# Radiotherapy for recurrent venous malformation involving the thigh and pelvic organs while preserving organ function: a case report

**Authors:** Doyoon Kim, Jihoon Maeng, Sunghyun Nam, Hyungsoon Kim, Won Sik Ham, Seo Hee Choi, Jaeho Cho

PMC · DOI: 10.3389/fcvm.2025.1615584 · Frontiers in Cardiovascular Medicine · 2026-02-11

## TL;DR

Radiotherapy successfully treated a woman's recurring pelvic venous malformation without harming her fertility.

## Contribution

This case report highlights radiotherapy as a viable, organ-preserving treatment for complex venous malformations.

## Key findings

- Radiotherapy provided durable disease control and symptom relief over five years.
- Ovarian function was preserved, with normal anti-Müllerian hormone levels and regular menstrual cycles.
- Intensity-modulated radiotherapy reduced lesion size and improved quality of life.

## Abstract

Venous malformations (VMs) are congenital vascular anomalies that cause significant pain and dysfunction. Although surgery is the primary treatment, no standardized guidelines exist for extensive or recurrent cases in which surgery is not feasible. Additionally, the role of radiotherapy (RT) in the management of VMs remains unclear.

A 24-year-old woman with extensive, recurrent VM involving the pelvic cavity, right thigh, and buttocks underwent multiple surgeries and sclerotherapy for over 10 years; however, the disease progressed, infiltrating the pelvic organs, and posed a risk to fertility. The patient presented with severe pain, ureteral obstruction, and menstrual irregularities, all of which significantly affected her quality of life. Considering the high morbidity associated with further surgery, definitive RT was performed. The patient received intensity-modulated radiotherapy (IMRT) at a total dose of 43 Gy in 20 fractions, preceded by ovarian transposition to preserve fertility.

After the treatment, the patient experienced remarkable symptom relief, including pain resolution and improvement in menstrual regularity. Follow-up imaging over five years demonstrated a continued reduction in the lesion size. The menstrual cycles remained regular, and anti-Müllerian hormone levels remained within the normal range.

This case demonstrates the potential of RT as an effective treatment for extensive, recurrent pelvic VMs. RT achieves durable disease control while preserving ovarian function, highlighting its role as a viable alternative in select cases.

## Linked entities

- **Diseases:** venous malformation (MONDO:0003083)

## Full-text entities

- **Genes:** ACVRL1 (activin A receptor like type 1) [NCBI Gene 94] {aka ACVRLK1, ALK-1, ALK1, HHT, HHT2, ORW2}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, TEK (TEK receptor tyrosine kinase) [NCBI Gene 7010] {aka CD202B, GLC3E, TIE-2, TIE2, VMCM, VMCM1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, GNAQ (G protein subunit alpha q) [NCBI Gene 2776] {aka CMAL, G-ALPHA-q, GAQ, SWS}, AMH (anti-Mullerian hormone) [NCBI Gene 268] {aka MIF, MIS}
- **Diseases:** heterotopic ossification (MESH:D009999), arteriovenous malformation (MESH:D001165), thigh lesions (MESH:D009059), speech difficulties (MESH:D013064), VM (MESH:C563977), embolization (MESH:D004617), diarrhea (MESH:D003967), tenderness (MESH:D063806), vascular malformations (MESH:D054079), vascular pathologies (MESH:D005598), ovarian damage (MESH:D010049), gastrointestinal and urinary tract toxicity (MESH:D014570), hemangiomas (MESH:D006391), ureteral obstruction (MESH:D014517), urinary dysfunction (MESH:D001745), migraines (MESH:D008881), Vascular Anomalies (MESH:D020785), proptosis (MESH:D005094), gastrointestinal or genitourinary toxicity (MESH:D000091642), visual field defects (MESH:D005128), muscle contracture (MESH:D003286), functional impairment (MESH:D003072), intravascular coagulopathy (MESH:D004211), thrombosis (MESH:D013927), inflammation (MESH:D007249), Premature ovarian failure (MESH:D016649), skin lesions (MESH:D012871), flank pain (MESH:D021501), pain (MESH:D010146), lymphatic malformation (MESH:D008209), keloids (MESH:D007627), infertility (MESH:D007246), malignancies (MESH:D009369), sexual dysfunction (MESH:D012735), gastrointestinal toxicity (MESH:D005767), vascular lesion (MESH:D014652), thyroid ophthalmopathy (MESH:D049970), pelvic venous insufficiency (MESH:D014689), hydronephrosis (MESH:D006869), toxicities (MESH:D064420)
- **Chemicals:** aspirin (MESH:D001241), bleomycin (MESH:D001761), ROS (MESH:D017382), ethanol (MESH:D000431), anti (-), Sirolimus (MESH:D020123)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932492/full.md

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Source: https://tomesphere.com/paper/PMC12932492