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Challenges in diagnosing COVID-19 related disease in pediatric patients with rheumatic disease.
Sener, Seher; Basaran, Ozge; Lacinel Gurlevik, Sibel; Kaya Akca, Ummusen; Atalay, Erdal; Kasap Cuceoglu, Muserref; Balik, Zeynep; Batu, Ezgi Deniz; Bilginer, Yelda; Ozsurekci, Yasemin; Ozen, Seza.
  • Sener S; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Basaran O; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Lacinel Gurlevik S; Division of Pediatric Infectious Diseases, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Kaya Akca U; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Atalay E; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Kasap Cuceoglu M; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Balik Z; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Batu ED; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Bilginer Y; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
  • Ozsurekci Y; Division of Pediatric Infectious Diseases, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Ozen S; Division of Pediatric Rheumatology, Department of Pediatrics, Hacettepe University, Ankara, Ankara, Turkey.
Mod Rheumatol ; 32(6): 1108-1113, 2022 Oct 15.
Article in English | MEDLINE | ID: covidwho-1546003
ABSTRACT

OBJECTIVES:

Multisystem inflammatory syndrome in children (MIS-C) is a rare but severe condition associated with coronavirus disease 2019. Here we aimed to raise awareness for the symptoms of MIS-C in patients with rheumatic diseases, emphasizing the challenges of the differential features.

METHODS:

We retrospectively evaluated the demographic and clinical characteristics, laboratory and imaging findings, treatments, and outcomes of six MIS-C patients with previous rheumatic disease.

RESULTS:

Three of the patients had familial Mediterranean fever (FMF), one had juvenile dermatomyositis, one had systemic juvenile idiopathic arthritis (JIA), and another patient had oligoarticular JIA. All FMF patients presented with fever and abdominal pain, two also had chest pain. The patient with systemic JIA presented with fever, rash, and myalgia. All patients had elevated inflammatory markers and high d-dimer levels. Chest imaging of two FMF patients showed infiltrations compatible with pneumonia. One FMF patient had mildly decreased systolic functions with a shortening fraction of 48% in his echocardiography. Intravenous immunoglobulin and methylprednisolone were administered to all patients. Anakinra was given to four patients.

CONCLUSIONS:

Clinical and laboratory signs of MIS-C may overlap with the findings of various rheumatic diseases, and this may cause a delay in diagnosis.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Familial Mediterranean Fever / Arthritis, Juvenile / Rheumatic Diseases / Collagen Diseases / COVID-19 Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Child / Humans Language: English Journal: Mod Rheumatol Year: 2022 Document Type: Article Affiliation country: Mr

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Familial Mediterranean Fever / Arthritis, Juvenile / Rheumatic Diseases / Collagen Diseases / COVID-19 Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Child / Humans Language: English Journal: Mod Rheumatol Year: 2022 Document Type: Article Affiliation country: Mr