References of "Mokhtar, I"
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See detailVulvar basal cell carcinoma
Kharfi, M.; Mokhtar, I.; Fazaa, B. et al

in European Journal of Dermatology (1992), 2

Vulva is an uncommon localization for basal cell carcinomas. We report three cases and review the literature. There is often a long delay before patients seek medical attention for these lesions. Moreover ... [more ▼]

Vulva is an uncommon localization for basal cell carcinomas. We report three cases and review the literature. There is often a long delay before patients seek medical attention for these lesions. Moreover the clinical aspect is often indistinctive and misleading. The gross polymorphism of vulvar neoplasms therefore calls for biopsy of any suspicious areas. Surgical excision or Moh's chemotherapy are the treatments of choice for vulvar basal cell carcinomas. The recurrence rate remains quite high even when the lesion looks completely resected. [less ▲]

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See detailCongenital sebaceous trichofolliculoma
Kharfi, M.; Fazaa, B.; Mokhtar, I. et al

in Giornale Internazionale Dermatologia Pediatrica (1992), 4(1), 33-35

We report the clinical and histological presentation of a sebaceous trichofolliculoma present on the dorsum of the nose of a 1-year-old boy. This lesion was present since birth and appears to be the forst ... [more ▼]

We report the clinical and histological presentation of a sebaceous trichofolliculoma present on the dorsum of the nose of a 1-year-old boy. This lesion was present since birth and appears to be the forst reported cas of a congenital sebaceous trichofolliculoma. [less ▲]

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See detailGranulomatous rosacea and demodicidosis
Kharfi, M.; Zarrouk, H.; Nikkels, Arjen ULg et al

in African journal of Dermatology (1991), 4(2), 39-43

Granulomatous rosacea is a rare disease sometimes mistaken for sarcoidosis or tuberculosis. We briefly review the historical evolution of the concept of this disease. We document this study with twelve ... [more ▼]

Granulomatous rosacea is a rare disease sometimes mistaken for sarcoidosis or tuberculosis. We briefly review the historical evolution of the concept of this disease. We document this study with twelve clinico-pathological confrontations, and we emphasize the resemblance with granulomatous demodicidosis. [less ▲]

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