coronary aneurysm/abdominal pain

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Asymptomatic coronary aneurysms in a patient with eosinophilic granulomatosis with polyangiitis who developed a digital gangrene

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Logi sisse

A 33-year-old male with a history of bronchial asthma and allergic rhinitis was diagnosed with eosinophilic granulomatosis with polyangiitis (EGPA) eight years ago. The diagnosis was based on the presence of fever, remarkable eosinophilia, and painful digital ulcer. His signs and symptoms improved

Kawasaki's disease in northern Italy: a multicenter retrospective study of 250 patients.

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Logi sisse

OBJECTIVE To evaluate (i) the clinical course and outcome in a cohort of 250 children affected with Kawasaki disease (KD) in northern Italy; (ii) the prevalence of coronary aneurysms and their correlation with treatment; and (iii) the prevalence of incomplete and atypical KD in the series as a

Aneurysm of the right atrial appendage in an elderly patient.

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Logi sisse

A 72-year-old male patient presented with a complaint of pain in both legs during short walks of less than 50 meters. Physical examination showed weak arterial pulses in both lower extremities. Electrocardiographic and telecardiographic evaluations were normal. A previous abdominal ultrasonography

[Effective combination therapy of plasma exchange and subsequent cyclophosphamide pulses for catastrophic antiphospholipid antibody syndrome: a case report].

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Logi sisse

A 7-year-old girl with catastrophic antiphospholipid antibody syndrome was described. She firstly admitted to the local hospital with the complaints of persistent fever and abdominal pain, and was diagnosed as systemic lupus erythematosus with the laboratory findings as follows; positive for

Kawasaki disease triggered by parvovirus infection: an atypical case report of two siblings.

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Logi sisse

There are reports of the familial occurrence of Kawasaki disease but only a few reports described Kawasaki disease in siblings. However, the familial cases were not simultaneous. In these patients the idea of infective agents as trigger must be

Myocardial infarction in Kawasaki disease: clinical analyses in 195 cases.

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Logi sisse

We analyzed clinical data from 195 patients (141 boys) with myocardial infarction complicating Kawasaki disease, collected from 74 major hospitals in Japan. The myocardial infarction usually occurred within the first year of illness, but 27.2% of the patients had myocardial infarction more than 1

Kawasaki disease shock syndrome: Unique and severe subtype of Kawasaki disease.

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Logi sisse

BACKGROUND Kawasaki disease shock syndrome (KDSS) is an uncommon presentation of Kawasaki disease (KD). KDSS has been associated with more severe markers of inflammation, coronary abnormalities and i.v. immunoglobulin (IVIG) resistance. METHODS A retrospective, descriptive study of children with

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Herbal & Natural Medicine

Kõige täiuslikum ravimtaimede andmebaas, mida toetab teadus

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