Evidence map›Paper›PMID 38124308›Full record

ArticleInternational journal of surgical pathology2024

Multinodal Cervical Angiomyomatous Hamartoma.

Georgia Mackay, James Johnston, Sameer Mallick, Vinod Khanijow

Open access · hybridAbstract readCase Reports
In one paragraph

Article in International journal of surgical pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 67% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 1 country.

Georgia MackayDepartment of Health Science, The University of Auckland Faculty of Medical and Health Sciences, Auckland, New Zealand.ORCID 0000-0002-9466-1461
James JohnstonDepartment of Surgery, The University of Auckland, Auckland, New Zealand.
Sameer MallickDepartment of ORL Head and Neck Surgery, Auckland District Health Board, Auckland, New Zealand.
Vinod KhanijowDepartment of Pathology, Auckland City Hospital, Auckland, New Zealand.
University of Auckland · NZAuckland City Hospital · NZAuckland District Health Board · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiomyomatous hamartoma (AMH) is a rare benign lesion of the lymph nodes. Angiomyomatous hamartoma tends to be found in inguinal lymph nodes, and usually in a single lymph node. We present a rare care case of a 53-year-old presenting with a neck lump, found to be AMH involving multiple lymph nodes in her neck. To our knowledge, this is the first case presenting with multiple nodes in this location. There are a limited number of case reports describing magnetic resonance imaging (MRI) features of AMH lesions located in inguinal and head and neck regions. Our MRI findings revealed the mass had intermediate T1 enhancement, high T2 signal enhancement, and high post-gadolinium enhancement and fat saturation of the lesion. Angiomyomatous hamartoma is a histological diagnosis, distinguished from other similar nodal vascular lesions by a number of key features: including the presence of central nodal distribution, muscular blood vessel walls, adipose tissue, and HMB45 negative staining. Early recognition of this benign lesion may have implications for a patient's clinical course and surgical requirements.

Indexed as

HamartomaMagnetic Resonance ImagingAngiomyomaHumansLymph NodesMiddle AgedNeckangiomyomatous hamartomabenign neck masscervical lymphadenopathylymph node

Identifiers

PMID38124308
PMCPMC11337725
OpenAlexW4388849750

What OpenQuestion holds

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LicenceCC BY
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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.