# Case Report: A patient with metastatic fumarate hydratase-deficient renal cell carcinoma associated with leiomyomatosis: real-world clinical insights on systemic therapy and liver-directed SBRT

**Authors:** Huili James Chong, Alastair Murray, Kwang Jeat Chong

PMC · DOI: 10.3389/fonc.2026.1729830 · Frontiers in Oncology · 2026-02-18

## TL;DR

This case report details the treatment journey of a rare kidney cancer patient, highlighting challenges in managing the disease and the role of combined therapies.

## Contribution

The paper provides real-world clinical insights into systemic therapy and liver-directed SBRT for a rare renal cancer subtype.

## Key findings

- The patient achieved a favorable response to bevacizumab and erlotinib but experienced renal impairment.
- SBRT was effectively used during a treatment pause to target liver metastases.
- Multidisciplinary collaboration is crucial for managing this rare tumor.

## Abstract

Fumarate hydratase-deficient renal cell carcinoma is a rare type of renal cell carcinoma often associated with hereditary leiomyomatosis and renal cell carcinoma syndrome. These tumors tend to exhibit an aggressive behavior and metastasize at an early stage. We describe the case of a 41-year-old woman of Chinese ethnicity who presented with progressive left flank pain and macroscopic hematuria. Computed tomography (CT) scan of the abdomen showed a large renal mass occupying the entire left kidney, left renal vein and inferior vena cava (IVC) tumor thrombus extension, left renal hilar lymphadenopathy, and indeterminate iliac bony and multiple large uterine fibroids. The patient underwent radical nephrectomy, caval thrombectomy and IVC reconstruction, total abdominal hysterectomy, and bilateral salpingo-oophorectomies. Histopathological examination revealed metastatic fumarate hydratase-deficient renal cell carcinoma associated with uterine leiomyomatosis with R1 resection margin at IVC. Owing to the lack of uniformly agreed guidelines for the management of this tumor, close surgical surveillance was advised. The patient subsequently developed postoperative liver metastases and sought self-funded medical care abroad. She subsequently received bevacizumab and erlotinib and achieved a favorable response. However, the patient experienced renal impairment with proteinuria following treatment, and the next cycle of systemic therapy was delayed. During this pause, we proceeded with stereotactic body radiation therapy (SBRT) to the remaining solitary liver metastasis. This case illustrates the practical challenges faced in treating fumarate hydratase-deficient renal cell carcinoma, including the lack of established systemic treatment guidelines and management of treatment-related adverse events. It highlights the value of integrating radiotherapy during interruptions in systemic therapy and the importance of multidisciplinary collaboration in this rare tumor.

## Linked entities

- **Chemicals:** erlotinib (PubChem CID 176870)

## Full-text entities

- **Genes:** FH (fumarate hydratase) [NCBI Gene 2271] {aka FMRD, HLRCC, HsFH, LRCC, MCL, MCUL1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, VIM (vimentin) [NCBI Gene 7431], VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, GATA3 (GATA binding protein 3) [NCBI Gene 2625] {aka HDR, HDRS}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, PAX8 (paired box 8) [NCBI Gene 7849] {aka PAX-8}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** proteinuria (MESH:D011507), Tumor necrosis (MESH:D009369), kidney tumors (MESH:D007680), rhabdoid (MESH:D018335), lymphopenia (MESH:D008231), renal (MESH:D006030), bony lesion (MESH:D000070896), inferior vena cava (IVC) tumor thrombus (MESH:C563013), bony (MESH:D018213), metabolic acidosis (MESH:D000138), cysts (MESH:D003560), hypertriglyceridemia (MESH:D015228), FH deficient (MESH:C538191), RCC (MESH:D002292), dominant (MESH:C566739), renal mass (MESH:C536030), Uterine leiomyomas (OMIM:150699), cutaneous leiomyomatosis (MESH:D018231), iliac bone lesion (MESH:D001847), Hypodense lesion (MESH:C565408), renal vein tumor thrombus (MESH:D013927), liver metastases (MESH:D009362), renal impairment (MESH:D007674), musculoskeletal back pain (MESH:D059352), abdominal and pelvic varices (MESH:D014648), Hypodense liver lesion (MESH:D008107), fibroids (MESH:D007889), lymphadenopathy (MESH:D008206), acneiform rash (MESH:D005076), anemia (MESH:D000740), HLRCC (MESH:C535516), iliac lesion (MESH:D017543), diarrhea (MESH:D003967), deficient (MESH:D007153), hematuria (MESH:D006417), blood (MESH:D006402), flank pain (MESH:D021501)
- **Chemicals:** Quinapril (MESH:D000077583), nitrite (MESH:D009573), fumarate (MESH:D005650), alcohol (MESH:D000438), bilirubin (MESH:D001663), Losartan (MESH:D019808), bevacizumab (MESH:D000068258), ketones (MESH:D007659), FDG (MESH:D019788), creatinine (MESH:D003404), glucose (MESH:D005947), erlotinib (MESH:D000069347), 2SC (MESH:C511650), sodium bicarbonate (MESH:D017693), tislelizumab (MESH:C000707970), 2-succincysteine (-), lenvatinib (MESH:C531958), axitinib (MESH:D000077784), sintilimab (MESH:C000632826)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956536/full.md

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Source: https://tomesphere.com/paper/PMC12956536