Bentounes, N K Le Hingrat, Q Planquette, B Darnige, L Khider, L Sanchez, O Smadja, D M Mauge, L Lê, M P Mirault, T
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Published in
La Revue de medecine interne
Nowadays, thanks to highly active antiretroviral therapy (HAART), human immunodeficiency virus (HIV) infection is transforming into a chronic disease. The life expectancy of people living with HIV (PWH) has increased, as well as their risk of developing several co-morbidities, in particular cardiovascular diseases. In addition, the incidence of ven...
Ferreira De Matos, C De Almeida Chaves, S Potin, P Syrykh, C Piel-Julian, M-L Sailler, L Moulis, G
Published in
La Revue de medecine interne
Castleman disease is a rare lymphoproliferation, which may mimic systemic lupus. Conversely, systemic lupus sometimes presents like an hematological malignancy. In these cases, a "Castleman-like" histology has been exceptionally described. A 55-year-old female treated by methotrexate for systemic lupus with skin and joint involvement presented weig...
De Fontcuberta, Pedro Vandenhende, Marie-Anne Laux, Miranda Tourbier, Benjamin Paz, Rafael Bonnet, Fabrice Meriglier, Etienne
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La Revue de medecine interne
Hearing loss is a rare manifestation in giant cell arteritis. The different types of deafness are possible with a predominance of sensorineural deafness. We report a 75-year-old woman who presented with typical manifestations of giant cell arteritis associated concomitantly with the occurrence of bilateral mixed hearing loss confirmed on the audiog...
Stammler, R Ackermann, F Vasse, M Verrat, A David, A Horodyckid, C Gratieux, J Marroun, I Groh, M Roumier, M
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Published in
La Revue de medecine interne
Chlorpromazine is a commonly used drug in several medical conditions associated with a wide range of side effects. Few cases of hemostatic disorder have been reported in the literature. A 39-year-old man had previously been diagnosed with a cavernous malformation of the medulla oblongata. Chlorpromazine was started to treat persistent hiccups. Twen...
de Sainte Marie, B Arnal, P Seguier, J Faucher, B Gaigne, L Briantais, A Bermudez, J Ebbo, M Schleinitz, N Andre, B
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Published in
La Revue de medecine interne
Schiller, D
Published in
La Revue de medecine interne
Perrard, N Pokeerbux, M R Quesnel, B Duployez, N Fenwarth, L Preudhomme, C Lefèvre, G Baillet, C Launay, D Terriou, L
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Published in
La Revue de medecine interne
Heterozygous germline mutations of GATA2 gene (guanine-adenine-thymine-adenine binding protein 2) are hereditary mutations that can be pathogenic, sometimes occurring sporadically, responsible for a florid clinical-biological picture, sometimes serious and quickly leading to the death. We reported two women and one man with germline mutations in th...
Erraoui, K Nassar, K Janani, S
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La Revue de medecine interne
Ochronosis, also known as alkaptonuria, is a rare autosomal recessive disease. It is caused by a lack of homogentisic acid oxidase, which causes homogentisic acid deposition in the tissues. We report a 69-year-old patient who presented with chronic mechanical low back and radicular pain. The clinical examination revealed lumbar lordosis loss, lumba...
Gomes de Pinho, Q de Sainte Marie, B Seguier, J Ebbo, M Schleinitz, N
Published in
La Revue de medecine interne
Jabbourri, R Aniq Filali, R Tazi, N
Published in
La Revue de medecine interne