Cutaneous horn: A rare subtype of juvenile xanthogranuloma

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منابع مشابه

A Cutaneous Horn-Like Form of Juvenile Xanthogranuloma

Vol. 28, No. 6, 2016 783 Received August 25, 2015, Revised October 16, 2015, Accepted for publication November 5, 2015 Corresponding author: Kyung Ho Lee, Department of Dermatology, Bucheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 327 Sosa-ro, Wonmi-gu, Bucheon 14647, Korea. Tel: 82-32-340-2115, Fax: 82-32-340-2118, E-mail: [email protected] This is an O...

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Juvenile xanthogranuloma: a rare benign histiocytic disorder

Juvenile xanthogranuloma (JXG) is a rare histiocytic disorder that typically affects children. The clinical presentation of this disease is characterized by single or, rarely, multiple yellow and brown skin nodules, most often found on the face and neck. Internal organ involvement has been sporadically observed in JXG and is associated with an increased risk of serious complications. We report ...

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Juvenile Xanthogranuloma.

Juvenile xanthogranuloma is a rare disorder which may be present at birth, or appears in infancy. It can also occur in adults of all ages, appears with lesions that may be solitary or multiple nodules several millimeters in diameter. The predilection sites are head and neck, but it may occur on the extremities and trunk also. Internal organs such as lung, kidney, gastrointestinal tract etc. can...

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Juvenile xanthogranuloma: dermoscopic pattern.

Palmer and Bowling [1] have recently described the dermoscopic features in 3 cases of juvenile xanthogranuloma (JXG). A dermoscopic pattern characterized by orange-yellow background with ‘clouds’ of paler yellow deposits was observed in all patients. We have had recent occasion to observe many cases of single and multiple JXG and noted a further constant dermoscopic feature, namely branched and...

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Juvenile Xanthogranuloma: Report of a Case.

JUVENILE xanthogranuloma, also commonly known as naevoxantho-endothelioma, was first described as a skin disease in 1909 (McDonaugh, 1909), but it was not until forty years later that the first intra-ocular case was reported in America (Blank, Eglick, and Beerman, 1949). Some twenty to thirty cases have since been described (Sanders, 1962), but our case is the first to be reported in the United...

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ژورنال

عنوان ژورنال: Clinical Case Reports

سال: 2019

ISSN: 2050-0904,2050-0904

DOI: 10.1002/ccr3.2549