Results 61 to 70 of about 319,608 (239)

Imaging features of neonatal systemic juvenile xanthogranuloma: A case report and review of the literature [PDF]

, 2020
Juvenile xanthogranuloma (JXG) is the most common non-Langerhans cell histiocytic disorder in children. This report describes the case of a 28-day-old boy that presented with multiple subcutaneous nodular lesions on the trunk and extremities, and ...
Deng, Xicheng, He, Siping, Jin, Ke, McKinstry, Robert C, Wang, Yong, Zhou, Zhengzhen   +5 more
core   +2 more sources

Bilateral anterior uveitis as a presenting feature of Juvenile Xanthogranuloma in a neonate

American Journal of Ophthalmology Case Reports, 2023
Purpose: To report a case of diffuse xanthogranuloma presenting as bilateral anterior uveitis in a neonate. Observations: A neonate was brought by the parents with complaints of redness, watering, and photophobia in both eyes for 10 days.
Brajesh Lahri, Zakir Hussain, Neerja Gupta, Shikha Gupta, Abhishek Singh, Viney Gupta   +5 more
doaj   +1 more source

Juvenile Xanthogranuloma

Health & Medical Journal, 2020
Juvenile xanthogranuloma is the most common form of non-Langerhans-cells histiocytosis or non-X histiocytosis. Most often affecting infants and young children.A case of  juvenile xanthogranuloma in a 3-month-old male infant has been reported.
Irma Primawati
semanticscholar   +1 more source

Robustness of a convolutional neural network trained on dermoscopic images and challenged with close‐up images

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives Deep learning‐convolutional neural networks (DL‐CNNs) have demonstrated high diagnostic accuracy within the domain of dermoscopy. However, many clinical settings lack dermoscopic devices, requiring reliance on close‐up images. This study evaluates the robustness of a DL‐CNN trained on dermoscopic images when challenged
Anastasia Sophie Vollmer, Julia Katharina Winkler, Katharina Susanne Kommoss, Wilhelm Stolz, Albert Rosenberger, Alexander Enk, Holger Andreas Haenssle   +6 more
wiley   +1 more source

Endoscopic treatment of mediastinal pancreatic pseudocyst using lumen apposing metal stents - Case report [PDF]

, 2023
Mediastinal pancreatic pseudocyst (PP) is a rare complication of acute alcoholic pancreatitis. Endoscopic drainage has become widely used in the management of PPs and novel lumen apposing metal stents (LAMS) could provide more effective ...
Kralj, Dominik, Kukić, Sandro, Pavić, Tajana   +2 more
core   +2 more sources

The Clinicopathologic Spectrum of Rosai–Dorfman–Destombes Disease in Adults: An Analysis of 16 Cases

European Journal of Haematology, EarlyView.
ABSTRACT Rosai–Dorfman–Destombes disease (RDD) is a rare histiocytic proliferation with protean clinical manifestations, resulting from the accumulation of activated histiocytes within nodal and extra‐nodal tissues. The diagnosis can be missed, particularly when biopsies are obtained from extra‐nodal sites, where histological features may be less ...
Mark Trinder, Collin Pryma, Emily Leung, Graham W. Slack, Pedro Farinha, Sean Young, Neval Ozkaya, Mollie Carruthers, Luke Y. C. Chen   +8 more
wiley   +1 more source

Management of pediatric uveitis [PDF]

, 2014
Pediatric uveitis is a topic of special interest not only because of the unique diagnostic and therapeutic challenges but also because of the lifetime burden of vision loss if the problem is not adequately treated, as well as the economic and ...
Foster, C. Stephen, Freitas-Neto, Clovis A., Wentworth, Bailey A.   +2 more
core   +1 more source

A Rare Case of Juvenile Xanthogranuloma in 8 Months Old Baby with Dyslipidemia

Bioscientia Medicina : Journal of Biomedicine and Translational Research, 2021
Background: Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis disease of childhood. But due to rarity of non Langerhans cell hystiosis itself, the exact prevalence of juvenile xanthogranuloma remain unknown with only a few ...
J. Saiful, Rina Gustia
semanticscholar   +1 more source

Epidermal Nevi and Epidermal Naevus Syndromes

JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.
ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini, Beatrice Carcano, Michela Brena   +2 more
wiley   +1 more source

Dermatofibroma: a curious tumor. [PDF]

, 2012
A tumor, such as a dermatofibroma, causes consternation among many patients, but it rarely creates problems on its own. Also called a histiocytoma, it remains one of the most common mesenchymal growths.
Lambert, Peter C, Lambert, W Clark, Parish, Lawrence, Yazdanian, Shideh   +3 more
core   +1 more source