Xanthogranulomatous osteomyelitis of the humerus in a pediatric patient with Alagille syndrome: a case report and literature review
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DOI: 10.1007/s00256-017-2707-5
Abstract: Xanthogranulomatous osteomyelitis (XO) is an exceedingly rare disease characterized by infiltration of histiocytes and foamy macrophages. Both on gross examination and on radiographs, XO can mimic malignancy. We describe the case of a 5-year-old female… read more here.
Keywords: xanthogranulomatous osteomyelitis; alagille syndrome; patient alagille; humerus ... See more keywords
An Adult Patient with Alagille Syndrome Showing Mainly Renal Failure and Vascular Abnormality without Liver Manifestation
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DOI: 10.2169/internalmedicine.4780-20
Abstract: Alagille syndrome is an inherited multisystemic disorder. We herein report an atypical case of a Japanese adult patient with Alagille syndrome. He had been diagnosed with Alagille syndrome as an infant based on a liver… read more here.
Keywords: adult patient; syndrome showing; alagille syndrome; patient alagille ... See more keywords
Epidermoid cyst in a patient with Alagille syndrome: Coincidence or connection?
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DOI: 10.25259/sni_611_2020
Abstract: Background: Alagille syndrome is a rare genetic syndrome, which arises due to defects in the Notch signaling pathway, resulting in liver, cardiopulmonary, renal, skeletal, and ophthalmologic problems, among others. Epidermoid cysts are rare congenital benign… read more here.
Keywords: cyst patient; epidermoid cyst; alagille syndrome; patient alagille ... See more keywords