Evidence map›Paper›PMID 35585974›Full record

ArticleFrontiers in immunology2022

The First Case Report of Preschool-Onset SS/SLE Coexisting With NMOSD of Chinese Origin.

Liqun Liu, Li Tang, Lu Zhang, Xingfang Li, Peng Huang, Jie Xiong, Yangyang Xiao, Lingjuan Liu

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Liqun LiuDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Li TangDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Lu ZhangDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Xingfang LiDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Peng HuangDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Jie XiongDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Yangyang XiaoDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Lingjuan LiuDepartment of Pediatrics, The Second Xiangya Hospital of Central South University, Changsha, China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune connective tissue disease (CTD), the main features of which are multiple serum autoantibodies and extensive involvement of multiple systems. The onset age of patients varies from childhood to middle age, with nearly 1/5 in childhood. Sjogren's syndrome (SS) is also an autoimmune disease characterized by high-degree lymphocytic infiltration of exocrine glands, usually occurring in middle-aged and older women, and rarely in childhood. Neuromyelitis optica spectrum disorder (NMOSD) is an immune-mediated inflammatory demyelinating disease of the central nervous system (CNS) mainly involving the optic nerve and spinal cord. The coexistence of NMOSD and SLE and/or SS is well recognized by both neurologists and rheumatologists, but cases in children have been rarely reported. In this paper, we reported a case of a girl with onset at age 5 clinically featured by recurrent parotid gland enlargement, pancytopenia, hypocomplementemia, multiple positive serum antibodies, and cirrhosis. She was initially diagnosed with SS/SLE overlap syndrome at age 5. Four years later, the patient suffered a sudden vision loss and was examined to have positive AQP4 antibodies in serum and cerebrospinal fluid (CSF), and long segmental spinal swelling, in line with the diagnostic criteria for NMOSD. Up to now, the current patient is of the youngest onset age to develop SS/SLE coexisting with NMOSD, also with cirrhosis. It is important for clinicians to be aware of the possibility of CTDs coexisting with NMOSD in children, especially in those with positive anti-multiple autoantibodies, and to decrease the rate of missed diagnosis.

Indexed as

Connective Tissue DiseasesLupus Erythematosus, SystemicNeuromyelitis OpticaSjogren's SyndromeAgedAutoantibodiesChildChild, PreschoolChinaFemaleHumansLiver CirrhosisMiddle AgedAutoantibodiesAQP-4child SS/SLE overlap syndrome with NMOSDneuromyelitis optica spectrum disorderSjogren’s syndromesystemic lupus erythematosus

Identifiers

PMID35585974
PMCPMC9108358
OpenAlexW4225265424

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.