{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["50(12)"],"submitter":["Harrabi F"],"pubmed_abstract":["Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of inheritance. This congenital disease is characterized by a wide spectrum of clinical manifestations and degree of severity. This case report describes a female patient in her early 20s who presented with a complaint of lumbosciatica-like pain evolving for several months. The condition initially escaped the attention of clinicians until a lumbar computed tomography scan and spinal magnetic resonance imaging were performed. The patient was then transferred to the general surgery department, where a clinical diagnosis of NF1 was established. The clinical manifestations were specific for this disease, including café-au-lait macules, plexiform neurofibroma, and a history of neurofibromatosis in he"],"journal":["The Journal of international medical research"],"pagination":["3000605221139716"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9751173"],"repository":["biostudies-literature"],"pubmed_title":["A fortuitous discovery of a neurofibroma in a female patient with type 1 neurofibromatosis: a case report."],"pmcid":["PMC9751173"],"pubmed_authors":["Harrabi F","Methnani J","Abdelkader M","Amine SM","Houssem A","Mehdi BL","Ali BA","Mohamed BM"],"additional_accession":[]},"is_claimable":false,"name":"A fortuitous discovery of a neurofibroma in a female patient with type 1 neurofibromatosis: a case report.","description":"Neurofibromatosis type 1 (NF1) is a neurocutaneous condition with an autosomal dominant pattern of inheritance. This congenital disease is characterized by a wide spectrum of clinical manifestations and degree of severity. This case report describes a female patient in her early 20s who presented with a complaint of lumbosciatica-like pain evolving for several months. The condition initially escaped the attention of clinicians until a lumbar computed tomography scan and spinal magnetic resonance imaging were performed. The patient was then transferred to the general surgery department, where a clinical diagnosis of NF1 was established. The clinical manifestations were specific for this disease, including café-au-lait macules, plexiform neurofibroma, and a history of neurofibromatosis in he","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Dec","modification":"2026-05-28T20:55:59.43Z","creation":"2024-10-18T02:23:20.758Z"},"accession":"S-EPMC9751173","cross_references":{"pubmed":["36510447"],"doi":["10.1177/03000605221139716"]}}