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

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

PMC · DOI: 10.3390/jcm14196741 · 2025-09-24

## TL;DR

A 28-year-old man with a rare thyroid condition called amyloidosis was diagnosed after a biopsy failed to identify the cause of his symptoms.

## Contribution

The paper presents a rare clinical case of systemic amyloidosis involving the thyroid in a young patient.

## Key findings

- Thyroid amyloidosis was confirmed through histopathological examination after a biopsy failed to identify the cause.
- The patient exhibited symptoms like neck enlargement, voice alteration, and weight loss.
- The case highlights the difficulty in diagnosing benign thyroid enlargement caused by amyloid deposits.

## 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.

## Linked entities

- **Diseases:** systemic amyloidosis (MONDO:0017816), medullary carcinoma (MONDO:0015277), papillary carcinoma (MONDO:0006509)

## Full-text entities

- **Diseases:** neck circumference enlargement (MESH:D006258), dysphagia (MESH:D003680), Thyroid amyloidosis (MESH:D000686), medullary carcinoma (MESH:D018276), decreased appetite (MESH:D001068), Systemic Amyloidosis (MESH:D009101), amyloid (MESH:C000718787), papillary carcinoma (MESH:D002291), weight loss (MESH:D015431), benign thyroid enlargement (MESH:D013959), voice alteration (MESH:D014832), goitre (MESH:D006042), Thyroid (MESH:D013966), fever (MESH:D005334)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12524822/full.md

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Source: https://tomesphere.com/paper/PMC12524822