Evidence map›Paper›PMID 41473361›Full record

ArticleSouth Asian journal of cancer2025

Follicular Dendritic Cell Sarcoma of the Thyroid Gland: A Rare Case Report.

Mayadevi Poojari, Irappa Madabhavi, Jaydeep Pol, Sharad Desai

Abstract readCase Reports
In one paragraph

Article in South Asian journal of cancer, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mayadevi PoojariDepartment of Radiation Oncology, Mahatma Gandhi Cancer Hospital, Miraj, Maharashtra, India.
Irappa MadabhaviDepartment of Medical and Pediatric Oncology and Hematology, J. N. Medical College, Belgaum, Karnataka, India.
Jaydeep PolDepartment of Oncopathology, Mahatma Gandhi Cancer Hospital, Miraj, Maharashtra, India.
Sharad DesaiDepartment of Surgical Oncology, Mahatma Gandhi Cancer Hospital, Miraj, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Follicular dendritic cell sarcoma (FDCS) is a rare neoplasm of antigen-presenting cells within the reticuloendothelial system primarily originating in lymph nodes, but in almost one-third of the patients, extranodal sites are involved including oral cavity, tonsil, gastrointestinal tract, soft tissue, and breast. The thyroid gland is an extremely rare location for FDCS and very few cases are reported in the literature. Case Report: Here, we present a 39-year-old man who presented with a swelling in the neck for 3 months and difficulty in breathing for 15 days. Following left hemi-thyroidectomy, histopathologically and immunohistologically, he was diagnosed as FDCS of thyroid arising in Castleman's disease. He received adjuvant radiation treatment. The patient had favorable prognosis with no evidence of disease for 6 years after treatment till date. Conclusion: The aim of this report was to present the rare site of FDCS arising in the thyroid gland, the vital role of immunohistochemistry in diagnosis, and effectiveness of multimodality treatment for favorable prognosis.

Indexed as

Castleman's diseaseextranodalfollicular dendritic cell sarcomaradiotherapythyroidthyroidectomy

Identifiers

PMID41473361
PMCPMC12747740

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.