Mode
Text Size
Log in / Sign up

KAT6B::KANSL1 fusion identified in uterine mesenchymal neoplasm with no recurrence at 8 monthsA rare genetic fusion explains a woman's uterine growth

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Interpret KAT6B::KANSL1 fusion as a preliminary finding; 8-month follow-up is insufficient for prognosis.

This is a single case report of a 47-year-old woman with a 7-year history of a presumed uterine fibroid. She underwent laparoscopic myomectomy and completion hysterectomy with bilateral salpingo-oophorectomy, and received letrozole. Molecular analysis identified an in-frame KAT6B::KANSL1 fusion involving KAT6B exon 3 and KANSL1 exon 11. At 8 months of follow-up, no clinical or radiologic recurrence was detected.

The report focuses on the molecular finding and short-term recurrence assessment. No effect size, absolute numbers, p-values, or confidence intervals were reported. Safety data, including adverse events, serious adverse events, discontinuations, and tolerability, were not reported. Funding and conflicts of interest were also not reported.

The authors note that the limited follow-up does not permit conclusions regarding long-term biological behavior or endocrine treatment benefit. Practice relevance was not reported. The findings are exploratory and hypothesis-generating only, and should not be used to guide clinical decisions.

How this fits prior evidence

This case report describes a KAT6B::KANSL1 fusion in a uterine mesenchymal neoplasm, a molecular finding not addressed in prior coverage. Prior items focused on letrozole in ovulation disorder FET, short-term preoperative letrozole in ER+/HER2- breast cancer, AI plus celecoxib in ER-positive breast cancer, ctDNA dynamics in advanced HR+ HER2- breast cancer, and HOMA-IR in PCOS. This report does not confirm or extend those findings; it addresses a distinct disease context and provides no comparative or long-term outcome data.

Imagine living for years with a growth in your uterus, only to have it labeled as a common fibroid. For one 47-year-old woman, this was her reality for seven years. However, surgery and testing eventually revealed that her condition was actually a rare type of growth called a uterine mesenchymal neoplasm.

Doctors identified a specific genetic change called a KAT6B::KANSL1 fusion. This is a piece of genetic material that joined together in a way it shouldn't have. This discovery helps clarify why her growth behaved differently than a typical fibroid. After her surgery and a period of treatment with letrozole, no signs of the growth returned during an 8-month follow-up.

While this case provides a clear look at how genetics can change a diagnosis, it is just one case. Because the follow-up period was only 8 months, doctors cannot yet say how the condition will behave over many years or how well the hormone treatment will work in the long run.

What this means for you:
A rare genetic fusion was found in a patient whose growth was previously thought to be a common fibroid.

Common questions

What was the specific cause of the growth?

Doctors found a specific genetic change called a KAT6B::KANSL1 fusion. This involves a piece of genetic material joining together at a specific point. This finding helped identify the growth as a uterine mesenchymal neoplasm rather than a common fibroid.

Was the condition still present after treatment?

After the patient underwent surgery and was treated with letrozole, no clinical or radiologic recurrence of the growth was detected during an 8-month follow-up period.

Is this a common finding for uterine growths?

This was a single case report. Because it is a rare genetic fusion, it is not a common finding, and the short follow-up period means more information is needed to understand long-term behavior.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedOct 2026
View Original Abstract ↓
KAT6B/A::KANSL1 fusion-positive uterine mesenchymal neoplasms are rare and may show overlapping endometrial stromal and smooth muscle features. We report a 47-year-old woman with regular menses, no dysmenorrhea, and a 7-year history of a presumed uterine fibroid. She underwent laparoscopic myomectomy at an outside hospital in November 2024. The fragmented specimen was interpreted as an endometrial stromal tumor with smooth muscle differentiation, but the tumor–myometrium interface could not be assessed, and an endometrial stromal nodule could not be distinguished from low-grade endometrial stromal sarcoma. Subsequent pelvic magnetic resonance imaging showed postoperative changes, possible residual leiomyomas, and heterogeneous enhancement at the uterine fundus. Pelvic computed tomography showed heterogeneous uterine enhancement without definite extrauterine disease. Because the original specimen was fragmented and a potentially malignant uterine mesenchymal neoplasm could not be excluded, completion hysterectomy with bilateral salpingo-oophorectomy was performed. The hysterectomy specimen contained multiple residual intramyometrial nodules with marked regional heterogeneity. One component showed fascicular smooth muscle morphology and diffuse desmin and h-caldesmon expression, whereas other nodules showed tongue-like myometrial infiltration, focal intravascular growth, spiral arteriole-like vessels, and diffuse ER, PR, CD10, and SMA expression. Whole-transcriptome sequencing identified an in-frame KAT6B::KANSL1 fusion involving KAT6B exon 3 and KANSL1 exon 11. Because the tumor expressed ER and PR, postoperative letrozole was administered for 30 days, after which surveillance was selected following review of the final pathologic and molecular findings. At 8 months after completion surgery, no clinical or radiologic recurrence was detected; this limited follow-up does not permit conclusions regarding long-term biological behavior or endocrine treatment benefit.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.