Acquired Immunodeficiency Syndrome Revealed by Oral Kaposi's Sarcoma

<p>Kaposi's sarcoma is the malignant proliferation of the endothelial cell vessels. It is a systemic, malignant and multifactor disease. It usually presents initially as violaceous cutaneous lesions. Outside of a known context of an immune deficiency, an isolated oral lesions may not thin...

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Asıl Yazarlar: Hanane Atarguine (Yazar), Soundous Benmoussa (Yazar), Fayçal Abbad (Yazar), Ouafa Hocar (Yazar), Fatima Ihbibane (Yazar), Hanane Rais (Yazar), Noura Tassi (Yazar), Nadia Akhdari (Yazar), Said Amal (Yazar)
Materyal Türü: Kitap
Baskı/Yayın Bilgisi: International Journal of Oral and Craniofacial Science - Peertechz Publications, 2016-02-10.
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042 |a dc 
100 1 0 |a Hanane Atarguine  |e author 
700 1 0 |a  Soundous Benmoussa  |e author 
700 1 0 |a  Fayçal Abbad  |e author 
700 1 0 |a  Ouafa Hocar  |e author 
700 1 0 |a  Fatima Ihbibane  |e author 
700 1 0 |a  Hanane Rais  |e author 
700 1 0 |a  Noura Tassi  |e author 
700 1 0 |a  Nadia Akhdari  |e author 
700 1 0 |a  Said Amal  |e author 
245 0 0 |a Acquired Immunodeficiency Syndrome Revealed by Oral Kaposi's Sarcoma 
260 |b International Journal of Oral and Craniofacial Science - Peertechz Publications,   |c 2016-02-10. 
520 |a <p>Kaposi's sarcoma is the malignant proliferation of the endothelial cell vessels. It is a systemic, malignant and multifactor disease. It usually presents initially as violaceous cutaneous lesions. Outside of a known context of an immune deficiency, an isolated oral lesions may not think to Kaposi's sarcoma. Hence the interest of the histological and immunohistochemical study. This paper reviews one such case of Kaposi's sarcoma in a 42-year-old woman who present an isolated pigmented lesions of the tongue, related to Kaposi's sarcoma, without cutaneous or visceral involvement, and which led to the discovery of acquired immunodeficiency syndrome (HIV). The stabilization was obtained with antiretroviral triple therapy.</p> 
540 |a Copyright © Hanane Atarguine et al. 
546 |a en 
655 7 |a Case Report  |2 local 
856 4 1 |u https://doi.org/10.17352/2455-4634.000010  |z Connect to this object online.