Leukoencephalopathy: unusual sonographic finding in a neonate with incontinentia pigmenti.
نویسندگان
چکیده
ncontinentia pigmenti (IP) is a rare X-linked dominant neurocutaneous syndrome chiefly involving the ectodermal tissues, such as the skin, teeth, hair, eyes, and central nervous system (CNS).1 The diagnosis is usually made when the pathognomonic skin lesions are present; these typically appear in 4 stages: erythematous vesicular rash, verrucous patches, swirling hyperpigmentation, and atrophic scarring. The exact pathogenesis and timing of neurologic involvement are not well known. It often manifests in the neonatal period with seizures paralleling the eruption of the vesicular rash.1 White matter abnormalities have been reported in IP.2–6 However, to our best knowledge, the sonographic characterization of white matter involvement has rarely been described. We report a case of IP with hyperechogenicity of the white matter on cranial sonography. The aim of this report is to suggest that IP should be considered as one etiology of leukoencephalopathy in neonates with vesicular eruption.
منابع مشابه
Diffuse cortical necrosis in a neonate with incontinentia pigmenti and an encephalitis-like presentation.
Incontinentia pigmenti is a rare neurocutaneous disorder that may present with neurologic symptoms, in addition to a characteristic vesicular rash within the first days of life. We describe a neonate girl presenting with a rash and an encephalopathy who was first thought to suffer from a viral infection and was only later recognized as being affected by incontinentia pigmenti. Cerebral MR imagi...
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Incontinentia pigmenti (IP) is an uncommon X-linked dominant genodermatosis characterized by four cutaneous stages and frequent association with dental (90%), central nervous system (33%) and ocular (35%) anomalies. The exact pathogenesis of this disorder remains unknown.Herein, we report a newborn girl with inflammatory vesiculobullous and warty skin lesions and a positive family history of IP...
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Incontinentia Pigmenti, also known as Bloch-Sulzberger syndrome, is a rare X-linked dominant disorder considered to be lethal in males. The syndrome usually presents at birth or shortly thereafter and the skin rash evolves in the classic four stages of vesicular, verrucous, hyperpigmented, and hypopigmented lesions following a blaschko linear distribution. Here we present an unusual case of Inc...
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عنوان ژورنال:
- Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine
دوره 29 5 شماره
صفحات -
تاریخ انتشار 2010