Evidence map›Paper›PMID 33415591›Full record

ArticleJournal of the Egyptian National Cancer Institute2021

Renal angiomyoadenomatous tumor (RAT): a rare distinct entity with diagnostic challenges-a case report.

Ankur Majumder, Ravi Hari Phulware, Arvind Ahuja, Anurag Singla, Pawan Kumar

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Journal of the Egyptian National Cancer Institute, 2021. 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
1.2field-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

0 citing papers in PubMed, 12 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

5 authors at 3 institutions in 1 country.

Ankur MajumderDepartment of Pathology, ABVIMS, PGIMER, RML Hospital, New Delhi, India.
Ravi Hari PhulwareDepartment of Pathology, All India Institute of Medical Sciences (AIIMS), Room no. C-2, Level 3, Rishikesh, India. ravipaarti@gmail.com.ORCID https://orcid.org/0000-0002-5136-7254
Arvind AhujaDepartment of Pathology, ABVIMS, PGIMER, RML Hospital, New Delhi, India.
Anurag SinglaDepartment of Urology and Renal Transplant, PGIMER, ABVIMS, RML Hospital, New Delhi, India.
Pawan KumarDepartment of Radiology, Goa Medical College, Bambolim, Goa, India.
Vardhman Mahavir Medical College & Safdarjung Hospital · INAll India Institute of Medical Sciences Rishikesh · INGoa Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRenal angiomyoadenomatous tumor (RAT) is a recently described rare renal neoplasm with variations in the presentation, gross, and microscopic findings, and having a benign course and good prognosis. It is characterized microscopically by the admixture of three components-epithelial cells arranged in tubules and nests, angiomyomatous stroma, and capillary-sized interconnecting vascular channels in close association with the epithelial cell clusters. Microscopically, these tumors can be confused with clear cell carcinoma, papillary carcinoma, mixed epithelial and stromal tumors, and angiomyolipoma. RAT differs from conventional clear cell carcinomas, which can rarely be associated with an identical leiomyomatosis stroma occasionally forming abortive vascular structures. RAT is a distinct morphologic entity, being different morphologically, immunohistochemically, and genetically from all renal tumors including conventional clear cell carcinoma and mixed epithelial and stromal tumor of the kidney. CASE PRESENTATION: Here, we report a case of a 21-year-old man with renal angiomyoadenomatous tumor, a rare neoplasm with only a few previous cases reported in the literature. Unlike our case, most tumors have been identified in middle-aged males; they present as well-circumscribed, encapsulated tan-brown masses with variably prominent cystic areas.

conclusionDiagnosis of RAT is challenging because of the rarity of the disease and common presenting symptoms to other renal pathology and is supplemented with histopathology and immunohistochemistry. A multidisciplinary team approach for diagnosis and management along with long-term follow-up are warranted.

Indexed as

Carcinoma, PapillaryCarcinoma, Renal CellKidney NeoplasmsBiomarkers, TumorHumansImmunohistochemistryMaleYoung AdultBiomarkers, TumorMixed epithelial and stromal tumor, Case reportRare renal tumorRenal angiomyoadenomatous tumorRenal cell carcinoma

Identifiers

PMID33415591
PMCPMC13314370
OpenAlexW3120038096

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