Zobrazeno 1 - 10
of 240
pro vyhledávání: '"Mouna, Snoussi"'
Publikováno v:
Acta Medica Iranica, Vol 61, Iss 4 (2023)
A 52‐year‐old woman developed progressive infiltrated purple and hyperpigmented cutaneous lesions in the face, thighs, armpits, chest, and abdomen evolving forone year. Histopathological examination showed large histiocytes exhibiting intact infl
Externí odkaz:
https://doaj.org/article/ad9bd5aa49044f249426931ac423b6b5
Autor:
Donia Chebbi, Sameh Marzouk, Imen Krichen, Ikram El Ahmer, Mouna Snoussi, Chifa Dammak, Faten Frikha, Raida Ben Salah, Choumous Kallel, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Acquired hemophilia A (AHA) is a potentially life‐threatening hemorrhagic disorder with many etiologies. We report the first case in the literature describing the association of AHA with adult‐onset Still's disease (AOSD).
Externí odkaz:
https://doaj.org/article/daa42fd1724343808b78e7030a7b8129
Autor:
Mouna Snoussi, Abir Derbel, Yosr Hentati Hentati, Zeineb Mnif, Sameh Marzouk, Zouheir Bahloul
Publikováno v:
European Journal of Case Reports in Internal Medicine (2023)
Rosai-Dorfman disease (RDD) is an uncommon lymphoproliferative disorder; RDD with oropharyngeal involvement is extremely rare, especially in adults. A 65-year-old woman with a complaint of progressive dyspnoea since 2016 presented with laryngeal invo
Externí odkaz:
https://doaj.org/article/19bd45596b924830a2cb73ea371b5d6b
Publikováno v:
Monaldi Archives for Chest Disease (2022)
One of the most common interstitial lung diseases in antisynthetase syndrome is nonspecific interstitial pneumonia (NSIP). A 49-year-old woman presented with slow progression exertional dyspnea, myalgia, and arthralgia. The radiological findings indi
Externí odkaz:
https://doaj.org/article/145ca8d022ab47878049594905f72a08
Autor:
Imen Chabchoub, Mouna Snoussi, Rania Ammar, Raida Ben Salah, Chifa Dammak, Faten Frikha, Mounir Bouaziz, Tahia Boudawara, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Guillain–Barré syndrome (GBS) and polymyositis (PM) are two rare autoimmune diseases, one of which affects the peripheral nervous system and other the muscle. We report the case of a young woman with no previous medical history who was ho
Externí odkaz:
https://doaj.org/article/651a94b8972941d48a776b0653229cdf
Autor:
Olfa Frikha, Raida Ben Salah, Ansar Mefteh, Faten Frikha, Mouna Snoussi, Sameh Marzouk, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Agranulocytosis is a rare acute condition characterized by severe a
Externí odkaz:
https://doaj.org/article/bdb3a4dda1584b9a97d3518a228ecbb3
Autor:
Donia Chebbi, Chifa Damak, Faten Frikha, Walid Abid, Mohamed Rebai, Mouna Snoussi, Raida Ben Salah, Sameh Marzouk, Abdessalem Hentati, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Pulmonary artery aneurysm must be evoked in front of any hemoptysis in a patient with Behçet disease as it requires urgent immunosuppressive therapy and often surgery.
Externí odkaz:
https://doaj.org/article/a907ce10286a4388b4e0db47b67694db
Autor:
Nedia Moussa, Tasnim Znegui, Mouna Snoussi, Rahma Gargouri, Zouhaier Bahloul, Sourour Abid, Samy Kammoun
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Hughes-Stovin syndrome is a very rare condition with no defined diagnostic criteria. We present the case of a 26-year-old man who had haemoptysis revealing Hughes-Stovin syndrome. We will consider the aetiology, therapeutic and evolutionary aspects o
Externí odkaz:
https://doaj.org/article/d0b70fba2f3741c4a0db73a6a7599de1
Publikováno v:
The Pan African Medical Journal, Vol 39, Iss 30 (2021)
Les pneumopathies infiltrantes diffuses (PID) constituent une manifestation fréquente des connectivites. Elles peuvent être révélatrices de la maladie ou survenir au cours du suivi. Le syndrome des anti-synthétases (SAS) est une connectivite aut
Externí odkaz:
https://doaj.org/article/25800c4fb9014673b619c1e65c9aeac5
Autor:
Mariem Ghribi, Faten Frikha, Abir Derbel, Sameh Marzouk, Raida Ben Salah, Mouna Snoussi, Zouhir Bahloul
Publikováno v:
PAMJ Clinical Medicine, Vol 3, Iss 191 (2020)
L´atteinte neurologique pseudotumorale au cours de la maladie de Behçet est rare. Quelques cas ont été rapportés dans la littérature. L´imagerie par résonance magnétique, montre un aspect pseudotumoral de localisation capsulothalamique. Le t
Externí odkaz:
https://doaj.org/article/1fa1dc683c7644ca805429ce456668b2