Spontaneous Regression of Infantile Hepatic Hemangioendothelioma

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منابع مشابه

Clinical features of infantile hepatic hemangioendothelioma

PURPOSE Infantile hepatic hemangioendothelioma (IHHE) is the most common type of hepatic vascular tumor in infancy. We conducted this study to review our clinical experience of patients with IHHE and to suggest management strategies. METHODS We retrospectively analyzed the medical records of 23 IHHE patients (10 males, 13 females) treated at the Asan Medical Center between 1996 and 2009. RE...

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Infantile Hepatic Hemangioendothelioma (IHHE) – An Unusual Presentation

Hepatic tumours are relatively rare in children, accounting for 1% 4% of all paediatric solid tumors, commonest amongst them are hepatoblastoma, neuroblastoma, and vascular tumors (hemangioendothelioma/haemangiomas). Infantile Hepatic hemangioendothelioma (IHHE) is classically characterised by hepatomegaly, jaundice, congestive cardiac failure with high cardiac output, skin haemangiomas, haemol...

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Infantile hepatic hemangioendothelioma: a clinicopathologic study in a Chinese population.

AIM To investigate whether the clinicopathologic features of infantile hemangioendothelioma (IHE) of the liver in a Chinese population are similar to the features observed in other races. METHODS The clinical data, radiological findings, histopathological changes and outcome of 12 cases of IHE diagnosed by the Department of Pathology, West China Hospital over the last 10 years were analyzed r...

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Infantile Hepatic Hemangioendothelioma Associated With Congestive Heart Failure

Infantile hepatic hemangioendothelioma (IHH) is rare which can regress spontaneously. Arteriovenous shunts within hemangiomas, however, may result in pulmonary artery hypertension (PAH) and congestive heart failure (CHF).The authors report 2 young infants suffering from multifocal IHH associated with CHF were both treated with glucocorticoid and transcatheter arterial embolization (TAE), but ha...

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Infantile hemangioma or kaposiform hemangioendothelioma?

We read with interest the letter sent by Yoon et al (1) about transarterial embolization of a cervicofacial hemangioma associated with Kasabach–Merritt (KM) syndrome in a premature neonate. There are some facets of the letter that warrant further comments, namely the association of the KM phenomenon with vascular tumors and the use of proper consensus-approved terminology adopted by the Interna...

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ژورنال

عنوان ژورنال: Journal of Medical Ultrasound

سال: 2013

ISSN: 0929-6441

DOI: 10.1016/j.jmu.2013.04.003