Publication:
A rare case of cutaneous vascular phenomena and fulminant cardiac involvement in paediatric multisystem inflammatory syndrome in children following asymptomatic COVID-19 exposure in a 7-year-old child

dc.contributor.authorTorun E.
dc.contributor.authorKaradoğan M. T.
dc.contributor.authorYURTSEVER İ.
dc.contributor.authorSert A.
dc.contributor.authorYOZGAT Y.
dc.date.accessioned2025-09-10T21:50:25Z
dc.date.issued2025-01-01
dc.description.abstractMultisystem inflammatory syndrome in children is a systemic disorder that involves incessant fever, extreme inflammation, and organ dysfunction, which is at first associated with exposure to COVID-19. This case, however, presents a unique twist. A 7-year-old paediatric patient, initially presenting with fever and rash, exhibited a polymorphous rash varying from macular to maculopapular, with a cutis marmorata-like appearance, particularly on the extremities. What followed was a rapid deterioration, with the patient developing tachypnoeic respiration and moderate hypotension (80/35 mm Hg). Elevated D-dimer levels, troponin, ferritin, a low platelet count, a low albumin level, and lymphopenia were detected, further complicating the case. This unique case challenges our understanding of multisystem inflammatory syndrome in children and prompts further investigation. Despite the severity of the case, the patient’s condition improved significantly with treatment. The patient’s COVID-19 polymerase chain reaction test was negative, but the COVID-19 immunoglobulin G test was positive. Transthoracic echocardiography demonstrated a mild/moderate systolic dysfunction of the left ventricular (Ejection fraction 52%, SF 25%), echogenicity of coronary vessels, and a first-degree mitral insufficiency was detected. Thorax CT showed pulmonary oedema. Milrinone and noradrenaline were promptly started for hemodynamic support. Intravenous immunoglobulin, methylprednisolone, favipiravir, and anakinra were started for his treatment. On the second day of hospitalisation, the patient’s condition was ameliorated. On the 10th day of hospitalisation, the patient was discharged from the hospital, marking a successful recovery from a complex and severe case. This successful recovery serves as a beacon of hope in the management of multisystem inflammatory syndrome in children.
dc.identifier.citationTorun E., Karadoğan M. T., YURTSEVER İ., Sert A., YOZGAT Y., "A rare case of cutaneous vascular phenomena and fulminant cardiac involvement in paediatric multisystem inflammatory syndrome in children following asymptomatic COVID-19 exposure in a 7-year-old child", Cardiology in the Young, 2025
dc.identifier.doi10.1017/s1047951125101431
dc.identifier.issn1047-9511
dc.identifier.pubmed40785500
dc.identifier.scopus105013030814
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105013030814&origin=inward
dc.identifier.urihttps://hdl.handle.net/20.500.12645/41147
dc.identifier.wosWOS:001546663800001
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectKardiyoloji
dc.subjectSağlık Bilimleri
dc.subjectMedicine
dc.subjectInternal Medicine Sciences
dc.subjectChild Health and Diseases
dc.subjectCardiovascular
dc.subjectHealth Sciences
dc.subjectKlinik Tıp (Med)
dc.subjectKlinik Tıp
dc.subjectKalp ve Kalp Damar Sistemleri
dc.subjectPediatri
dc.subjectClinical Medicine (Med)
dc.subjectClinical Medicine
dc.subjectCardiac & Cardiovascular Systems
dc.subjectPediatrics
dc.subjectPediatri, Perinatoloji ve Çocuk Sağlığı
dc.subjectKardiyoloji ve Kardiyovasküler Tıp
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectCardiology and Cardiovascular Medicine
dc.subjectcardiogenic shock
dc.subjectCOVID-19
dc.subjectmultisystem inflammatory syndrome in children
dc.subjectpaediatrics
dc.titleA rare case of cutaneous vascular phenomena and fulminant cardiac involvement in paediatric multisystem inflammatory syndrome in children following asymptomatic COVID-19 exposure in a 7-year-old child
dc.typeArticle
dspace.entity.typePublication
local.avesis.id820a16f4-9c17-47b7-94ee-1f1fa2cdc182

Files