Publications by authors named "A Q Al-Awad"
Article Synopsis
- * A 24-year-old woman developed a persistent cough and chest discomfort three weeks after laparoscopic ovarian surgery, leading to the discovery of a hydatid cyst via chest X-ray and CT scans.
- * Following the surgical removal of the cyst and subsequent antiparasitic treatment with albendazole, the patient had a smooth recovery with no symptoms during follow-up.
Evans syndrome is a rare autoimmune disorder characterized by autoimmune hemolytic anemia (AIHA) and immune thrombocytopenia (ITP), often linked with systemic lupus erythematosus (SLE). We present a case of a 25-year-old female with a history of rheumatoid arthritis (RA) who presented with new SLE symptoms, including left-sided weakness, pallor, and a photosensitive rash. Laboratory tests confirmed Evans syndrome, and MRI showed a cerebral infarction.
View Article and Find Full Text PDFArticle Synopsis
- Bacterial meningitis is a rare but serious risk associated with spinal surgery, particularly following open procedures that can expose cerebrospinal fluid.
- Documented cases have mostly stemmed from these open surgeries, whereas none have been reported from endoscopic techniques until now.
- The text presents a unique case where a patient developed bacterial meningitis after an endoscopic procedure for lumbar disc herniation, which necessitated multiple surgeries for resolution.
Jeune syndrome, a rare autosomal recessive disorder, is characterized by skeletal abnormalities, particularly a narrow, bell-shaped chest, leading to severe respiratory distress in newborns. This case report details a full-term female neonate presenting with significant respiratory challenges, typical skeletal features, and early-onset renal dysfunction. Despite normal initial imaging, persistent renal abnormalities were observed, underscoring the need for early diagnosis, vigilant monitoring, and a multidisciplinary management approach to optimize outcomes for patients with Jeune syndrome.
View Article and Find Full Text PDFArticle Synopsis
- * A reported case involves a female neonate born at 30 weeks who experienced severe respiratory distress and displayed the characteristic skin features of IPS, requiring intensive medical interventions.
- * Early diagnosis, genetic testing for FATP4 mutations, and coordinated care significantly improved the infant's condition, leading to her discharge after 4 weeks, marking the first documented case of IPS in Iraq.