Results 41 to 50 of about 5,669 (178)

Diffuse normolipemic plane xanthoma associated with monoclonal gammopathy

Dermatology Practical & Conceptual, 2015
Diffuse normolipemic plane xanthoma (DNPX) was first described by Altman and Winkelmann in 1962. It is a rare and non-inherited form of xanthomatosis. Clinically, the dermatosis is characterized by the presence of symmetric yellowish-orange plaques that ...
Yoon K. Cohen, David J. Elpern
doaj   +1 more source

Multiple histiocytic foam cell nodules of the tongue in a Shih Tzu dog

Veterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract An uncommon histiocytic lesion of the tongue was described in an 11‐year‐7‐month‐old male Shih Tzu dog that presented with multiple nodules on the upper lip and tongue, with further dissemination on the ventral lingual surface observed during sedation.
Hugo Henrique Rocon Gregório, Liandra Guidolini Roni, Aluisio Miguel Filho, Haide Valeska Scheid, Clairton Marcolongo‐Pereira   +4 more
wiley   +1 more source

An Unusual Case of Xanthoma of Bilateral Achilles Tendon with Gouty Infiltration: A Rare Case Report

Indian Journal of Radiology and Imaging, 2023
Achilles tendon xanthoma is a benign and rare disease with a high incidence in patients having familial hypercholesterolemia. Patients present with or without pain and thickened tendons. Gout is seen in patients with hyperuricemia.
Heena M. Khatoon, Annapurna Srirambhatla, Abhimanyu Sharma, Poojitha Sankepally, Abhishek J. Arora   +4 more
doaj   +1 more source

Bleeding Disorders in Children With Genetic Diseases: A Narrative Review

Acta Paediatrica, Volume 115, Issue 5, Page 1015-1024, May 2026.
ABSTRACT Aim The lack of data on bleeding risk assessment in children with genetic diseases is concerning given their increased care needs and risk of haemorrhagic complications compared to the general population. Identification of haemostatic disorders is crucial for implementing preventive measures and mitigating bleeding risk.
Raphaelle Cagol, Mariam Sbeity Barakat, Marjolaine Willems, Tasnime Akbaraly, Biron‐Andreani Christine, Isabelle Diaz, Alexandre Theron   +6 more
wiley   +1 more source

The Genetic Landscape of Hereditary Spastic Paraplegia in Greece

Clinical Genetics, Volume 109, Issue 5, Page 837-846, May 2026.
We investigated 112 Greek index‐cases with hereditary spastic paraplegia collected over > 25 years using NGS and MLPA. We identified a causative variant in 68 patients (60.7%), including 7 novel causative variants. This study presents a comprehensive overview of the phenotypic and genotypic spectrum of HSP in the Greek population.
Georgios Koutsis, Viorica Chelban, Chrisoula Kartanou, Zoi Kontogeorgiou, Chrysoula Koniari, Nikolaos Ragazos, Charalampos Voudommatis, Kristina Zhelcheska, David S. Lynch, Reza Maroofian, Ehsan Barkhordari, Rahema Mohammad, Ioannis Zaganas, Minas Drakos, Georgia Xiromerisiou, Efthymios Dardiotis, Leonidas Stefanis, Marios Panas, Henry Houlden, Georgia Karadima   +19 more
wiley   +1 more source

Eruptive xanthomas [PDF]

Advances in Dermatology and Allergology, 2013
Xanthomas are localized lipid deposits in the skin, tendons and subcutaneous tissue associated with lipid abnormality. The hyperlipidemia responsible for this disorder can be caused by a primary genetic defect, a secondary disorder, or both. That kind of skin exanthema may be the first signal of cardiovascular risk.
Zaremba, Joanna, Zaczkiewicz, Andrzej, Placek, Waldemar   +2 more
openaire   +2 more sources

PCSK9 Inhibitors Reduce Oxidative Stress Biomarkers in Heterozygous Familial Hypercholesterolemia

Journal of Cellular and Molecular Medicine, Volume 30, Issue 10, May 2026.
ABSTRACT Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, such as alirocumab and evolocumab, effectively reduce LDL‐C levels, improve cardiovascular outcomes, and are well tolerated in the treatment of heterozygous familial hypercholesterolemia (HeFH).
Agnieszka Woźniak‐Szczepocka, Agnieszka Pawlos, Paulina Gorzelak‐Pabiś, Marlena Broncel, Bożena Bukowska, Ewelina Woźniak   +5 more
wiley   +1 more source

Childhood Pseudoxanthomatousmastocytosis; Report of two cases

Indian Journal of Dermatopathology and Diagnostic Dermatology, 2018
Cutaneous mastocytosis (CM) is a mast cell proliferative disorder that commonly affects pediatric population. It has various clinical forms such as urticaria pigmentosa, solitary mastocytoma, telangiectasia macularis eruptiva perstans, diffuse CM, and ...
Bhabani S. T. P. Singh, Tapaswini Tripathy, Bikash Ranjan Kar, Surabhi Singh   +3 more
doaj   +1 more source

Novel and Simple Punch Treatment for Xanthelasma Palpebrarum: A Preliminary Case Series

Journal of Cosmetic Dermatology, Volume 25, Issue 5, May 2026.
ABSTRACT Background Xanthelasma palpebrarum (XP) is a common cutaneous condition of the eyelid, which compromises eyelid aesthetics. Non‐surgical treatments are often limited by multiple sessions and high cost. Surgical treatment, although effective, is constrained by the limited availability of eyelid skin and the risk of ectropion.
Hui Cheng, Wende Yao, Yun Bai, Xinyi Li, Xiaojing Li   +4 more
wiley   +1 more source

A Case Of Diabetes Mellitus With Xanthoma Disseminatum

Indian Journal of Dermatology, 2002
Xanthoma Disseminatum is a rare, benign, normolipaemic form of histiocytoxanthomatosis affecting the skin and mucous membranes and known to be associated with diabetes insipidus, multiple myeloma or other paraproteinaemias.
Balasaraswathy P, Kakkilaya B.S, Shetty K. M, Parameswaraiah S   +3 more
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