scholarly journals A rare case of ileocolic intussusception due to severe endometriosis

2020 ◽  
Vol 2020 (6) ◽  
Author(s):  
Luca Benigno ◽  
Loriana Lisarelli ◽  
Rosita Sortino ◽  
Joerg Neuweiler ◽  
Thomas Steffen

Abstract Intestinal intussusception is a rare cause of intestinal obstruction; intestinal intussusception associated with endometriosis is very rare. The varied clinical presentations make the diagnosis demanding. In this article, we report the case of a young female patient with an intestinal obstruction due to intussusception. The successive histologic examination of the resected sample showed advanced endometriosis. This is a very rare entity with only a few similar cases reported in the literature.

2021 ◽  
Vol 22 ◽  
Author(s):  
Le Hoan ◽  
Le Minh Hang ◽  
Le Tuan Linh ◽  
Thieu Thi Tra My ◽  
Tran Ngoc Minh ◽  
...  

2016 ◽  
Vol 6 (12) ◽  
pp. 1043-1045
Author(s):  
P Poudel ◽  
B Bajracharya ◽  
S Bhattacharya ◽  
D Bajracharya ◽  
S Singh ◽  
...  

Odontogenic myxofibroma is a rare, benign tumor, which is considered to be the variant of odontogenic myxoma. It is locally infiltrative, aggressive and has high recurrence rate. Only 24 specific cases of myxofibroma have been reported since 1950 and only two cases have been reported with excessive calcifications till 2012. Here, we report a rare case of Odontogenic myxofibroma with calcifications in 53 years old female patient who presented with the chief complain of swelling. The final diagnosis of Odontogenic myxofibroma was established after histopathological and immunohistochemical examination.


2021 ◽  
Vol 34 ◽  
pp. 101436
Author(s):  
Mahmoud Moawad ◽  
Najla Ben Ghashir ◽  
Quatullah Rustum ◽  
Hamid Toussi

2020 ◽  
Vol 7 (3) ◽  
pp. 15-17
Author(s):  
Hardik Dodia ◽  
Karnadev Solanki ◽  
Bhaumik Shah

Cysticercosis is caused by Taenia solium larvae infestation. Isolated oral cysticercosis is a very rare presentation of this disease. Here is a case of masseter cysticercosis in a young woman who presented with painful cheek swelling. Diagnosis is confirmed with history, clinical examination and MRI.  Luckily patient got cured with conservative management.    


Vascular ◽  
2020 ◽  
pp. 170853812097909
Author(s):  
Christian Renz ◽  
Nader Tehrani ◽  
Lillian Malach ◽  
Michael Soult ◽  
Matthew Blecha ◽  
...  

Objective Fibromuscular dysplasia rarely involves vessels other than the renal and carotid arteries. We present a case of a rare fibromuscular dysplasia involving multiple vascular beds in a young female patient with history of spontaneous coronary artery (SCAD). Methods This is a case report with review of the literature using PubMed search for other cases of fibromuscular dysplasia that involves multiple vascular beds and its association with SCAD. The patient agreed to publish her case including her images. Results Fibromuscular dysplasia involving multiple vascular beds in a young female patient with prior coronary dissection is rarely reported in the literature. Conclusion Fibromuscular dysplasia affecting multiple vascular beds is rare but should be suspected in patients with SCAD, particularly young female patients.


2015 ◽  
Vol 4 (9) ◽  
pp. 205846011559918 ◽  
Author(s):  
Abhishek J Arora ◽  
Richa Arora

Ossification of the Achilles tendon is a rare clinical entity comprising of one or more segments of variable sized ossified masses in the fibrocartilaginous substance of the tendon. The etiology of ossification of the Achilles tendon is multifactorial with recurrent trauma and surgery comprising major predisposing factors, with others being metabolic, systemic, and infectious diseases. The possibility of a genetic predisposition towards this entity has also been raised, but has not yet been proven. We present a rare case of ossification of the bilateral Achilles tendons without any history of trauma or surgery in a 48-year-old female patient.


2013 ◽  
Vol 12 (4) ◽  
pp. 312-314 ◽  
Author(s):  
Fabio Augusto Cypreste Oliveira ◽  
Carlos Eduardo de Sousa Amorelli ◽  
Fabio Lemos Campedelli ◽  
Werther Sales ◽  
Maria Cunha Ribeiro Amorelli ◽  
...  

Schwannoma is a rare cause of benign tumors of the larynx. The first-choice treatment is surgical resection. The objective of this paper is to report on a rare case of a young female patient who suffered severe intraoperative hemorrhaging during surgical resection of a laryngeal Schwannoma and needed emergency embolization.


2014 ◽  
Vol 27 (2) ◽  
pp. 118-120 ◽  
Author(s):  
Mansur Rahnama ◽  
Anna Szyszkowska ◽  
Marta Pulawska ◽  
Joanna Szczerba-Gwozdz

Abstract The study presents a case of the rarely occurring totally retained fourth molar teeth simultaneously in maxilla and mandible. The appearance of supernumerary teeth is a relatively uncommon dental anomaly and it is rare for patients to have impacted fourth molars in two quadrant. The aim of this work is to describe the presence of unilateral (right) fourth molars in the maxilla and the mandible in a young female patient aged 24 years. Orthopantomogram revealed impacted lower third molars but also unerupted unilateral (right) upper and lower fourth molars. Before orthodontic treatment, the patient was subsequently admitted for removal of third and fourth impacted upper and lower molars under local anesthesia.


2016 ◽  
Vol 4 (1) ◽  
pp. 432
Author(s):  
Richa Jaiman ◽  
Neelabh Agrawal ◽  
Dipt Kumar ◽  
Chandrodaya Kumar ◽  
Abhishek Pathak ◽  
...  

Aggressive angiomyxoma is a rare benign neoplasm usually involving the pelvic region. It is six times more common in females than males. It occurs almost exclusively in adult females. The term aggressive signifies the neoplastic character of the blood vessels, its locally invasive nature, and the high risk of local recurrence. Here we report a rare case of an eighteen year old female, who had a vulvar swelling for over two years, which turned out to be aggressive angiomyxoma after wide local excision on histopathological examination.


Author(s):  
Albandri Alowid ◽  
Bashayer Helaby ◽  
Lujain Alqarni

This report presents a rare case of multiple Cl.VI carious lesions developed in a young female patient due to full-time wearing of an Essix retainer combined with poor oral hygiene and high acidic intake. The demineralization during orthodontic retention and the hygiene instructions, including the retainer cleaning protocol, are highlighted.


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