Lokesh Nehete

ORCID: 0000-0003-0228-6324
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About
Contact & Profiles
Research Areas
  • Neurofibromatosis and Schwannoma Cases
  • Bone Tumor Diagnosis and Treatments
  • Meningioma and schwannoma management
  • Oral and Maxillofacial Pathology
  • Head and Neck Surgical Oncology
  • Teratomas and Epidermoid Cysts
  • Adrenal and Paraganglionic Tumors
  • Fetal and Pediatric Neurological Disorders
  • Osteomyelitis and Bone Disorders Research
  • Elbow and Forearm Trauma Treatment
  • CNS Lymphoma Diagnosis and Treatment
  • Infectious Diseases and Tuberculosis
  • Facial Nerve Paralysis Treatment and Research
  • Legionella and Acanthamoeba research
  • Cleft Lip and Palate Research
  • Spinal Fractures and Fixation Techniques
  • Vascular Malformations and Hemangiomas
  • Hedgehog Signaling Pathway Studies
  • Pelvic and Acetabular Injuries
  • Soft tissue tumor case studies
  • Spinal Hematomas and Complications
  • Spinal Dysraphism and Malformations
  • Spine and Intervertebral Disc Pathology
  • Hip disorders and treatments
  • Heme Oxygenase-1 and Carbon Monoxide

All India Institute of Medical Sciences Raipur
2018-2024

National Institute of Mental Health and Neurosciences
2016-2018

Abstract Concurrent occurrence of brain tumors in the same location is very unusual and has been noted patients with neurofibromatosis. Two lesions, occurring close contact but different histology, are called contiguous tumors. Schwannoma meningioma two common histologies reported to present as tumor. We cerebellopontine angle. The magnetic resonance imaging characteristics both cases demonstrate important findings that should be identified raise possibility discuss surgical implications...

10.1055/s-0037-1608873 article EN Journal of Neurological Surgery Part A Central European Neurosurgery 2017-12-14

We are reporting two patients of fatal and rapidly progressive amoebic encephalitis in immunocompetent host from poor socioeconomic status. Both these patient had acute neurological worsening preoperatively did not respond to subsequent surgical decompression. Biopsy report confirmed acanthamoebic cerebral infection.

10.1080/02688697.2018.1485873 article EN British Journal of Neurosurgery 2018-07-23

This report presents an extremely rare case of papillary meningioma with prominent flow voids and increased perfusion parameters on MRI in a 28-year-old male presenting headache. knowledge helped the neurosurgeon to minimise intra-operative blood loss achieve favourable post-surgical outcome.

10.4102/sajr.v28i1.2778 article EN cc-by South African Journal of Radiology 2024-03-22

We report a case of biopsy-proven retrobulbar lymphangioma in 14-year-old girl. She presented with chief complaints swelling the left eye for 2 months. The patient underwent imaging evaluation and it was diagnosed as cavernous hemangioma, radiologically. However, later on, surgery, specimen sent histopathology which revealed to be lymphangioma.

10.4103/ajns.ajns_165_18 article EN cc-by-nc-nd Asian Journal of Neurosurgery 2018-10-23

The most feared complication while inserting C2 screws is vertebral artery injury. This article proposes predicting the position of on a true lateral X-ray axis vertebra from background information acquired computed tomography (CT) scan utilizing fluoroscopy.Spiral CT scans 33 vertebrae were performed 16-slice scanner X-rays then obtained before and after painting grooves with barium. space available for transarticular pedicle screw insertion above groove in isthmus was calculated as ratio...

10.4103/sni.sni_109_18 article EN cc-by-nc-sa Surgical Neurology International 2018-01-01

A diffuse neurofibroma, a variant of most commonly occurs in young adults and involves the head neck. In absence neurofibromatosis, associated calvarial defect with these swellings is rarely seen.An 18-year-old woman presented history rapidly progressive painless large swelling over bilateral parieto-occipital region scalp. It was soft boggy brownish discoloration overlying skin. Imaging study showed brilliantly enhancing lesion involving scalp extending into extradural region. She underwent...

10.25259/sni_213_2020 article EN cc-by-nc-sa Surgical Neurology International 2020-10-02

An 8-year-old boy presented with a history of progressive left hemiparesis for 3 weeks associated mild headache but normal vision and have no familial neurofibromatosis.

10.47739/2573-1289.brainscience.1021 article EN JSM brain science. 2020-10-23

Background: Alobar holoprosencephaly is a rare disorder of brain development. Most the cases have facial abnormalities and survival such children usually not prolonged. Case Description: We are reporting 2-month-old female child presented with seizures delayed developmental milestones. Interestingly, she has no abnormality which quite unusual. The management difficult individualized. Conclusion: counseling parents should be done regarding severity outcome congenital disease also importance...

10.4103/jpn.jpn_250_20 article EN Journal of Pediatric Neurosciences 2022-01-01
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