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Featured researches published by H. Marrak.


Skin Pharmacology and Physiology | 2005

Acebutolol-induced subacute cutaneous lupus erythematosus.

Samy Fenniche; Asma Dhaoui; F. Ben Ammar; Rym Benmously; H. Marrak; I. Mokhtar

Beta-blocking medications are rarely associated with drug-induced lupus erythematosus syndrome and have never been incriminated as a cause of subacute lupus erythematosus (SCLE). We present herein the first case of SCLE induced by acebutolol. A 57-year-old woman presented with a 1-month history of a cutaneous eruption of the photoexposed areas. One month ago, the patient had started a treatment with oral acebutolol to cure a hypertension of 1-year evolution. Physical examination revealed erythematous scaly annular plaques, involving the face, arms and trunk. Immunologic serology findings revealed a positive titer of antinuclear antibodies up to 1/1,280 with positivity of antihistone and Ro/SSA antibodies. Acebutolol was stopped, and the lesions cleared completely 4 months later. Literature data, along with our case, suggest a link between acebutolol therapy and the onset of a lupus syndrome. Although this is the first report of acebutolol-induced SCLE, we should be aware of this occurrence, and avoidance of acebutolol is recommended in patients with stigmata of lupus erythematosus


Annales De Dermatologie Et De Venereologie | 2004

Hémangioendothéliome épithélioïde cutané

Samy Fenniche; Rym Benmously; H. Marrak; Olfa Khayat; F. Ben Ammar; Achraf Debbiche; M. Ben Ayed; I. Mokhtar

Resume Introduction L’hemangioendotheliome epithelioide est une tumeur des tissus mous prenant naissance a partir de l’endothelium vasculaire. Elle est consideree comme une tumeur de bas grade de malignite. La localisation a la peau est tres rare et fait souvent partie d’une atteinte multisystemique. Observation Une femme de 34 ans, consultait pour un nodule cutane erythemato-violace, douloureux, siegeant a l’avant-bras droit et evoluant depuis 6 mois. Une echographie abdominale avait ete pratiquee 1 mois avant l’apparition du nodule cutane, du fait de douleurs epigastriques et etait normale. Les examens histologiques et immunohistochimiques cutanes permettaient de poser le diagnostic d’hemangioendotheliome epithelioide. Le bilan d’extension, comprenant des examens radiologiques, echographiques, un scanner thoraco-abdominal et une imagerie par resonance magnetique, revelait la presence de nodules hepatiques. Le traitement consistait en une exerese large et complete de la tumeur. Apres un an d’evolution, aucune recidive locale n’etait observee et les localisations hepatiques etaient stables. Discussion L’hemangioendotheliome epithelioide appartient au groupe des tumeurs vasculaires epithelioides ayant en commun un aspect morphologique epithelioide des cellules tumorales endotheliales. La localisation a la peau est rare et a notre connaissance, seulement 20 cas d’hemangioendotheliome epithelioide avec atteinte cutanee ont ete rapportes dans la litterature. L’hemangioendotheliome epithelioide cutane peut rester isole ou rentrer dans le cadre d’une maladie multifocale avec des atteintes viscerales associees. Ainsi, la decouverte de lesions cutanees impose la pratique d’un bilan d’extension a la recherche de localisations profondes. L’hemangioendotheliome epithelioide etant considere comme une tumeur de bas grade de malignite, l’integrite du foie chez cette malade, observee un mois avant l’apparition de la maladie, est en faveur d’une maladie multicentrique plutot que de localisations metastatiques hepatiques d’une tumeur cutanee primitive.


International Journal of Dermatology | 2013

Tongue hyperpigmentation during PEG-interferon-alfa/ribavirin therapy in a non-Caucasian patient with chronic hepatitis C: a case report and review of the literature

Rym Benmously Mlika; Nadia Kerkeni; H. Marrak; Samy Fenniche; Incaf Mokhtar; Achraf Debbiche

Morphol 2002; 10: 7–14. 3 Wu YH, Chen HC, Hsiao PF, et al. Hydroa vacciniforme-like Epstein-Barr virus-associated monoclonal T-lymphoproliferative disorder in a child. Int J Dermatol 2007; 46: 1081–1086. 4 Quintanilla-Martinez L, Kimura H, Jaffe ES. EBV-positive T-cell lymphoproliferative disorders of childhood. In: Swerdlow SH, Campo E, Harris NL, et al., eds. WHO Classification of Tumors of Hematopoietic and Lymphoid Tissues. Lyon: IARC Press, 2008: 278–280. 5 Oono T, Arata J, Masuda T, Ohtsuki Y. Coexistence of hydroa vacciniforme and malignant lymphoma. Arch Dermatol 1986; 122: 1306–1309. 6 Feng S, Jin P, Zeng X. Hydroa vacciniforme-like primary cutaneous CD8-positive T-cell lymphoma. Eur J Dermatol 2008; 18: 364–365. 7 Doeden K, Hernan MK, Perez E, et al. Hydroa-like lymphoma with CD56 expression. J Cutan Pathol 2008; 35: 488–494. 8 Xu Z, Lian S. Epstein-Barr virus-associated hydroa vacciniforme-like cutaneous lymphoma in seven Chinese children. Pediatr Dermatol 2010; 27: 463–469. 9 Cohen JI, Kimura H, Nakamura S, et al. Epstein-Barr virus-associated lymphoproliferative disease in nonimmunocompromised hosts: a status report and summary of an international meeting, 8–9 September 2008. Ann Oncol 2009; 20: 1472–1482. 10 Lyssel J, Wiegleb Edstrom D, Linde A, et al. Antiviral therapy in children with hydroa vacciniforme. Acta Derm Venereol 2009; 89: 393–397.


International Journal of Dermatology | 2013

Unilateral upper limb skin sarcoid reaction after homolateral mastectomy for breast cancer

Talel Badri; Nadia Kerkeni; H. Marrak; Elhem Khelifa; Rym Benmously-Mlika; Incaf Mokhtar; Samy Fenniche

in patients with familial benign chronic pemphigus (Hailey–Hailey disease). J Am Acad Dermatol 1989; 21: 506–510. 3 Remitz A, Lauerma AI, Stubb S, et al. Darier’s disease, familial benign chronic pemphigus (Hailey–Hailey disease) and contact hypersensitivity. J Am Acad Dermatol 1990; 22: 134. 4 Pónyai G, Kárpáti S, Ablonczy E, et al. Benign familial chronic pemphigus (Hailey–Hailey) provoked by contact sensitivity in two patients. Contact Derm 1999; 40: 168– 169. 5 Walker SL, Beck MH. Undiagnosed Hailey–Hailey disease causing painful erosive changes during patch testing. Br J Dermatol 2005; 153: 253–254.


Dermatology Online Journal | 2006

Childhood cutaneous tuberculosis: a 20-year retrospective study in Tunis.

Rym Benmously Mlika; Tounsi J; Samy Fenniche; Hajlaoui K; H. Marrak; I. Mokhtar


Dermatology Online Journal | 2005

Syphilis presenting as erosive papules on the palate

Rym Benmously Mlika; Samy Fenniche; Elhem Khelifa; H. Marrak; Achraf Debbiche; Olfa Khayat; Mohamed Ben Ayed; Incaf Mokhtar


Dermatology Online Journal | 2008

Erythematous nodule of the eyelid.

Rym Benmously-Mlika; Elhem Khelifa; Achraf Debbiche; H. Marrak; Mohamed Ben Ayed; Incaf Mokhtar; Samy Fenniche


Journal De Mycologie Medicale | 2003

Chromomycose : À propos d'une observation

H. Marrak; N. Mnajja; Samy Fenniche; M Fourati; M. Zghal; E. Chaker; M. Ben Ayed; I. Mokhtar


Tunisie médicale | 2011

Prurit chez le sujet âgé: Etude de 208 cas

Nedra Sliti; Rim Benmously; Sami Fenniche; H. Marrak; Selima Ben Jannet; Incaf Mokhtar


Annales De Dermatologie Et De Venereologie | 2008

Xanthomes tubéreux révélant une hypercholestérolémie familiale homozygote

Houda Hammami; Rym Benmously; H. Marrak; A. Debbiche; Anissa Souissi; M. Ben Ayed; Samy Fenniche; I. Mokhtar

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