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Case Report: Bilateral Sensorineural Hearing Loss Faradhifa Karima Ardianti; Fivien Fedriani
Medula Vol 17 No 1 (2026): Medula
Publisher : CV. Jasa Sukses Abadi

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.53089/medula.v17i1.1921

Abstract

Sensorineural hearing loss (SNHL) is a hearing disorder caused by damage to the cochlea, auditory nerve, or central auditory pathways connecting the ear to the brain. It is the most common type of hearing impairment, affecting more than 5% of the global population, and its prevalence continues to increase with aging. The etiology of SNHL is multifactorial, including age-related degeneration, noise exposure, infection, vascular disorders, and autoimmune diseases. This case report describes a 63-year-old man with a history of Autoimmune Hemolytic Anemia (AIHA) who developed sudden bilateral hearing loss after receiving a transfusion of two units of blood. The hearing loss was preceded by tinnitus and was occasionally accompanied by vertigo without other associated symptoms. Ear, nose, and throat examinations were unremarkable. The whisper test indicated severe hearing loss, while tuning fork tests could not be performed because the patient was unable to perceive the sound. Pure-tone audiometry confirmed severe bilateral sensorineural hearing loss, and the patient was advised to use hearing aids. The diagnosis was established through comprehensive history taking, physical examination, hearing assessment, and audiometric evaluation. The underlying pathophysiology was considered to involve age-related cochlear degeneration aggravated by systemic autoimmune inflammation. Prognosis depends on the severity and underlying etiology of hearing loss. This case highlights the importance of comprehensive clinical evaluation, audiometry, and appropriate management to determine disease severity, improve communication, prevent complications, and optimize the patient's quality of life.
Karsinoma Nasofaring Pada Pasien Pria Usia 51 Tahun Faiq Razaan; Fivien Fedriani
Medula Vol 17 No 1 (2026): Medula
Publisher : CV. Jasa Sukses Abadi

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.53089/medula.v17i1.1942

Abstract

Nasopharyngeal carcinoma is a malignant epithelial tumor arising from the nasopharynx and remains one of the most common head and neck cancers in Indonesia. Its etiology is multifactorial, involving Epstein-Barr virus infection, genetic susceptibility, and environmental exposures such as smoking and consumption of preserved foods. Because early symptoms are often nonspecific, many patients present at an advanced stage. This case report describes the clinical manifestations, risk factors, and diagnostic approach in a 51-year-old man with nasopharyngeal carcinoma and orbital infiltration. The patient presented with a progressively enlarging neck mass for nine months accompanied by hearing loss, tinnitus, epistaxis, diplopia, right-sided facial numbness, nausea, and fatigue. Physical examination revealed cervical lymphadenopathy, right ptosis, anisocoria, multiple cranial nerve deficits, and unilateral hearing impairment. Head computed tomography demonstrated a mass extending to adjacent structures with compression of the optic nerve, while histopathological examination of the nasopharyngeal biopsy revealed keratinizing squamous cell carcinoma, confirming the diagnosis of nasopharyngeal carcinoma with orbital infiltration. The patient had a long history of heavy smoking and frequent consumption of salted fish, both recognized risk factors for this malignancy. Initial management consisted of symptomatic and supportive treatment, followed by referral to a tertiary oncology center for definitive chemoradiotherapy. This case highlights the importance of early recognition of persistent cervical lymphadenopathy and cranial nerve involvement to facilitate timely diagnosis, appropriate staging, and improved clinical outcomes in patients with nasopharyngeal carcinoma.