ReviewBMC pediatrics2019
The various clinical spectra of juvenile xanthogranuloma: imaging for two case reports and review of the literature.
Review in BMC pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed, 44 citations in OpenAlex.
- Ultrasonography of pediatric cutaneous and subcutaneous masses.Pediatric radiology · 2026Review
- A case report of a blueberry muffin baby caused by congenital self-healing indeterminate cell histiocytosis.BMC pediatrics · 2023Article
- Disseminated Juvenile Xanthogranuloma with a Novel MYH9-FLT3 Fusion Presenting as a Blueberry Muffin Rash in a Neonate.AJP reports · 2023Article
- Neuroimaging in Pediatric Patients with Juvenile Xanthogranuloma of the CNS.AJNR. American journal of neuroradiology · 2022Article
- [Benign skin neoplasms in children].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2022Review
- Progressive nodular histiocytosis in a 9-year-old boy treated with cobimetinib.Pediatric dermatology · 2022Article
- Musculoskeletal imaging features of non-Langerhans cell histiocytoses.Skeletal radiology · 2021Review
- Lower Abdominal Juvenile Xanthogranuloma in an Infant: A Rare Site of Presentation.Kansas journal of medicineArticle
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundJuvenile xanthogranuloma (JXG) belongs to the heterogeneous group of non-Langerhans cell histiocytosis and is caused by an accumulation and proliferation of macrophages. In the majority of cases JXG is a disorder of early childhood presenting during the first 2 years of life. The typical presentation is a solitary reddish or yellowish skin papule or nodule with spontaneous regression and no need for treatment. CASE PRESENTATION: Two infants with an atypical presentation of JXG, one with multiple blueberry muffin rash-like skin lesions and the other with severe multi-systemic involvement, are reported. Diagnosis was established by skin biopsy including histological work-up and immunostaining, where markers for macrophages (CD68 and CD163) exhibited significant reactivity.
conclusionJXG is the most common of the non-Langerhans cell histiocytosis. The typical presentation is a solitary skin lesion. The purpose of this report is to familiarize paediatricians with an unusual variant of this entity in order to facilitate early diagnosis and raise awareness for possible visceral complications and associated medical conditions.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.