Evidence map›Paper›PMID 41782043›Full record

ArticleJournal of medical case reports2026

Surgical excision of giant axillary cystic lymphangioma: a case report.

Wail Alqatta

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2026. 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

1 author.

Wail AlqattaDepartment of General and Visceral Surgery, Ibn Sina Hospital, Sanaa, Yemen. qattaw@yahoo.com.ORCID http://orcid.org/0000-0003-3438-6290

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCystic lymphangiomas are rare benign congenital malformations of the lymphatic system, usually diagnosed in childhood and rarely encountered in adults. Axillary involvement in adults is particularly uncommon and presents diagnostic and surgical challenges owing to proximity to neurovascular structures. CASE PRESENTATION: This report describes a case of a 22-year-old Yemeni female patient presenting with localized pain in the left breast and a progressively enlarging tender axillary swelling. Imaging revealed a unilocular, thin-walled cystic lesion measuring 13 × 8 cm, extending into the subpectoral space and closely abutting the axillary vessels without invasion. Complete excision was performed via a curvilinear axillary incision, requiring meticulous adhesiolysis to preserve neurovascular integrity. Histopathology confirmed cystic lymphangioma. The postoperative course was uneventful, and no recurrence was noted at 5 month follow-up.

conclusionAlthough predominantly a pediatric entity, cystic lymphangioma should be considered in the differential diagnosis of adult axillary masses. Preoperative imaging is crucial for surgical planning, and complete surgical excision offers excellent outcomes with minimal functional impairment.

Indexed as

AxillaLymphangioma, CysticDiagnosis, DifferentialFemaleHumansTomography, X-Ray ComputedTreatment OutcomeYoung AdultAxillaBenign tumorCase reportCystic lymphangiomaSurgical excision

Identifiers

PMID41782043
PMCPMC13069735

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LicenceCC BY-NC-ND
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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.