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Keratinocytes, Melanocytes, Merkel cells, Langerhans cells
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Langerhans cell
Langerhans cells give the skin the power to become beautiful by itself.
Copyright© Shiseido Co., Ltd. All rights reserved.
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AP1: SKIN: MELANOCYTES, LANGERHANS CELLS
MELANOCYTES, LANGERHANS CELLS
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Langerhans Cell Histiocytosis
In this pediatric patient, a large mass expands the inferior aspect of the orbit. Additional infiltrative masses are present in the mastoid and tympanic portions of the temporal bones bilaterally. This was diagnosed as Langerhans Cell Histiocytosis.
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Langerhans Cell Histiocytosis
Public Speaking video used during topic of Langerhan Cell Histiocytosis (LCH).
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Living with Langerhans Cell Histiocytosis
Ian, a rare disease patient, shares his story about living with Langerhans Cell Histiocytosis.
You can learn more about this disease on the NORD Rare Disease Database http://rarediseases.org/rare-disease-information/rare-diseases/byID/408/viewAbstract.
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Langerhans cell histiocytosis (Medical Condition)
Symptoms, risk factors and treatments of Langerhans cell histiocytosis (Medical Condition)
Langerhans cell histiocytosis is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes
This video contains general medical information If in doubt, always seek professional medical advice.
The medic
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*Langerhans Cells Research Project
Group Members: Gwyneth Choo (12), Claire Tan (11), Jasmine Chuah (10)
Class: 3T
- - -
MUSIC:
Au Revoir Simone - Tell Me (Clock Opera Remix)
PROGRAM:
Sony Vegas Pro 12.0
SOURCES:
- "Dendritic Cell Migration" by garlandscience http://www.youtube.com/watch?v=ZuccruG_79M
- http://en.wikipedia.org/wiki/Langerhans_cell
- http://en.wikipedia.org/wiki/Birbeck_granules
- http://en.wikipedia.org/wiki/Lan
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Overview of LCH in Children - Dr. Maarten Egeler MD, PhD
Dr. Egeler discusses an overview of Langerhans cell histiocytosis (LCH), its symptoms, diagnosis and treatment, as well as a description of the BRAF mutation and the importance of the relationship between the Histiocytosis Association and the Histiocyte Society.
Questions:
What is LCH? (in children)
What are the symptoms of LCH?
How is LCH diagnosed?
How is LCH treated?
Is LCH hereditary or genet
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Histopathology Lymph node--Langerhans cell histiocytosis (Ha
Histopathology Lymph node--Langerhans cell histiocytosis (Hand-Schuller-Christian disease)
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Langerhans Cell Histiocytosis and Monkeygrins.org
My two year old son (known as Picobaby) is currently undergoing treatment for Langerhans Cell Histiocytosis, and has just received a gift from the states.
Please check out www.monkeygrins.org and if you can spare anything at all dontate. They are doing a lovely thing.
You can find them on Facebook here: https://www.facebook.com/MonkeyGrins/
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Langerhans Cell Histiocytosis (LCH)
This is a story about Rylan! I did this video for a school project and also for friends and family! I hope you all enjoy! Much love and blessings!!!
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HISTIOCITOSIS DE CELULAS DE LANGERHANS/LANGERHANS CELL HYSTIOCITOSIS
Dra Lidia Ossorio García. Unidad DE Gestión de Dermatología Médico-Quirúrgica y Venereología. Hospital Universitario Puerta del Mar. Cádiz. Servicio Andaluz de Salud. Consejería de Igualdad, Salud y políticas sociales. Junta de Andalucía.
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LCH 101 Part 1 of 7
Learn about Langerhans Cell Histiocytosis (LCH) in this 7 part series presented by Dr. Ken McClain of Texas Children's Cancer Center.
Part 1
Introduction & clinical challenge
Symptoms (clinical presentation)
What is a histiocyte?
Where do histiocytes come from?
More information at www.HISTIO.org
Film/Editing by Don Johnson, proud parent of a Histio Warrior.
www.NotTheActor.com
-
Ryans fight against Langerhans Cell Histiocytosis (LCH).
This is the brave story of my son Ryans fight against a rare blood disease called Langerhans Cell Histiocytosis.
Ryan was born with Langerhans Cell Histocytosis, however it was not diagnosed until he was 4 months old (and had progressed to Multi System Langerhans Cell Histiocytosis in this time). The disease had really got hold of him at this stage and was killing him.
This video tells the story
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Batang may sakit na Langerhans Cell Histiocytosis, lumuwa ang mata at nagkasugat-sugat ang katawan
24 Oras is GMA Network’s flagship newscast, anchored by Mike Enriquez and Mel Tiangco. It airs on GMA-7 Mondays to Fridays at 6:30 PM (PHL Time) and on weekends at 5:30 PM. For more videos from 24 Oras, visit http://www.gmanetwork.com/24oras.
GMA News Online: http://www.gmanews.tv
Facebook: http://www.facebook.com/gmanews
Twitter: http://www.twitter.com/gmanews
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Deryn Blackwell defies odds to recover from leukaemia and Langerhans cell sarcoma
The 14-year-old is thought to be the only person to have developed both diseases - and then recover from them.
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Langerhans Cell Histiocytosis of the Pituitary Gland
This is a case of Langerhans Cell Histiocytosis, or LCH, of the pituitary gland and infundibulum in a 6-year-old male. The first image is sagittal T1-weighted with some motion degradation. There is thickening of the infundibulum and pituitary gland itself, with classic loss of the typically hyerintense posterior pituitary. The second image is a noncontrast coronal T1 correlate redemonstrating infu
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Little Noah's Big Battle with Langerhans Cell Histiocytosis, LCH
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Designing Dreams: Jared - The Legend - Living With Langerhans Cell Histiocytosis
If you'd like to donate: https://www.youcaring.com/other/designing-dreams/41580/donate#pp
We have exciting news for you all! We will be redoing a little boys room the weekend of July 18th.
Jared is a 12 year old boy who has Langerhans Cell Histiocytosis (LCH), a cancer-like condition. LCH involves a proliferation of Langerhans or abnormal cells deriving from the bone marrow, which can migrate f
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Overview of Pulmonary LCH - Dr. Robert Vassallo, MD
Dr. Vassallo gives an overview of Pulmonary Langerhans cell histiocytosis (PLCH) as well as the symptoms, diagnosis, treatment and long-term effects.
Questions:
What is pulmonary Langerhans cell histiocytosis (PLCH)?
What is the link between smoking and PLCH?
What are the symptoms of PLCH?
How is PLCH diagnosed?
What are the treatments for PLCH?
What are the long-term effects of PLCH?
What does
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langerhans cell histiocytosis by Heather Jones
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5 year old Daylen receiving chemo for Langerhans Cell Histiocytosis
My son receiving chemotherapy, fighting Langerhans Cell Histiocytosis!
He got diagnosed on May2014
With a rare disease called : Langerhans Cell Histiocytosis! He is very brave..
This is him getting accessed on his port on his chest with a large thick needle (although he does have numbing cream on to not feel directly) any child his age would be screaming in pain! But he is brave!!!! Let's get mor
Langerhans cell
Langerhans cells give the skin the power to become beautiful by itself.
Copyright© Shiseido Co., Ltd. All rights reserved....
Langerhans cells give the skin the power to become beautiful by itself.
Copyright© Shiseido Co., Ltd. All rights reserved.
wn.com/Langerhans Cell
Langerhans cells give the skin the power to become beautiful by itself.
Copyright© Shiseido Co., Ltd. All rights reserved.
- published: 01 Aug 2014
- views: 1381
Langerhans Cell Histiocytosis
In this pediatric patient, a large mass expands the inferior aspect of the orbit. Additional infiltrative masses are present in the mastoid and tympanic portion...
In this pediatric patient, a large mass expands the inferior aspect of the orbit. Additional infiltrative masses are present in the mastoid and tympanic portions of the temporal bones bilaterally. This was diagnosed as Langerhans Cell Histiocytosis.
wn.com/Langerhans Cell Histiocytosis
In this pediatric patient, a large mass expands the inferior aspect of the orbit. Additional infiltrative masses are present in the mastoid and tympanic portions of the temporal bones bilaterally. This was diagnosed as Langerhans Cell Histiocytosis.
- published: 14 Jul 2014
- views: 1205
Langerhans Cell Histiocytosis
Public Speaking video used during topic of Langerhan Cell Histiocytosis (LCH)....
Public Speaking video used during topic of Langerhan Cell Histiocytosis (LCH).
wn.com/Langerhans Cell Histiocytosis
Public Speaking video used during topic of Langerhan Cell Histiocytosis (LCH).
- published: 23 Feb 2012
- views: 2509
Living with Langerhans Cell Histiocytosis
Ian, a rare disease patient, shares his story about living with Langerhans Cell Histiocytosis.
You can learn more about this disease on the NORD Rare Disease D...
Ian, a rare disease patient, shares his story about living with Langerhans Cell Histiocytosis.
You can learn more about this disease on the NORD Rare Disease Database http://rarediseases.org/rare-disease-information/rare-diseases/byID/408/viewAbstract.
wn.com/Living With Langerhans Cell Histiocytosis
Ian, a rare disease patient, shares his story about living with Langerhans Cell Histiocytosis.
You can learn more about this disease on the NORD Rare Disease Database http://rarediseases.org/rare-disease-information/rare-diseases/byID/408/viewAbstract.
- published: 30 Sep 2011
- views: 6070
Langerhans cell histiocytosis (Medical Condition)
Symptoms, risk factors and treatments of Langerhans cell histiocytosis (Medical Condition)
Langerhans cell histiocytosis is a rare disease involving clonal p...
Symptoms, risk factors and treatments of Langerhans cell histiocytosis (Medical Condition)
Langerhans cell histiocytosis is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes
This video contains general medical information If in doubt, always seek professional medical advice.
The medical information is not advice and should not be treated as such. The medical information is provided without any representations or warranties, express or implied. We do not warrant or represent that the medical information on this websiteis true, accurate, complete, current or non-misleading
Music: 'Undaunted' Kevin Macleod CC-BY-3.0
Source/Images: "Langerhans cell histiocytosis" CC-BY-2.5 https://www.freebase.com/m/05s549
wn.com/Langerhans Cell Histiocytosis (Medical Condition)
Symptoms, risk factors and treatments of Langerhans cell histiocytosis (Medical Condition)
Langerhans cell histiocytosis is a rare disease involving clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes
This video contains general medical information If in doubt, always seek professional medical advice.
The medical information is not advice and should not be treated as such. The medical information is provided without any representations or warranties, express or implied. We do not warrant or represent that the medical information on this websiteis true, accurate, complete, current or non-misleading
Music: 'Undaunted' Kevin Macleod CC-BY-3.0
Source/Images: "Langerhans cell histiocytosis" CC-BY-2.5 https://www.freebase.com/m/05s549
- published: 10 May 2015
- views: 162
*Langerhans Cells Research Project
Group Members: Gwyneth Choo (12), Claire Tan (11), Jasmine Chuah (10)
Class: 3T
- - -
MUSIC:
Au Revoir Simone - Tell Me (Clock Opera Remix)
PROGRAM:
Sony Vega...
Group Members: Gwyneth Choo (12), Claire Tan (11), Jasmine Chuah (10)
Class: 3T
- - -
MUSIC:
Au Revoir Simone - Tell Me (Clock Opera Remix)
PROGRAM:
Sony Vegas Pro 12.0
SOURCES:
- "Dendritic Cell Migration" by garlandscience http://www.youtube.com/watch?v=ZuccruG_79M
- http://en.wikipedia.org/wiki/Langerhans_cell
- http://en.wikipedia.org/wiki/Birbeck_granules
- http://en.wikipedia.org/wiki/Langerin
- http://www.ncbi.nlm.nih.gov/pubmed/18792031
- http://emedicine.medscape.com/article/1100579-overview
[pictures:]
- http://3.bp.blogspot.com/-yEW70Hf5-TY/ULnBfiGTb9I/AAAAAAAAF1s/JOoQ-d5V1Zw/s1600/nm0307-245-F2.gif
- http://images.inmagine.com/400nwm/sciencephotolibrary/spl015/spl015178.jpg
- http://m1.acris-antibodies.com/images/11841-1-AP-IHC456.jpg
wn.com/Langerhans Cells Research Project
Group Members: Gwyneth Choo (12), Claire Tan (11), Jasmine Chuah (10)
Class: 3T
- - -
MUSIC:
Au Revoir Simone - Tell Me (Clock Opera Remix)
PROGRAM:
Sony Vegas Pro 12.0
SOURCES:
- "Dendritic Cell Migration" by garlandscience http://www.youtube.com/watch?v=ZuccruG_79M
- http://en.wikipedia.org/wiki/Langerhans_cell
- http://en.wikipedia.org/wiki/Birbeck_granules
- http://en.wikipedia.org/wiki/Langerin
- http://www.ncbi.nlm.nih.gov/pubmed/18792031
- http://emedicine.medscape.com/article/1100579-overview
[pictures:]
- http://3.bp.blogspot.com/-yEW70Hf5-TY/ULnBfiGTb9I/AAAAAAAAF1s/JOoQ-d5V1Zw/s1600/nm0307-245-F2.gif
- http://images.inmagine.com/400nwm/sciencephotolibrary/spl015/spl015178.jpg
- http://m1.acris-antibodies.com/images/11841-1-AP-IHC456.jpg
- published: 13 Feb 2014
- views: 364
Overview of LCH in Children - Dr. Maarten Egeler MD, PhD
Dr. Egeler discusses an overview of Langerhans cell histiocytosis (LCH), its symptoms, diagnosis and treatment, as well as a description of the BRAF mutation an...
Dr. Egeler discusses an overview of Langerhans cell histiocytosis (LCH), its symptoms, diagnosis and treatment, as well as a description of the BRAF mutation and the importance of the relationship between the Histiocytosis Association and the Histiocyte Society.
Questions:
What is LCH? (in children)
What are the symptoms of LCH?
How is LCH diagnosed?
How is LCH treated?
Is LCH hereditary or genetic?
Is there a cure for LCH?
What are the possibilities of reactivation?
Should I immunize my child?
What is the importance and relevance of the relationship between the Histiocyte Society and Histiocytosis Association?
What is the B-RAF mutation?
wn.com/Overview Of Lch In Children Dr. Maarten Egeler Md, Phd
Dr. Egeler discusses an overview of Langerhans cell histiocytosis (LCH), its symptoms, diagnosis and treatment, as well as a description of the BRAF mutation and the importance of the relationship between the Histiocytosis Association and the Histiocyte Society.
Questions:
What is LCH? (in children)
What are the symptoms of LCH?
How is LCH diagnosed?
How is LCH treated?
Is LCH hereditary or genetic?
Is there a cure for LCH?
What are the possibilities of reactivation?
Should I immunize my child?
What is the importance and relevance of the relationship between the Histiocyte Society and Histiocytosis Association?
What is the B-RAF mutation?
- published: 15 Jan 2014
- views: 1948
Histopathology Lymph node--Langerhans cell histiocytosis (Ha
Histopathology Lymph node--Langerhans cell histiocytosis (Hand-Schuller-Christian disease)...
Histopathology Lymph node--Langerhans cell histiocytosis (Hand-Schuller-Christian disease)
wn.com/Histopathology Lymph Node Langerhans Cell Histiocytosis (Ha
Histopathology Lymph node--Langerhans cell histiocytosis (Hand-Schuller-Christian disease)
- published: 11 May 2007
- views: 9339
Langerhans Cell Histiocytosis and Monkeygrins.org
My two year old son (known as Picobaby) is currently undergoing treatment for Langerhans Cell Histiocytosis, and has just received a gift from the states.
Plea...
My two year old son (known as Picobaby) is currently undergoing treatment for Langerhans Cell Histiocytosis, and has just received a gift from the states.
Please check out www.monkeygrins.org and if you can spare anything at all dontate. They are doing a lovely thing.
You can find them on Facebook here: https://www.facebook.com/MonkeyGrins/
wn.com/Langerhans Cell Histiocytosis And Monkeygrins.Org
My two year old son (known as Picobaby) is currently undergoing treatment for Langerhans Cell Histiocytosis, and has just received a gift from the states.
Please check out www.monkeygrins.org and if you can spare anything at all dontate. They are doing a lovely thing.
You can find them on Facebook here: https://www.facebook.com/MonkeyGrins/
- published: 31 Oct 2015
- views: 579
Langerhans Cell Histiocytosis (LCH)
This is a story about Rylan! I did this video for a school project and also for friends and family! I hope you all enjoy! Much love and blessings!!!...
This is a story about Rylan! I did this video for a school project and also for friends and family! I hope you all enjoy! Much love and blessings!!!
wn.com/Langerhans Cell Histiocytosis (Lch)
This is a story about Rylan! I did this video for a school project and also for friends and family! I hope you all enjoy! Much love and blessings!!!
- published: 05 May 2014
- views: 893
HISTIOCITOSIS DE CELULAS DE LANGERHANS/LANGERHANS CELL HYSTIOCITOSIS
Dra Lidia Ossorio García. Unidad DE Gestión de Dermatología Médico-Quirúrgica y Venereología. Hospital Universitario Puerta del Mar. Cádiz. Servicio Andaluz de ...
Dra Lidia Ossorio García. Unidad DE Gestión de Dermatología Médico-Quirúrgica y Venereología. Hospital Universitario Puerta del Mar. Cádiz. Servicio Andaluz de Salud. Consejería de Igualdad, Salud y políticas sociales. Junta de Andalucía.
wn.com/Histiocitosis De Celulas De Langerhans Langerhans Cell Hystiocitosis
Dra Lidia Ossorio García. Unidad DE Gestión de Dermatología Médico-Quirúrgica y Venereología. Hospital Universitario Puerta del Mar. Cádiz. Servicio Andaluz de Salud. Consejería de Igualdad, Salud y políticas sociales. Junta de Andalucía.
- published: 28 May 2015
- views: 694
LCH 101 Part 1 of 7
Learn about Langerhans Cell Histiocytosis (LCH) in this 7 part series presented by Dr. Ken McClain of Texas Children's Cancer Center.
Part 1
Introduction &...
Learn about Langerhans Cell Histiocytosis (LCH) in this 7 part series presented by Dr. Ken McClain of Texas Children's Cancer Center.
Part 1
Introduction & clinical challenge
Symptoms (clinical presentation)
What is a histiocyte?
Where do histiocytes come from?
More information at www.HISTIO.org
Film/Editing by Don Johnson, proud parent of a Histio Warrior.
www.NotTheActor.com
wn.com/Lch 101 Part 1 Of 7
Learn about Langerhans Cell Histiocytosis (LCH) in this 7 part series presented by Dr. Ken McClain of Texas Children's Cancer Center.
Part 1
Introduction & clinical challenge
Symptoms (clinical presentation)
What is a histiocyte?
Where do histiocytes come from?
More information at www.HISTIO.org
Film/Editing by Don Johnson, proud parent of a Histio Warrior.
www.NotTheActor.com
- published: 07 Jul 2007
- views: 14336
Ryans fight against Langerhans Cell Histiocytosis (LCH).
This is the brave story of my son Ryans fight against a rare blood disease called Langerhans Cell Histiocytosis.
Ryan was born with Langerhans Cell Histocytosis...
This is the brave story of my son Ryans fight against a rare blood disease called Langerhans Cell Histiocytosis.
Ryan was born with Langerhans Cell Histocytosis, however it was not diagnosed until he was 4 months old (and had progressed to Multi System Langerhans Cell Histiocytosis in this time). The disease had really got hold of him at this stage and was killing him.
This video tells the story of Ryans battle with this disease and his journey so far.
I really hope this video will raise awareness of this rare blood disease - Langerhans Cell Histiocytosis.
Update 17th April 2013:
Ryans review/scans/tests went very well in Our Ladys Childrens Hospital, Crumlin, Dublin.
After 2 years & 2 months of chemo, Ryan has finally finished! He will be closely monitored by his Consultant Oncologist for a long while yet with frequent checks ups/xrays/scans etc.
He will continue the TB medication for another few months until his immune system has built back up to a safe level for this medication to be stopped.
Please God the LCH will stay well away now that Ryan has finished chemotherapy.
He is doing really well, he is full of life and living life like a normal 2 & half year old little boy!
Update November 2013:
Ryan is now completely medication free. For 2 and half years, Ryan has been taking daily TB medication and 'Septrin' at weekends (to protect him against serious pnuemonia), Ryans immune system is now back to normal (confirmed by a special blood test called a CD4 blood test).
His medical care has now been transferred to our family GP (not the local hospital which is 30 mins away).
He will still have regular check ups/xray/abdominal ultrasound by his Consultant Oncologist in Our Ladys Childrens Hospital, Crumlin, Co. Dublin every couple of months.
He turned 3 years old in November 2013 and has started playschool two afternoons a week and he absolutely loves going.
Please God the LCH will stay away and let Ryan finaly live a 'normal' life.
wn.com/Ryans Fight Against Langerhans Cell Histiocytosis (Lch).
This is the brave story of my son Ryans fight against a rare blood disease called Langerhans Cell Histiocytosis.
Ryan was born with Langerhans Cell Histocytosis, however it was not diagnosed until he was 4 months old (and had progressed to Multi System Langerhans Cell Histiocytosis in this time). The disease had really got hold of him at this stage and was killing him.
This video tells the story of Ryans battle with this disease and his journey so far.
I really hope this video will raise awareness of this rare blood disease - Langerhans Cell Histiocytosis.
Update 17th April 2013:
Ryans review/scans/tests went very well in Our Ladys Childrens Hospital, Crumlin, Dublin.
After 2 years & 2 months of chemo, Ryan has finally finished! He will be closely monitored by his Consultant Oncologist for a long while yet with frequent checks ups/xrays/scans etc.
He will continue the TB medication for another few months until his immune system has built back up to a safe level for this medication to be stopped.
Please God the LCH will stay well away now that Ryan has finished chemotherapy.
He is doing really well, he is full of life and living life like a normal 2 & half year old little boy!
Update November 2013:
Ryan is now completely medication free. For 2 and half years, Ryan has been taking daily TB medication and 'Septrin' at weekends (to protect him against serious pnuemonia), Ryans immune system is now back to normal (confirmed by a special blood test called a CD4 blood test).
His medical care has now been transferred to our family GP (not the local hospital which is 30 mins away).
He will still have regular check ups/xray/abdominal ultrasound by his Consultant Oncologist in Our Ladys Childrens Hospital, Crumlin, Co. Dublin every couple of months.
He turned 3 years old in November 2013 and has started playschool two afternoons a week and he absolutely loves going.
Please God the LCH will stay away and let Ryan finaly live a 'normal' life.
- published: 17 Jun 2012
- views: 5966
Batang may sakit na Langerhans Cell Histiocytosis, lumuwa ang mata at nagkasugat-sugat ang katawan
24 Oras is GMA Network’s flagship newscast, anchored by Mike Enriquez and Mel Tiangco. It airs on GMA-7 Mondays to Fridays at 6:30 PM (PHL Time) and on weekends...
24 Oras is GMA Network’s flagship newscast, anchored by Mike Enriquez and Mel Tiangco. It airs on GMA-7 Mondays to Fridays at 6:30 PM (PHL Time) and on weekends at 5:30 PM. For more videos from 24 Oras, visit http://www.gmanetwork.com/24oras.
GMA News Online: http://www.gmanews.tv
Facebook: http://www.facebook.com/gmanews
Twitter: http://www.twitter.com/gmanews
wn.com/Batang May Sakit Na Langerhans Cell Histiocytosis, Lumuwa Ang Mata At Nagkasugat Sugat Ang Katawan
24 Oras is GMA Network’s flagship newscast, anchored by Mike Enriquez and Mel Tiangco. It airs on GMA-7 Mondays to Fridays at 6:30 PM (PHL Time) and on weekends at 5:30 PM. For more videos from 24 Oras, visit http://www.gmanetwork.com/24oras.
GMA News Online: http://www.gmanews.tv
Facebook: http://www.facebook.com/gmanews
Twitter: http://www.twitter.com/gmanews
- published: 05 Nov 2014
- views: 2292
Deryn Blackwell defies odds to recover from leukaemia and Langerhans cell sarcoma
The 14-year-old is thought to be the only person to have developed both diseases - and then recover from them....
The 14-year-old is thought to be the only person to have developed both diseases - and then recover from them.
wn.com/Deryn Blackwell Defies Odds To Recover From Leukaemia And Langerhans Cell Sarcoma
The 14-year-old is thought to be the only person to have developed both diseases - and then recover from them.
- published: 24 Feb 2014
- views: 1339
Langerhans Cell Histiocytosis of the Pituitary Gland
This is a case of Langerhans Cell Histiocytosis, or LCH, of the pituitary gland and infundibulum in a 6-year-old male. The first image is sagittal T1-weighted w...
This is a case of Langerhans Cell Histiocytosis, or LCH, of the pituitary gland and infundibulum in a 6-year-old male. The first image is sagittal T1-weighted with some motion degradation. There is thickening of the infundibulum and pituitary gland itself, with classic loss of the typically hyerintense posterior pituitary. The second image is a noncontrast coronal T1 correlate redemonstrating infundibular thickening as well as enlargement of the pituitary gland itself. The third image is with T2 weighting in the coronal plane redemonstrating thickening of the pituitary stalk. The fourth through sixth images are multi planar postcontrast T1-weighted sequences demonstrating avid post contrast enhancement of the markedly enlarged infundibulum and pituitary gland itself. LCH is a reactive clonal disease of the monocyte-macrophage system, and may affect almost any organ system. LCH CNS involvement may fall into one of several forms such as: osseous lesions with or without soft tissue components, intra-cranial extra-axial lesions, such as in the hypothalamic-pituitary region, meninges, or circumventricular organs, intracranial intra-axial lesions and cerebral atrophy. Langerhans cell histiocytosis is the most common cause of infundibular thickening in childhood. Diabetes insipidus is the typical clinical presentation of hypothalamic-pituitary involvement.
wn.com/Langerhans Cell Histiocytosis Of The Pituitary Gland
This is a case of Langerhans Cell Histiocytosis, or LCH, of the pituitary gland and infundibulum in a 6-year-old male. The first image is sagittal T1-weighted with some motion degradation. There is thickening of the infundibulum and pituitary gland itself, with classic loss of the typically hyerintense posterior pituitary. The second image is a noncontrast coronal T1 correlate redemonstrating infundibular thickening as well as enlargement of the pituitary gland itself. The third image is with T2 weighting in the coronal plane redemonstrating thickening of the pituitary stalk. The fourth through sixth images are multi planar postcontrast T1-weighted sequences demonstrating avid post contrast enhancement of the markedly enlarged infundibulum and pituitary gland itself. LCH is a reactive clonal disease of the monocyte-macrophage system, and may affect almost any organ system. LCH CNS involvement may fall into one of several forms such as: osseous lesions with or without soft tissue components, intra-cranial extra-axial lesions, such as in the hypothalamic-pituitary region, meninges, or circumventricular organs, intracranial intra-axial lesions and cerebral atrophy. Langerhans cell histiocytosis is the most common cause of infundibular thickening in childhood. Diabetes insipidus is the typical clinical presentation of hypothalamic-pituitary involvement.
- published: 07 Jul 2015
- views: 95
Designing Dreams: Jared - The Legend - Living With Langerhans Cell Histiocytosis
If you'd like to donate: https://www.youcaring.com/other/designing-dreams/41580/donate#pp
We have exciting news for you all! We will be redoing a little boys ...
If you'd like to donate: https://www.youcaring.com/other/designing-dreams/41580/donate#pp
We have exciting news for you all! We will be redoing a little boys room the weekend of July 18th.
Jared is a 12 year old boy who has Langerhans Cell Histiocytosis (LCH), a cancer-like condition. LCH involves a proliferation of Langerhans or abnormal cells deriving from the bone marrow, which can migrate from skin to lymph nodes and can result in bone lesions as well as multisystem disease. He has a specific neurodegenerative type which affects his central nervous system leaving which has resulted in some physical limitations, cognitive issues etc. His speech at times is slurred. He is currently undergoing chemo for LCH. He has been getting chemo for a little over two years. His balance is off, so he needs somebody close by because he could fall at any time. He has had 133 chemo treatments so far and has never cried or had a negative attitude about any of it. At the moment he goes to school for half days where he must use a wheelchair. Jared is limited to what he can do because of mobility issues. His favorite things are Transformers, Legos too, and the Three Stooges. Jared's favorite colors are green and red. He holds a lot of emotions inside. When his mother told him about Designing Dreams, he said he was so excited he was about to burst! We are giving him something to think about besides his next treatment or hospital appointment, and he could not be more deserving of it!
Read more about Designing Dreams...
Our principle activity is to annually/semiannually redesign critically ill children's bedrooms at their home. We decorate, paint murals, and help design children's dream rooms to inspire hope and happiness in their lives.
Designing Dreams is a student organization founded at the University of Minnesota-Twin Cities that is managed entirely through student involvement. Our mission is to be a beacon of happiness and inspiration to critically ill children. We seek to inspire hope in the lives of these children by incorporating aspects of design to make their dream bedroom a reality. We would like to provide an optimistic and encouraging outlook for the young patients and their families through the hardships they are facing.
We promote the formation of supportive relationships between University students and within the Minneapolis and greater Midwest community of hospitals, business, and organizations with which we partner. Members who participate in the Dream Team efforts of Designing Dreams will be able to utilize their creativity, determined work ethic, passion for children, health, and the medical community, and any artistic design abilities (though none are required to join!).
wn.com/Designing Dreams Jared The Legend Living With Langerhans Cell Histiocytosis
If you'd like to donate: https://www.youcaring.com/other/designing-dreams/41580/donate#pp
We have exciting news for you all! We will be redoing a little boys room the weekend of July 18th.
Jared is a 12 year old boy who has Langerhans Cell Histiocytosis (LCH), a cancer-like condition. LCH involves a proliferation of Langerhans or abnormal cells deriving from the bone marrow, which can migrate from skin to lymph nodes and can result in bone lesions as well as multisystem disease. He has a specific neurodegenerative type which affects his central nervous system leaving which has resulted in some physical limitations, cognitive issues etc. His speech at times is slurred. He is currently undergoing chemo for LCH. He has been getting chemo for a little over two years. His balance is off, so he needs somebody close by because he could fall at any time. He has had 133 chemo treatments so far and has never cried or had a negative attitude about any of it. At the moment he goes to school for half days where he must use a wheelchair. Jared is limited to what he can do because of mobility issues. His favorite things are Transformers, Legos too, and the Three Stooges. Jared's favorite colors are green and red. He holds a lot of emotions inside. When his mother told him about Designing Dreams, he said he was so excited he was about to burst! We are giving him something to think about besides his next treatment or hospital appointment, and he could not be more deserving of it!
Read more about Designing Dreams...
Our principle activity is to annually/semiannually redesign critically ill children's bedrooms at their home. We decorate, paint murals, and help design children's dream rooms to inspire hope and happiness in their lives.
Designing Dreams is a student organization founded at the University of Minnesota-Twin Cities that is managed entirely through student involvement. Our mission is to be a beacon of happiness and inspiration to critically ill children. We seek to inspire hope in the lives of these children by incorporating aspects of design to make their dream bedroom a reality. We would like to provide an optimistic and encouraging outlook for the young patients and their families through the hardships they are facing.
We promote the formation of supportive relationships between University students and within the Minneapolis and greater Midwest community of hospitals, business, and organizations with which we partner. Members who participate in the Dream Team efforts of Designing Dreams will be able to utilize their creativity, determined work ethic, passion for children, health, and the medical community, and any artistic design abilities (though none are required to join!).
- published: 28 Jun 2014
- views: 1085
Overview of Pulmonary LCH - Dr. Robert Vassallo, MD
Dr. Vassallo gives an overview of Pulmonary Langerhans cell histiocytosis (PLCH) as well as the symptoms, diagnosis, treatment and long-term effects.
Questions...
Dr. Vassallo gives an overview of Pulmonary Langerhans cell histiocytosis (PLCH) as well as the symptoms, diagnosis, treatment and long-term effects.
Questions:
What is pulmonary Langerhans cell histiocytosis (PLCH)?
What is the link between smoking and PLCH?
What are the symptoms of PLCH?
How is PLCH diagnosed?
What are the treatments for PLCH?
What are the long-term effects of PLCH?
What does the future hold for patients with PLCH?
wn.com/Overview Of Pulmonary Lch Dr. Robert Vassallo, Md
Dr. Vassallo gives an overview of Pulmonary Langerhans cell histiocytosis (PLCH) as well as the symptoms, diagnosis, treatment and long-term effects.
Questions:
What is pulmonary Langerhans cell histiocytosis (PLCH)?
What is the link between smoking and PLCH?
What are the symptoms of PLCH?
How is PLCH diagnosed?
What are the treatments for PLCH?
What are the long-term effects of PLCH?
What does the future hold for patients with PLCH?
- published: 15 Jan 2014
- views: 900
5 year old Daylen receiving chemo for Langerhans Cell Histiocytosis
My son receiving chemotherapy, fighting Langerhans Cell Histiocytosis!
He got diagnosed on May2014
With a rare disease called : Langerhans Cell Histiocytosis! ...
My son receiving chemotherapy, fighting Langerhans Cell Histiocytosis!
He got diagnosed on May2014
With a rare disease called : Langerhans Cell Histiocytosis! He is very brave..
This is him getting accessed on his port on his chest with a large thick needle (although he does have numbing cream on to not feel directly) any child his age would be screaming in pain! But he is brave!!!! Let's get more awareness on LCH!
wn.com/5 Year Old Daylen Receiving Chemo For Langerhans Cell Histiocytosis
My son receiving chemotherapy, fighting Langerhans Cell Histiocytosis!
He got diagnosed on May2014
With a rare disease called : Langerhans Cell Histiocytosis! He is very brave..
This is him getting accessed on his port on his chest with a large thick needle (although he does have numbing cream on to not feel directly) any child his age would be screaming in pain! But he is brave!!!! Let's get more awareness on LCH!
- published: 24 Feb 2015
- views: 107