Results 31 to 40 of about 5,669 (178)

Cutaneous xanthoma causing hypercalcaemia in a cat

open access: yesJournal of Feline Medicine and Surgery Open Reports, 2022
Case summary A 5-year-old male neutered cat weighing 3.56 kg presented owing to the development of two masses over the dorsal cervical and cranial thoracic areas, as well as weight loss, inappetence and vomiting.
Doris Ma   +2 more
doaj   +1 more source

Sitosterolemia With Atherosclerosis in a Child: A Case Report

open access: yesFrontiers in Pediatrics, 2021
Introduction: Sitosterolemia is a rare condition in children and is often misdiagnosed as familial hypercholesterolemia. Serious complications can result if not treated promptly and effectively.
Hongjun Ba   +9 more
doaj   +1 more source

Assessment of Antimicrobial Resistance in M. leprae Strains From Kiribati

open access: yesTropical Medicine &International Health, EarlyView.
ABSTRACT Objectives Kiribati has one of the highest rates of leprosy worldwide. A nationwide screening and chemoprophylaxis program for household leprosy contacts was introduced in 2018. In 2022, population‐wide screening and rifamycin‐based treatment or chemoprophylaxis for leprosy and tuberculosis was introduced as part of the PEARL and COMBINE ...
Patrick O. Campbell   +10 more
wiley   +1 more source

A Case of Xanthoma of Bilateral Tendoachilles Reconstructed with Fascia Lata Graft X [PDF]

open access: yesJournal of Orthopedics and Joint Surgery
Aims and background: Cerebrotendinous xanthoma is an autosomal recessive disorder characterized by a lack of production of primary bile acids and accumulation of cholestanol in various tissues like the brain, spinal cord, peripheral nerves, eyes, and ...
S Jaikish, Balaji Sambandam
doaj   +1 more source

Nerve Ultrasound Detects Peripheral Nerve Enlargement in Cerebrotendinous Xanthomatosis

open access: yesMuscle &Nerve, Volume 73, Issue 6, Page 1082-1088, June 2026.
ABSTRACT Introduction/Aims Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive disorder caused by variants in the CYP27A1 gene, resulting in cholestanol accumulation in various tissues, including peripheral nerves. Polyneuropathy is common but often under‐recognized in CTX.
Antonio Edvan Camelo‐Filho   +8 more
wiley   +1 more source

Eruptive xanthomas

open access: yesDermatology Online Journal, 2008
A 26-year-old woman presented for evaluation of multiple, red-yellow papules that had been appearing over the course of 2 months on the extensor surfaces of the upper extremities, dorsal aspects of the hands, thighs, and buttocks. Serum lipid evaluation showed hypertriglyceridemia in a patient with a recent history of pancreatitis.
Merola, Joseph F   +3 more
openaire   +4 more sources

Oral verruciform xanthoma: The great imitator

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2020
Oral Verruciform xanthoma (OVX) is an uncommon benign muco-cutaneous lesion having various concepts regarding its etiopathogenesis. Intraorally, this usually occurs on the gingiva and alveolar mucosa.
Sweety Lalawat   +3 more
doaj   +1 more source

Cytologic and Histological Features Distinguishing Myxoid Meningioma From Chordoid Meningioma: A Case Report

open access: yesDiagnostic Cytopathology, Volume 54, Issue 5, Page E127-E130, May 2026.
ABSTRACT Meningiomas are the most common primary brain tumors worldwide and are classified into 15 subtypes in the 5th edition of the WHO classification. Myxoid meningioma, characterized by the presence of a mucinous matrix within the tumor, is a rare metaplastic meningioma subtype classified as WHO grade 1.
Tatsuya Aso   +4 more
wiley   +1 more source

Transverse colon xanthoma: Rare yet important

open access: yesSaudi Journal for Health Sciences, 2019
Colonic xanthomas are rare, benign lesions of the gastrointestinal tract characterized by a foamy cell containing lipid in the lamina propria and mucosa. They have been commonly described in the stomach and rectosigmoid region in few case reports.
Sameer Ahmed Ansari   +3 more
doaj   +1 more source

GPIHBP1 Autoantibody‐Related Hypertriglyceridemia in Children: A Report of Two Cases and a Review of Pediatric Cases From the Literature

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 5, May 2026.
We report two young children with severe hypertriglyceridemia lacking monogenic causes. Both were ANA‐positive, with confirmed anti‐GPIHBP1 antibodies. Immunosuppressive therapy (hydroxychloroquine ± prednisolone) effectively reduced triglycerides. GPIHBP1 autoantibody‐related hypertriglyceridemia is an important pediatric cause, requiring accurate ...
Rai‐Hseng Hsu   +4 more
wiley   +1 more source

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