Publications by authors named "Ashraf Chadli Debbiche"
Article Synopsis
- Hemangiomas of the small intestine, though rare, can cause serious issues like intussusception, especially in young people, making diagnosis before surgery quite difficult.!* -
- A case involving a 3-month-old girl highlighted the severity of this condition, as she presented with symptoms of abdominal pain and bleeding, ultimately requiring surgical resection to remove the affected portion of the intestine.!* -
- Post-surgery, the patient had no complications, indicating that while rare, early recognition and surgical intervention for hemangiomas could lead to positive outcomes, despite the challenges in diagnosis provided typical methods.!*
Cutaneous lesions may represent the initial sign of various neoplasms in children, including histiocytosis, neuroblastomas, and lymphomas. Primary cutaneous lymphoblastic lymphomas are rare and involve mostly the B-cell phenotype. Herein, we report a case of isolated, primary B-lymphoblastic lymphoma in a 7-month-old infant and emphasize the importance of early diagnosis.
View Article and Find Full Text PDFIntroduction: Several theses are supported, every year, in the Faculty of Medicine of Tunis but their scientific become is this day unknown. The most part of specialities have not bibliometric data.
Objectives: This work had for objectives to study the still unknown future of theses of Tunis Faculty of Medecine during 2004-2005, in terms of publication in indexed reviews and to determine the predictive factors of their publication.
Xeroderma Pigmentosum (XP) is a rare recessive autosomal cancer prone disease, characterized by UV hypersensitivity and early appearance of cutaneous and ocular malignancies. We investigated four unrelated patients suspected to be XP-C. To confirm linkage to XPC gene, genotyping and direct sequencing of XPC gene were performed.
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