Publications by authors named "Nedim Hasic"
Article Synopsis
- * The patient showed symptoms of hyperaldosteronism and malignant hypertension, prompting the medical team to evaluate her conditions, leading to the surgical removal of the affected adrenal gland and a portion of the stomach.
- * Post-surgery, the patient had a successful recovery, remained stable without complications, and highlighted the need for a team approach in managing complex medical cases.
Female adnexal tumors of probable Wolffian origin (FATWOs) are extremely rare tumors, with only around 100 cases published worldwide. FATWOs are most frequently found in the broad ligament, but these can also appear in the mesosalpinx, Fallopian tube, ovary, paravaginal region or peritoneum. We present a case of a 68-year-old female with a history of painless abdominal distension and frequent urination, with palpable big abdominal mass.
View Article and Find Full Text PDFCholedochal cysts (CCs) are rare congenital anomalies in the form of cystic dilatation of any part of the biliary tree, and they rarely reach the size over 10 cm. We present a case of a 51-year-old female with a one-year history of abdominal pain and palpable mass in the epigastrium and right upper abdomen. Diagnosis of giant CC was made using magnetic resonance cholangiopancreatography.
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