Cardiac Juvenile Xanthogranuloma in an Infant Presenting with Pericardial Effusion [PDF]
Juvenile xanthogranuloma is a rare histiocytic disorder of childhood mainly affecting skin and rarely deep soft tissues and viscera. We report a 2‐month‐old infant who presented with respiratory distress secondary to a large pericardial effusion ...
Aggarwal, Sanjeev +3 more
core +1 more source
CASES OF DISSEMINATED AND GIANT JUVENILE XANTHOGRANULOMA IN CHILDREN
Juvenile xanthogranuloma is the most common clinical variant of the class II histiocytosis. This article presents two clinical observationsof papulonodular juvenile xanthogranuloma, specification of epidemiological data, clinical and histological ...
E. I. Pil'gui +5 more
doaj +1 more source
New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]
The existence of thromboangiitis obliterans as a clinical entity has been a matter of debate for many years. In contrast to other immunovasculitides there is no organ involvement while peripheral vessels are affected.
Berlit, Peter +3 more
core +1 more source
A Multifaceted Approach to Treatment of Recalcitrant Cutaneous Periorbital Juvenile Xanthogranuloma [PDF]
Purpose: To demonstrate novel treatments for patients with high juvenile xanthogranuloma ( JXG) eyelid lesion burden. Case Report: A 14-year-old girl was referred to the oculoplastic surgery service for management of worsening extensive bilateral eyelid ...
Feng, Shu +4 more
core +2 more sources
C.E. Credit. Xanthogranuloma of the Palate in an Adult: A Case Report with Differential Diagnosis
Background Solitary oral mucosal xanthogranuloma, previously termed juvenile xanthogranuloma, is exceedingly rare in adults. Extracutaneous lesions are similarly rarely seen; and the condition generally affects infants and children.Methods This case ...
Hardev M. Singh +3 more
doaj +1 more source
The Impact of Hybrid Therapy on Langerhans Cell Histiocytosis of the Mandible in an Older Male: A Case Report and Literature Review. [PDF]
Background The unusual disorder known as Langerhans cell histiocytosis (LCH), which is most frequently observed in children and young adults, is caused by the clonal proliferation of Langerhans cells. This disease is classified into several types depending on the extent of the lesion.
Matsumoto Y +3 more
europepmc +2 more sources
Baby with neonatal systemic juvenile xanthogranuloma born within a cross-cousin marriage
Juvenile xanthogranuloma is a non-Langerhans cell histiocytosis seen most commonly in childhood and adolescence. Extracutaneous involvement is rare. We report an interesting and extremely rare case of systemic (skin, lung, spleen, and colon) “juvenile ...
Hikmet Tekin Nacaroglu +6 more
doaj +1 more source
Erdheim-Chester Disease: a comprehensive review of the literature [PDF]
Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected.
Mirra Manevich-Mazor +2 more
core +1 more source
Three different ophthalmic presentations of juvenile xanthogranuloma [PDF]
Three cases of juvenile xanthogranuloma from two ophthalmology departments were reviewed. Clinical histories, ophthalmic examination, physical examination, investigations, and treatment of these cases are described.
Fan, Dorothy S.P. +4 more
core +1 more source
Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children [PDF]
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Barbi, Egidio +6 more
core +1 more source

