Evidence map›Paper›PMID 31253137›Full record

ArticleDiagnostic pathology2019

Hyaline vascular variant of unicentric Castleman disease of the tonsil: a case report.

Ping Li, Huaipu Liu, Hao Li, Ang Li, Guangyin Yu, Weihua Yin

Open access · goldAbstract readCase Reports
In one paragraph

Article in Diagnostic pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 27% of its field
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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Hyaline Vascular Variant of Castleman Disease of the Tonsil in an Adolescent: A case Report.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2024
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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

6 authors at 2 institutions in 1 country.

Ping LiDepartment of Pathology, Shenzhen Hospital of Peking University, 1120 Lianhua road, Shenzhen, 518036, China.
Huaipu LiuDepartment of Cardiothoracic Surgery, Shenzhen Children's Hospital, 7019 Yitian road, Shenzhen, 518038, China.
Hao LiDepartment of Pathology, Shenzhen Hospital of Peking University, 1120 Lianhua road, Shenzhen, 518036, China.
Ang LiDepartment of Pathology, Shenzhen Hospital of Peking University, 1120 Lianhua road, Shenzhen, 518036, China.
Guangyin YuDepartment of Pathology, Shenzhen Hospital of Peking University, 1120 Lianhua road, Shenzhen, 518036, China.
Weihua YinDepartment of Pathology, Shenzhen Hospital of Peking University, 1120 Lianhua road, Shenzhen, 518036, China. bdyyblksgs@163.com.
Peking University Shenzhen Hospital · CNShenzhen Children's Hospital · CN

Funding

Sanming Project of Medicine in Shenzhen SZSM201812088Shenzhen Science and Technology Innovation Commission No.JCYJ20170303155657876
6 · The paper itself

Abstract

backgroundCastleman disease (CD) is a lymphoproliferative disorder with an unknown etiology. The disease may be unicentric (UCD) or multicentric (MCD), and three histopathologic variants have been described: hyaline vascular (HV), plasma cell (PC), and mixed type. Extranodal CD is rare. Herein, we report a case of CD presenting as a tonsillar mass, which has not been documented in the literature. CASE PRESENTATION: The patient was a 32-year-old man. Laryngoscopy revealed tonsillar hypertrophy, and the patient underwent a low-temperature plasma tonsillectomy. Microscopic examination of permanent sections showed lymphoid follicular hyperplasia, a portion of which appeared to be a fusion of nodular hyperplasia (composed of lymphoid follicles of variable size and shape). These distinctive follicles with atrophic hyalinized germinal centers and a broad mantle zone of small lymphocytes formed concentric rings (so-called onion-skin arrangement). Medium-sized vessels and a plethora of capillaries were present in the center of the lymphatic follicles, mantle zones, and interfollicular areas. A characteristic lollipop appearance was also observed due to the onion-skin arrangement of the expanded mantle zone lymphocytes with a vessel penetrating the germinal center. No aberrant lymphoid population was present based on CD3, CD5, CD20, CD79α, CD21, CD23, bcl-2, cyclin D1, and ki-67 immunostaining. Tests for human herpesvirus (HHV)-8 and Epstein Barr virus (EBV)-encoded small RNA (EBER) were negative. Therefore, a diagnosis of an HV variant UCD was rendered. The patient was treated by local excision without any other therapy based on the diagnosis. At the 7-month follow up, the patient had no recurrent symptoms or masses.

conclusionWe present an unusual case of a tonsil presenting hyaline vascular Castleman disease (HVCD). This study aims to highlight CD as a differential diagnosis that should be considered by otolaryngologists and pathologists for lymphoproliferative disorders of the tonsil.

Indexed as

AdultCastleman DiseaseDiagnosis, DifferentialGerminal CenterHumansHyalinImmunohistochemistryLymph NodesLymphocytesLymphoid TissueLymphoproliferative DisordersMalePalatine TonsilCastleman disease (CD)Hyaline vascular variantLymphoproliferative disorderTonsilUnicentric Castleman disease (UCD)

Identifiers

PMID31253137
PMCPMC6599372
OpenAlexW2955458844

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Registered trials

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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.