Thyroid Lump Study: What People With MS Should Know
By MS Buddy ·
Summarized from Endocrine pathology, Oct 2026 · PubMed. AI-generated summary. Not medical advice.
Research by André Lametti, Raja Seethala and 6 colleagues at the University of Pittsburgh Medical Center in the United States.
Key Takeaway
Certain signs in thyroid lumps may help doctors recognize tumors that are usually low risk, but this study does not change MS care.
What They Found
Researchers studied 51 removed thyroid lumps with a marker called IMP3 and compared them with 113 similar lumps without it.,Nearly all lumps with IMP3 were types of thyroid tumors considered low risk.,Under a microscope, these lumps often had a distinct mix of small and large spaces, clear-looking cells, and unusually shaped cell centers.,Another marker, called HBME-1, was absent in almost all of the IMP3 lumps tested, which may give doctors another clue when identifying them.,The groups did not show a clear difference in how long people stayed free of returning disease, but the study could not settle that question.
Who Should Care and Why
This study is about thyroid lumps, not MS, so it does not suggest a new way to treat MS or manage its symptoms.,It may matter to a person with MS who also has a thyroid lump, because the lump deserves its own careful diagnosis.,Some of these low-risk tumors can look more concerning under a microscope than they turn out to be, like a harmless-looking object casting a frightening shadow.,The signs described here may help the doctor who examines tissue identify the tumor more accurately.,If you have a thyroid lump, ask your care team what the test results mean for you rather than changing your MS treatment based on this study.
Important Considerations
This was a study of removed thyroid lumps, not a study of people with MS.,Follow-up was fairly short for most people, so the researchers cannot be sure how often these tumors may return years later.,One tumor returned after it was not fully removed, which is a reminder that your own diagnosis and treatment plan matter more than a tumor marker alone.
AI-generated summary — for informational purposes only, not medical advice
Read the original abstract
Published in Endocrine pathology by et al.. Reproduced from the PubMed record.
IGF2BP3 fusion results in IGF2BP3 (IMP3) overexpression, driving a subset of RAS-like indolent thyroid tumors, typically noninvasive follicular thyroid neoplasm with papillary like nuclear features (NIFTP) or minimally invasive encapsulated follicular variant of papillary thyroid carcinoma (miEFVPTC). These also have distinct morphologic features that have yet to be characterized. We assessed 51 cases of surgically resected thyroid nodules with IMP3 positivity or IGF2BP3 overexpression (IMP3+) and compared them to 113 pathologically similar cases without IMP3 positivity (IMP3-) within the same time frame (2014-2025). IMP3+ cases were diagnosed as miEFVPTC (n=36), NIFTP (n=14), with only one follicular adenoma. On comparative morphologic analysis, key features selectively noted in IMP3+ tumors included: low power "pale blue" optical clarity, condensation of cellularity at the nodule periphery, microfollicles interspersed between macrofollicles, perifollicular sclerosis, clear cytoplasm, perinuclear indentation by cytoplasmic vacuoles, "squared-off" nuclei, prominent single nuclear grooves, grade 3 nuclei, and background chronic lymphocytic thyroiditis. Oncocytic cytoplasm and solid/trabecular/insular growth were exclusive to the IMP3- group. Only one of 34 (2.9%) tested cases was weakly HBME-1 positive in the IMP3+ group. A multiple logistic regression model predicting IMP3 status included microfollicles interspersed between macrofollicles, clear cytoplasm, perinuclear indentation by cytoplasmic vacuoles, "squared-off" nuclei, and background chronic lymphocytic thyroiditis (AUC: 0.957, AIC: 63.858, BIC: 81.109). Adding HBME-1 status resulted in a slightly more discriminatory model (AUC: 0.987, AIC: 58.087, BIC: 78.214). No significant difference in disease-free survival was observed between IMP3+ and IMP3- groups (log-rank p = 0.348), although analysis was limited by short follow-up and very few events. In the IMP3+ group (median follow up: 23.3 months), one case recurred 155 months after incomplete excision. IMP3-positive/IGF2BP3-overexpressing thyroid tumors have a RAS-like profile and likely indolent clinical behavior. We demonstrate that they have distinct cytomorphologic features that allow for recognition. The exaggerated overt nuclear features may lead to misclassification as more aggressive subtypes (i.e. conventional). HBME-1 negativity is characteristic and can aid in recognition of IMP3+ tumors.
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