID41095829
PMCPMC12524822

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