Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
BMC Neurol ; 23(1): 181, 2023 May 05.
Artículo en Inglés | MEDLINE | ID: mdl-37147571

RESUMEN

BACKGROUND: We report a patient with a novel c.737 C > T variant (p.Ser246Leu) of the TPM3 gene presenting with adult-onset distal myopathy. CASE PRESENTATION: A 35-year-old Chinese male patient presented with a history of progressive finger weakness. Physical examination revealed differential finger extension weakness, together with predominant finger abduction, elbow flexion, ankle dorsiflexion and toe extension weakness. Muscle MRI showed disproportionate fatty infiltration of the glutei, sartorius and extensor digitorum longus muscles without significant wasting. Muscle biopsy and ultrastructural examination showed a non-specific myopathic pattern without nemaline or cap inclusions. Genetic sequencing revealed a novel heterozygous p.Ser246Leu variant (c.737C>T) of the TPM3 gene which is predicted to be pathogenic. This variant is located in the area of the TPM3 gene where the protein product interacts with actin at position Asp25 of actin. Mutations of TPM3 in these loci have been shown to alter the sensitivity of thin filaments to the influx of calcium ions. CONCLUSION: This report further expands the phenotypic spectrum of myopathies associated with TPM3 mutations, as mutations in TPM3 had not previously been reported with adult-onset distal myopathy. We also discuss the interpretation of variants of unknown significance in patients with TPM3 mutations and summarise the typical muscle MRI findings of patients with TPM3 mutations.


Asunto(s)
Miopatías Distales , Tropomiosina , Masculino , Humanos , Adulto , Tropomiosina/genética , Tropomiosina/metabolismo , Miopatías Distales/patología , Actinas/genética , Músculo Esquelético/patología , Mutación , Debilidad Muscular , Paresia/patología
3.
Australas J Dermatol ; 61(3): e346-e350, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31965571

RESUMEN

We report an unusual case of drug-associated granulomatous CD30+ T-cell pseudolymphoma secondary to amlodipine. A 55-year-old Chinese man presented with a 6-month eruption of disseminated erythematous dermal papulonodules and annular infiltrated plaques over his neck and limbs symmetrically. Histopathology revealed a perivascular and interstitial infiltrate of histiocytes, eosinophils and morphologically normal lymphocytes associated with CD30 expression. The eruption improved rapidly after discontinuation of amlodipine and did not recur.


Asunto(s)
Amlodipino/efectos adversos , Antihipertensivos/efectos adversos , Granuloma/inducido químicamente , Seudolinfoma/inducido químicamente , Erupciones por Medicamentos/etiología , Granuloma/patología , Humanos , Antígeno Ki-1/metabolismo , Masculino , Persona de Mediana Edad , Seudolinfoma/patología , Linfocitos T/metabolismo
5.
J Cardiovasc Dev Dis ; 10(12)2023 Dec 18.
Artículo en Inglés | MEDLINE | ID: mdl-38132666

RESUMEN

Endovascular therapy (EVT) has revolutionized the management of acute ischaemic strokes with large vessel occlusion, with emerging evidence suggesting its benefit also in large infarct core volume strokes. In the last two years, four randomised controlled trials have been published on this topic-RESCUE-Japan LIMIT, ANGEL-ASPECT, SELECT2 and TENSION, with overall results showing that EVT improves functional and neurological outcomes compared to medical management alone. This review aims to summarise the recent evidence presented by these four trials and highlight some of the limitations in our current understanding of this topic.

SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA