601 results match your criteria: "Aleppo University.[Affiliation]"

A nationwide survey in the USA reported that healthcare workers had the highest prevalence of short sleep duration compared with other professions. Moreover, several studies have reported poor sleep quality among healthcare professionals and described insufficient sleep as a potential driver of reduced physician well-being. This study aims to explore sleep quality and mental health issues among Syrian medical residents, with the goal of informing targeted interventions to enhance their well-being and professional performance.

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Extraction and characterization of spherical nanocellulose from sesame husks.

Heliyon

January 2025

Department of Food Engineering Technologies, Faculty of Technical Engineering, Aleppo University, Syria.

The objective of this study was to extract and characterize nanocellulose from sesame husks, which are typically discarded as waste by sesame processing facilities. However, these husks are rich in cellulose, presenting a valuable potential source for nanocellulose. Sesame husk cellulose (SHC) was initially isolated through a multi-step process that removed oil, hemicellulose, and lignin.

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Introduction: The COVID-19 pandemic has significantly impacted global healthcare systems. Vaccination is an effective strategy to battle the disease. Policies and distribution frameworks have varied widely across countries.

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Successful surgical management of Leriche syndrome in a 30-year-old female patient: A rare case report.

Int J Surg Case Rep

January 2025

Department of Vascular Surgery, Faculty of Medicine, Aleppo University Hospital, University of Aleppo, Aleppo, Syria.

Introduction And Importance: Leriche syndrome (LS), or aortoiliac occlusive disease, is a rare form of peripheral arterial disease leading to claudication, impotence, and diminished femoral pulses due to atheromatous obstruction of the infrarenal aorta and common iliac arteries. Early identification is crucial as untreated LS can result in severe complications. Treatment primarily involves surgical interventions, with endovascular options considered as alternatives.

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Bickerstaff Brainstem Encephalitis (BBE) is a rare immunologic condition characterized by CNS inflammation, presenting with ataxia, external ophthalmoplegia, altered consciousness, and quadriplegia. A 25-year-old male with no significant medical history exhibited symptoms of blurred vision, diplopia, facial numbness, and imbalance following a respiratory infection. Brain MRI revealed hyperintense lesions in the cerebral peduncle and pons on T2-weighted/FLAIR sequences but not on T1-weighted sequences, indicative of demyelination.

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Trichobezoars are accumulations of undigested hair. Usually, this disorder follows a psychiatric etiology; however, sometimes a nonpsychiatric etiology, such as pica, can also be suspected. Rapunzel syndrome is a rare type of trichobezoar in which the hair is usually confined to the stomach and small intestine.

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Novel Otolaryngological and Radiological Manifestations in GAPO Syndrome.

Ear Nose Throat J

December 2024

Department of Otorhinolaryngology, Al Mouwasat University Hospital, Damascus University, Damascus, Syria.

GAPO syndrome is an exceptionally-rare autosomal recessive disorder characterized by growth retardation, alopecia, pseudoanodontia, and optic abnormalities, with fewer than 60 cases reported globally. We present the first documented case in Syria, highlighting novel otolaryngological and radiological findings that expand the clinical spectrum of this syndrome. A 27-year-old male presented with chronic right-sided otalgia, unilateral conductive hearing loss, and persistent sinonasal symptoms.

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Ectopic pregnancy, the implantation of a fertilized zygote outside the uterine cavity, presents with abdominal pain and vaginal bleeding. Diagnosis relies on clinical signs, and treatment involves surgery or methotrexate in selected cases. A 24-year-old woman at 37 weeks of gestation underwent elective cesarean delivery under general anesthesia, revealing an unexpected broad ligament ectopic pregnancy.

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Intravascular leiomyoma (IVL) with intracardiac extension (ICE) represents an exceedingly rare diagnosis of a cardiac mass. We present the case of a 42-year-old woman with recurrent syncopal episodes. Cardiac investigations revealed an extensive, mobile mass stretching from the inferior vena cava (IVC) through the right heart to the bifurcation of the pulmonary artery.

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Introduction: Cancer poses a significant burden in Africa, where limited resources and infrastructure compound the challenges of managing the disease. Undernutrition, a critical concern among cancer patients, can profoundly affect treatment outcomes and overall prognosis. Despite its importance, the prevalence of undernutrition among African cancer patients remains poorly understood.

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Introduction: Post-intubation tracheal rupture (PiTR) is an extremely uncommon disorder. Pneumothorax, pneumomediastinum, hemorrhage, cutaneous emphysema, and sepsis are common clinical presentations that eventually result in organ failure and mediastinitis. Endoscopy and computed tomography (CT) are considered the gold standards for assessment and diagnosis.

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Article Synopsis
  • The spleen develops from mesenchymal cells in the dorsal mesentery during embryogenesis, and accessory spleens are common anomalies that can be mistaken for tumors; this case is the first report of three accessory spleens found in Syria in a patient who had a prior splenectomy.
  • A 33-year-old male experienced right-sided abdominal pain, and after medical evaluation, imaging tests showed a lobulated mass in the right adrenal gland and elevated levels of metanephrine, suggesting a pheochromocytoma; laparoscopic surgery ultimately revealed multiple accessory spleens without signs of cancer.
  • The case emphasizes the importance of considering accessory spleens in patients with masses near the adrenal glands, as they can complicate diagnosis and treatment
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Article Synopsis
  • Ulcerative colitis is a chronic inflammatory condition affecting the gastrointestinal tract and can lead to complications in multiple body systems, including autoimmune disorders like Takayasu arteritis and ankylosing spondylitis.
  • A case study highlights a 32-year-old man with a long history of ulcerative colitis who also developed ankylosing spondylitis and Takayasu's disease, showing significant improvement after treatment with infliximab.
  • The report emphasizes the importance of recognizing these coexisting conditions to improve diagnosis and treatment outcomes for patients with complex autoimmune diseases.
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Effective communication of scientific knowledge plays a crucial role in the advancement of medical research and health care. Technological advancements have introduced large language models such as Chat Generative Pre-Trained Transformer (ChatGPT), powered by artificial intelligence (AI), which has already shown promise in revolutionizing medical writing. This study aimed to conduct a detailed evaluation of ChatGPT-3.

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Intraoperative diagnosis of Amyand's hernia, a case report.

Int J Surg Case Rep

November 2024

Faculty of Medicine, Aleppo University, Stemosis for Scientific Research, Syria.

Introduction: Hernia forms when an organ or its fascia protrudes through the continuing cavity's wall. Amyand's hernia describes an inguinal hernia containing an appendix, regardless of inflammation.

Presentation Of Case: Our patient was complaining of an increasing lump in the inguinal area.

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Article Synopsis
  • Pulsed-field ablation (PFA) is a new technique for treating atrial fibrillation (AF) that targets heart tissue more selectively than traditional thermal methods like radiofrequency and cryoablation.
  • A systematic review of 17 studies with 2,255 patients found that PFA significantly lowers AF recurrence, procedure time, heart rate changes, and risks of certain complications like phrenic nerve palsy and esophageal lesions.
  • However, PFA is also linked to a higher risk of pericardial tamponade, indicating it has both benefits and potential risks compared to thermal ablation.
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Article Synopsis
  • - This meta-analysis compares two breast reconstruction techniques, Deep Inferior Epigastric Perforator (DIEP) flaps and Latissimus Dorsi (LD) flaps, to evaluate patient satisfaction and complication rates to help guide clinical decisions.
  • - The analysis included 13 studies with a total of 2,128 patients, showing that DIEP flaps resulted in higher breast satisfaction and physical well-being scores, while also having lower seroma incidence compared to LD flaps.
  • - Although DIEP flaps were associated with increased risk of complications such as skin flap necrosis and wound dehiscence, they overall provided better patient satisfaction outcomes than LD flaps.
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  • Retroperitoneal liposarcomas (RPLPSs) are uncommon tumors arising from mesenchymal cells in the peritoneal cavity, with renal cases being especially rare; only 45 instances have been documented.* -
  • A case study of a 44-year-old woman revealed that she had RPLPS, identified due to symptoms like hirsutism and an abdominal mass, which was confirmed via imaging and needle biopsy; she successfully underwent surgery.* -
  • RPLPSs are primarily asymptomatic until they grow large, categorized into five subtypes, and while they seldom metastasize, they often recur; they can compress nearby structures like the adrenal gland.*
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Article Synopsis
  • Radiocontrast agents can be iodinated or noniodinated, with iodinated agents further classified into low and high molecular weight categories, where low molecular weight agents (LOCM) have become more common due to safety concerns but still have severe side effects.
  • In a case study, a 62-year-old woman suffered a hypertensive crisis after receiving Iohexol during a CT scan for acute brain issues, leading to her critical condition and eventual death despite medical intervention.
  • The case highlights a rare adverse reaction to a low molecular weight contrast agent, suggesting that severe blood pressure spikes can occur without typical catecholamine-related causes, adding to the complexity of handling such reactions in patients.
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Griscelli syndrome: a diagnostic challenge of a rare disease: a case report.

Ann Med Surg (Lond)

October 2024

Department of Gastroenterology & Interventional Endoscopy Pediatric, Damascus University, Pediatric Hospital and Syrian Specialty Hospital, Damascus, Syria.

Introduction: Griscelli syndrome (GS) is a rare autosomal recessive genetic disorder that primarily manifests as hair and skin hypopigmentation, with three types differentiated by their specific genetic defects as well as by their clinical features. Clinically, GS type 1 is characterized by early neurological alterations, while GS type 2 is characterized by immunodeficiency and could present with neurological symptoms, and type 3 is characterized by a chromosomal anomaly without a specific clinical profile besides hypopigmentation. This article details the challenges faced in the diagnosis of a patient with GS who presents with neurological symptoms followed by immunological deficits.

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Article Synopsis
  • PASH syndrome is an autoimmune condition that causes skin problems like acne and painful sores, which get worse over time.
  • A 36-year-old man had severe symptoms including skin ulcers and struggled to find effective treatments until he improved using Infliximab.
  • Treating PASH syndrome is tricky because it can be linked to other health issues, and doctors need to try different therapies to see what works best for each patient.
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Corticosteroid-induced bradycardia following high-dose methylprednisolone administration: a case report.

Ann Med Surg (Lond)

October 2024

Division of Cardiology, Department of Internal Medicine, Faculty of Medicine, University of Aleppo, Aleppo, Syria.

Article Synopsis
  • Corticosteroids, although effective in treating inflammation and modifying immune responses, can lead to several side effects like high blood sugar, hypertension, and bradycardia (slow heart rate).
  • A case study details a 43-year-old woman with multiple sclerosis who developed symptomatic bradycardia after receiving high doses of methylprednisolone, which resolved after 36 hours once the medication was stopped.
  • While bradyarrhythmias like bradycardia are rare compared to tachyarrhythmias, they are important to monitor, and corticosteroid-induced bradycardia typically resolves on its own and often occurs without clear reasons.
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The increasing popularity of prolonged-release dosage forms, owing to their ability to provide continuous drug release after administration, has significantly improved patient compliance and overall quality of life. However, achieving prolonged release beyond 24 h frequently requires the use of invasive methods, including injections or implants, which may prove challenging for people suffering from needle phobia. This study introduces atorvastatin (ATR) microparticles (MPs) or nanocrystal (NCs) dissolving microarray patches (D-MAPs) as a noninvasive alternative for intradermal drug delivery over a two-week period for the management of hyperlipidemia.

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Endoscopic therapy for gastrointestinal angiodysplasia.

Cochrane Database Syst Rev

September 2024

Division of Neurology, Department of Internal Medicine, Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic.

This is a protocol for a Cochrane Review (intervention). The objectives are as follows: To assess the benefits and harms of the different endoscopic management approaches for gastrointestinal angiodysplasia in symptomatic adults.

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