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Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report

RATIONALE: A predominant Th2 immune response is suggested in the pathogenesis of both minimal change disease (MCD) and membranous nephropathy (MN); however, consecutive development of the 2 diseases in a patient is extremely rare. PATIENT CONCERN: A Japanese man, who developed nephrotic syndrome in...

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Autores principales: Kojima, Aki, Uchida, Takahiro, Sugisaki, Kentaro, Koizumi, Minami, Aoki, Ken, Mukae, Mitsuya, Yamada, Muneharu, Oda, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578765/
https://www.ncbi.nlm.nih.gov/pubmed/37832087
http://dx.doi.org/10.1097/MD.0000000000035470
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author Kojima, Aki
Uchida, Takahiro
Sugisaki, Kentaro
Koizumi, Minami
Aoki, Ken
Mukae, Mitsuya
Yamada, Muneharu
Oda, Takashi
author_facet Kojima, Aki
Uchida, Takahiro
Sugisaki, Kentaro
Koizumi, Minami
Aoki, Ken
Mukae, Mitsuya
Yamada, Muneharu
Oda, Takashi
author_sort Kojima, Aki
collection PubMed
description RATIONALE: A predominant Th2 immune response is suggested in the pathogenesis of both minimal change disease (MCD) and membranous nephropathy (MN); however, consecutive development of the 2 diseases in a patient is extremely rare. PATIENT CONCERN: A Japanese man, who developed nephrotic syndrome in his 50s and was diagnosed with MCD by renal biopsy, experienced a relapse of proteinuria approximately 3 years later during long-term steroid treatment. Since the proteinuria was resistant to increase in steroid dosage, repeat renal biopsy was performed, which revealed a small amount of glomerular subepithelial immune deposits containing immunoglobulin (Ig)G (dominantly IgG4). Immunostaining for thrombospondin-type-1-domain-containing-7A (THSD7A) was positive on the glomerular capillary walls, whereas that for other causative antigens of MN, such as phospholipase A2 receptor or neural epidermal growth factor-like 1 protein, was negative. Detailed examination found no associated condition, including malignancies and allergic diseases. DIAGNOSIS: The diagnosis of THSD7A-associated idiopathic MN was made. INTERVENTIONS AND OUTCOMES: He received further increased dose of steroids. Thereafter he maintained clinical improvement because his urinary protein level was decreased. LESSONS: The present case suggested that histological transition from MCD to MN is possible and repeat biopsy would be crucial for accurate diagnosis.
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spelling pubmed-105787652023-10-17 Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report Kojima, Aki Uchida, Takahiro Sugisaki, Kentaro Koizumi, Minami Aoki, Ken Mukae, Mitsuya Yamada, Muneharu Oda, Takashi Medicine (Baltimore) 5200 RATIONALE: A predominant Th2 immune response is suggested in the pathogenesis of both minimal change disease (MCD) and membranous nephropathy (MN); however, consecutive development of the 2 diseases in a patient is extremely rare. PATIENT CONCERN: A Japanese man, who developed nephrotic syndrome in his 50s and was diagnosed with MCD by renal biopsy, experienced a relapse of proteinuria approximately 3 years later during long-term steroid treatment. Since the proteinuria was resistant to increase in steroid dosage, repeat renal biopsy was performed, which revealed a small amount of glomerular subepithelial immune deposits containing immunoglobulin (Ig)G (dominantly IgG4). Immunostaining for thrombospondin-type-1-domain-containing-7A (THSD7A) was positive on the glomerular capillary walls, whereas that for other causative antigens of MN, such as phospholipase A2 receptor or neural epidermal growth factor-like 1 protein, was negative. Detailed examination found no associated condition, including malignancies and allergic diseases. DIAGNOSIS: The diagnosis of THSD7A-associated idiopathic MN was made. INTERVENTIONS AND OUTCOMES: He received further increased dose of steroids. Thereafter he maintained clinical improvement because his urinary protein level was decreased. LESSONS: The present case suggested that histological transition from MCD to MN is possible and repeat biopsy would be crucial for accurate diagnosis. Lippincott Williams & Wilkins 2023-10-13 /pmc/articles/PMC10578765/ /pubmed/37832087 http://dx.doi.org/10.1097/MD.0000000000035470 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5200
Kojima, Aki
Uchida, Takahiro
Sugisaki, Kentaro
Koizumi, Minami
Aoki, Ken
Mukae, Mitsuya
Yamada, Muneharu
Oda, Takashi
Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report
title Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report
title_full Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report
title_fullStr Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report
title_full_unstemmed Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report
title_short Histological transition from minimal change disease to THSD7A-associated membranous nephropathy in a patient receiving long-term steroid treatment: A case report
title_sort histological transition from minimal change disease to thsd7a-associated membranous nephropathy in a patient receiving long-term steroid treatment: a case report
topic 5200
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578765/
https://www.ncbi.nlm.nih.gov/pubmed/37832087
http://dx.doi.org/10.1097/MD.0000000000035470
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