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Dive into the research topics where Manish Jaiswal is active.

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Featured researches published by Manish Jaiswal.


Asian Spine Journal | 2013

Concept of Gunshot Wound Spine

Manish Jaiswal; Radhey Shyam Mittal

Gunshot wound (GSW) to the spine which was earlier common in the military population is now being increasingly noted in civilians due to easy availability of firearms of low velocity either licensed or illegal combined with an increased rate of violence in the society. Contributing to 13% to 17% of all spinal injuries, the management of complex injury to the spine produced by a GSW remains controversial. Surgery for spinal cord injuries resulting from low velocity GSWs is reserved for patients with progressive neurologic deterioration, persistent cerebrospinal fluid fistulae, and sometimes for incomplete spinal cord injuries. Surgery may also be indicated to relieve active neural compression from a bullet, bone, intervertebral disk, or a hematoma within the spinal canal. Spinal instability rarely results from a civilian GSW. Cauda equina injuries from low velocity GSWs have a better overall outcome after surgery. In general, the decision to perform surgery should be made on consideration of multiple patient factors that can vary over a period of time. Although there have been plenty of individual case reports regarding GSW to the spine, a thorough review of unique mechanical and biological factors that affect the final outcome has been lacking. We review the key concepts of pathogenesis and management of GSW to the spine and propose an algorithm to guide decision making in such cases.


Journal of Neurosciences in Rural Practice | 2013

Acute traumatic orbital encephalocele: A case report with review of literature.

Manish Jaiswal; I Vijay Sundar; Ashok Gandhi; Devendra Purohit; Radhey Shyam Mittal

Orbital roof fractures after a blunt injury are an uncommon complication of trauma. Traumatic encephaloceles in the orbital cavity are even rarer, with only 15 cases published till date. Raised intraorbital pressure leading to irreversible damage to the optic nerve can be prevented by early diagnosis and management. Orbital computed tomography (CT) with thin axial and coronal sections is helpful in trauma patients with a concurrent orbital trauma. Decompression of the orbital roof is the key step in surgical treatment and should be performed in every case. Repairing the orbital roof has to be performed to avoid transmission of variation in the intracranial pressure to the orbit. We present a case of traumatic orbital encephalocele who underwent surgical treatment via a frontobasal approach with evacuation of the contused herniated brain and reconstruction of the orbital roof using temporalis fascia which is readily available in contrast to costly materials like titanium mesh, screws, bone powder, fibrin glue, and so on, which are not easily available in every hospital. Rapid resolution of proptosis and visual symptoms along with excellent cosmetic outcome was seen at follow-ups after three and nine months. We emphasize the early diagnosis of this rare condition and also emergency treatment to prevent permanent visual loss as well as to achieve good cosmetic results.


Pediatric Neurosurgery | 2015

Occipital Post-Traumatic Intradiploic Arachnoid Cyst Converted to Pseudomeningocele after Re-Trauma: A Rare Complication of Rare Pathology

Manish Jaiswal; Ashok Gandhi; Achal Sharma; Rashmi Mittal

Background: Growing skull fracture (GSF)/pseudomeningocele is a rare complication of head injury in children. Post-traumatic intradiploic arachnoid cyst (PTIAC) is a variant but it is extremely rare. PTIACs are usually asymptomatic or with mild symptoms like headache. The rupture of PTIAC due to re-trauma leading to pseudomeningocele formation has not been seen or reported before. Patient and Method: We present a case of occipital PTIAC where pseudomeningocele developed after re-trauma, and discuss the pathogenesis and management. Result: En masse removal of the ruptured PTIAC was performed along with dural-defect repair. The post-operative recovery was good. Conclusion: PTIAC is an extremely rare occurrence as a variant of GSF. It is usually asymptomatic, but it may rupture with trivial trauma due to a thinned-out outer table and then converts into pseudomengocele. En masse excision with dural-defect repair gives good results in cases of ruptured PTIAC due to re-trauma.


Pediatric Neurosurgery | 2017

Disappearance of the Hemorrhagic Component of the Frontal Contusion Possibly due to Redistribution of the Hematoma within the Subarachnoid Space: A Case Report

Mohd Faheem; Manish Jaiswal; Bal Krishna Ojha; Anil Chandra; Sunil Kumar Singh; Chhitij Srivastava; Noor Us Saba

Posttraumatic hemorrhagic contusions are a common sequel of traumatic brain injuries. They occur in around 8% of all traumatic brain injuries. Spontaneous resolution of acute subdural and acute extradural hematomas, although rare, is a recognized entity, but spontaneous resolution of the hemorrhagic component of a contusion within 24 h has not been reported in the literature. We present a patient in whom the hemorrhagic component of her contusion resolved spontaneously over a period of 24 h after injury. The rarity of this case prompted us to this study.


Pediatric Neurosurgery | 2017

Extra-Axial Cerebellopontine Angle Medulloblastoma in an Infant

Mukesh Kumar Bhaskar; Manish Jaiswal; Bal Krishna Ojha; Sunil Kumar Singh; Anil Chandra; Mukta Meel; Mohd Faheem

Medulloblastoma is a common tumor of the posterior fossa, representing 20-25% of all pediatric neoplasms. It commonly occurs in the midline (cerebellar vermis) and rarely at the cerebellopontine angle. Most of them are intra-axial, and an extra-axial location of this tumor is very rare. Extra-axial cerebellopontine angle medulloblastoma is extremely uncommon and has never been reported in an infant. We report an extra-axial cerebellopontine angle medulloblastoma in a 1-year-old child.


Pediatric Neurosurgery | 2016

Giant Interfrontal Encephalocele in an Infant: A Rare Entity

Mohd Faheem; Sunil Kumar Singh; Bal Krishna Ojha; Anil Chandra; Chhitij Srivastava; Manish Jaiswal; Qazi Zeeshan

Interfrontal encephalocele is one of the rare varieties of anterior encephalocele, and a giant interfrontal encephalocele is extremely rare. The authors could find only one case report of giant interfrontal encephalocele in the literature. Anterior encephaloceles are more prevalent in South-East Asia and some northern parts of India. Giant encephalocele poses a great challenge to neurosurgeons and neuroanesthetists during surgery, as these infants usually have a low birth weight and a large sac, thus making the infant prone to hypothermia and blood loss among other risks. We encountered a patient with a giant interfrontal encephalocele aged 1 month. The rarity of this case prompted us to this report.


Asian journal of neurosurgery | 2016

Primary non-Hodgkin's lymphoma of the skull with extra and intracranial extension presenting with bulky scalp mass lesion

Manish Jaiswal; Ashok Gandhi; Devendra Purohit; Shashi Singhvi; Radhey Shyam Mittal

Primary non-Hodgkins lymphoma (NHL) of the cranium with extra- and intracranial extension without systemic or skeletal manifestation in a non-immunocompromised patient is extremely rare. These lesions are most of the time misdiagnosed because they mimic other conditions like meningioma. Here, we report a case presented with huge bulky scalp mass which on magnetic resonance imaging (MRI) brain showed involvement of scalp, cranial vault, meninges, and the brain parenchyma, mimicking a meningioma. After gross total resection, biopsy and CD marker study revealed primary non-Hodgkins diffuse large B-cell lymphoma (DLBCL). Malignant NHL should be considered in differential diagnosis of bulky scalp mass lesion.


Asian journal of neurosurgery | 2016

Ganglioglioma of conus medullaris in a patient of neurofibromatosis type 1: A novel association?

Ilangovan Vijay Sundar; Manish Jaiswal; Devendra Purohit; Rashmi Mittal

Ganglioglioma of the conus region is quite rare with only 12 reported cases. Ganglioglioma shares biologic features with neurofibromatosis leading to suggestions that the co-existence of the two diseases may be more than coincidental. We report a case of ganglioglioma of the conus medullaris in a patient of neurofibromatosis and explore the possible association of the two diseases.


Romanian Neurosurgery | 2014

Traumatic acute posterior fossa subdural hematoma – A case report and review of literature

Manish Jaiswal; I Vijay Sundar; Ashok Gandhi; Devendra Purohit; Rashmi Mittal

Abstract Traumatic subdural hematomas of the posterior fossa are rare but dangerous neurosurgical emergencies that require prompt diagnosis and management to avoid the uniformly poor outcome. We present a case of a teenager with severe TBI and acute subdural hematoma of the posterior fossa that deteriorated rapidly before surgery but eventually made a good recovery. We also the review the literature concerning traumatic posterior fossa subdural hematomas [PFSDH].


Romanian Neurosurgery | 2014

Outcome of operative intervention in intramedullary spinal cord tumours

Manish Jaiswal; Radhey Shyam Mittal

Abstract Objective: The authors analysed the outcome of intramedullary spinal cord tumour surgery, focusing on the preoperative & postoperative neurological status and influence of preoperative gait status on postoperative gait. Methods: Retrospective analysis of medical records of 53 intramedullary tumour patients, operated at our institute between Jan 2006 and July 2012 was done. Pre - and postoperative neurological status was determined. Preoperative MRI was done. Ambulatory status were evaluated using the modified McCormick Scale. All the patients were operated using standard microsurgical techniques. Extent of resection was quantified by direct visualization with microscope as: gross resection, subtotal resection, partial resection, and biopsy. Results: 73.5% of the patients were in 40-60 years of age group (age range, 5-81 years; mean age 41 years). Region most commonly affected was thoracic (40%). The preoperative McCormick grade was I in 20 (37.7%), II in 16 (30.1%), III in 7 (13.2%), IV in 9 (16.9%), and V in 1 (1.88%) patients. Gross resection was possible in 54.7% of cases. Gross resection rate was significantly higher in good preoperative gait (grade - I). Histologically 41.5% of the lesions were ependymomas. Overall postoperative neurological status improved in 16 (30.3%) of the patients, remained unchanged in 27 (50.9%) of cases, and deteriorated in 10 (18.8%) patients. Conclusions: Better final outcome of walking ability correlated with good preoperative gait. Higher Gross resection rate was found in cases at an early stage. We favor early and optimal resection of tumour to give least morbidity and better quality of life.

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Dive into the Manish Jaiswal's collaboration.

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Anil Chandra

King George's Medical University

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Bal Krishna Ojha

King George's Medical University

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Sunil Kumar Singh

King George's Medical University

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Chhitij Srivastava

King George's Medical University

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Mohd Faheem

King George's Medical University

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Rashmi Mittal

All India Institute of Medical Sciences

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Harsha A. Huliyappa

King George's Medical University

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Mukesh Kumar Bhaskar

King George's Medical University

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Somil Jaiswal

King George's Medical University

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Ankur Bajaj

King George's Medical University

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