Zobrazeno 1 - 10
of 186
pro vyhledávání: '"Ines, Chelly"'
Autor:
Ghassen Gader, Meissa Hamza, Ftima Zarraa, Ines Chelly, Ihsen Zammel, Mouna Rkhami, Mohamed Badri
Publikováno v:
Caspian Journal of Internal Medicine, Vol 15, Iss 2, Pp 354-359 (2024)
Background: Intracranial inflammatory pseudotumours (IPT) are rare entities that frequently lead to misdiagnosis with malignant lesions. The identification of these lesions is difficult, but important to avoid inadvertent iatrogenicity and to adjust
Externí odkaz:
https://doaj.org/article/8f4d7a34ea9341d88358172e269c3962
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 12 (2024)
This report describes a case of facial hyperpigmentation in a patient with Crohn’s disease receiving adalimumab, a tumor necrosis factor (TNF)-alpha inhibitor. The onset of hyperpigmentation coincided with adalimumab administration, and its discont
Externí odkaz:
https://doaj.org/article/9c7a40f0ecfb449cbe762904135452e4
Autor:
Dorsaf Elinkichari, Mariem Tabka, Asmahane Souissi, Fatimazahra Alaoui, Ines Chelly, Slim Haouet, Mourad Mokni
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract Morphea is an auto‐immune disease, and its association with other immune‐mediated diseases should not come as a surprise. Dermatologists should be aware of its possible coexistence with severe systemic involvement.
Externí odkaz:
https://doaj.org/article/e09d574aa09d4ee0a4313af382cd26e6
Publikováno v:
Urology Case Reports, Vol 48, Iss , Pp 102400- (2023)
Urinary tract endometriosis (UTE) is a very rare but serious form of infiltrating endometriosis because of the risk of urinary tract obstruction and loss of renal function. We report the case of A 42-year-old female patient admitted for intense right
Externí odkaz:
https://doaj.org/article/2a2b1321dd324727a719b1b80484a2d8
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3339-3342 (2020)
Externí odkaz:
https://doaj.org/article/a29f46c831224f3aa87fe742d301eb41
Autor:
Wissal Abdelli, Asmahen Souissi, Fatima Alaoui, Wiem Sassi, Ines Chelly, Slim Haouat, Mourad Mokni
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Rapp–Hodgkin syndrome (RHS) is a rare condition that is characterized by ectodermal dysplasia and palatal abnormalities. Palmoplantar keratoderma (PPK) is an unusual manifestation of hidrotic ED. Ulcerations on the palms are also not commo
Externí odkaz:
https://doaj.org/article/604c18e5a7274eeb9b5b8fda915431ce
Autor:
Wissal Abdelli, Fatima Alaoui, Asmahen Souissi, Wiem Sassi, Ines Chelly, Slim Haouet, Mourad Mokni
Publikováno v:
Clinical Case Reports, Vol 9, Iss 12, Pp n/a-n/a (2021)
Abstract Necrolytic migratory erythema (NME) is a rare cutaneous paraneoplastic manifestation of glucagonoma. We report a case of a woman with a 6‐year history of delayed diagnosis of glucagonoma. This case highlights the atypical clinical features
Externí odkaz:
https://doaj.org/article/a13a95e96c9a48b6b1b94e87a6e71b59
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1450-1452 (2021)
Abstract Primary umbilical endometriosis is unusual clinical presentation of endometriosis. Its diagnosis can be challenging due to lack of knowledge. This condition should be listed in the differential diagnosis of umbilical disorders.
Externí odkaz:
https://doaj.org/article/6514792cbd3a42fe9ea2588da448ae94
Publikováno v:
Indian Journal of Neurosurgery, Vol 06, Iss 03, Pp 228-231 (2017)
Extraventricular locations of neurocytoma are extremely rare, especially in the spinal cord, which has been reported in only sporadic cases. In this article, we report a new pediatric case of a spinal neurocytoma in a 12-year-old girl and briefly rev
Externí odkaz:
https://doaj.org/article/d507296c45534f8d84e78dfedb00f867
Autor:
Amal Chamli, Asmahane Souissi, Refka Frioui, Fatima Alaoui, Wiem Sassi, Asma Raboudi, Ines Chelly, Mourad Mokni
Publikováno v:
International Journal of Rheumatic Diseases.