Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranuloma

Liat Samuelov, Michael Kinori, Sarah L. Chamlin, Annette Wagner, Brandi M. Kenner-Bell, Amy S. Paller, Lacey L. Kruse, Anthony J. Mancini*

*Corresponding author for this work

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Background/Objectives: Cutaneous juvenile xanthogranuloma is an uncommon, usually benign disease affecting infants and young children. Ocular and other systemic involvement have been reported, but their incidence is unclear, and the utility of routine screening is not well established. Our aim was to characterize the risk of ocular and systemic complications in children with cutaneous juvenile xanthogranuloma. Methods: In this retrospective study, we reviewed the medical charts of children with cutaneous juvenile xanthogranuloma seen at Ann and Robert H. Lurie Children's Hospital, Chicago, Illinois, between January 2000 and December 2015. A comprehensive literature review was also performed. Results: Of 338 children with cutaneous juvenile xanthogranuloma, 76 (median age 6 months, 51% female) met inclusion criteria. The most frequently involved site was the head and neck region (40%). In 39 patients (51%), there was a single lesion. Multiple lesions (>5) were evident in 20 patients (26%). Most cutaneous juvenile xanthogranulomas were micronodular (77%). None of the patients had ocular involvement. One patient had multiple asymptomatic hepatic nodules on imaging that regressed spontaneously within several months. Literature review of pediatric cutaneous juvenile xanthogranuloma series, including our cohort, revealed that the incidence of ocular manifestations is 0.24% (7/2949) and of systemic manifestations is 0.75% (22/2949). Conclusion: Cutaneous juvenile xanthogranulomas are generally limited to the skin. Because eye involvement is rare, a routine eye examination is of low yield and probably not warranted in children with no ocular or visual symptoms. New recommendations for systemic screening could not be drawn from this study.

Original languageEnglish (US)
Pages (from-to)329-335
Number of pages7
JournalPediatric Dermatology
Volume35
Issue number3
DOIs
StatePublished - May 1 2018

Fingerprint

Juvenile Xanthogranuloma
Skin
Eye Manifestations
Incidence
Neck
Retrospective Studies
Head
Pediatrics

Keywords

  • cutaneous juvenile xanthogranuloma
  • micronodular and macronodular juvenile xanthogranuloma
  • ocular juvenile xanthogranuloma
  • systemic juvenile xanthogranuloma

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Dermatology

Cite this

@article{827fb45021a147b9bbf025bd57b983fe,
title = "Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranuloma",
abstract = "Background/Objectives: Cutaneous juvenile xanthogranuloma is an uncommon, usually benign disease affecting infants and young children. Ocular and other systemic involvement have been reported, but their incidence is unclear, and the utility of routine screening is not well established. Our aim was to characterize the risk of ocular and systemic complications in children with cutaneous juvenile xanthogranuloma. Methods: In this retrospective study, we reviewed the medical charts of children with cutaneous juvenile xanthogranuloma seen at Ann and Robert H. Lurie Children's Hospital, Chicago, Illinois, between January 2000 and December 2015. A comprehensive literature review was also performed. Results: Of 338 children with cutaneous juvenile xanthogranuloma, 76 (median age 6 months, 51{\%} female) met inclusion criteria. The most frequently involved site was the head and neck region (40{\%}). In 39 patients (51{\%}), there was a single lesion. Multiple lesions (>5) were evident in 20 patients (26{\%}). Most cutaneous juvenile xanthogranulomas were micronodular (77{\%}). None of the patients had ocular involvement. One patient had multiple asymptomatic hepatic nodules on imaging that regressed spontaneously within several months. Literature review of pediatric cutaneous juvenile xanthogranuloma series, including our cohort, revealed that the incidence of ocular manifestations is 0.24{\%} (7/2949) and of systemic manifestations is 0.75{\%} (22/2949). Conclusion: Cutaneous juvenile xanthogranulomas are generally limited to the skin. Because eye involvement is rare, a routine eye examination is of low yield and probably not warranted in children with no ocular or visual symptoms. New recommendations for systemic screening could not be drawn from this study.",
keywords = "cutaneous juvenile xanthogranuloma, micronodular and macronodular juvenile xanthogranuloma, ocular juvenile xanthogranuloma, systemic juvenile xanthogranuloma",
author = "Liat Samuelov and Michael Kinori and Chamlin, {Sarah L.} and Annette Wagner and Kenner-Bell, {Brandi M.} and Paller, {Amy S.} and Kruse, {Lacey L.} and Mancini, {Anthony J.}",
year = "2018",
month = "5",
day = "1",
doi = "10.1111/pde.13437",
language = "English (US)",
volume = "35",
pages = "329--335",
journal = "Pediatric Dermatology",
issn = "0736-8046",
publisher = "Wiley-Blackwell",
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TY - JOUR

T1 - Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranuloma

AU - Samuelov, Liat

AU - Kinori, Michael

AU - Chamlin, Sarah L.

AU - Wagner, Annette

AU - Kenner-Bell, Brandi M.

AU - Paller, Amy S.

AU - Kruse, Lacey L.

AU - Mancini, Anthony J.

PY - 2018/5/1

Y1 - 2018/5/1

N2 - Background/Objectives: Cutaneous juvenile xanthogranuloma is an uncommon, usually benign disease affecting infants and young children. Ocular and other systemic involvement have been reported, but their incidence is unclear, and the utility of routine screening is not well established. Our aim was to characterize the risk of ocular and systemic complications in children with cutaneous juvenile xanthogranuloma. Methods: In this retrospective study, we reviewed the medical charts of children with cutaneous juvenile xanthogranuloma seen at Ann and Robert H. Lurie Children's Hospital, Chicago, Illinois, between January 2000 and December 2015. A comprehensive literature review was also performed. Results: Of 338 children with cutaneous juvenile xanthogranuloma, 76 (median age 6 months, 51% female) met inclusion criteria. The most frequently involved site was the head and neck region (40%). In 39 patients (51%), there was a single lesion. Multiple lesions (>5) were evident in 20 patients (26%). Most cutaneous juvenile xanthogranulomas were micronodular (77%). None of the patients had ocular involvement. One patient had multiple asymptomatic hepatic nodules on imaging that regressed spontaneously within several months. Literature review of pediatric cutaneous juvenile xanthogranuloma series, including our cohort, revealed that the incidence of ocular manifestations is 0.24% (7/2949) and of systemic manifestations is 0.75% (22/2949). Conclusion: Cutaneous juvenile xanthogranulomas are generally limited to the skin. Because eye involvement is rare, a routine eye examination is of low yield and probably not warranted in children with no ocular or visual symptoms. New recommendations for systemic screening could not be drawn from this study.

AB - Background/Objectives: Cutaneous juvenile xanthogranuloma is an uncommon, usually benign disease affecting infants and young children. Ocular and other systemic involvement have been reported, but their incidence is unclear, and the utility of routine screening is not well established. Our aim was to characterize the risk of ocular and systemic complications in children with cutaneous juvenile xanthogranuloma. Methods: In this retrospective study, we reviewed the medical charts of children with cutaneous juvenile xanthogranuloma seen at Ann and Robert H. Lurie Children's Hospital, Chicago, Illinois, between January 2000 and December 2015. A comprehensive literature review was also performed. Results: Of 338 children with cutaneous juvenile xanthogranuloma, 76 (median age 6 months, 51% female) met inclusion criteria. The most frequently involved site was the head and neck region (40%). In 39 patients (51%), there was a single lesion. Multiple lesions (>5) were evident in 20 patients (26%). Most cutaneous juvenile xanthogranulomas were micronodular (77%). None of the patients had ocular involvement. One patient had multiple asymptomatic hepatic nodules on imaging that regressed spontaneously within several months. Literature review of pediatric cutaneous juvenile xanthogranuloma series, including our cohort, revealed that the incidence of ocular manifestations is 0.24% (7/2949) and of systemic manifestations is 0.75% (22/2949). Conclusion: Cutaneous juvenile xanthogranulomas are generally limited to the skin. Because eye involvement is rare, a routine eye examination is of low yield and probably not warranted in children with no ocular or visual symptoms. New recommendations for systemic screening could not be drawn from this study.

KW - cutaneous juvenile xanthogranuloma

KW - micronodular and macronodular juvenile xanthogranuloma

KW - ocular juvenile xanthogranuloma

KW - systemic juvenile xanthogranuloma

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U2 - 10.1111/pde.13437

DO - 10.1111/pde.13437

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JO - Pediatric Dermatology

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