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Articoli di riviste sul tema "Calcifications cutanées"

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Autore: Grafiati
Pubblicato: 22 giugno 2024

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1

Vignes, S., B. Wechsler, C. Francès e JC Piette. "Des calcifications sous-cutanées". La Revue de Médecine Interne 18, n. 2 (febbraio 1997): 167–68. http://dx.doi.org/10.1016/s0248-8663(97)84683-8.

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2

Avenel, G., J. Bernet, L. Lahaxe, H. Lévesque e I. Marie. "Des calcifications sous-cutanées et un syndrome dysmorphique". La Revue de Médecine Interne 31, n. 3 (marzo 2010): 238–40. http://dx.doi.org/10.1016/j.revmed.2009.02.009.

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3

Ben Ghorbel, I., A. Sioud Dhrif, K. Chelaifa, M. Miled e M. H. Houman. "Calcifications sous-cutanées au cours d'un lupus érythémateux systémique". La Revue de Médecine Interne 27, n. 4 (aprile 2006): 350–52. http://dx.doi.org/10.1016/j.revmed.2005.12.003.

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4

Durox, H., J. Berger, A. Sparsa, J. M. Bonnetblanc, P. Colombeau, V. Guigonis, L. Fourcade e C. Bédane. "Prise en charge des calcifications sous-cutanées par lithotripsie extra-corporelle". La Revue de Médecine Interne 30 (giugno 2009): S84—S85. http://dx.doi.org/10.1016/j.revmed.2009.03.156.

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5

Sparsa, A., N. Lesaux, J. Bonnetblanc, S. Blaise, P. Soria, V. Lebrun-Ly, P. Colombeau, E. Vidal e C. Bedane. "P94 - Traitement de calcifications sous-cutanées de CREST syndrome par lithotritie extra-corporelle". Annales de Dermatologie et de Vénéréologie 132 (ottobre 2005): 126–27. http://dx.doi.org/10.1016/s0151-9638(05)79823-9.

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6

Colboc, H., J. Fontaine, D. Bazin, V. Frochot, E. Letavernier, M. Daudon, N. Laporte et al. "Caractérisation clinique, chimique et morphologique des calcifications cutanées dans les ulcères de jambe". Annales de Dermatologie et de Vénéréologie 147, n. 12 (dicembre 2020): A173—A174. http://dx.doi.org/10.1016/j.annder.2020.09.190.

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7

Ammouri, W., H. Harmouche, K. Ainouch, S. Hamaz, Z. Tazi Mezalek, M. Aouni e M. Adnaoui. "Mastite simulant une mastite carcinomateuse associée à des calcifications sous-cutanées au cours d’un lupus systémique. À propos d’un cas". La Revue de Médecine Interne 30 (dicembre 2009): S444. http://dx.doi.org/10.1016/j.revmed.2009.10.329.

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8

Wilson, Perry R. "PORPHYRIA CUTANEA TARDA WITH CUTANEOUS "SCLERODERMA" AND CALCIFICATION". Australasian Journal of Dermatology 30, n. 2 (agosto 1989): 93–96. http://dx.doi.org/10.1111/j.1440-0960.1989.tb00427.x.

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9

Rey, J., C. Della Volpe, A. Labarelle, K. Solere, D. Chouquet, F. Fourquet, S. Hesse e J. J. Bonerandi. "Calcifications du cuir chevelu au cours d'une porphyrie cutanée tardive associée a une hepatite C". La Revue de Médecine Interne 22 (dicembre 2001): 499s—500s. http://dx.doi.org/10.1016/s0248-8663(01)80166-1.

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10

Küçükuysal, Ceren, e Selim Kapur. "Mineralogical, geochemical and micromorphological evaluation of the Plio-Quaternary paleosols and calcretes from Karahamzall, Ankara (Central Turkey)". Geologica Carpathica 65, n. 3 (1 giugno 2014): 243–55. http://dx.doi.org/10.2478/geoca-2014-0014.

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Abstract (sommario):
Abstract We present the mineralogical, micromorphological, and geochemical characteristics of the paleosols and their carbonates from Karahamzall, Ankara (Central Turkey). The paleosols include calcretes of powdery to nodular forms and alternate with channel deposits. The presence of pedofeatures, such as clay cutans, floating grains, circumgranular cracks, MnO linings, secondary carbonate rims, traces of past bioturbation and remnants of root fragments are all the evidence of pedogenesis. Bw is the most common soil horizon showing subangular-angular blocky to granular or prismatic microstructures. Calcretes, on the other hand, are evaluated as semi-mature massive, nodular, tubular or powdery forms. The probable faunal and floral passages may also imply the traces of life from when these alluvial deposits were soil. The presence of early diagenetic palygorskite and dolomite together with high salinization, high calcification and low chemical index of alteration values are evidence of the formation of calcretes under arid and dry conditions. δ13C compositions of the carbonates ranging from -7.11 ‰ to -7.74 ‰ VPDB are comformable with the world pedogenic carbonates favouring the C4 vegetation; likely δ18O compositions of the carbonates are between -3.97 ‰ and -4.91 ‰ which are compatible with the paleosols formed under the influence of meteroic water in the vadose zone
11

Theodorou, Daphne J., e Stavroula J. Theodorou. "Syndrome de l’huile toxique et calcifications diffuses du tissu sous-cutané". Revue du Rhumatisme, aprile 2024. http://dx.doi.org/10.1016/j.rhum.2024.04.012.

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12

"Sclerodermoid changes and dystrophic calcification: A unique presentation of porphyria cutanea tarda". Journal of the American Academy of Dermatology 74, n. 5 (maggio 2016): AB130. http://dx.doi.org/10.1016/j.jaad.2016.02.509.

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13

"Extensive calcifications of the scalp in a patient with porphyria cutanea tarda secondary to hepatitis C virus infection". Journal of the European Academy of Dermatology and Venereology 21, n. 2 (febbraio 2007). http://dx.doi.org/10.1111/j.1468-3083.2006.01860.x.

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14

Rey, J., S. Hesse e JJ Bonerandi. "Extensive calcifications of the scalp in a patient with porphyria cutanea tarda secondary to hepatitis C virus infection". Journal of the European Academy of Dermatology and Venereology, 3 novembre 2006, 070209222700117—??? http://dx.doi.org/10.1111/j.1468-3083.2007.01860.x.

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15

Rahmatika, Amira Suryani, Trisniartami Setyaningrum, Sawitri Sawitri, Evy Ervianti e Damayanti Damayanti. "Cutaneous Manifestations in End-Stage Renal Disease (ESRD)". Qanun Medika - Medical Journal Faculty of Medicine Muhammadiyah Surabaya 8, n. 01 (9 gennaio 2024). http://dx.doi.org/10.30651/jqm.v8i01.19371.

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Abstract (sommario):
Skin can reflect systemic conditions due to abnormalities in internal organs, including kidney disorders. Cutaneous manifestations are common in patients with end-stage renal disease (ESRD). It can be severe and negatively impact a patient's quality of life. Clinicians can effectively manage ESRD by closely examining the patient's skin and nails, improving the patient's quality of life, and reducing mortality and morbidity. Clinicians can be more aware of ESRD by examining the patient's skin and nails closely so proper management can be performed and the patient's quality of life can be improved. This review aims to increase understanding of common cutaneous manifestations in ESRD for early recognition and better management. Cutaneous manifestations in ESRD are divided into specific and nonspecific manifestations. Specific manifestations include acquired perforating dermatosis (APD), bullous disease (porphyria cutanea tarda and pseudoporphyria), metastatic calcification (calcinosis cutis and calcific uremic arteriolopathy), and nephrogenic systemic fibrosis. Nonspecific manifestations include pruritus, xerosis, skin pigmentation changes, nail disorders, purpura, hair disorders, oral mucosal changes, skin infections, and other skin manifestations. These manifestations range from benign and asymptomatic to serious conditions that negatively impact life quality. In conclusion, Early detection and treatment of cutaneous manifestations in patients with ESRD are crucial for reducing morbidity and mortality and also improving patients' quality of life.

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