Evidence map›Paper›PMID 30083234›Full record

ArticleThyroid research2018

A rare malignant thyroid carcinosarcoma with aggressive behavior and DICER1 gene mutation: a case report with literature review.

Jing Yang, Carmen Sarita-Reyes, David Kindelberger, Qing Zhao

Open access · goldAbstract readCase Reports
In one paragraph

Article in Thyroid research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Thyroid carcinosarcoma masquerading as a paraesophageal abscess in a Cane Corso dog.The Canadian veterinary journal = La revue veterinaire canadienne · 2023
    Article
  9. Primary Thyroid Neoplasm with Fetal Morphology Associated withThyroid : official journal of the American Thyroid Association · 2022
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Poorly differentiated thyroid carcinoma of childhood and adolescence: a distinct entity characterized by DICER1 mutations.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  19. Expanding the spectrum of dicer1-associated sarcomas.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  20. The Histological Spectrum of DICER1-Associated Neoplasms.Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
    Review
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

4 authors at 1 institution in 1 country.

Jing YangDepartment of Pathology and Laboratory Medicine, Boston University Medical Center, 670 Albany St. Biosquare III, Boston, MA 02118 USA.
Carmen Sarita-ReyesDepartment of Pathology and Laboratory Medicine, Boston University Medical Center, 670 Albany St. Biosquare III, Boston, MA 02118 USA.
David KindelbergerDepartment of Pathology and Laboratory Medicine, Boston University Medical Center, 670 Albany St. Biosquare III, Boston, MA 02118 USA.
Qing ZhaoDepartment of Pathology and Laboratory Medicine, Boston University Medical Center, 670 Albany St. Biosquare III, Boston, MA 02118 USA.ORCID 0000-0003-2716-8383
Boston University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalignant biphasic tumor also known as carcinosarcoma is an uncommon neoplasm that is composed of both malignant epithelial and mesenchymal components. Most reported cases of carcinosarcoma affect the female genital tract; however, other sites including head and neck, lung, and breast have been described. Carcinosarcoma of the thyroid is an extremely rare and aggressive malignancy with an ominous clinical course similar to anaplastic carcinoma. CASE PRESENTATION: We report a case of a 45-year-old female who was found to have a biphasic thyroid carcinosarcoma. Her clinical course declined significantly shortly after she underwent a total thyroidectomy and she developed distant metastases to the lungs. Histopathological features of the primary and metastatic tumor were identical. The tumor is composed of an intimately intermixed epithelial component of poorly differentiated follicular thyroid carcinoma and a spindle cell sarcoma with rhabdomyosarcoma differentiation. Molecular analysis using a next-generation sequencing based assay revealed a

conclusionTo our knowledge, the E1705K point mutation within the

Indexed as

Biphasic tumorCarcinosarcomaDICER1 mutationLung metastasisThyroid

Identifiers

PMID30083234
PMCPMC6069891
OpenAlexW2887659392

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.