An atypical presentation of Kawasaki disease: a 10-year-old boy with acute exudative tonsillitis and bilateral cervical lymphadenitis

Yap, C. K.; Lin, Lung–Huang; Wang, Nan-Koong

doi:10.6061/clinics/2012(06)25

Cited by 17 publications

(4 citation statements)

References 13 publications

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“…The differential diagnosis for neoplastic neck masses include benign tumors, such as haemangiomas, teratomas, plexiform neurofibromas, juvenile nasopharyngeal angiofibromas (JNA), and Langerhans cell histiocytosis (LCH), as well as malignant tumors, such as Hodgkin's lymphoma (HL) and non-Hodgkin's lymphomas (NHL), rhabdomyosarcoma (RMS), thyroid malignances, nasopharyngeal carcinomas (NPC), salivary gland tumors, neuroblastoma, and metastasis. 4 5 6…”

Section: Discussionmentioning

confidence: 99%

Chondromesenchymal Hamartoma in Ectopic Thyroid Tissue in a Neonate

Szepesi

Juhász

Kover

et al. 2019

European J Pediatr Surg Rep

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Section: Discussionmentioning

confidence: 99%

Chondromesenchymal Hamartoma in Ectopic Thyroid Tissue in a Neonate

Szepesi

Juhász

Kover

et al. 2019

European J Pediatr Surg Rep

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“…Yaygın veya 1,5 cm'den küçük LAP, bilateral servikal lenfadenopati, aksiller veya inguinal LAP'ta olabilir 9,12,20,66,69 .…”

Section: Diğer Organ Ve Sistem Tutulumlarıunclassified

Kawasaki Hastalığında Görülen Sıra Dışı Klinik Durumlar

Güvenç

Oflaz

2020

Arşiv Kaynak Tarama Dergisi

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Kawasaki disease is the most frequent reason for acquired heart diseases in developed countries. The disease may develop with many clinical pictures and the most important disease-related complication is coronary arterial aneurysm. The sooner the diagnosis is made and treatment is initiated, the lower the risk for its complications to arise. Atypical Kawasaki disease is characterized by organ and system involvement, which do not clinically meet the disease criteria, are unexpected or not frequently seen under normal circumstances. Approximately 7-10% of the patients show atypical involvement. In atypical patients, coronary arterial involvement is more frequent as a result of late diagnosis. This article presents the clinical conditions that may be seen as a result of atypical Kawasaki disease in the light of literature data.

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“…But all patients do not have symptoms that meet the classic diagnostic criteria of KD. 13 Atypical KD is mostly seen in young infants less than 6 months of age, who are unfortunately at the greatest risk of developing coronary disease. These patients may have only prolonged fever as a sole clinical feature or sometimes associated with subtle clinical signs along with fever.…”

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confidence: 99%

A 3 Month Old Child with Atypical Kawasaki Disease

Salim¹,

Afroze

2021

Bangladesh J Med Sci

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Background: Kawasaki Disease (KD) is an autoimmune vasculitis of unknown etiology that occurs predominantly in infants and young children with special predilection to coronary arteries. Case Presentation: We report the case of a 3-month-old child with an atypical form of KD, characterized by prolonged fever and non- specific symptoms, who developed an aneurysm of the left anterior descending coronary artery. Conclusion: This case report underlines the challenges in recognizing atypical forms of the illness in young infants with minor features, who are at higher risk of long term cardiac complications. Bangladesh Journal of Medical Science Vol.20(3) 2021 p.665-668

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An atypical presentation of Kawasaki disease: a 10-year-old boy with acute exudative tonsillitis and bilateral cervical lymphadenitis

Cited by 17 publications

References 13 publications

Chondromesenchymal Hamartoma in Ectopic Thyroid Tissue in a Neonate

Chondromesenchymal Hamartoma in Ectopic Thyroid Tissue in a Neonate

Kawasaki Hastalığında Görülen Sıra Dışı Klinik Durumlar

A 3 Month Old Child with Atypical Kawasaki Disease

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