The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis

<table class="fixed-width table-group" id="tab1"><tr><td><table class="table"><colgroup><col style="width:27.47em"/></colgroup><tr><td class="thead-hr" colspan="1"><hr/></td></tr><tr><td class="align_left">(1) Six or more pigmentations greater than 5 mm before puberty and greater than 15 mm after puberty (cafe au lait)</td></tr><tr><td class="align_left">(2) One plexiform neurofibroma or more than two neurofibromas of any type</td></tr><tr><td class="align_left">(3) Axillary or inguinal freckling</td></tr><tr><td class="align_left">(4) Optic glioma</td></tr><tr><td class="align_left">(5) Two or more “Lisch” nodules (iris hamartoma)</td></tr><tr><td class="align_left">(6) Bone lesions</td></tr><tr><td class="align_left">(7) Presence of at least one of these clinical findings in first-degree relatives</td></tr><tr class="table-tr"><td colspan="1"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

<div>Neurofibromatosis Type 1 diagnostic criteria.</div>

Case Reports in Urology

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Table 1

Table 1: The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis 