دورية أكاديمية
Giant gluteal and vesical plexiform neurofibromas in a patient with neurofibromatosis type 1: a case report.
| العنوان: | Giant gluteal and vesical plexiform neurofibromas in a patient with neurofibromatosis type 1: a case report. |
|---|---|
| المؤلفون: | Sassi, Imen1 (AUTHOR) imen.sassi.mail@gmail.com, Bouida, Mohamed Amine1 (AUTHOR), Hasnaoui, Anis2 (AUTHOR), Zemni, Ines1 (AUTHOR), Ben Dhieb, Tarek1 (AUTHOR) |
| المصدر: | Journal of Medical Case Reports. 1/13/2024, Vol. 18 Issue 1, p1-4. 4p. |
| مصطلحات موضوعية: | *NEUROFIBROMA, *NEUROFIBROMATOSIS 1, *BENIGN tumors, *BUTTOCKS, *GENETIC disorders, *BLADDER, *NEUROCUTANEOUS disorders |
| مستخلص: | Background: Neurofibromatosis type 1 is a neurocutaneous genetic disorder caused by mutations in the NF1 gene, resulting in the formation of benign tumors called neurofibromas. The most common type of tumor seen in patients with neurofibromatosis type 1 is the slow-growing and benign neurofibroma, with a subtype called plexiform neurofibroma being particularly common and causing pain, functional impairment, and cosmetic disfigurement. Case presentation: We report the case of a 20-year-old North African female patient with a history of neurofibromatosis type 1 who presented with a growing mass in her right gluteal region, which was later diagnosed as a giant cutaneous neurofibroma. Imaging studies revealed infiltration in several regions, including the urinary bladder wall, resulting in significant bilateral hydronephrosis. The patient is currently being monitored, and no excisional procedures are planned. Conclusions: Neurofibromatosis type 1 can cause a variety of clinical symptoms, including the development of large plexiform neurofibromas. It is important to closely monitor patients with neurofibromatosis type 1 for the early detection of neurofibromas. Early detection and prompt surgical intervention are essential for preventing complications. [ABSTRACT FROM AUTHOR] |
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