2018
DOI: 10.1155/2018/2302918
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The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis

Abstract: Neurofibromatosis Type 1 (Von Recklinghausen disease) is a common, autosomal dominant hereditary disorder characterized by involvement of multiple tissues derived from the neural crest. Urinary system involvement in neurofibromatosis is a rare condition. Leiomyoma of the bladder is a rare benign mesenchymal tumor. In this case, our experience and approach regarding the bladder leiomyoma development in a patient diagnosed with neurofibromatosis are presented and the literature data has been reviewed.

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Cited by 3 publications
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“…Several endocrine alterations and genomic mutations have been associated with an increased risk of bladder leiomyoma [10,11]; however, our patient did not screen positive for any of them.…”
Section: Discussioncontrasting
confidence: 75%
“…Several endocrine alterations and genomic mutations have been associated with an increased risk of bladder leiomyoma [10,11]; however, our patient did not screen positive for any of them.…”
Section: Discussioncontrasting
confidence: 75%
“…As recent studies have shown promise in establishing best practices for evaluation and management, we reviewed the related studies on the last five years between 2016 and 2021. To review the features of bladder leiomyoma such as symptoms, diagnosis tools, treatment and prognosis, a literature search of PubMed and the Web of Science was conducted, which included 22 cases of bladder leiomyomas in 17 publications as shown in Table 1 (1,(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18). The symptoms vary according to the location of the tumor, and may even be asymptomatic (Table 1).…”
Section: Discussionmentioning
confidence: 99%