-
Je něco špatně v tomto záznamu ?
Protracted febrile myalgia syndrome in children with familial Mediterranean fever - systematic review and a case report
T. Hospach, F. Blankenburg, A. Heinkele, T. von Kalle, Y. Uziel, T. Kallinich, K. Rücklová
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu kazuistiky, časopisecké články, systematický přehled
NLK
BioMedCentral
od 2007-12-01
BioMedCentral Open Access
od 2007
Directory of Open Access Journals
od 2007
Free Medical Journals
od 2007
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2007-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2003
Springer Nature OA/Free Journals
od 2007-12-01
- MeSH
- dítě MeSH
- familiární středomořská horečka * komplikace diagnóza MeSH
- horečka * diagnóza etiologie MeSH
- lidé MeSH
- magnetická rezonanční tomografie metody MeSH
- myalgie * diagnóza etiologie MeSH
- syndrom MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- systematický přehled MeSH
INTRODUCTION: Protracted febrile myalgia syndrome (PFMS) is a rare manifestation of familial Mediterranean fever (FMF), characterized by myalgia, fever and elevated inflammatory markers lasting several weeks. As the hallmark of FMF are short episodes of disease symptoms, the long duration of PFMS may lead to a delayed diagnosis and treatment. OBJECTIVES: 1. To perform a review of literature and rheumatology textbooks focused on clinical features and treatment of PFMS in children. 2. To present our own case. METHODS: All articles in Pub Med generated using the keywords "protracted febrile myalgia" and information on PFMS in seven rheumatology textbooks were collected. The systematic review was supplemented with our own case presentation. RESULTS: In total, 18 articles with 78 pediatric patients (including our own) were retrieved. More than half of the patients presented with PFMS as the first manifestation of FMF. All complained of myalgia, 65% of abdominal pain and 26% had a rash. Corticosteroids (CS) were effective in 77%. In all CS-refractory cases, anakinra was shown efficient. MRI was used in 5 patients and showed myositis in all of them. The scrutiny of seven rheumatology textbooks showed that PFMS presenting with myalgia was mentioned in six. Possible accompanying symptoms were described only once, the long duration of symptoms twice, the efficacy of corticosteroids three times and anakinra only once. The presented 6 year old patient manifested with fever, myalgia, abdominal pain and petechial rash lasting 6 weeks. She had undergone multiple diagnostic procedures before her parents mentioned a positive family history for FMF. The subsequent genetic testing confirmed a homozygosity for M694V pathogenic variant in the MEFV gene. CONCLUSION: The long duration of PFMS may be misleading to clinicians especially if PFMS occurs at manifestation of FMF. The fact that more than half of the reported patients experienced PFMS as the presenting symptom of FMF is one of the key findings of our study. Our case presentation demonstrates the importance of genetic testing early in suspected autoinflammatory diseases. Furthermore, MRI may be an important diagnostic tool showing myositis in PFMS.
Charité University Medicine Berlin Germany
Charles University Prague Czech Republic
Faculty of Medicine Tel Aviv University Tel Aviv Israel
Radiologic Institute Olgahospital Klinikum Stuttgart Stuttgart Germany
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24018948
- 003
- CZ-PrNML
- 005
- 20241024111155.0
- 007
- ta
- 008
- 241015s2024 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1186/s12969-024-01019-6 $2 doi
- 035 __
- $a (PubMed)39256780
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Hospach, Toni $u Centre for Pediatric Rheumatology, Olgahospital Klinikum Stuttgart, Kriegsbergstr. 60, Stuttgart, 70174, Germany
- 245 10
- $a Protracted febrile myalgia syndrome in children with familial Mediterranean fever - systematic review and a case report / $c T. Hospach, F. Blankenburg, A. Heinkele, T. von Kalle, Y. Uziel, T. Kallinich, K. Rücklová
- 520 9_
- $a INTRODUCTION: Protracted febrile myalgia syndrome (PFMS) is a rare manifestation of familial Mediterranean fever (FMF), characterized by myalgia, fever and elevated inflammatory markers lasting several weeks. As the hallmark of FMF are short episodes of disease symptoms, the long duration of PFMS may lead to a delayed diagnosis and treatment. OBJECTIVES: 1. To perform a review of literature and rheumatology textbooks focused on clinical features and treatment of PFMS in children. 2. To present our own case. METHODS: All articles in Pub Med generated using the keywords "protracted febrile myalgia" and information on PFMS in seven rheumatology textbooks were collected. The systematic review was supplemented with our own case presentation. RESULTS: In total, 18 articles with 78 pediatric patients (including our own) were retrieved. More than half of the patients presented with PFMS as the first manifestation of FMF. All complained of myalgia, 65% of abdominal pain and 26% had a rash. Corticosteroids (CS) were effective in 77%. In all CS-refractory cases, anakinra was shown efficient. MRI was used in 5 patients and showed myositis in all of them. The scrutiny of seven rheumatology textbooks showed that PFMS presenting with myalgia was mentioned in six. Possible accompanying symptoms were described only once, the long duration of symptoms twice, the efficacy of corticosteroids three times and anakinra only once. The presented 6 year old patient manifested with fever, myalgia, abdominal pain and petechial rash lasting 6 weeks. She had undergone multiple diagnostic procedures before her parents mentioned a positive family history for FMF. The subsequent genetic testing confirmed a homozygosity for M694V pathogenic variant in the MEFV gene. CONCLUSION: The long duration of PFMS may be misleading to clinicians especially if PFMS occurs at manifestation of FMF. The fact that more than half of the reported patients experienced PFMS as the presenting symptom of FMF is one of the key findings of our study. Our case presentation demonstrates the importance of genetic testing early in suspected autoinflammatory diseases. Furthermore, MRI may be an important diagnostic tool showing myositis in PFMS.
- 650 _2
- $a dítě $7 D002648
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a familiární středomořská horečka $x komplikace $x diagnóza $7 D010505
- 650 12
- $a horečka $x diagnóza $x etiologie $7 D005334
- 650 _2
- $a magnetická rezonanční tomografie $x metody $7 D008279
- 650 12
- $a myalgie $x diagnóza $x etiologie $7 D063806
- 650 _2
- $a syndrom $7 D013577
- 655 _2
- $a kazuistiky $7 D002363
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a systematický přehled $7 D000078182
- 700 1_
- $a Blankenburg, Friederike $u Centre for Pediatric Rheumatology, Olgahospital Klinikum Stuttgart, Kriegsbergstr. 60, Stuttgart, 70174, Germany
- 700 1_
- $a Heinkele, Anita $u Centre for Pediatric Rheumatology, Olgahospital Klinikum Stuttgart, Kriegsbergstr. 60, Stuttgart, 70174, Germany
- 700 1_
- $a von Kalle, Thekla $u Radiologic Institute, Olgahospital Klinikum Stuttgart, Stuttgart, Germany
- 700 1_
- $a Uziel, Yosef $u Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
- 700 1_
- $a Kallinich, Tillmann $u Charité, University Medicine, Berlin, Germany
- 700 1_
- $a Rücklová, Kristina $u Centre for Pediatric Rheumatology, Olgahospital Klinikum Stuttgart, Kriegsbergstr. 60, Stuttgart, 70174, Germany. k.ruecklova@klinikum-stuttgart.de $u Charles University, Prague, Czech Republic. k.ruecklova@klinikum-stuttgart.de $1 https://orcid.org/0000000245184881
- 773 0_
- $w MED00165373 $t Pediatric rheumatology online journal $x 1546-0096 $g Roč. 22, č. 1 (2024), s. 85
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39256780 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20241015 $b ABA008
- 991 __
- $a 20241024111149 $b ABA008
- 999 __
- $a ok $b bmc $g 2201662 $s 1230921
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 22 $c 1 $d 85 $e 20240910 $i 1546-0096 $m Pediatric rheumatology online journal $n Pediatr Rheumatol Online J $x MED00165373
- LZP __
- $a Pubmed-20241015