ArticleCureus2026
Pelvic Lymphangioma: The Purpose of a Clinical Case.
Article in Cureus, 2026. 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
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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.
- Giant Recurrent Retroperitoneal and Ischioanal Lymphangioma in an Adult: A Case Report.Reports (MDPI) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Lymphangioma is a benign vascular malformation characterized by abnormal proliferation of lymphatic vessels, resulting in the formation of lymphatic masses or cysts. Pelvic lymphangiomas may remain asymptomatic for long periods and are often discovered incidentally during imaging studies performed for other reasons. When symptomatic, they may cause manifestations related to compression of adjacent structures, such as abdominal pain and distension, urinary retention, or gastrointestinal symptoms. We report the clinical case of a 37-year-old male patient with no relevant medical history who presented to the emergency department twice within two months due to urinary retention. As part of the etiological study, a computed tomography (CT) scan revealed a large, lobulated pelvic mass of uncertain characterization, raising suspicion for a necrotic mass, fluid collection, lymphangioma, or another cause. Subsequently, pelvic magnetic resonance imaging (MRI) supported the diagnostic hypothesis of lymphangioma. The patient was referred to the Portuguese Institute of Oncology (IPO), Lisbon, where he underwent elective surgery. Histopathological examination confirmed the diagnosis of pelvic lymphangioma.
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Registered trials
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