Badr Kabila

ORCID: 0009-0004-1908-4272
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About
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Research Areas
  • Abdominal vascular conditions and treatments
  • Biliary and Gastrointestinal Fistulas
  • Infectious Disease Case Reports and Treatments
  • Hemostasis and retained surgical items
  • Surgical Sutures and Adhesives
  • Cancer Diagnosis and Treatment
  • Pituitary Gland Disorders and Treatments
  • RNA regulation and disease
  • Cerebrospinal fluid and hydrocephalus
  • Histiocytic Disorders and Treatments
  • Diverticular Disease and Complications
  • Genital Health and Disease
  • Hereditary Neurological Disorders
  • Infectious Diseases and Mycology
  • Vascular Malformations and Hemangiomas
  • MXene and MAX Phase Materials
  • Intracranial Aneurysms: Treatment and Complications
  • Assisted Reproductive Technology and Twin Pregnancy
  • Diagnosis and treatment of tuberculosis
  • Tumors and Oncological Cases
  • Actinomycetales infections and treatment
  • Spinal Dysraphism and Malformations
  • Vascular anomalies and interventions
  • Pharmacological Effects and Toxicity Studies
  • Fetal and Pediatric Neurological Disorders

Mohammed V University
2023-2025

Institut National d'Oncologie
2024

Centre Hospitalier Ibn Sina
2023

10.1016/j.visj.2025.102272 article EN Visual Journal of Emergency Medicine 2025-04-01

Abstract Background Cavitary lung lesions are frequent findings on imaging, with the most common sources being malignancies and infections. They have multiple etiologies differential diagnoses, which can overlapping imaging characteristics, posing a diagnostic difficulty. Main body of abstract This article is an educational pictorial essay highlighting pitfalls diagnoses cavities, focusing typical patterns, clinical biological contexts each etiology, illustrated by images that were extracted...

10.1186/s43055-023-01098-7 article EN cc-by The Egyptian Journal of Radiology and Nuclear Medicine 2023-09-04

Meningocele is a rare congenital malformation of the central nervous system resulting from herniation meninges containing cerebrospinal fluid through bony defect in skull. It part neural tube closure anomalies. The overall incidence meningocele 0.8 to 3 per 10 000 live births; it varies based on geographical location and race, with predominance occipital localization. Among diagnostic methods, computed tomography (CT) magnetic resonance imaging (MRI) remain crucial examinations. Prenatal...

10.1177/2333794x231204498 article EN cc-by-nc Global Pediatric Health 2023-01-01

Acute disseminated encephalomyelitis (ADEM) is an acute and rapidly progressive auto-immune demyelinating disorder in the central nervous system. It a rare disease but more frequently observed pediatric population. We report case of monophasic postvaccination ADEM, which presented with paraparesis associated fever. showed favorable evolution under corticosteroids, without recurrence after 3 years follow-up. The diagnosis was established due to context MRI abnormalities characteristics. This...

10.1016/j.radcr.2023.08.107 article EN cc-by-nc-nd Radiology Case Reports 2023-11-10

The brown tumor is a non-neoplastic lesion resulting from an abnormality in bone metabolism the context of primary, secondary, or tertiary hyperparathyroidism. They can affect any structure and be single multiple. are usually located on long bones, pelvis, ribs, collarbones. Facial localization rare found only 4.5% tumors dominated by mandibular involvement. treatment depends several elements: etiology, location, symptomatology. It regress disappear after hyperparathyroidism, thus avoiding...

10.1177/2333794x231219168 article EN cc-by-nc Global Pediatric Health 2023-01-01

Abstract The Buschke-Lowenstein Tumor is a giant condyloma acuminatum caused by human papillomavirus, most commonly types 6 or 11. It rare condition with an estimated frequency of 0.1% in the general population. Transmission primarily occurs through sexual contact. particularly affects men, predominantly appearing on penis, characterized its deep-seated growth, potential for degeneration, and tendency to recur after treatment. Surgery preferred We present case a50-year-old patient history...

10.1093/omcr/omae034 article EN cc-by-nc Oxford Medical Case Reports 2024-04-01

Abstract A pheochromocytoma is a tumor that typically originates within the chromaffin cells of adrenal glands, resulting in excessive production catecholamines. Cystic forms are exceptional and pose diagnostic challenge, especially those non-secreting. The most prevalent symptom associated with this condition arterial hypertension, which can be either persistent or, more commonly, intermittent. Ménard triad, comprising headaches, sweating, palpitations, may accompany episodes hypertension....

10.1093/omcr/omae033 article EN cc-by-nc Oxford Medical Case Reports 2024-04-01

10.1016/j.visj.2024.102105 article EN Visual Journal of Emergency Medicine 2024-09-13

The “Mercedes-Benz” sign is a term used to describe triradiate pattern of gas found within gallstones. This was initially observed on abdominal radiographs and later confirmed computed tomography. It allows the differentiation with causes gallbladder such as emphysematous cholecystitis, biliary-enteric fistula, sphincterotomy, cholangitis from gas-forming organisms.

10.4103/amhs.amhs_115_23 article EN cc-by-nc-sa Archives of Medicine and Health Sciences 2024-09-01

Rhinoscleroma is a rare benign granulomatous disease in children, the pathogen of which Klebsiella rhinoscleromatis. almost always affects respiratory tract, nasal cavities are most common site, but can also be found over entire extent tree, clinically patient often presents with obstruction other non-specific signs, Histology basis diagnosis rhinoscleroma. Early and appropriate medical treatment improves prognosis prevents progression to disabling sequelae. We present case 9-year-old child...

10.1177/2333794x231210673 article EN cc-by-nc Global Pediatric Health 2023-01-01

A subcutaneous mass in the anterior region of thorax, (presternal region). Subcutaneous metastases ovarian cancer are rare, occurring 0.9% to 5.8% cases. They usually a late manifestation that arises several years after initial diagnosis and often serve as poor prognostic indicator. Their presence suggests reported median survival ranging from 3 18 months. can be categorized into umbilical metastases, commonly referred Sister Joseph's nodules (SJN) most prevalent type, non-SJN cutaneous...

10.1016/j.radcr.2024.06.097 article EN cc-by-nc-nd Radiology Case Reports 2024-07-27

Mesenchymal hamartoma (MH) is a benign liver tumor accounting for 3% to 8% of all tumors in children, commonly manifesting before 3 years life. Distinguishing MH from hepatoblastoma and other relies on imaging alpha-fetoprotein (which usually within normal range MH), histologic examination. We report case hepatic associated with elevated alpha-fetoprotein, leading misdiagnosis the administration chemotherapy. draw attention diagnostic difficulty pitfalls related elevation setting tumor, we...

10.1177/2333794x231193560 article EN cc-by-nc Global Pediatric Health 2023-01-01
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