Evidence map›Paper›PMID 37632898›Full record

ArticleJMIR dermatology2022

Cutaneous Angiomyolipoma-A Distinct Entity That Should Be Separated From Classic Angiomyolipoma: Complete Review of Existing Cases and Defining Fundamental Features.

Natalia Gabriela Sanchez, Alfonsina Angelica Ávila Romay, Eduwiges Martínez Luna, Alvaro Lezid Padilla Rodríguez

Abstract readCase Reports
In one paragraph

Article in JMIR dermatology, 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  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

4 authors.

Natalia Gabriela SanchezDIGIPATH: Digital Pathology Laboratory, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-6657-2544
Alfonsina Angelica Ávila RomayClínica Dermatología Integral Medica Sur, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-3382-8459
Eduwiges Martínez LunaClínica Dermamedics, Morelia, Michoacán, Mexico.ORCID https://orcid.org/0000-0001-9939-1491
Alvaro Lezid Padilla RodríguezDIGIPATH: Digital Pathology Laboratory, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-7008-6047

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous angiomyolipoma is a rare mesenchymal tumor that is demographically, clinically, and immunohistochemically distinct from its renal and extrarenal counterparts. We present a case of cutaneous angiomyolipoma in the right retroauricular area of a 35-year-old male patient and provide a broad systematic review of the literature and the largest compilation of cutaneous angiomyolipomas reported to date. According to the findings presented in this review, we conclude that cutaneous angiomyolipoma should be completely separated from renal and extrarenal angiomyolipomas and therefore be considered a distinct entity in the classification of skin tumors.

Indexed as

angiomyolipomacutaneous angiomyolipomacutaneous mesenchymal tumorsHMB-45

Identifiers

PMID37632898
PMCPMC10334929

What OpenQuestion holds

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Registered trials

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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.