Evidence map›Paper›PMID 41094570›Full record

ReviewWorld journal of surgical oncology2025

Rare abdominal wall clear cell carcinoma in endometriosis: case report and literature review of diagnostic and therapeutic considerations.

Davut Dayan, Lisa Wisniewski, Andrea Formentini, Marko Kornmann, Sarah Bette, Florian Ebner, Wolfgang Janni, Stefan Lukac, Lea Traub, Fabienne Schochter

Abstract readCase ReportsReview
In one paragraph

Review in World journal of surgical oncology, 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

10 authors.

Davut DayanDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany. Davut.dayan@uniklinik-ulm.de.ORCID http://orcid.org/0000-0003-1589-2016
Lisa WisniewskiDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany.
Andrea FormentiniDepartment of Visceral Surgery, University Hospital Ulm, Ulm, Germany.
Marko KornmannDepartment of Visceral Surgery, University Hospital Ulm, Ulm, Germany.
Sarah BetteInstitute of Pathology, University Hospital Ulm, 89081, Ulm, Germany.
Florian EbnerDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0003-2066-5344
Wolfgang JanniDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0001-5911-2400
Stefan LukacDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0002-9336-2267
Lea TraubDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany.
Fabienne SchochterDepartment of Obstetrics and Gynaecology, University Hospital Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0003-3675-6494

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndometriosis of the abdominal wall is exceptionally rare, with malignant transformation to clear cell carcinoma being of even greater rarity. In this paper, the importance of accurate diagnosis and appropriate treatment is emphasized, including the possibility of mesh reconstruction of the abdominal wall. CASE PRESENTATION: A 53-year-old woman presented with a rapidly enlarging abdominal wall tumor, 19 years after undergoing a caesarean section. Prior to her referral to our facility, a peripheral hospital had already performed tumor resection with mesh-based abdominal wall reconstruction. Tumor histology had revealed endosalpingiosis without evidence of malignancy. However, a year later, the patient exhibited a relapse accompanied by renewed rapid growth. Both punch and open biopsies revealed endosalpingiosis. Due to its rapid growth, a total resection of the tumor was performed. This necessitated the removal of a significant portion of the abdominal wall musculature and fascia. The abdominal wall was then reconstructed using a two-layer mesh. Final histological examination revealed a clear cell carcinoma that had arisen from endometriosis. Following the complete healing, the patient received adjuvant platinum-based chemotherapy and radiation to the inguinal area.

conclusionClear cell carcinoma of the abdominal wall arising from endometriosis is a rare and highly aggressive form of malignant transformation with a high rate of recurrence and metastasis. In rapidly growing abdominal wall tumors following gynaecological surgery, the objective should be radical resection. In addition to this, the selection of appropriate reconstruction procedures is crucial to achieving optimal oncological and functional results. Examples of such reconstruction procedures include a two-layer mesh reconstruction. This case aims to raise awareness of this rare and highly aggressive malignancy and to discuss diagnostic challenges and therapeutic strategies, including complex abdominal wall reconstruction.

Indexed as

Abdominal NeoplasmsAbdominal WallAdenocarcinoma, Clear CellEndometriosisFemaleHumansMiddle AgedPlastic Surgery ProceduresPrognosisClear cell carcinoma of the abdominal wallEndometriosisEndosalpingiosisManagement of abdominal wall reconstructionRecurrent abdominal wall tumors

Identifiers

PMID41094570
PMCPMC12529844

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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.