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Peer-reviewedCC BY 4.0Frontiers in Immunology

Case Report: A rare case of biopsy-proven lupus nephritis complicated by Graves’ disease in a 39-year-old man

  1. 1Department of Endocrinology, Shengjing Hospital of China Medical University
  2. 2Department of Nephrology, Shengjing Hospital of China Medical University

Abstract

Hyperthyroidism and systemic lupus erythematosus (SLE) are both common diseases in internal medicine. Among them, Graves’ disease (GD) is the most frequent cause of hyperthyroidism, while lupus nephritis (LN) represents one of the most severe organ manifestations of SLE. Basic research suggests that GD and SLE may share overlapping genetic and immunological pathways; however, whether these shared mechanisms contribute to their clinical coexistence remains uncertain. Clinical studies or case reports on their coexistence are currently limited, and we cannot effectively manage cases of co-occurrence based on authoritative guidelines or expert consensus. In this study, we report a 39-year-old male patient with biopsy-proven ISN/RPS Class IV + V LN concomitant with GD. The patient was treated with a combination of glucocorticoids, mycophenolate mofetil, and hydroxychloroquine for LN, along with methimazole for GD, supplemented by symptomatic therapy including antihypertensive and heart rate controlling agents, etc. The patient demonstrated early clinical and laboratory improvement during follow-up, although the limited follow-up precluded assessment of an established renal response.

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BibTeX
@article{wang2026case,
  title = {{Case Report: A rare case of biopsy-proven lupus nephritis complicated by Graves’ disease in a 39-year-old man}},
  author = {Xichang Wang and Xiaoguang Shi and Beiru Zhang and Mi Tian},
  journal = {Frontiers in Immunology},
  year = {2026},
  month = oct,
  doi = {10.3389/fimmu.2026.1908289},
  url = {https://www.frontiersin.org/articles/10.3389/fimmu.2026.1908289/full},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Case Report: A rare case of biopsy-proven lupus nephritis complicated by Graves’ disease in a 39-year-old man
AU  - Xichang Wang
AU  - Xiaoguang Shi
AU  - Beiru Zhang
AU  - Mi Tian
PY  - 2026
DA  - 2026/10/28
JO  - Frontiers in Immunology
DO  - 10.3389/fimmu.2026.1908289
UR  - https://www.frontiersin.org/articles/10.3389/fimmu.2026.1908289/full
AB  - Hyperthyroidism and systemic lupus erythematosus (SLE) are both common diseases in internal medicine. Among them, Graves’ disease (GD) is the most frequent cause of hyperthyroidism, while lupus nephritis (LN) represents one of the most severe organ manifestations of SLE. Basic research suggests that GD and SLE may share overlapping genetic and immunological pathways; however, whether these shared mechanisms contribute to their clinical coexistence remains uncertain. Clinical studies or case reports on their coexistence are currently limited, and we cannot effectively manage cases of co-occurrence based on authoritative guidelines or expert consensus. In this study, we report a 39-year-old male patient with biopsy-proven ISN/RPS Class IV + V LN concomitant with GD. The patient was treated with a combination of glucocorticoids, mycophenolate mofetil, and hydroxychloroquine for LN, along with methimazole for GD, supplemented by symptomatic therapy including antihypertensive and heart rate controlling agents, etc. The patient demonstrated early clinical and laboratory improvement during follow-up, although the limited follow-up precluded assessment of an established renal response.
SN  - 1664-3224
ER  -