TP53

joined 3 days ago
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WHO: Here are 28 different histologic features, many of which are subjective in determining presence/absence let alone quantifying and then combining together to provide a tiered grade.

 

For all of you histology and clinical laboratory nerds, there is now a pathology community on mander.xyz. This will be the third pathology community on Lemmy, with the other two currently being unmaintained. Drop by for some pretty purple/pink stuff.

 

Welcome! This is the mander.xyz pathology community. The goal of this community is to provide a space for the discussion of pathology as a field as well as share interesting (non-identified) cases and approaches to diagnosis.

Interesting cases should follow this format as closely as possible (please copy/paste):

**Clinical**: [insert brief clinical information here; omit age and sex/gender unless relevant to the case, and if it is relevant, provide decade age ranges such as 0-1 years, 1-10, 11-20... 81-90. Do not give an age greater than 90.]

**Histology**: [insert either a link to a de-identified whole slide image or take de-identified histology still images and upload them as images; please use captions as appropriate.

**Special/ancillary testing**:

[Enter any special or ancillary testing here. These can sometimes spoil the diagnosis, so wrap them in spoiler text to help users self-test using the already provided information first]

**Diagnosis**:

[Enter diagnosis and explanation here]

4
submitted 3 days ago* (last edited 3 days ago) by TP53@mander.xyz to c/pathology@mander.xyz
 

Clinical: Pharyngeal mass

Histology:

Approximately 20% of the tumor looks like this.

Approximately 80% of the tumor looks like this. The mitotic rate is less than 10/10 high-power fields (at most 5 figures/1mm^2^). Necrosis was not seen.

Special/ancillary testing:

Testing performed on a region like image #2 above:

  • Smooth muscle actin: scattered positive
  • Desmin: scattered positive
  • CD34: positive (non-specific)
  • S100: negative
  • SOX10: negative
  • AE1/AE3: negative
  • STAT6: negative
  • ALK1: negative
  • beta-catenin: negative
  • MUC4: negative
  • MDM2: strongly positive in most tumor cells
  • CDK4: strongly positive in most tumor cells

Diagnosis:

Following immunohistochemical testing, we had a differential diagnosis of cellular well-differentiated liposarcoma (WDLPS) and a low-grade dedifferentiated liposarcoma (DDLPS). In the 5th edition of the WHO classification of soft tissue and bone tumors, they note that "low-grade DDLPS is virtually indistinguishable from cellular WDLPS". Which is fun to read when you're trying to sign out a case like this.

We identified a helpful publication (Graham et al., 2023) that stratified tumors like this into 1) classic WDLPS without the non-lipocytic components like we see in this case, 2) tumors with non-lipocytic areas and < 5 mitotic figures/10 HPF, and 3) tumors with non-lipocytic areas and 5 or more mitotic figures/10 HPF. They found that groups 1 and 2 performed similarly while group 3 tended to have a worse disease-specific survival compared to groups 1 and 2. Since we had at least 5 mitotic figures/10 HPF, after consultation with multiple pathologists, we felt that this was most in keeping with an FNCLCC intermediate-grade dedifferentiated liposarcoma (DDLPS).