Objective: To gain information about the indications for and complications of conventional nephrectomy as practiced in a teaching hospital of Pakistan.
Methods: Medical records of patients who underwent nephrectomy during five years period from January 2001 to December 2005 were studied with regards to clinical presentation, indication for nephrectomy, histopathological report, post-operative complications and mortality. The indications for nephrectomy were divided into benign and malignant conditions.
Results: Out of 154 nephrectomies, 118 (76.6%) were performed for benign condition and 36 (23%) for malignant etiology. In the benign group, majority (i.e. 53.3%) of the patients had kidneys removed due to renal stone. Other conditions in this group included chronic pyelonephritis (20%), neglected ureteropelvic junction obstruction (16%), renal tuberculosis (7.6%) and iatrogenic (2.5%). Thirty-six (23%) patients had nephrectomy for malignant conditions i.e. renal cell carcinoma. Malignant tumors were more common in males while benign conditions necessitating nephrectomy were predominant in female patients. Patients with benign conditions were much younger (mean age 32 years) than patients in malignant group (mean age 52.8 years). Nephrectomy for malignant disease had a higher rate of complications (13.8%) than for benign conditions (7.6%). The re-operation rate was 1.29% for all patients who underwent nephrectomy. Two patients, one in each group, died post-operatively and the overall 30-day mortality was 1.29%
Conclusion: The mean age of the patients undergoing nephrectomy for benign and malignant conditions was lower than reported from western countries. In our series there was a much higher rate of nephrectomy performed for benign conditions. Renal stone related etiology was the major indication for nephrectomy. Malignant renal tumours affected patients at a remarkably younger age and clear cell renal carcinoma was the predominant histological variety. Nephrectomy for malignant conditions had a higher rate of complications than for benign conditions while there was no difference in the overall mortality.
Download full-text PDF |
Source |
---|
Int J Surg Case Rep
December 2024
Department of Surgical Oncology, Regional Hospital of Jendouba, Jendouba, Tunisia.
Introduction: Rosai-Dorfman disease (RDD) is a rare histiocytic neoplasm. It most commonly presents with bilateral cervical lymphadenopathy. We report the fourth case in the literature of RDD presenting as isolated axillary lymphadenopathy.
View Article and Find Full Text PDFSci Rep
December 2024
ICAR-Indian Grassland and Fodder Research Institute, Jhansi, 284 003, India.
Sugarcane is a major industrial crop highly susceptible to parasitic weed (Striga spp.), causing a 38% reduction in cane yield due to a longer lag phase of 20-40 days, and wider spacing. Herbicides with a longer retention and slow-release nature could allow Striga seeds to germinate and be killed before attaching to the host.
View Article and Find Full Text PDFInt J Surg Case Rep
December 2024
Department of Outpatient, Zaozhuang Municipal Hospital, 41th, Zaozhuang, China. Electronic address:
Introduction: This case report discusses the clinical manifestations, diagnosis and treatment of idiopathic scrotal calcinosis, and reviews the literature of similar cases, providing important reference for the diagnosis and treatment of this rare disease.
Case Presentation: Idiopathic scrotal calcinosis is a rare condition characterized by calcium deposition in the skin of the scrotum. We present a case of a 67-year-old male patient with idiopathic scrotal calcinosis, a rare condition characterized by calcium deposition in the skin of the scrotum.
J Pers Med
December 2024
Radiological Sciences Section, Department of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, AOUP "Paolo Giaccone", Via del Vespro 129, 90127 Palermo, Italy.
Nasal and paranasal sinus masses can arise from a wide range of conditions, both benign and malignant, as well as congenital or acquired. Diagnosing these masses is often challenging, requiring a combination of nasal endoscopy, imaging studies, and histopathological analysis. Initial imaging frequently involves computed tomography or cone beam computed tomography (CBCT) to evaluate the bony anatomy of the nasal cavity and surrounding sinuses, while magnetic resonance imaging (MRI) is typically used for detailed assessment of soft tissues and to aid in differential diagnosis when the findings are inconclusive.
View Article and Find Full Text PDFDiseases
December 2024
Department of Pediatrics, Dokkyo Medical University, Tochigi 321-0293, Japan.
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by mutations in the TSC1 and TSC2 genes, leading to the dysregulation of the mammalian target of rapamycin (mTOR) pathway. This dysregulation results in the development of benign tumors across multiple organ systems and poses significant neurodevelopmental challenges. The clinical manifestations of TSC vary widely and include subependymal giant cell astrocytomas (SEGAs), renal angiomyolipomas (AMLs), facial angiofibromas (FAs), and neuropsychiatric conditions such as autism spectrum disorder (ASD).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!