Evidence map›Paper›PMID 32007865›Full record

ArticleInternational journal of surgery case reports2020

Lipomatous tumors of adrenal gland: A case series of 5 patients and review of the literature.

Abdullah Mahmoud Alkhalifa, Mohammed Yousef Aldossary, Ammar Jamal Abusultan, Abdullah Saleh AlQattan, Mohammed Alsomali, Fatimah Alquraish, Njoud Alkhaldi, Jamal Y Alsaeed, Abdulaziz M Alwosaibei, Mohammed Alqambar and 1 more

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Article in International journal of surgery case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 10 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

11 authors at 3 institutions in 1 country.

Abdullah Mahmoud AlkhalifaImam Abdulrahman Bin Faisal University, P.O. Box 1982, Al-Khobar, Dammam 31441, Saudi Arabia.
Mohammed Yousef AldossaryDepartment of General Surgery, Surgical Oncology Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia. Electronic address: Dossarym@kfsh.med.sa.
Ammar Jamal AbusultanImam Abdulrahman Bin Faisal University, P.O. Box 1982, Al-Khobar, Dammam 31441, Saudi Arabia.
Abdullah Saleh AlQattanDepartment of General Surgery, Surgical Oncology Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
Mohammed AlsomaliDepartment of Pathology and Laboratory Medicine, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
Fatimah AlquraishDepartment of General Surgery, King Abdulaziz Airbase Armed Forces Hospital, Dhahran, Saudi Arabia.
Njoud AlkhaldiDepartment of Internal Medicine, Endocrine Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
Jamal Y AlsaeedDepartment of Internal Medicine, Endocrine Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
Abdulaziz M AlwosaibeiDepartment of Internal Medicine, Endocrine Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
Mohammed AlqambarDepartment of Internal Medicine, Endocrine Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
Osama Habib AlsaifDepartment of General Surgery, Surgical Oncology Section, King Fahad Specialist Hospital-Dammam, Saudi Arabia.
King Fahad Specialist Hospital · SAImam Abdulrahman Bin Faisal University · SAArmed Forces Hospital · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionLipomatous tumors of the adrenal glands are a diverse group of tumors characterized by the composition of adipose tissue. This group of tumors include myelolipomas, angiomyolipomas (AML), lipomas, and teratomas. They are usually benign, non-functioning tumors, and they account for 5% of all primary adrenal tumors. This study aimed to elucidate the management of the initial size of the adrenal mass and symptoms of presentation. We provide a succinct literature review regarding angiomyolipomas tumors of the adrenal glands. PRESENTATION OF CASES: Here, we report 5 cases of lipomatous tumors of the adrenal glands. All 5 tumors were non-functioning. Four of them were myelolipoma, and one was AML. Two cases of myelolipoma presented with flank pain, while the rest of the 3 cases presented with hypochondrium pain. Three cases of myelolipoma were managed with laparoscopic adrenalectomy, one case of myelolipoma was converted from laparoscopic to open adrenalectomy because of abdominal adhesions, and the last case was AML and was managed with open adrenalectomy. All patients had an uneventful recovery with regular follow-up. DISCUSSION: Myelolipoma, the most common lipomatous tumor of the adrenal gland, consists of a mixture of bone morrow element and adipose tissue. AML consists of a mixture of a thick-walled blood vessel, smooth muscle, and adipose tissue. They mimic many different benign and malignant tumors on radiography, and the histopathological examination is still needed to confirm the diagnosis. There is still controversy in the management of these tumors. Usually, the management is individualized on each case. Reporting of these tumors are increasing due the wide-spread use of modern imaging modalities.

conclusionAdrenal lipomatous tumors are uncommon but with the increase use of imaging modalities their detection has increased. Further studies are needed to establish guidelines in the management of these tumors, especially that they can mimic malignant conditions.

Indexed as

Adrenal glandAngiomyolipomaMyelolipomaTumor

Identifiers

PMID32007865
PMCPMC7000441
OpenAlexW3004365172

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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.