Evidence map›Paper›PMID 26644887›Full record

ArticleCaspian journal of internal medicine2015

Isolated thrombocytopenia; A report of a rare presentation of childhood systemic lupus erythematosus (SLE).

Ahmad Tamaddoni, Behnaz Yousefghahari, Afshin Khani, Mohammadreza Esmaeilidooki, Rahim Barari Sawadkouhi, Iraj Mohammadzadeh

Abstract readCase Reports
In one paragraph

Article in Caspian journal of internal medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ahmad TamaddoniNon-Communicable Pediatric Diseases Research Center, Babol University of Medical Sciences, Babol, Iran.
Behnaz YousefghahariDepartment of Rheumatology, Ayatollah Rouhani Hospital, Babol University of Medical Sciences, Babol, Iran.
Afshin KhaniStudent Research Committee, Babol University of Medical Sciences, Babol, Iran.
Mohammadreza EsmaeilidookiNon-Communicable Pediatric Diseases Research Center, Babol University of Medical Sciences, Babol, Iran.
Rahim Barari SawadkouhiNon-Communicable Pediatric Diseases Research Center, Babol University of Medical Sciences, Babol, Iran.
Iraj MohammadzadehNon-Communicable Pediatric Diseases Research Center, Babol University of Medical Sciences, Babol, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) has various presentations in children. Hematologic abnormalities is common in childhood onset of SLE, however, isolated thrombocytopenia is relatively rare. Thus, we present a child with isolated thrombocytopenia as a rare presentation of SLE. CASE PRESENTATION: A 12-year-old boy with chief complaints of loss of appetite, weight loss, decreased platelet count (8000/µL) and lymph node enlargement was referred to our hospital. Biopsy of lymph node showed reactive lymphadenopathy. Investigations regarding infectious disease was negative. Platelet count remained low after low dose steroidned therapy. Antinuclear antibody (ANA) and anti-double stranded DNA antibody screening tests were positive with titer of 1/62 and 1/54, respectively. Therefore, juvenile SLE was considered as the final diagnosis and raising the dose of prednisolone to 2mg/kg/day was associated with increasing platelet count to 40000/µL and a week later to 96000/µL.

conclusionThe findings of this study indicate that in cases with isolated thrombocytopenia refractory to conventional dose of steroids, SLE should be considered. This study justifies serum ANA and anti DNA assessment in children with thrombocytopenia.

Indexed as

PediatricsSystemic Lupus ErythematosusThrombocytopenia

Identifiers

PMID26644887
PMCPMC4650795

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