TY - JOUR
T1 - A case of neuron-derived neurotrophic factor-positive, syphilis-related membranous nephropathy that achieved spontaneous remission
AU - Yoshida, Yuko
AU - Ueki, Kenji
AU - Matsukuma, Yuta
AU - tsuchimoto, akihiro
AU - Ataka, Eri
AU - Okamoto, Hirofumi
AU - Torisu, Kumiko
AU - Hara, Yuichirou
AU - Ikeda, Hirofumi
AU - Kitazono, Takanari
AU - Nakano, Toshiaki
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Japanese Society of Nephrology 2024.
PY - 2024
Y1 - 2024
N2 - Neuron-derived neurotrophic factor (NDNF) was discovered as a target antigen in membranous nephropathy (MN) caused by syphilis. However, there have been few reports of NDNF-positive MN in Japan. A 19-year-old female patient was admitted to our hospital with nephrotic syndrome and acute kidney injury. After admission, she presented with a skin rash and was serologically positive for syphilis. Kidney biopsy showed MN positive not only for immunoglobulin (Ig) G, but also for IgA and complement C1q. IgG subclass analysis revealed positivity for IgG1 and IgG3. Immunohistochemistry for glomerular NDNF was positive, and a diagnosis of syphilis-related MN was confirmed. Prior to treatment of the infection, her urinary protein decreased to achieve complete remission and her kidney function improved. Benzylpenicillin was administered, and no recurrence of nephrotic syndrome or kidney dysfunction was observed thereafter. This case illustrates the importance of considering syphilis infection when encountering a case of nephrotic syndrome with skin rash. In addition, urinalysis of syphilitic patients should be performed to avoid missing MN that may be in spontaneous remission. Further elucidation of the pathogenesis of NDNF-positive, syphilis-related MN in Japan is needed.
AB - Neuron-derived neurotrophic factor (NDNF) was discovered as a target antigen in membranous nephropathy (MN) caused by syphilis. However, there have been few reports of NDNF-positive MN in Japan. A 19-year-old female patient was admitted to our hospital with nephrotic syndrome and acute kidney injury. After admission, she presented with a skin rash and was serologically positive for syphilis. Kidney biopsy showed MN positive not only for immunoglobulin (Ig) G, but also for IgA and complement C1q. IgG subclass analysis revealed positivity for IgG1 and IgG3. Immunohistochemistry for glomerular NDNF was positive, and a diagnosis of syphilis-related MN was confirmed. Prior to treatment of the infection, her urinary protein decreased to achieve complete remission and her kidney function improved. Benzylpenicillin was administered, and no recurrence of nephrotic syndrome or kidney dysfunction was observed thereafter. This case illustrates the importance of considering syphilis infection when encountering a case of nephrotic syndrome with skin rash. In addition, urinalysis of syphilitic patients should be performed to avoid missing MN that may be in spontaneous remission. Further elucidation of the pathogenesis of NDNF-positive, syphilis-related MN in Japan is needed.
KW - Acute kidney injury
KW - Jarisch–Herxheimer reaction
KW - Membranous nephropathy
KW - Neuron-derived neurotrophic factor
KW - Spontaneous remission
KW - Syphilis
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U2 - 10.1007/s13730-024-00960-5
DO - 10.1007/s13730-024-00960-5
M3 - Article
AN - SCOPUS:85213725996
SN - 2192-4449
JO - CEN case reports
JF - CEN case reports
ER -