Juvenile xanthogranuloma: a case report and review of the literature
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چکیده
منابع مشابه
Juvenile xanthogranuloma: case report and review of the literature.
The present case report describes a juvenile xanthogranuloma in a five-month-old girl. A circumscribed papule was located below the right nasal ala and above the right vermilion border. The lesion was histologically diagnosed as a juvenile xanthogranuloma after surgical resection of the mass. Juvenile xanthogranuloma is an uncommon diagnosis, with the head, neck and trunk being the most common ...
متن کاملCase Reports on Juvenile Xanthogranuloma and Brief Review of Literature
Juvenile xanthogranuloma is an unusual, self-limiting dermatological disorder occurring especially in infants, late childhood and rarely in adults. It belongs to the broad group of non-Langerhans cell histiocytosis. It usually appears as solitary or multiple papules, macules or nodules several millimeters in diameter with the head and neck being the most common site of involvement and vulva bei...
متن کاملSolitary juvenile xanthogranuloma in cervical spine: case report and review of the literature.
Solitary juvenile xanthogranuloma (JXG) in the spinal column is extremely rare. Here, we report and characterize the case of xanthogranuloma of the upper cervical spine. A 18-year-old male presented with neck pain for 3 months, along with progressive quadriparesis and sensory loss of 2 months duration with urinary retention. Motor examination revealed spastic quadriparesis with power of 2/5 in ...
متن کاملJuvenile 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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Malakoplakia is a rare disease with undefined etiology that has been almost exclusively reported in urology and pathology journals. We are presenting a case of colonic malakoplakia in an I8-year old young man who was referred to us with a four-year history of intermittent rectorrhagia. The pathological examination of the endoscopically resected specimen revealed pathognomonic features of ma...
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ژورنال
عنوان ژورنال: BMC Research Notes
سال: 2014
ISSN: 1756-0500
DOI: 10.1186/1756-0500-7-174