Evidence map›Paper›PMID 41057940›Full record

ArticleJournal of medical case reports2025

A previously unreported triad of poorly differentiated thyroid carcinoma, parathyroid adenoma, and paraganglioma: random coincidence or hidden genetic etiology-a case report.

Ankush Nayyar, Praneeth Potluri, Kshitij Charaya

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Article in Journal of medical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers 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

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ankush NayyarDepartment of Pathology and Research and Publications Department, Indus Hospitals, Mohali, India. ankush.nayyar@gmail.com.ORCID http://orcid.org/0000-0002-9108-1349
Praneeth PotluriDepartment of ENT Surgery, Indus International Hospital, Mohali, India.
Kshitij CharayaDepartment of ENT Surgery, Indus International Hospital, Mohali, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeoplasms arising simultaneously from the thyroid, parathyroid, and paraganglionic tissues are exceptionally rare. To our knowledge, no previous case has documented the synchronous occurrence of poorly differentiated thyroid carcinoma, parathyroid adenoma, and cervical paraganglioma. This report highlights the diagnostic and embryologic significance of this rare triad. CASE PRESENTATION: A 79-year-old South Asian woman presented with a slowly progressive anterior neck swelling. Imaging showed a mass in the left thyroid lobe with vascular displacement. Total thyroidectomy with neck dissection was performed. Histology revealed poorly differentiated thyroid carcinoma with insular architecture and high mitotic activity. Adjacent to the tumor, a parathyroid adenoma was identified. A separate encapsulated lesion near the internal jugular vein showed a Zellballen pattern consistent with paraganglioma. Immunohistochemistry confirmed all three components. There was no history of familial endocrine neoplasia.

conclusionThis case presents a unique triad of poorly differentiated thyroid carcinoma, parathyroid adenoma, and paraganglioma-an association not previously reported. Their coexistence in a single patient may reflect a shared embryologic origin from neural crest derivatives. Recognition of such unusual combinations can aid in accurate diagnosis, prevent misinterpretation of tumor margins, and guide appropriate surgical and follow-up decisions.

Indexed as

AdenomaNeoplasms, Multiple PrimaryParagangliomaParathyroid NeoplasmsThyroid NeoplasmsAgedFemaleHumansNeck DissectionThyroidectomyParagangliomaParathyroid adenomaPoorly differentiated thyroid cancer

Identifiers

PMID41057940
PMCPMC12506355

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