Jump to content
In this section we have spot diagnoses posted on a daily basis since June 2010, now over 4000! You can review the archived cases and read the suggested diagnoses by users and the final comment by the contributors.
Case are uploaded each week day by 10 am UK time with the correct diagnosis will generally be posted at 8 pm UK time. Why not view the most recent spot diagnosis and proffer a diagnosis?

Case Number : Case 2901 - 19 August 2021 Posted By: Dr. Richard Carr

Please read the clinical history and view the images by clicking on them before you proffer your diagnosis.
Submitted Date :
   (0 reviews)

F18. Cheek. IDN?


  Report Record

User Feedback


Krishnakumar subramanian

Posted

Intradermal melanocytic nevus with a focus of nevoid melanoma

Share this comment


Link to comment
share_externally

BAPOMA. 
Nuclear Bap1 loss. And my first spot on morphology features.  

Share this comment


Link to comment
share_externally

I agree BAP1 inactivate nevus, BAP1 is nuclear stain and it seems to be loss of nuclear stain

Share this comment


Link to comment
share_externally

Krishnakumar subramanian

Posted

ki 67 is low and P16 is preserved, it is not a melanoma

But BAPomas have epidermal flattening with only dermal component.  I agree there is nuclear loss of BAP1

BAPOMA, will wait for Dr Carr's input

Share this comment


Link to comment
share_externally

Dr. Richard Carr

Posted

Well done for not being fooled by the cytoplasmic pattern of BAP1 staining which is uncommon (although actually quite common in mesothelioma from a little google-ing). Agree with BAPoma / MBAIT.

I suggested they enquire about the possibility of the familial syndrome.

We've seen p16 in a mainly, highly aberrant, weak cytoplasmic distribution (about 10% of SCC)  and even a case of p53 in which there was aberrant cytoplasmic staining in addition to the normal nuclear only pattern. Remarkably I've also seen a recent case of p16 (E2H6) antibody completely negative in the background internal controls (in two separate specimens from the same patient) and completely normal staining in the background internal controls for another different p16 antibody. Please look out for this as it would be a big catch to interpret the tumour as pathologically "null" when the patient has a native p16 protein which does not stain for the antibody in the expected background internal controls (melanocytes, epithelia, macrophages etc). If you do find a similar case let me know as it needs writing up.

Share this comment


Link to comment
share_externally



Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Add a comment...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...

×
×
  • Create New...