Uncommon features of giant colonic diverticula.

Dis Colon Rectum

Published: December 1983

Two patients with giant colonic diverticula were operated upon within one week. Uncommon features of this rare condition were observed in both patients: 1) the diverticulum was located outside the sigmoid colon, 2) smooth-muscle fibers and ganglion cells were present in the wall of the diverticulum, and 3) free perforation into the peritoneal cavity was the presenting symptom. Barium enema in one patient showed no communication between the diverticulum and the colonic lumen, despite evidence of such communication on histologic examination. Both patients were successfully treated by simple excision of the diverticulum without colonic resection.

Download full-text PDF

Source
http://dx.doi.org/10.1007/BF02554756DOI Listing

Publication Analysis

Top Keywords

uncommon features
8
giant colonic
8
colonic diverticula
8
diverticulum colonic
8
features giant
4
colonic
4
diverticula patients
4
patients giant
4
diverticula operated
4
operated week
4

Similar Publications

Cystic cuboid adenomatous malformations (CCAM) are congenital pulmonary lesions, usually benign, that can progress into malignancy. Bronchopulmonary sequestration (BPS) is another type of malformation that consistsof an ectopic pulmonary tissue mass that doesn't participate in blood-gas exchanges, with vascularization provided by anomalous branches of the thoracic aorta. Hybrid lesions are lesions that have histological features of CCAM but with systemic vascularization, a pathognomonic sign of BPS.

View Article and Find Full Text PDF

Classification and Pixel Change Detection of Brain Tumor Using Adam Kookaburra Optimization-Based Shepard Convolutional Neural Network.

NMR Biomed

February 2025

Department of Computer Science and Engineering Koneru Lakshmaiah Education Foundation, Vijayawada, India.

The uncommon growth of cells in the brain is termed as brain tumor. To identify chronic nerve problems, like strokes, brain tumors, multiple sclerosis, and dementia, brain magnetic resonance imaging (MRI) is normally utilized. Identifying the tumor on early stage can improve the patient's survival rate.

View Article and Find Full Text PDF

Witteveen-Kolk Syndrome With Cleft Palate: A Case Report and Review of the Literature.

Cleft Palate Craniofac J

January 2025

Department of Plastic Reconstructive and Aesthetic Surgery, Research and Application Center for the Treatment of Cleft Lip and Palate and Craniomaxillofacial Deformities, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Witteveen-Kolk syndrome (WITKOS) is an exceptionally uncommon genetic and neurodevelopmental disorder, characterized by developmental delay, mild intellectual disability, and craniofacial dysmorphic features. Although cleft palate (CP) has rarely been reported in WITKOS, CP in this condition has not been assessed in detail. Here, we present a case of WITKOS with a CP.

View Article and Find Full Text PDF

Gamna-Gandy (GG) bodies are sclerosiderotic nodules composed of iron pigment and calcium, that have been described predominantly in the spleens of patients with sickle cell disease. Their formal depiction in the kidney is mainly limited to case reports and small series. We aimed to investigate the incidence of GG bodies and associated clinicopathologic features in consecutive nephrectomies performed for renal tumors.

View Article and Find Full Text PDF

Background: Undifferentiated pleomorphic sarcoma, previously called malignant fibrous histiocytoma, is a type of malignant mesenchymal tumor (sarcoma) of soft tissue and sometimes bone. It is uncommon in the oral cavity and very sporadic in the maxillary sinus. Microscopic diagnosis of this malignancy in the maxillary sinus can be very challenging, because there is a range of features that may overlap with other benign and malignant tumors.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!