Evidence map›Paper›PMID 37363587›Full record

ArticleAnnals of medicine and surgery (2012)2023

Epithelioid angiosarcoma of the adrenal gland with metastasis: a case report and literature review.

Mahmoud Noman, Almotazbellah M M Zeer, Zahraa M M Zeer, Raed Daas, Yousef Hamamra

Open access · diamondAbstract read
In one paragraph

Article in Annals of medicine and surgery (2012), 2023. 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
0.9field-weighted citation impact, top 21% 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, 4 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

5 authors at 2 institutions in 2 countries.

Mahmoud NomanFaculty of Medicine, Al-Quds University.ORCID 0009-0003-2446-7166
Almotazbellah M M ZeerFaculty of Medicine, Al-Quds University.ORCID 0000-0001-9525-6997
Zahraa M M ZeerFaculty of Medicine, Al-Quds University.
Raed DaasAugusta Victoria Hospital, Jerusalem, Palestine.
Yousef HamamraAugusta Victoria Hospital, Jerusalem, Palestine.
Al-Quds University · PSAugusta Victoria Hospital · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary adrenal epithelioid angiosarcoma is an exceptionally rare condition, with only 51 cases reported in the literature since 1988. Case presentation: We report a case of a 59-year-old male patient who presented with a 4-month history of left flank pain and anemia. Radiographic imaging identified a 14 cm mass lesion in the left suprarenal region, which showed heterogeneous enhancement. The patient underwent total adrenalectomy with tumor-free surgical margins. Histological sections showed features consistent with an epithelioid tumor, and immunohistochemical staining confirmed the diagnosis of epithelioid angiosarcoma of the left adrenal gland. Discussion: Primary adrenal epithelioid angiosarcoma is a very rare entity. It was first described by Kareti Conclusion: In cases of rare malignancies, interdisciplinary collaboration is crucial for determining the optimal management strategy.

Indexed as

adjuvant therapyadrenal glandangiosarcomacase reportimmunohistochemistry

Identifiers

PMID37363587
PMCPMC10289494
OpenAlexW4376602508

What OpenQuestion holds

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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.