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325 results on '"Litaiem, Noureddine"'

2. Extracting Color Name Features Utilized for Skin Disease Characterization and Comparing It to Other Representations Describing the ABCD Dermatological Criteria for Melanoma Inspection

Author

Daghrir, Jinen, Tlig, Lotfi, Bouchouicha, Moez, Moreau, Eric, Litaiem, Noureddine, Zeglaoui, Faten, Sayadi, Mounir, Filipe, Joaquim, Editorial Board Member, Ghosh, Ashish, Editorial Board Member, Prates, Raquel Oliveira, Editorial Board Member, Zhou, Lizhu, Editorial Board Member, Maciaszek, Leszek A., editor, Mulvenna, Maurice D., editor, and Ziefle, Martina, editor

Published
2023
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7. Nail Alterations From Musical Instruments: Insights for Dermatologists Treating Musicians.

Author

Ghannem, Azza, Litaiem, Noureddine, Slouma, Maroua, and Zeglaoui, Faten

Subjects
PERFORMANCE practice (Music performance), MEDICAL personnel, MUSICAL instruments, SURFACE plates, NAILS (Anatomy)
Abstract

Long-term practice and performance with a musical instrument predispose musicians to several skin conditions and nail disorders. We conducted a comprehensive literature search of the PubMed, Scopus, and Google Scholar databases for articles on nail alterations in musicians. Complications were divided into modifications of the nail surface and nail plate, soft-tissue abnormalities, and periungual tissue and distal pulp disorders. Health care professionals should be aware of these various modifications related to the use of musical instruments and provide preventive measures. [ABSTRACT FROM AUTHOR]

Published
2024
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10. Cutaneous involvement in Rosai–Dorfman disease: clinical and dermoscopic features.

Author

Litaiem, Noureddine, Trimech, Ranim, Daoud, Yosr, Gara, Soumaya, Slouma, Maroua, Jones, Meriem, and Zeglaoui, Faten

Subjects
*NON-langerhans-cell histiocytosis, *SKIN diseases, *DELAYED diagnosis, *TEMPORAL lobe, *DISEASE remission, *ERDHEIM-Chester disease
Abstract

The article discusses cutaneous involvement in Rosai-Dorfman disease (RDD), a rare non-Langerhans cell histiocytosis. The study describes the clinical, dermoscopic, and therapeutic features of cutaneous RDD (CRDD) based on nine cases identified in North Africa. The article emphasizes the importance of recognizing characteristic features of CRDD, such as asymptomatic red-brown to yellow papules, nodules, or plaques, and highlights the use of dermoscopy in aiding diagnosis. Treatment options for CRDD include systemic corticosteroids, with observation being indicated in some cases of remarkable remission. [Extracted from the article]

Published
2024
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11. Collective human intelligence vs. artificial intelligence: a comparative analysis for melanoma diagnosis in darker skin tones.

Author

Litaiem, Noureddine, Sboui, Karama, Daghrir, Jinen, Khouladi, Asma, Tlig, Lotfi, Bouchouicha, Moez, Sayadi, Mounir, and Zeglaoui, Faten

Subjects
*ARTIFICIAL neural networks, *ARTIFICIAL intelligence, *CONVOLUTIONAL neural networks, *MAJORITIES, *NEVUS, *MELANOMA
Abstract

The study compared the diagnostic performance of a deep learning (DL) model and collective human intelligence (CoHI) in diagnosing melanoma in patients with darker skin tones. The DL model showed higher sensitivity but lower specificity compared to CoHI, indicating the need for more inclusive training datasets for accurate diagnosis in diverse populations. The study highlighted the importance of training artificial intelligence models on diverse skin tones to ensure equitable and accurate diagnosis for all individuals. [Extracted from the article]

Published
2024
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24. Keratoacanthoma arising within a linear epidermal nevus

Author

Litaiem, Noureddine, Toumi, Asma, and Zeglaoui, Faten

Subjects
Nevus, Health
Abstract

Byline: Noureddine. Litaiem, Asma. Toumi, Faten. Zeglaoui A 22-year-old male with an existing linear epidermal nevus on the nape of his neck, was referred for a dermatological evaluation of a [...]

Published
2020

31. Becker Nevus Syndrome: A Rare Entity but Important to Recognize.

Author

LITAIEM, NOUREDDINE, CHABBOUH, AMEL, CHABCHOUB, INES, NACEUR, RADHI BEN, MOKNI, MOURAD, and ZEGLAOUI, FATEN

Subjects
*SKELETAL muscle, *NEVUS, *SYNDROMES, *WOMEN patients, *EARLY diagnosis
Abstract

Becker's nevus syndrome is defined by the association of a Becker nevus with homolateral breast hypoplasia or more rarely skeletal cutaneous or muscle deformities. Early diagnosis is important, especially in female patients to prevent and treat breast hypoplasia. We report two cases of Becker nevus syndrome with serious functional impairment and discuss possible treatment options. [ABSTRACT FROM AUTHOR]

Published
2024

37. End of the road for terbinafine? Think of compliance to treatment

Author

Litaiem, Noureddine, Karray, Manel, Bouhlel, Sabrine, Bacha, Takwa, and Zeglaoui, Faten

Subjects
Health
Abstract

Byline: Noureddine. Litaiem, Manel. Karray, Sabrine. Bouhlel, Takwa. Bacha, Faten. ZeglaouiSir,We read with interest the publication entitled 'End of the road for terbinafine? Results of a pragmatic prospective cohort study [...]

Published
2019

45. Maintenance Phototherapy for the Treatment of Early-stage Mycosis Fungoides

Author

Gara, Soumaya, Litaiem, Noureddine, Bacha, Takwa, Jmour, Yosra, and Zeglaoui, Faten

Subjects
Case Report
Abstract

Mycosis fungoides (MF) is the most common type of cutaneous T cell lymphoma. Phototherapy is a first-line treatment option of early stages MF. The present study aimed at assessing the efficacy of phototherapy in Tunisian patients with MF treated with phototherapy and evaluate the efficacy of maintenance phase.

Published
2021

47. Acute localized exanthematous pustulosis: Clinical features, pathophysiology, and therapy

Author

Hichem Belhajali, Jameleddine Zili, Zeglaoui Faten, Litaiem Noureddine, Lahouel Ines, Jones Meriem, Idoudi Safa, and Njima Manel

Subjects
medicine.medical_specialty, business.industry, Dermatology, General Medicine, Disease, Acute generalized exanthematous pustulosis, medicine.disease, Pathophysiology, Pathogenesis, Hypersensitivity reaction, Acute Generalized Exanthematous Pustulosis, Humans, Medicine, Acute Localized Exanthematous Pustulosis, Good prognosis, business, Rare disease
Abstract

Acute localized exanthematous pustulosis (ALEP) is a rare disease characterized by the acute onset of multiple localized non-follicular, pinhead-sized pustules. ALEP is considered a localized form of acute generalized exanthematous pustulosis but its pathogeny is not well identified. We performed a systematic review of the literature of all publications regarding ALEP cases using the term "acute localized exanthematous pustulosis," to provide an update on this disease and its management. Results and conclusion ALEP is an uncommon skin condition attributed primarily to a hypersensitivity reaction to a systemic drug (classical or herbal); though a contact mechanism has been reported. It may be misdiagnosed as infectious or inflammatory disease but the clinico-pathological correlation in addition to the rapid response to withdrawal of the culprit agent supports this diagnosis. The pathogenesis of ALEP is still unclear, and there are no standardized treatment guidelines to manage this disease. Both AGEP and ALEP have a good prognosis if an early diagnosis is made.

Published
2021
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