its good to see you uploading dr bolin, you are the best

Doctor ur number one in KZfaq but u need to enhance the exhibit of your slides to get professional I would like to thank u lot u helped my wife we are seeing u from Africa

I have the Langerhans cell sarcoma

great video!

Thank you Dr

what resource is best for reading medical case studies , from the most common conditions to some interesting ones ?

thank you

I need help understanding my Adult Pulmonary Langerhans Cell Hystoidcytosis. I was diagnosed in 2014. I had a small snipped of my lung taken and sent to the Mayo Clinic and they initially as well as Kaiser Permanente pathologist not diagnose me. I then had lung surgery and they determined that I have APLCH. With COVID-19 I am considered as a vulnerable part of the population and have stayed home due to being afraid of the consequences. Has there been any research pertaining to how this affects those of us who have APLCH? I am being asked to go back to the office but am scared so bad of being exposed.

Dr Bolin, please do one on ectopic pregnancy 😊

I had histiocytosis x as a child. I was diagnosed at just a few weeks old back in 1970. I have a large dent in my skull as a result of this disease.

As someone who had LCH at 15 and a relapse at 22. I've been 18 years "free of it". There was no lymph node, bone or bone marrow involvement. As it turns out, I'm type O-, can I safely donate blood?

Nice video sir

You sound like a young doctor. Langahans cell is german terminology. And I suffered with this when I was 14 in my jaw x

I love your videos and I love u more . But please dr ; we need to understand what is the exact pathophysiology for each symptoms not just in this video (since as u said ; it is poorly understood) but in all videos. I can not keep the clinical features without deep knowledge from where these features are come . Thank u again

Ty for sharing. This disease got me at age 34, it is attacking my skins an both lungs. It took a lung biopsy to diagnose it from Mayo Clinic

I had Langerhans Cell Histiocytosis and there isn’t a Dr. out there that doesn’t need to know what it is. We’re misdiagnosed and half of us are dead before you all figure it out! I was really unlucky with it and had MDS, Monosomy 7 as well. But, luckily i’m in Northern Va. and Hopkins saved my life. I suggest you look into the research Kettering and TX Children’s is doing. I didn’t do 12 months of chemo for 3 years straight for something that is small. Then the MDS. Please do yourself a favor and research it. I’m not a Dr. and I know more than you!