Solitary juvenile xanthogranuloma in the lung of a young adult

Lin, Lisa; Salisbury, Elizabeth; Gardiner, I T; Varikatt, Winny

doi:10.1097/pat.0b013e328348900d

Cited by 8 publications

(4 citation statements)

References 12 publications

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“…12,19,20 Histiocytic infiltrations of the dermis have been detected in the skin biopsies; moreover, lung and colon biopsies confirmed the diagnosis of JXG histopathologically and immunohistochemically.…”

Section: Discussionmentioning

confidence: 68%

“…Although these extracutaneous lesions are of a benign nature, significant problems may arise due to pressure effects and possible clinical misdiagnosis as malignant entities. 3,4,12,13 Involvement of the central nervous system and liver was reported to be related to death. 3,4,14,15 Pulmonary involvement usually manifests as bilateral, diffuse, asymptomatic micro-or macronodules.…”

Section: Discussionmentioning

confidence: 99%

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Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

Nacaroğlu

Can

Karkıner

et al. 2015

Dermatologica Sinica

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Section: Discussionmentioning

confidence: 68%

Section: Discussionmentioning

confidence: 99%

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

Nacaroğlu

Can

Karkıner

et al. 2015

Dermatologica Sinica

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“…53 JXG occurs primarily in childhood, often presenting in the first year of life, with occasional reports of the disease presenting in the adult population. 54 In the vast majority of cases, JXG is a cutaneous disorder, with the characteristic lesion being a red-brown papular cutaneous nodule.…”

Section: Pulmonary Langerhans Cell Histiocytosismentioning

confidence: 99%

Cardiothoracic manifestations of primary histiocytoses

Vargas¹,

Richards²,

Ocazionez³

et al. 2016

The British Journal of Radiology

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The objectives of this article were: (1) to review common and rare manifestations of systemic and pulmonary Langerhans cell histiocytosis, Rosai-Dorfman disease, Erdheim-Chester disease and juvenile xanthogranuloma; (2) to provide the reader with important pathologic, epidemiologic and clinical features of these diseases. The histiocytoses are a diverse group of diseases which typically manifest with multiorgan involvement. Understanding the pathologic, epidemiologic and clinical features of these entities can help the radiologist suggest an accurate diagnosis of histiocytosis when typical imaging features are encountered.

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“…Extracutaneous JXGs in the central nervous system, lungs, heart, liver, testicles, bone marrow, and blood cells are rare [7,8,9,10,11,12]. Ocular involvement in patients with cutaneous JXG is the most common symptom in extracutaneous JXG [2,13,14,15].…”

Section: Introductionmentioning

confidence: 99%

Multiple Juvenile Xanthogranuloma of the Eyelids

2017

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Juvenile xanthogranuloma (JXG) is a rare and benign tumor in infants. A solitary lesion on the eyelid has been reported in patients with JXG. We report a 15-year-old boy with multiple involvement of JXG on both eyelids. A mass on the left inner canthus was resected because of disturbance of the visual field and a risk of malignancy in terms of central ulceration in the lesion. The mass was examined by light microscopy. The mass had Touton giant cells with a wreath of nuclei surrounded by foamy histiocytes. No malignancy was observed. The mass showed no recurrence after resection.

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Solitary juvenile xanthogranuloma in the lung of a young adult

Cited by 8 publications

References 12 publications

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage

Cardiothoracic manifestations of primary histiocytoses

Multiple Juvenile Xanthogranuloma of the Eyelids

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