## Abstract ## BACKGROUND: In pediatric patients, a cutaneous nodule is usually diagnosed by performing an excisional biopsy, but fineβneedle cytology (FNC) is a safer and noninvasive diagnostic method widely used to obtain diagnostic specimens with little stress to the patient. The authors compar
Cytologic features of deep juvenile xanthogranuloma
β Scribed by Ronald T. Grenko; Joshua Z. Sickel; Catherine S. Abendroth; Robert E. Cilley
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 720 KB
- Volume
- 15
- Category
- Article
- ISSN
- 8755-1039
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β¦ Synopsis
Juvenile xanthogranuloma (JXG) is a rare lesion of the skin and deep tissues whose cytologic features have not previously been published. We report on 2 cases of JXG in patients aged 5 days and 5 yr who presented with an axillary mass and enlarged supraclavicular lymph node, respectively. Fine-needle aspiration and touch imprints made from the surgical biopsies yielded cellular specimens composed of histiocytes, multinucleated Touton-type giant cells, and variable admixtures of lymphocytes and eosinophils. One lesion was composed primarily of benignappearing histiocytes with aahixed multinucleated giant cells and a f a v lymphocytes. The second lesion consisted of a few histiocytes, occasional Touton giant cells, many lymphocytes
, and scatteredfibroblasts. The histiocytes were CD68-positive and S l Oo-nrgative. Histologic follow-up confirmed the diagnosis of juvenile xanthogranuloma. One patient was lost to follow-up: the other is alive without evidence of recurrence 1 yr afer surgery. We conclude that deep JXG has characteristic and diagnostic cytologic features.
π SIMILAR VOLUMES
## Abstract ## Background Juvenile xanthogranulomatosis (JXG) is a relatively rare macrophage proliferative disorder. It usually presents as a localized cutaneous lesion but may affect other organs. Until now it has never been described in the subglottic region of the larynx. ## Methods We repor