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Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report

RATIONALE: Detection of aquaporin-4 (AQP4) antibody in cerebrospinal fluid (CSF) was not suggested for the diagnosis of neuromyelitis opica spectrum disorders (NMOSD). However, some patients with NMOSD have only AQP4 antibody positive in CSF but not in serum with unknown cause. Besides, it is rarely...

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Autores principales: Jin, Haiqiang, Hao, Hongjun, Nan, Ding, Luo, Jingjing, Wang, Lei, Gao, Feng, Huang, Yining
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380749/
https://www.ncbi.nlm.nih.gov/pubmed/30732138
http://dx.doi.org/10.1097/MD.0000000000014229
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author Jin, Haiqiang
Hao, Hongjun
Nan, Ding
Luo, Jingjing
Wang, Lei
Gao, Feng
Huang, Yining
author_facet Jin, Haiqiang
Hao, Hongjun
Nan, Ding
Luo, Jingjing
Wang, Lei
Gao, Feng
Huang, Yining
author_sort Jin, Haiqiang
collection PubMed
description RATIONALE: Detection of aquaporin-4 (AQP4) antibody in cerebrospinal fluid (CSF) was not suggested for the diagnosis of neuromyelitis opica spectrum disorders (NMOSD). However, some patients with NMOSD have only AQP4 antibody positive in CSF but not in serum with unknown cause. Besides, it is rarely reported that NMOSD complicated with renal clear cell carcinoma. So, the relationship between AQP4-Ab, NMOSD and malignant tumors warrants an investigation. PATIENTS CONCERNS: A 31-year-old female presented in our hospital with chief complaints of urinary retention and weakness in bilateral lower extremities for more than 10 days. DIAGNOSES: The patient was diagnosed as NMOSD by neuroimaging and laboratory examination, with AQP4 antibody positive only in CSF. Besides, asymptomatic clear cell carcinoma was also found in left kidney. INTERVENTIONS: The patient underwent 2-month immunosuppressive therapy for NMOSD at first, including intravenous administration of immunoglobulin (IVIG) and methylprednisone, with oral drugs of predisone and tacrolimus. After that, Partial nephrectomy of left kidney was performed. OUTCOMES: The patient demonstrated almost complete remission for NMOSD after immunosuppressive therapy, and the renal tumor was cured by partial nephrectomy. LESSON: This case indicates that neuromyelitis optica (NMO)-IgG positive only in CSF could have potential association with the etiology of NMOSD, and renal clear cell carcinoma could be found complicated with NMOSD coincidently. Besides, it is necessary to examine NMO-IgG in CSF for patients suspicious with NMOSD, even when the serum test is negative, especially for those with complicated malignant tumors.
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spelling pubmed-63807492019-03-04 Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report Jin, Haiqiang Hao, Hongjun Nan, Ding Luo, Jingjing Wang, Lei Gao, Feng Huang, Yining Medicine (Baltimore) Research Article RATIONALE: Detection of aquaporin-4 (AQP4) antibody in cerebrospinal fluid (CSF) was not suggested for the diagnosis of neuromyelitis opica spectrum disorders (NMOSD). However, some patients with NMOSD have only AQP4 antibody positive in CSF but not in serum with unknown cause. Besides, it is rarely reported that NMOSD complicated with renal clear cell carcinoma. So, the relationship between AQP4-Ab, NMOSD and malignant tumors warrants an investigation. PATIENTS CONCERNS: A 31-year-old female presented in our hospital with chief complaints of urinary retention and weakness in bilateral lower extremities for more than 10 days. DIAGNOSES: The patient was diagnosed as NMOSD by neuroimaging and laboratory examination, with AQP4 antibody positive only in CSF. Besides, asymptomatic clear cell carcinoma was also found in left kidney. INTERVENTIONS: The patient underwent 2-month immunosuppressive therapy for NMOSD at first, including intravenous administration of immunoglobulin (IVIG) and methylprednisone, with oral drugs of predisone and tacrolimus. After that, Partial nephrectomy of left kidney was performed. OUTCOMES: The patient demonstrated almost complete remission for NMOSD after immunosuppressive therapy, and the renal tumor was cured by partial nephrectomy. LESSON: This case indicates that neuromyelitis optica (NMO)-IgG positive only in CSF could have potential association with the etiology of NMOSD, and renal clear cell carcinoma could be found complicated with NMOSD coincidently. Besides, it is necessary to examine NMO-IgG in CSF for patients suspicious with NMOSD, even when the serum test is negative, especially for those with complicated malignant tumors. Wolters Kluwer Health 2019-02-08 /pmc/articles/PMC6380749/ /pubmed/30732138 http://dx.doi.org/10.1097/MD.0000000000014229 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Research Article
Jin, Haiqiang
Hao, Hongjun
Nan, Ding
Luo, Jingjing
Wang, Lei
Gao, Feng
Huang, Yining
Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report
title Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report
title_full Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report
title_fullStr Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report
title_full_unstemmed Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report
title_short Neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: A case report
title_sort neuromyelitis optica spectrum disorder coincident with renal clear cell carcinoma: a case report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380749/
https://www.ncbi.nlm.nih.gov/pubmed/30732138
http://dx.doi.org/10.1097/MD.0000000000014229
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