Results 21 to 30 of about 6,887 (246)

Disseminated juvenile xanthogranulomas with ocular involvement: A case report and literature review

open access: yesSAGE Open Medical Case Reports, 2022
Cutaneous juvenile xanthogranuloma is an uncommon disorder usually arising during infancy. Systemic involvement of juvenile xanthogranuloma remains rare, and there are no published guidelines to date on screening extracutaneous manifestations in these ...
Nadine Sophie Maalouf   +5 more
doaj   +1 more source

C.E. Credit. Xanthogranuloma of the Palate in an Adult: A Case Report with Differential Diagnosis

open access: yesJournal of the California Dental Association, 2023
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

An analysis of clinical and pathological features of 32 cases of juvenile xanthogranuloma

open access: yesPifu-xingbing zhenliaoxue zazhi, 2020
Objective: To summarize the clinical and histopathological features of juvenile xanthogranuloma (JXG). Methods: The clinical manifestations and histopathological findings of 32 children with juvenile xanthogranuloma diagnosed and treated in our hospital ...
Cui HU   +6 more
doaj   +1 more source

Oral Juvenile Xanthogranuloma: a case report of gingival hyperplasia and osteolysis in male adult patient

open access: yesBMC Oral Health, 2022
Background Juvenile Xanthogranuloma (JXG) is a non-hereditary, self-limiting disease which is usually presented in infancy or early childhood and in males over females.
Long Chen, Lin Feng, Lingling E
doaj   +1 more source

Stroke‐Like Migraine Attacks After Radiation Therapy (SMART) Syndrome: A Case Report and Review of a Rare Delayed Complication of Cranial Irradiation [PDF]

open access: yesClin Case Rep
ABSTRACT SMART syndrome is a rare, delayed complication of cranial irradiation that can mimic stroke, tumor recurrence, or autoimmune encephalitis. Early recognition based on clinical‐radiologic features is critical to avoid misdiagnosis and unnecessary interventions since conservative management often leads to complete recovery.
Jha S   +4 more
europepmc   +2 more sources

Case series of volar juvenile xanthogranuloma: Clinical observation of a peripheral rim of hyperkeratosis [PDF]

open access: yes, 2014
Juvenile xanthogranuloma is a benign histiocytic tumor predominantly occurring in children as yellowish papules on the head and trunk. Presentations on the volar surfaces are rare and may cause diagnostic confusion with pyogenic granuloma, eccrine poroma
Amadi, Ugochukwu   +7 more
core   +1 more source

Parasellar xanthogranulomas [PDF]

open access: yesJournal of Neurosurgery, 2015
OBJECT Xanthogranulomas are rare inflammatory masses most often found in the skin and eye. The incidence of intracranial xanthogranulomas is 1.6%–7%, with those found in the sellar and parasellar region being exceedingly rare and their etiology controversial.
Redi, Rahmani   +5 more
openaire   +2 more sources

Cardiac Juvenile Xanthogranuloma in an Infant Presenting with Pericardial Effusion [PDF]

open access: yes, 2012
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

open access: yesПедиатрическая фармакология, 2014
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]

open access: yes, 1984
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

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