Publications by authors named "Yosra Soua"

Unlabelled: Introduction-Aim: The third cycle of medical studies (TCMS) lasts 3 years for the specialty of family medicine (FM) in Tunisia. The members of the FM committee of the Faculty of Medicine of Monastir (FMM) aimed to detail the learning objectives (LO) of residents in FM.

Method: We used the Delphi method in 2 rounds including a group of experts called FM Learning Objectives Writing Group (FMLOWG) at the FMM.

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A 61-year-old woman presented with a 3-year history of painless soft-tissue mass on the right sole. The patient reported gradual growth, with a rapid increase in size over the past few months, leading to difficulty in walking. She had no history of past trauma.

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We report a new case of chronic recurrent annular neutrophilic dermatosis in a woman. Through our observation, we aim to make the clinician aware of this rare entity, in order to consider it among the diagnostic hypotheses of annular dermatosis, with centrifugal, recurrent, and chronic evolution.

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Article Synopsis
  • - A newborn boy weighing 4500g was delivered via C-section at 41 weeks due to fetal distress, shortly after which he exhibited respiratory issues and required ventilation support, followed by convulsions diagnosed as hypoxic-ischemic encephalopathy.
  • - Subsequent examination revealed firm, nodular lesions on his body, diagnosed as subcutaneous fat necrosis, accompanied by laboratory results indicating low levels of calcium, magnesium, and potassium.
  • - Treatment involved vitamin and electrolyte supplementation, which led to improved calcium levels, but resulted in hypertriglyceridemia; after managing complications with medication, the infant showed complete recovery from fat necrosis and normalized growth by the end of two months.
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Bullous morphea is a rare variant of localized scleroderma characterized by occasional intermittent blisters. Lichen sclerosus is a chronic inflammatory disease. The coexistence of morphea and lichen sclerosus has been reported in different sites in the same patient and more rarely in the same lesion.

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Lichen planus pigmentosus is uncommon in childhood and its treatment is often challenging. We report a case of cutaneous lichen planus pigmentosus in a 10-year-old boy, without oral mucosal involvement, two months after an amalgam dental restoration. The diagnosis was based on the histopathological examination of a skin biopsy, the positive patch test to mercury, and the improvement after amalgam removal.

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Background: Fixed drug eruption (FDE) represents a drug-related cutaneous reaction. Many drugs been associated with this clinical entity, with continually evolving documentation of implicated agents and clinical presentations. A bullous form can occur although it is rare.

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