ArticleInternational cancer conference journal2022
Urachal mucinous cystic tumor of low malignant potential in a polymorbid female: a case report and review of the literature.
Article in International cancer conference journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 7 citations in OpenAlex.
- Urachal Mucinous Cystic Tumour of Low Malignant Potential With Incidental Clinical Presentation: A Case Report With Clinicopathologic Features and Review of the Literature.Case reports in pathology · 2026Article
- Case report: Fistula formation of a urachal cyst 6 years after prostatectomy.Urology case reports · 2025Article
- Urachal Mucinous Cystic Tumour of Low Malignant Potential: A Case Report With Literature Review.Cureus · 2025Article
- Rare urachal mucinous cystic tumor of low malignant potential with peritoneal pseudomyxoma: A case report.Experimental and therapeutic medicine · 2023Article
- Article
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Neoplasms of the urachus are exceedingly rare, representing 0.17% of all bladder cancers. The mucinous cystic tumor of low malignant potential (MCTLMP) subtype is particularly rare with just 25 previous cases reported in the literature. Although rare, MCTLMPs are important to identify due to potential devastating complications and good cure rates with surgical removal. We present a 43 year old female with a nuanced constellation of comorbidities and confirmed MCTLMP following a workup for abdominal pain and irritative lower urinary tract symptoms. Notably, this tumor did not change in size over a 3-year course of serial imaging prior to surgical excision. This urachal MCTLMP represents roughly the 26th and one of the smallest of its subtype reported in the literature. This case illustrates the diagnosis and management of this rare urachal MCTLMP. Individual patient medical history, clinical considerations, and neoplasm characteristics are examined. Although rare, the potential for increased malignancy and potential complications necessitates surgical management and further investigation by the academic community.
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