Evidence map›Paper›PMID 35198182›Full record

ArticleAnnals of medicine and surgery (2012)2022

Giant symptomatic adrenal myelolipoma: A case report.

Abdelbassir Ramdani, Asmae Aissaoui, Tariq Bouhout, Amal Bennani, Hanane Latrech, Badr Serji, Tijani El Harroudi

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2022. 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
0.9field-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, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 1 institution in 1 country.

Abdelbassir RamdaniSurgical Oncology Department, Mohammed VI University Hospital, Regional Oncology Center, Oujda, Morocco.
Asmae AissaouiMohammed First University Oujda, Faculty of Medicine and Pharmacy Oujda, Oujda, Morocco.
Tariq BouhoutSurgical Oncology Department, Mohammed VI University Hospital, Regional Oncology Center, Oujda, Morocco.
Amal BennaniMohammed First University Oujda, Faculty of Medicine and Pharmacy Oujda, Oujda, Morocco.
Hanane LatrechMohammed First University Oujda, Faculty of Medicine and Pharmacy Oujda, Oujda, Morocco.
Badr SerjiSurgical Oncology Department, Mohammed VI University Hospital, Regional Oncology Center, Oujda, Morocco.
Tijani El HarroudiSurgical Oncology Department, Mohammed VI University Hospital, Regional Oncology Center, Oujda, Morocco.
Mohamed I University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAdrenal myelolipomas are rare non-functioning benign tumors composed of adipose and hematopoietic tissues. Most AMLs are discovered incidentally and represent the second most common adrenal incidentaloma. CASE PRESENTATION: A 58-years-old female patient, obese with a history of diabetes and blood hypertension presented with complaints of pain in the left flank. Abdominopelvic computed tomography showed a giant well-defined mass of the left adrenal gland with fat density suggesting adrenal myelolipoma. The patient underwent open left adrenalectomy. The pathological study confirmed the diagnosis of adrenal myelolipoma. DISCUSSION: Most AMLs are asymptomatic, remain stable in size, or grow slowly. Mass effect symptoms and spontaneous rupture are observed more in larger AMLs. The most common symptoms observed are abdominal discomfort/pain, hypochondrial pain, and flank pain. Most of the AMLs are discovered incidentally and the radiological features are accurate in diagnosing AML in up to 90% of the cases, CT is more sensitive for detection than other imaging modalities. The open surgery approach is the standard treatment of choice for giant AML (>10cm) while the minimally invasive approach has been used in only a few cases.

conclusionThe therapeutic management is discussed on a case-by-case basis. Surgical treatment is indicated for larger, symptomatic, or rapidly growing AMLs. Meanwhile smaller and asymptomatic AMLs are managed conservatively.

Indexed as

Adrenal myelolipomaCase reportEndocrine surgery

Identifiers

PMID35198182
PMCPMC8844840
OpenAlexW4210858751

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.