Work

Neurofibromatosis type 2: A challenging case report and multidisciplinary management approach

Year: 2025

Type: article

Abstract: Neurofibromatosis type 2 (NF2) is a genetic disorder characterised by multiple benign tumours in the nervous system. We present the case of a 16-year-old female with NF2, seen on April 29, 2023, at Nishtar Hospital, Multan, exhibiting symptoms such as swollen left eye, chronic headache, decreased vision, bilateral hearing loss, tinnitus, and gait issues. Diagnostic evaluation, including Magnetic Resonance Imaging (MRI), confirmed NF2 diagnosis based on National Institutes of Health (NIH) and Manchester criteria. Surgical resection is the primary treatment, but the patient refused and opted for herbal treatment due to personal and socioeconomic reasons. The report highlights the challenges in NF2 management and the importance of patient preferences.

Source: Journal of the Pakistan Medical Association

DOI: 10.47391/jpma.21415

Authors: Muhammad Usman, Syed Muhammad Salman Hassan, Maria Batool, Ramisha Chaudhary, Salman Ahmed Malik

Institution: Nishtar Medical College and Hospital

Language: English

Topic: Neurofibromatosis and Schwannoma Cases

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $650