Evidence map›Paper›PMID 40385878›Full record

ArticleCureus2025

Percutaneous Breast Biopsy: Local Tumor Spread, Ontogenetic Compartments, and Cell Transgression/Reverse Morphogenesis Theory.

Eduardo De Faria Castro Fleury, Marcia G Tavares, Veronica J Ayres

Abstract read
In one paragraph

Article in Cureus, 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.

Eduardo De Faria Castro FleuryRadiology, MD duFLE Diagnósticos, São Paulo, BRA.
Marcia G TavaresNuclear Medicine, Instituto Brasileiro de Controle do Câncer, São Paulo, BRA.
Veronica J AyresGynecology, Faculdade de Medicina do ABC, Sao Paulo, BRA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Observing patients submitted to percutaneous biopsy at our service who had post-biopsy breast magnetic resonance imaging scans for breast carcinoma staging, we observed tumor extension through the biopsy tract in some lesions, compromising skin and subcutaneous tissue. This study aimed to evaluate tumor extension through the biopsy tract in patients diagnosed with breast carcinoma undergoing neoadjuvant chemotherapy with a radioactive seed marker to locate the original tumor area by retrospectively analyzing MRI, ultrasonography, and histological reports. Methods We evaluated tumor extension through a biopsy tract in consecutive patients included in a prospective observational study protocol to assess the applicability of radioactive seed localization before breast surgery. Sixty-two patients included in the radioactive seed protocol were retrospectively evaluated. The abnormal enhancement in the biopsy tract was assessed by magnetic resonance imaging scans performed for clinical staging and seed localization as proposed in the original study protocol, with complementary target ultrasonography of the findings and ultrasound-guided biopsy of the suspected lesion. Results Four of the 62 patients in the protocol had abnormal enhancement in the biopsy tract, and three patients had a positive biopsy for carcinoma in the tract. The lesions that showed extension along the tract were luminal A, luminal B, and luminal hybrid carcinomas, with an average diameter of 3.9 cm. Conclusions Our study has shown the possibility of tumor extension through the biopsy tract in patients undergoing diagnostic percutaneous breast biopsy for breast cancer. These findings are crucial for understanding the biopsy procedures' potential risks and clinical implications.

Indexed as

breast cancermorphogenesisneedle biopsyontogenetic anatomypost-biopsy changetumor prognostic factors

Identifiers

PMID40385878
PMCPMC12085805

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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.