Evidence map›Paper›PMID 41465905›Full record

ReviewMedicine2025

Clinicopathological observation of adult malignant ectodermal mesenchymoma: A case report and literature review.

Le Xie, Yingxin Huang, Rongjun Mao

Abstract readCase ReportsReview
In one paragraph

Review in Medicine, 2025. 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
–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

0 citing papers in PubMed.

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

3 authors.

Le XieDepartment of Pathology, The Eighth Clinical Medical College of Guangzhou University of Chinese Medicine, Foshan, Guangdong, China.ORCID 0009-0008-9191-855
Yingxin HuangDepartment of Pathology, The Eighth Clinical Medical College of Guangzhou University of Chinese Medicine, Foshan, Guangdong, China.
Rongjun MaoDepartment of Pathology, The Eighth Clinical Medical College of Guangzhou University of Chinese Medicine, Foshan, Guangdong, China.ORCID 0009-0004-0728-7160

Funding

Foshan's 14th Five-Year Plan Key Medical Specialties Project FSZD145010
6 · The paper itself

Abstract

rationaleMalignant ectomesenchymoma (MEM) is a relatively rare soft tissue tumor, which predominantly occurs in infants or children under 15 years of age. The classic sites of occurrence are the pelvic perineal region and genitourinary system. Compared to pediatric cases, adult cases exhibit certain differences in clinicopathological features and are more prone to misdiagnosis. A thorough comprehension of their clinicopathologic features is crucial for precise diagnosis and effective management. PATIENT CONCERNS: A 23-year-old male had a lesion located on the right side of his head and face, and the disease course lasted 13 months. A retrospective analysis was conducted on the clinicopathological data, histopathological features, immunophenotype, and molecular pathological changes. DIAGNOSES: The tumor was composed of embryonal rhabdomyosarcoma and undifferentiated neuroectodermal components. Immunohistochemistry showed positivity for rhabdomyosarcoma markers such as Desmin, MyoD1, and Myogenin in the rhabdomyosarcomatous component and positivity for neuroectodermal markers, including synaptophysin and chromogranin A in the neuroectodermal component. No specific molecular alterations were detected in genetic testing.

interventionsThis is a case of initial misdiagnosis, multimodal comprehensive treatment combining surgery with chemotherapy was the primary therapeutic approach, However, poor clinical outcomes were observed. OUTCOMES: Despite aggressive treatments, the patient died of the disease after 1 year of follow-up. LESSONS: Adult MEM is a biphenotypic sarcoma composed of rhabdomyosarcoma and neuroectodermal tissues. Morphological and immunohistochemical interpretation is crucial for diagnosis. treatment approaches and prognosis are correlated with the completeness of tumor resection and the differentiation degree of both components.

Indexed as

MesenchymomaRhabdomyosarcoma, EmbryonalSoft Tissue NeoplasmsFatal OutcomeHumansMaleYoung Adultclinicopathologymalignant ectomesenchymomaprognosistreatment

Identifiers

PMID41465905
PMCPMC12746915

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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.