Oh look, It's Brain Surgery !

A medical related blog to this beautiful branch of the medicine world. In here you will find medical cases, usefull data, interactive and graphic explanations about diseases and procedures and much more. Welcome and enjoy!
fuckyeahmedicalstuff:


attherisk:
This is my niece Cailyn, she’s three years old and was recently diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) . This is a very rare form of tumor diagnosed in only 200 children a year in the united states. The tumor is sitting on her brain stem and is inoperable. She just finished her first round of radiation, but other wise there is not much else the doctors can do. UNLESS she gets to take part in an experimental treatment in NY. My brother is in the Navy, and their insurance will not cover the cost. 
I am asking that my followers help me out with a signal boost for Cailyn, whether it be for prayers or donating to her fund to help her recieve treatment. The average length of survival with this type of cancer is 9 months, with about 30% making it a year, and less than 10% making it 2 years. 
You can donate to her fund by following this link, where you can also read more about her illness: Cailyn’s Pediatric Brain Tumor Foundation

Spread the word. Donate. Save a life.

fuckyeahmedicalstuff:

attherisk:

This is my niece Cailyn, she’s three years old and was recently diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) . This is a very rare form of tumor diagnosed in only 200 children a year in the united states. The tumor is sitting on her brain stem and is inoperable. She just finished her first round of radiation, but other wise there is not much else the doctors can do. UNLESS she gets to take part in an experimental treatment in NY. My brother is in the Navy, and their insurance will not cover the cost. 

I am asking that my followers help me out with a signal boost for Cailyn, whether it be for prayers or donating to her fund to help her recieve treatment. The average length of survival with this type of cancer is 9 months, with about 30% making it a year, and less than 10% making it 2 years. 

You can donate to her fund by following this link, where you can also read more about her illness: Cailyn’s Pediatric Brain Tumor Foundation

Spread the word. Donate. Save a life.

(via fuckyeahmedicalstuff)

Anonymous asked: I'm just gonna go ahead and assume that you're a neurosurgeon. Could you please describe the daily life of a neurosurgeon? I've been very interested lately in the career. Thanks!

I’m not a neurosurgeon…yet. I’m a general practitioner currently working in the primary care health area and preparing myself to postulate to neurosurgery residency in the near future ;)

fuckyeahmedicalstuff:


attherisk:
This is my niece Cailyn, she’s three years old and was recently diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) . This is a very rare form of tumor diagnosed in only 200 children a year in the united states. The tumor is sitting on her brain stem and is inoperable. She just finished her first round of radiation, but other wise there is not much else the doctors can do. UNLESS she gets to take part in an experimental treatment in NY. My brother is in the Navy, and their insurance will not cover the cost. 
I am asking that my followers help me out with a signal boost for Cailyn, whether it be for prayers or donating to her fund to help her recieve treatment. The average length of survival with this type of cancer is 9 months, with about 30% making it a year, and less than 10% making it 2 years. 
You can donate to her fund by following this link, where you can also read more about her illness: Cailyn’s Pediatric Brain Tumor Foundation

Spread the word. Donate. Save a life.

fuckyeahmedicalstuff:

attherisk:

This is my niece Cailyn, she’s three years old and was recently diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) . This is a very rare form of tumor diagnosed in only 200 children a year in the united states. The tumor is sitting on her brain stem and is inoperable. She just finished her first round of radiation, but other wise there is not much else the doctors can do. UNLESS she gets to take part in an experimental treatment in NY. My brother is in the Navy, and their insurance will not cover the cost. 

I am asking that my followers help me out with a signal boost for Cailyn, whether it be for prayers or donating to her fund to help her recieve treatment. The average length of survival with this type of cancer is 9 months, with about 30% making it a year, and less than 10% making it 2 years. 

You can donate to her fund by following this link, where you can also read more about her illness: Cailyn’s Pediatric Brain Tumor Foundation

Spread the word. Donate. Save a life.

(via fuckyeahmedicalstuff)

Diffuse Intrinsic Pontine Glioma (DIPG).

fuckyeahmedicalstuff:

A Diffuse Intrinsic Pontine Glioma (DIPG) is a tumor located in the pons (middle) of the brain stem. The brain stem is the bottom most portion of the brain, connecting the cerebrum with the spinal cord. The majority of brain stem tumors occur in the pons (middle brain stem), are diffusely infiltrating (they grow amidst the nerves), and therefore are not able to be surgically removed. Glioma is a general name for any tumor that arises from the supportive tissue called glia, which help keep the neurons (“thinking cells”) in place and functioning well. The brain stem contains all of the “wires” converging from the brain to the spinal cord as well as important structures involved in eye movements, face and throat muscle control and sensation.

 

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valetallica:

fuckyeahmedicalstuff:

force-ofnature:

fuckyeahmedicalstuff:


attherisk:
This is my niece Cailyn, she’s three years old and was recently diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) . This is a very rare form of tumor diagnosed in only 200 children a year in the united states. The tumor is sitting on her brain stem and is inoperable. She just finished her first round of radiation, but other wise there is not much else the doctors can do. UNLESS she gets to take part in an experimental treatment in NY. My brother is in the Navy, and their insurance will not cover the cost. 
I am asking that my followers help me out with a signal boost for Cailyn, whether it be for prayers or donating to her fund to help her recieve treatment. The average length of survival with this type of cancer is 9 months, with about 30% making it a year, and less than 10% making it 2 years. 
You can donate to her fund by following this link, where you can also read more about her illness: Cailyn’s Pediatric Brain Tumor Foundation
Everyone, I know this kid’s aunt. This is legitimate. I need your help. Please, spread the word, and if you can, donate to her foundation. Help save a kid’s life.  

Come on guys, please spread the word, and help! This is important.

Legitimate or not, at least I’m doing my part. 

Legitimate. I know this little girl’s aunt. It’s awful that we’ve been scammed so many times, that when someone REALLY needs us, we hesitate.  

This is a awful disease, with very poor outcome in most of cases. We should do everything in our power to fight this rare condition and help a little girl to live. At least try our best. Please help her, and spread the message.

valetallica:

fuckyeahmedicalstuff:

force-ofnature:

fuckyeahmedicalstuff:

attherisk:

This is my niece Cailyn, she’s three years old and was recently diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG) . This is a very rare form of tumor diagnosed in only 200 children a year in the united states. The tumor is sitting on her brain stem and is inoperable. She just finished her first round of radiation, but other wise there is not much else the doctors can do. UNLESS she gets to take part in an experimental treatment in NY. My brother is in the Navy, and their insurance will not cover the cost. 

I am asking that my followers help me out with a signal boost for Cailyn, whether it be for prayers or donating to her fund to help her recieve treatment. The average length of survival with this type of cancer is 9 months, with about 30% making it a year, and less than 10% making it 2 years. 

You can donate to her fund by following this link, where you can also read more about her illness: Cailyn’s Pediatric Brain Tumor Foundation

Everyone, I know this kid’s aunt. This is legitimate. 
I need your help. Please, spread the word, and if you can, donate to her foundation. Help save a kid’s life.  

Come on guys, please spread the word, and help! This is important.

Legitimate or not, at least I’m doing my part. 

Legitimate. I know this little girl’s aunt. 
It’s awful that we’ve been scammed so many times, that when someone REALLY needs us, we hesitate.  

This is a awful disease, with very poor outcome in most of cases. We should do everything in our power to fight this rare condition and help a little girl to live. At least try our best. Please help her, and spread the message.

Circle of Willis

Malformation of the Circle of Willis:
1. Unruptured aneurysm of the bifurcation of A. internal carotid artery;
2. Ruptured aneurysm of the bifurcation of A. basilar (location uncommon);
3. Two Aa. communicating before (instead of one);
4. Three Aa. brain before (instead of two) 

(via themightymelatonin)

   Pituitary Macroadenoma

 Post-mortem specimens showing a circumcribed nodular tumour arising from the anterior pituitary consistent with a macroadenoma. 

Source

(Source: themightymelatonin)

fuckyeahnarcotics:

Scoliosis is an abnormal curvature of the spine; the normal spine, when viewed from behind has no visible curve, when viewed from the side there will be a slight round back ‘kyphosis’ in the upper back and a mild swayback ‘lordosis’ in the lower back.

The surgical treatment of scoliosis involves a spinal fusion; this procedure removes the flexible elements of the spine, creating a solid block of bone throughout the fused area of the curve; this in most cases, is performed with the addition of an instrumentation system of rods, hooks, wires, and/or screws, the instrumentation system is used to correct the curvature of the spine as much as possible, as well as to maintain stability of the spine in the postoperative period while solidification of the fusion occurs, the surgical approach to the spine can be either through an incision on the back (posterior) or through an incision in the side (anterior); when doing a posterior spinal fusion the spinous processes, lamina, and transverse processes of the spine are exposed, it’s to these elements of the vertebra that the hooks, wires, or screws are placed to provide fixation of the rod to the spine, bone graft is applied to the exposed bony surfaces of the spine, which allow these vertebrae to subsequently grow together or fuse with bone connecting each of the vertebra to one another

fuckyeahnarcotics:

Vertebrectomy was first described in 1922 by MacLennan for the treatment of scoliosis through the posterior approach alone, this technique was subsequently used in the management of congenital, tumoral, infectious, deformity and traumatic disorders, Sharrard reported a technique of osteotomy excision of the spine in the treatment of myelomeningocele, this procedure consisted of a dural dissection, excision of myelomeningocele, osteotomy shortening of the spine, and internal instrumentation with Blount staples, many authors have used posterior vertebral column resection for severe spinal deformities; vertebrectomy for posttuberculous kyphosis can be carried out through an anterior, posterior, or combined approach, Reyes Sanchez described a technique of partial vertebrectomy shortening in the treatment of burst fractures, this technique consisted in resection of the proximal two thirds of the vertebra, the posterior arch and upper disc were also removed; that permitted short segmental instrumentation with a high fusion rate to our knowledge, complete vertebrectomy and spinal column shortening in the acute phase of thoracic spine fracture-dislocation has never been reported