ReviewRomanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
Primary cutaneous extraskeletal Ewing sarcoma of the plantar region: clinicopathological features and review of the literature.
Review in Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Spermatocytic Tumor Arising in a Cryptorchid Testis: A Case Report and Narrative Review.Journal of clinical medicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background∕Objectives: Primary cutaneous extraskeletal Ewing sarcoma (pcEES) is an exceptionally rare malignant small round cell tumor, with limited cases reported and challenging diagnosis due to overlapping clinicopathological features. We aimed to review its diagnostic and therapeutic aspects and present a rare plantar case. Study selection for review: A PubMed search was performed to evaluate current data regarding the epidemiology, diagnosis, differential diagnosis, and management of pcEES. Case presentation: A 62-year-old woman with recurrent pcEES of the left plantar region presented with severe pain, ulceration, superinfection, inguinal lymph node involvement, and suspected osseous invasion. Histopathology and immunohistochemistry supported the diagnosis. Due to advanced locoregional disease, left transfemoral amputation was performed. Conclusions: pcEES is a rare and diagnostically demanding malignancy that may show aggressive behavior despite superficial location. Early diagnosis and multidisciplinary management are essential.
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Registered trials
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 Socratic graph.