Sunil Samdani

ORCID: 0000-0003-0203-6624
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About
Contact & Profiles
Research Areas
  • Ear Surgery and Otitis Media
  • Hearing Loss and Rehabilitation
  • Voice and Speech Disorders
  • Sinusitis and nasal conditions
  • Hearing, Cochlea, Tinnitus, Genetics
  • Head and Neck Surgical Oncology
  • Cleft Lip and Palate Research
  • Antifungal resistance and susceptibility
  • Facial Nerve Paralysis Treatment and Research
  • Meningioma and schwannoma management
  • Tracheal and airway disorders
  • Veterinary medicine and infectious diseases
  • Tumors and Oncological Cases
  • Phonetics and Phonology Research
  • Diphtheria, Corynebacterium, and Tetanus
  • Airway Management and Intubation Techniques
  • Craniofacial Disorders and Treatments
  • Congenital Ear and Nasal Anomalies
  • Sarcoma Diagnosis and Treatment
  • Iron Metabolism and Disorders
  • Nasal Surgery and Airway Studies
  • Vascular Tumors and Angiosarcomas
  • Foreign Body Medical Cases
  • Otitis Media and Relapsing Polychondritis
  • Hemoglobinopathies and Related Disorders

Sawai ManSingh Medical College and Hospital
2016-2025

Abstract Objective To study the possible association between invasive fungal sinusitis (mucormycosis) and coronavirus disease. Methods A prospective observational was conducted at a tertiary care centre over four months, involving all patients with mucormycosis of paranasal sinuses suffering from or having history disease infection. Results Twenty-three presented mucormycosis, had an 2019. The ethmoids (100 per cent) were most common affected. Intra-orbital extension seen in 43.47 cent...

10.1017/s0022215121000992 article EN The Journal of Laryngology & Otology 2021-04-08

10.1016/j.ijporl.2016.04.024 article EN International Journal of Pediatric Otorhinolaryngology 2016-04-28

10.1016/j.ijporl.2017.10.032 article EN International Journal of Pediatric Otorhinolaryngology 2017-10-31

Abstract Objective To propose a new classification of inner-ear anomalies that is more clinically oriented and surgically relevant: the SMS (Sawai Man Singh) cochleovestibular malformations. Methods A retrospective multicentric study was conducted 436 cochlear implantations carried out in 3 Indian tertiary care institutes. Patients with anomalous anatomy were included classified, as per classification, into malformation types I, II, III IV, based on morphology, modiolus lamina cribrosa....

10.1017/s0022215119000884 article EN The Journal of Laryngology & Otology 2019-05-01

Intracranial epidermoid cysts constitute about 1% of all intracranial tumors. They are usually congenital in origin and thought to derive from ectodermal cell inclusions occurring during closure the neural tube. Twenty-five percent these found skull as intradiploic cysts. These congenital, slow growing, can grow large size without causing symptoms. We present a case cyst frontal bone developed due childhood trauma. The expanded eroded walls sinus proptosis, diplopia, restricted eye movements...

10.1097/scs.0b013e3182700a03 article EN Journal of Craniofacial Surgery 2013-03-01

Abstract Aim: To determine the extent of cholesteatoma by imaging and intraoperative findings in both pediatric adult category. Objectives: study disease (cholesteatoma); (a) Radiologically (HRCT-Temporal Bone) (b) Intraoperatively, to post-op hearing outcome healing period (dry cavity/ epithelization cavity) following surgery Materials Method: A prospective observational was conducted on 60 patients chronic otitis media with cholesteatoma. Each category had 30 patients, all which were...

10.4103/indianjotol.indianjotol_70_24 article EN Indian Journal of Otology 2024-10-01

BACKGROUND: Primary leiomyosarcoma of the tongue is an extremely rare malignant mesenchymal tumour that exhibits smooth muscle differentiation.Only 23 cases this neoplasm have been described in literature.CASE REPORT: This article describes a case report primary right lateral border 35-year-old male.The diagnosis was supported by histological findings and immunohistochemical positivity for desmin, vimentin actin.Hemiglossectomy with supraomohyoid neck dissection done three years follow-up,...

10.14260/jemds/2014/1852 article EN Journal of Evolution of Medical and Dental Sciences 2014-01-10

Introduction: Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis beta chains hemoglobin.Iron overload occurs thalassemia, with transfusion therapy being major cause. Deferoxamine continues to be mainstay remove excess iron patients requiring long-term transfusions.One most important complications deferoxamine is neurosensory toxicity, including sensorineural hearing loss (SNHL).Labyrinthine hemmorhage (LH) thought result from altered...

10.1080/14670100.2018.1522715 article EN Cochlear Implants International 2018-09-20
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