Evidence map›Paper›PMID 31105947›Full record

ArticleSAGE open medical case reports2019

Intranodal capillary-cavernous hemangioma: Report of a very rare case.

Jérôme Tessieras, Jinane Chenaye, Christophe Senechaud, Yara Banz

Open access · goldAbstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Capillary Hemangioma of the Maxillary Sinus: A Rare Cause of Massive Life-Threatening Epistaxis.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2023
    Article
  3. Intranodal Hemangioma: Case Report and Systematic Review.Journal of Indian Association of Pediatric Surgeons
    Article
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 2 institutions in 1 country.

Jérôme TessierasDepartment of Surgery, Bernese Jura Hospital, Saint-Imier, Switzerland.ORCID https://orcid.org/0000-0003-3141-6458
Jinane ChenayeBernese Jura Radiology Institute, Saint-Imier, Switzerland.
Christophe SenechaudDepartment of Surgery, Bernese Jura Hospital, Saint-Imier, Switzerland.
Yara BanzInstitute of Pathology, University of Bern, Bern, Switzerland.
Hôpital du Jura Bernois · CHUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation of capillaries and cavernous vessels filled with erythrocytes and lined by endothelial cells. Magnetic resonance imaging with enhanced and T2 STIR sequences is the most efficient imaging for diagnosing this type of hemangioma. Rarely, malignancy or another vascular lesion can be evoked as a differential diagnosis of mixed hemangioma. Treatment in this localization is often surgical, even if other possibilities exist for other areas. In this article, we describe a very rare case of intranodal capillary-cavernous hemangioma.

Indexed as

Capillary hemangiomacavernous hemangiomaintranodal tumorlymphadenopathyvascular malformation

Identifiers

PMID31105947
PMCPMC6501482
OpenAlexW2943789907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.