Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Soumaya Hamich"'
Autor:
Fatima Azzahra El gaitibi, MD, Mehdi Khallaayoune, MD, Soumaya Hamich, MD, Kaoutar Znati, MD, Mariame Meziane, MD, Karima Senouci, MD
Publikováno v:
JAAD Case Reports, Vol 8, Iss , Pp 74-76 (2021)
Externí odkaz:
https://doaj.org/article/c73626103f68442c8854ce153b16abd6
Autor:
Asmae Abdelmouttalib, Soumaya Hamich, Mariame Meziane, Nadia Ismaili, Laila Benzekri, Karima Senouci
Publikováno v:
Nasza Dermatologia Online, Vol 12, Iss e, Pp e78-e78 (2021)
Externí odkaz:
https://doaj.org/article/d00601ee4fe945489ff68a8bc25a6096
Autor:
Soumaya Hamich, Fatima Zahra El Gaitibi, Kaoutar Znati, Meriem Meziane, Nadia Ismaili, Laila Benzekri, Karima Senouci
Publikováno v:
Nasza Dermatologia Online, Vol 13, Iss 1, Pp 99-100 (2022)
We report the case of a 43-year-old male with a history of pulmonary tuberculosis cured one year previously and a 25-year-old history of smoking. The patient presented with a tumor of the scalp that had been evolving since the age of thirteen years,
Externí odkaz:
https://doaj.org/article/854613e6b9024f9bab8252d2a80b6748
Autor:
Asmae Abdelmouttalib, Sanae Sialiti, Soumaya Hamich, Kawtar Znati, Mariame Meziane, Nadia Ismaili, Leila Benzekri, Karima Senouci
Publikováno v:
Nasza Dermatologia Online, Vol 13, Iss 1, Pp 118-119 (2022)
Sir, CD8+ mycosis fungoides (MF) is a rare form of MF with an indolent course. Herein, we report a rare case of CD8+ fungoid mycosis preceded by lymphomatoid papulosis type D with an aggressive course. A 36-year-old female presented with several papu
Externí odkaz:
https://doaj.org/article/21eabb08db4541279e14459c695f33b6
Autor:
Asmae Abdelmouttalib, Soumaya Hamich, Amine Haouzi, Mariame Meziane, Nadia Ismaili, Leila Benzekri, Karima Senouci
Publikováno v:
Our Dermatology Online. 13:296-298
Epithelioid hemangioendothelioma (EHE) is an extremely rare sarcoma whose target may be different organs, including soft tissue. The spectrum of the disease is highly variable between indolent and aggressive with extended metastases. Herein, we repor
Autor:
Soumaya Hamich, R. El Bacha, Karima Senouci, Y. Saoiabi, L. Benzekri, F.Z. El Gaitibi, M. Meziane, N. Ismaili
Publikováno v:
La Presse Médicale Formation. 2:415-418
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 1:558-560
Publikováno v:
Our Dermatology Online. 12:419-421
Langerhans cell histiocytosis (LCH) is an uncommon systemic disease characterized by the infiltration of one organ or more by Langerhans cells. Its clinical presentation is heterogeneous and depends on the affected organs. We report the rare case of
Autor:
Michèle Sanchez, Hugo Tristani, Soumaya Hamich, Brigitte Lagrange, Martin Mazereeuw, Olivier Lavelle, Julien Rakotoson
Publikováno v:
Néphrologie & Thérapeutique. 16:431-436
Calciphylaxis is a rare and severe condition, characterized by calcification and thrombosis of small vessels, mainly affecting the skin. It is most often described in patients with end-stage renal disease on dialysis. Rarer cases of non-uremic calcip
Autor:
Gregory Cohen, Isabelle de Araujo, Niariantsoa Rakotomalala, Brigitte Lagrange, Franck Magnan, Julien Rakotoson, Anna Dellyes, Soumaya Hamich
Publikováno v:
Hématologie. 26:201-211