Evidence map›Paper›PMID 32430041›Full record

ReviewDiagnostic pathology2020

ALK-1-positive inflammatory myofibroblastic tumor of the thyroid complicated by Hashimoto's thyroiditis: report of a rare case and a literature review.

Cheng-Fang Li, Xing-Long Wu, Jin-Jing Wang, Kai Wang, Su-Yuan Zhang, Jia-Jia Huang, Han-Zhong Hu, Hong Zheng

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in Diagnostic pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Cheng-Fang LiDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Xing-Long WuDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Jin-Jing WangDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Kai WangDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Su-Yuan ZhangDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Jia-Jia HuangDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Han-Zhong HuDepartment of Ultrasonography, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China.
Hong ZhengDepartment of Pathology, the Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China. zhenghonghq@hotmail.com.
Zunyi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammatory myofibroblastic tumors (IMTs) of the thyroid are extremely rare soft-tissue tumors. In the literature, IMTs are sometimes called plasma cell granulomas (PCGs) or inflammatory pseudotumors, which often causes ambiguity. To date, 17 cases of PCGs and five cases of thyroid IMTs have been reported. These cases reveal that IMTs of the thyroid are often negative for the anaplastic lymphoma kinase (ALK-1) gene. To provide further information on this rare lesion, we present a case of an ALK-1-positive thyroid IMT and a review of IMTs of the thyroid. CASE PRESENTATION: A 34-year-old Chinese woman presented with a painless neck mass that had persisted for over a month. Ultrasonography revealed a 4.28 × 2.53 cm

conclusionsIMTs should be considered in the diagnosis when spindle cell proliferation accompanied by mature inflammatory cells is observed, spindle cells are mildly atypical, and myofibroblast differentiation is present in the thyroid. A uniform diagnostic term is crucial to avoid ambiguity. Clinicians and pathologists should be aware of the necessity for long-term follow-up, especially in ALK-positive cases. The therapeutic potential of ALK-1 positivity should be explored further.

Indexed as

Activin Receptors, Type IIAdultFemaleGranuloma, Plasma CellHashimoto DiseaseHumansThyroid DiseasesActivin Receptors, Type IIACVRL1 protein, humanALK-1-positiveCase reportHashimoto’s thyroiditisInflammatory myofibroblastic tumorPlasma cell granuloma

Identifiers

PMID32430041
PMCPMC7236920
OpenAlexW3026285777

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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.