ArticleCureus2024
Adult Mediastinal Lymphangioma Presenting As Persistent Chest Pain: A Case Report.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
2 citing papers in PubMed.
- Mediastinal Lymphangioma of the Adult: Case Report and Literature Review.Clinics and practice · 2026Article
- Idiopathic anterior mediastinal lymphangioma in a young adult: a rare case report and review of management.International journal of surgery case reports · 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
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mediastinal lymphangiomas are rare benign tumors arising from lymphatic system malformations, most commonly seen in pediatric populations. In adults, they are exceedingly rare and present diagnostic challenges due to nonspecific symptoms and imaging overlap with other mediastinal masses. Diagnosis is typically based on imaging, including CT and MRI, with histopathology confirming the diagnosis. Surgical resection is the treatment of choice, especially for symptomatic lesions. A 35-year-old female presented with persistent chest pain for two months. Imaging revealed a multiloculated cystic mass in the anterior mediastinum, which was consistent with a lymphangioma. The patient underwent video-assisted thoracoscopic surgery (VATS) for excision, and histopathology confirmed the diagnosis. Postoperatively, she had an uneventful recovery, and follow-up showed no recurrence at six months. This case emphasizes the importance of considering lymphangioma in the differential diagnosis of mediastinal masses, particularly in patients with persistent chest pain, and highlights the role of imaging and surgical management in achieving favorable outcomes.
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Registered trials
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