A 56-year-old man presented with headaches for 3 months and drooping eyelids for 2 months. On examination, he had complete opthalmoplegia of the right eye and partial palsy of the left eye. MRI of the brain showed basal meningitis. Cerebrospinal fluid analysis revealed lymphocytic pleocytosis. He was diagnosed with tuberculous meningitis based on these findings and started on anti-tubercular drugs and steroids. On follow-up, his eye palsies had improved with treatment.
The patient, an 11-year-old boy, presented with weakness of all four limbs and difficulty swallowing over the past 10 days. Examination found symmetrical weakness, hypotonia, diminished reflexes, and facial nerve palsy. Investigations including CSF analysis and nerve conduction study supported a diagnosis of Guillain-Barré syndrome. He was treated with IVIG and made gradual improvement over his hospital stay, with resolution of accompanying hypertension. He was discharged with advice for outpatient physiotherapy follow up.
- 49-year-old man presented with gradually worsening left-sided hearing loss, imbalance, facial numbness, and recent headache.
- Examination found left sensorineural hearing loss, cerebellar ataxia, reduced sensation in the left V1 and V2 dermatomes, and signs of increased intracranial pressure.
- This suggests a likely diagnosis of a left cerebellopontine angle benign lesion such as a vestibular schwannoma involving the left cerebellum and trigeminal nerve.
1. A 21-year-old female presented with progressive weakness on the right side of her body over 1.5 years, along with fever, headache, diplopia, and two seizures.
2. Neurological examination revealed spastic right hemiparesis, internuclear ophthalmoplegia, nystagmus, and ataxic gait.
3. MRI brain showed multiple enhancing lesions in the midbrain, left periventricular area, and left basal ganglia, suggestive of tuberculomas. She was diagnosed with multiple tuberculomas and treated with anti-tuberculosis therapy and steroids.
This document summarizes the case of a 38-year-old woman who presented with a 6-month history of headache and 3-month history of vision loss. Her examination revealed vitiligo, poliosis, hearing loss, and funduscopic findings of retinal detachment and sunset glow appearance, consistent with Vogt-Koyanagi-Harada syndrome. Investigations including MRI brain, audiometry, skin biopsy, and OCT confirmed the diagnosis of VKH. She was started on high-dose steroids and azathioprine for treatment.
This document presents a case of a 40-year-old female patient presenting with headaches, blurry vision, and behavioral changes. Imaging shows a left sphenoid wing meningioma. The planned procedure is a left pterional craniotomy and tumor removal. Key details include a thorough patient history and exam, MRI findings of the brain tumor, and descriptions of the surgical approach and anticipated complications.
A 56-year-old man presented with headaches for 3 months and drooping eyelids for 2 months. On examination, he had complete opthalmoplegia of the right eye and partial palsy of the left eye. MRI of the brain showed basal meningitis. Cerebrospinal fluid analysis revealed lymphocytic pleocytosis. He was diagnosed with tuberculous meningitis based on these findings and started on anti-tubercular drugs and steroids. On follow-up, his eye palsies had improved with treatment.
The patient, an 11-year-old boy, presented with weakness of all four limbs and difficulty swallowing over the past 10 days. Examination found symmetrical weakness, hypotonia, diminished reflexes, and facial nerve palsy. Investigations including CSF analysis and nerve conduction study supported a diagnosis of Guillain-Barré syndrome. He was treated with IVIG and made gradual improvement over his hospital stay, with resolution of accompanying hypertension. He was discharged with advice for outpatient physiotherapy follow up.
- 49-year-old man presented with gradually worsening left-sided hearing loss, imbalance, facial numbness, and recent headache.
- Examination found left sensorineural hearing loss, cerebellar ataxia, reduced sensation in the left V1 and V2 dermatomes, and signs of increased intracranial pressure.
- This suggests a likely diagnosis of a left cerebellopontine angle benign lesion such as a vestibular schwannoma involving the left cerebellum and trigeminal nerve.
1. A 21-year-old female presented with progressive weakness on the right side of her body over 1.5 years, along with fever, headache, diplopia, and two seizures.
2. Neurological examination revealed spastic right hemiparesis, internuclear ophthalmoplegia, nystagmus, and ataxic gait.
3. MRI brain showed multiple enhancing lesions in the midbrain, left periventricular area, and left basal ganglia, suggestive of tuberculomas. She was diagnosed with multiple tuberculomas and treated with anti-tuberculosis therapy and steroids.
This document summarizes the case of a 38-year-old woman who presented with a 6-month history of headache and 3-month history of vision loss. Her examination revealed vitiligo, poliosis, hearing loss, and funduscopic findings of retinal detachment and sunset glow appearance, consistent with Vogt-Koyanagi-Harada syndrome. Investigations including MRI brain, audiometry, skin biopsy, and OCT confirmed the diagnosis of VKH. She was started on high-dose steroids and azathioprine for treatment.
This document presents a case of a 40-year-old female patient presenting with headaches, blurry vision, and behavioral changes. Imaging shows a left sphenoid wing meningioma. The planned procedure is a left pterional craniotomy and tumor removal. Key details include a thorough patient history and exam, MRI findings of the brain tumor, and descriptions of the surgical approach and anticipated complications.
This case presentation describes a 30-year-old male who presented with gradual weakness in both lower limbs over 3 days. Initial treatment with analgesics and IV fluids provided no improvement. Nerve conduction studies revealed sensorimotor nerve affection in the lower limbs suggestive of Guillain-Barré syndrome. However, after admission the patient was found to be hypokalemic, which when corrected with IV potassium infusion resulted in rapid improvement of his weakness. Differential diagnoses discussed include various causes of secondary periodic paralysis and other entities that could cause acute generalized weakness.
A 60-year-old female presented with double vision, right eye drooping, numbness on the right side of her forehead, and diminished vision in her right eye over the past 5 weeks. On examination, she had partial paralysis of the right 3rd, 4th, and 6th cranial nerves as well as decreased sensation in the V1 distribution of the right trigeminal nerve. Imaging and labs were notable for normal findings except no response on visual evoked potentials in the right eye. She received pulse steroids with partial improvement of some cranial nerve deficits but no change in vision.
A 48-year-old female presented with double vision, inability to close her left eye, redness of the left eye, difficulty swallowing, and unsteadiness while walking over the past 3 days. On examination, she had right lateral rectus palsy, left facial weakness, gait ataxia, and proximal weakness of the lower limbs. Investigations showed multi-nodular goiter and demyelinating radiculopathy more severe in the lower limbs. She was diagnosed with Miller Fisher syndrome/Bickerstaff brainstem encephalitis overlap and treated with plasma exchange, with improvement of symptoms over time.
- The patient Laam, a 9 month old boy, presented with recurrent seizures for 1 month with delayed developmental milestones.
- His neurological exam and investigations including EEG and CT brain were suggestive of West Syndrome with bilateral cerebral atrophy possibly due to birth asphyxia.
- He was started on ACTH and antihypertensive treatment. Follow up showed improved seizure control but persistent hypertension requiring dose adjustment. Eye evaluation found pale optic discs and chorioretinal changes.
This document presents a pre-operative case of a 38-year-old female patient presenting with sudden severe headache for 2 months. Imaging revealed a subarachnoid hemorrhage from a ruptured aneurysm on the M1 segment of the right middle cerebral artery. The planned procedure is a right pterional craniotomy for clipping of the aneurysm. Key steps of the procedure are described, including skin incision, craniotomy, durotomy, sylvian fissure dissection, aneurysm dissection and clipping, closure, and potential complications.
A 57-year-old diabetic man presented with double vision for 6 days and difficulty walking for 4 days. On examination, he had bilateral eye muscle paralysis, weakness of the limbs, reduced reflexes, and an unsteady gait. Tests showed a motor nerve disorder and diabetes complications. He was diagnosed with Guillain-Barré syndrome (Miller Fisher variant), diabetes mellitus type 2, and white matter brain changes. He received treatment and showed improvement in the hospital.
- A 71-year old retired policeman presented with 3 months of gradually worsening lower back pain, lower limb weakness, and urinary/fecal incontinence. On examination, he had wasting and weakness predominantly in his left lower limb, absent ankle reflexes, and sensory loss up to the saddle area. Imaging and laboratory tests were ordered.
- The document describes the case of a 27-year old male who presented with 10 months of gradually worsening weakness and wasting of his right upper limb. On examination, he had muscle wasting and weakness isolated to his right forearm, hand, and thumb muscles.
- The provisional diagnosis was monomelic amyotrophy. Differential diagnoses included brachial plexopathy, intracranial lesion, or cervical cord compression. Investigations were ordered and the patient was started on physical therapy, occupational therapy, and medications to improve strength and function.
An 57-year-old hypertensive male presented with sudden onset right-sided weakness, slurred speech, and deviation of the mouth angle for 3 days. On examination, he was conscious and cooperative with upper motor neuron signs on the right side and exaggerated reflexes. Imaging showed an acute intracerebral hemorrhage in the left internal capsule compressing surrounding structures. The patient was diagnosed with a hemorrhagic stroke due to ruptured blood vessels caused by long-standing hypertension.
This case involves an 18-year-old female who presented with protrusion of the eyes, headaches, visual blurring, and weakness of all four limbs. Examination found signs of Graves' disease including exophthalmos and an enlarged thyroid. Testing found elevated thyroid hormones consistent with Graves' disease. Imaging found lesions in the brainstem and spinal cord characteristic of neuromyelitis optica spectrum disorder (NMOSD). She tested positive for NMO-IgG antibodies. The final diagnosis was Graves' disease with NMOSD, possibly associated with systemic lupus erythematosus. NMOSD must be distinguished from multiple sclerosis as they have different treatments and prognoses. This case demonstrates the association
1. The document presents a case study of a 74-year-old male patient diagnosed with Parkinson's disease. It includes details on the patient's history, examination findings, and management.
2. The objectives of the case study were to share knowledge with supervisors, get feedback, and improve presentation skills. Parkinson's disease causes abnormal movements and difficulties with walking.
3. Examination revealed symptoms of Parkinson's disease including a shuffling gait, masked facial expressions, tremors, and rigidity.
A 35-year-old diabetic woman presented with altered consciousness for 12 days. She had a history of vomiting and abdominal pain. Examinations revealed she was disoriented with hypertonia and exaggerated reflexes. Investigations showed hyponatremia that had since corrected. MRI brain showed changes consistent with osmotic demyelination syndrome. She was diagnosed with diabetes, osmotic demyelination from hyponatremia, and erosive gastritis. She was treated with insulin, omeprazole, rehabilitation and discharged with advice to follow up in neurology.
Long case examination done during MBBS and MD examination. Neurology case is mostly the long case. History, general examination , systemic examination, provisional diagnosis, investigation and final diagnosis are the sequential steps. Neurology examinations includes higher mental function, cranial nerve examination, motor and sensory system examination, cerebellar signs, gait, peripheral nerves, spine and skull and peripheral nerve examination.
A 47-year-old male presented with low back pain for 1.5 months, dimness of vision in both eyes for 15 days, and unintentional weight loss. Examinations revealed hepatomegaly, abdominal lymphadenopathy, and neurological deficits. Investigations showed abnormal liver function and imaging supported CNS tuberculosis. The patient deteriorated on anti-TB treatment due to increased liver enzymes. Further testing is needed to confirm the diagnosis and determine the best treatment approach.
This document provides a summary of clinical syndromes and neurological conditions for medical students. It includes tables comparing upper and lower motor neuron signs. It also provides descriptions of various conditions like herpes simplex encephalitis, Guillain-Barre syndrome, cauda equina syndrome, multiple sclerosis, motor neuron disease, myasthenia gravis, Parkinson's disease, and Bell's palsy. Example cases are presented and the appropriate diagnosis and investigations are discussed for each case. Overall the document serves as a review of key neurology topics for medical students.
- A 71-year-old diabetic and hypertensive male presented with gradual onset of lower back pain, lower limb weakness, and urinary incontinence over 3 months.
- On examination, he had asymmetrical lower limb weakness and wasting, absent ankle reflexes, and sensory loss below the knees.
- Imaging and laboratory tests were ordered to investigate the cause of his progressive neurological deficits.
A 61-year old male farmer presented with gradually worsening vision in both eyes over the past 2 months. He has a 15-year history of uncontrolled diabetes. Examination found cataracts and signs of proliferative diabetic retinopathy in both eyes, including laser scar marks, dot and blot hemorrhages, and tortuous blood vessels. The patient was previously treated with laser photocoagulation in both eyes for diabetic retinopathy. The provisional diagnosis was proliferative diabetic retinopathy in both eyes status post pan retinal photocoagulation, along with nuclear sclerosis cataracts.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
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This case presentation describes a 30-year-old male who presented with gradual weakness in both lower limbs over 3 days. Initial treatment with analgesics and IV fluids provided no improvement. Nerve conduction studies revealed sensorimotor nerve affection in the lower limbs suggestive of Guillain-Barré syndrome. However, after admission the patient was found to be hypokalemic, which when corrected with IV potassium infusion resulted in rapid improvement of his weakness. Differential diagnoses discussed include various causes of secondary periodic paralysis and other entities that could cause acute generalized weakness.
A 60-year-old female presented with double vision, right eye drooping, numbness on the right side of her forehead, and diminished vision in her right eye over the past 5 weeks. On examination, she had partial paralysis of the right 3rd, 4th, and 6th cranial nerves as well as decreased sensation in the V1 distribution of the right trigeminal nerve. Imaging and labs were notable for normal findings except no response on visual evoked potentials in the right eye. She received pulse steroids with partial improvement of some cranial nerve deficits but no change in vision.
A 48-year-old female presented with double vision, inability to close her left eye, redness of the left eye, difficulty swallowing, and unsteadiness while walking over the past 3 days. On examination, she had right lateral rectus palsy, left facial weakness, gait ataxia, and proximal weakness of the lower limbs. Investigations showed multi-nodular goiter and demyelinating radiculopathy more severe in the lower limbs. She was diagnosed with Miller Fisher syndrome/Bickerstaff brainstem encephalitis overlap and treated with plasma exchange, with improvement of symptoms over time.
- The patient Laam, a 9 month old boy, presented with recurrent seizures for 1 month with delayed developmental milestones.
- His neurological exam and investigations including EEG and CT brain were suggestive of West Syndrome with bilateral cerebral atrophy possibly due to birth asphyxia.
- He was started on ACTH and antihypertensive treatment. Follow up showed improved seizure control but persistent hypertension requiring dose adjustment. Eye evaluation found pale optic discs and chorioretinal changes.
This document presents a pre-operative case of a 38-year-old female patient presenting with sudden severe headache for 2 months. Imaging revealed a subarachnoid hemorrhage from a ruptured aneurysm on the M1 segment of the right middle cerebral artery. The planned procedure is a right pterional craniotomy for clipping of the aneurysm. Key steps of the procedure are described, including skin incision, craniotomy, durotomy, sylvian fissure dissection, aneurysm dissection and clipping, closure, and potential complications.
A 57-year-old diabetic man presented with double vision for 6 days and difficulty walking for 4 days. On examination, he had bilateral eye muscle paralysis, weakness of the limbs, reduced reflexes, and an unsteady gait. Tests showed a motor nerve disorder and diabetes complications. He was diagnosed with Guillain-Barré syndrome (Miller Fisher variant), diabetes mellitus type 2, and white matter brain changes. He received treatment and showed improvement in the hospital.
- A 71-year old retired policeman presented with 3 months of gradually worsening lower back pain, lower limb weakness, and urinary/fecal incontinence. On examination, he had wasting and weakness predominantly in his left lower limb, absent ankle reflexes, and sensory loss up to the saddle area. Imaging and laboratory tests were ordered.
- The document describes the case of a 27-year old male who presented with 10 months of gradually worsening weakness and wasting of his right upper limb. On examination, he had muscle wasting and weakness isolated to his right forearm, hand, and thumb muscles.
- The provisional diagnosis was monomelic amyotrophy. Differential diagnoses included brachial plexopathy, intracranial lesion, or cervical cord compression. Investigations were ordered and the patient was started on physical therapy, occupational therapy, and medications to improve strength and function.
An 57-year-old hypertensive male presented with sudden onset right-sided weakness, slurred speech, and deviation of the mouth angle for 3 days. On examination, he was conscious and cooperative with upper motor neuron signs on the right side and exaggerated reflexes. Imaging showed an acute intracerebral hemorrhage in the left internal capsule compressing surrounding structures. The patient was diagnosed with a hemorrhagic stroke due to ruptured blood vessels caused by long-standing hypertension.
This case involves an 18-year-old female who presented with protrusion of the eyes, headaches, visual blurring, and weakness of all four limbs. Examination found signs of Graves' disease including exophthalmos and an enlarged thyroid. Testing found elevated thyroid hormones consistent with Graves' disease. Imaging found lesions in the brainstem and spinal cord characteristic of neuromyelitis optica spectrum disorder (NMOSD). She tested positive for NMO-IgG antibodies. The final diagnosis was Graves' disease with NMOSD, possibly associated with systemic lupus erythematosus. NMOSD must be distinguished from multiple sclerosis as they have different treatments and prognoses. This case demonstrates the association
1. The document presents a case study of a 74-year-old male patient diagnosed with Parkinson's disease. It includes details on the patient's history, examination findings, and management.
2. The objectives of the case study were to share knowledge with supervisors, get feedback, and improve presentation skills. Parkinson's disease causes abnormal movements and difficulties with walking.
3. Examination revealed symptoms of Parkinson's disease including a shuffling gait, masked facial expressions, tremors, and rigidity.
A 35-year-old diabetic woman presented with altered consciousness for 12 days. She had a history of vomiting and abdominal pain. Examinations revealed she was disoriented with hypertonia and exaggerated reflexes. Investigations showed hyponatremia that had since corrected. MRI brain showed changes consistent with osmotic demyelination syndrome. She was diagnosed with diabetes, osmotic demyelination from hyponatremia, and erosive gastritis. She was treated with insulin, omeprazole, rehabilitation and discharged with advice to follow up in neurology.
Long case examination done during MBBS and MD examination. Neurology case is mostly the long case. History, general examination , systemic examination, provisional diagnosis, investigation and final diagnosis are the sequential steps. Neurology examinations includes higher mental function, cranial nerve examination, motor and sensory system examination, cerebellar signs, gait, peripheral nerves, spine and skull and peripheral nerve examination.
A 47-year-old male presented with low back pain for 1.5 months, dimness of vision in both eyes for 15 days, and unintentional weight loss. Examinations revealed hepatomegaly, abdominal lymphadenopathy, and neurological deficits. Investigations showed abnormal liver function and imaging supported CNS tuberculosis. The patient deteriorated on anti-TB treatment due to increased liver enzymes. Further testing is needed to confirm the diagnosis and determine the best treatment approach.
This document provides a summary of clinical syndromes and neurological conditions for medical students. It includes tables comparing upper and lower motor neuron signs. It also provides descriptions of various conditions like herpes simplex encephalitis, Guillain-Barre syndrome, cauda equina syndrome, multiple sclerosis, motor neuron disease, myasthenia gravis, Parkinson's disease, and Bell's palsy. Example cases are presented and the appropriate diagnosis and investigations are discussed for each case. Overall the document serves as a review of key neurology topics for medical students.
- A 71-year-old diabetic and hypertensive male presented with gradual onset of lower back pain, lower limb weakness, and urinary incontinence over 3 months.
- On examination, he had asymmetrical lower limb weakness and wasting, absent ankle reflexes, and sensory loss below the knees.
- Imaging and laboratory tests were ordered to investigate the cause of his progressive neurological deficits.
A 61-year old male farmer presented with gradually worsening vision in both eyes over the past 2 months. He has a 15-year history of uncontrolled diabetes. Examination found cataracts and signs of proliferative diabetic retinopathy in both eyes, including laser scar marks, dot and blot hemorrhages, and tortuous blood vessels. The patient was previously treated with laser photocoagulation in both eyes for diabetic retinopathy. The provisional diagnosis was proliferative diabetic retinopathy in both eyes status post pan retinal photocoagulation, along with nuclear sclerosis cataracts.
Similar to case - Autoimmune encephalitis post covid .pptx (20)
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kol...rightmanforbloodline
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Versio
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
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Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
3. Main complain:
gait disorder.
•3 months ago, the patient complains of vertigo,
dysarthria, blurred vision and gait disorder which
development gradually over these months.
•No sensory symptoms or weakness.
•No dysphagia or dyspnea.
•No previous infection, vaccines, toxins exposure.
4. •he was conscious, oriented, and reactive.
•Cranial nerves: normal.
•Nystagmus: Multidirectional gaze-evoked nystagmus.
•Cerebellar signs: positive ( bilateral / upper and lower)
•Ataxic gait and dysarteria with trunk ataxia.
•Romberg sign: not detected.
•Planter reflex: bilateral flextion.
Iower left
Lower right
Upper left
Upper right
5/5
5/5
5/5
5/5
Strength
normal
normal
normal
normal
Tone
brisk
brisk
brisk
brisk
Reflexes
13. •The patient discharged with these
recommendations:
•Corticosteroid and tapering for about 2 months.
• Repeat consult and MRI after finishing
corticosteroid or when developing other
symptoms.
14. Follow up:
•4 months later, the same complain with some
relapse when he stopped corticosteroid.
•No other symptoms developed.
•We repeated MRI and csf aspiration.