scholarly journals Emergency embolization after resection of a laryngeal Schwannoma

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 ◽  
...  
Keyword(s):  
Female Patient ◽  
Surgical Resection ◽  
Rare Case ◽  
Young Female ◽  
Benign Tumors ◽  
First Choice

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.

scholarly journals A Rare Case of Pancreatic Endometriosis Masquerading as Pancreatic Mucinous Neoplasm

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Barton Huang ◽  
Annie Mooser ◽  
Danielle Carpenter ◽  
Grace Montenegro ◽  
Carrie Luu
Keyword(s):  
Distal Pancreatectomy ◽  
Female Patient ◽  
Surgical Resection ◽  
Rare Case ◽  
Cystic Lesions ◽  
Common Condition ◽  
Mucinous Neoplasm ◽  
Endometriotic Cyst

Endometriosis is a relatively common condition among women, and pancreatic endometriosis has been reported on rare occasions. Such pancreatic lesions are difficult to diagnose and distinguish from other cystic lesions of the pancreas preoperatively. This report describes a case of pancreatic endometriosis in a 51-year-old female patient. Imaging demonstrated an enlarging cyst with findings concerning for a mucinous neoplasm. The patient underwent robotic distal pancreatectomy and splenectomy. Histopathology revealed an endometriotic cyst. Pancreatic endometriosis can be difficult to distinguish from other lesions of the pancreas. Surgical resection should be undertaken in cases where malignancy is suspected.

scholarly journals A Rare Case of Kikuchi-Fujimoto Disease in a Young Female Patient

2021 ◽  
Vol 22 ◽  
Author(s):  
Le Hoan ◽  
Le Minh Hang ◽  
Le Tuan Linh ◽  
Thieu Thi Tra My ◽  
Tran Ngoc Minh ◽  
...  
Keyword(s):  
Female Patient ◽  
Rare Case ◽  
Young Female

scholarly journals Rare case presentation of leiomyoma of bladder neck with tuberculous pelvic lymphadenitis in a young female patient

2021 ◽  
Vol 34 ◽  
pp. 101436
Author(s):  
Mahmoud Moawad ◽  
Najla Ben Ghashir ◽  
Quatullah Rustum ◽  
Hamid Toussi
Keyword(s):  
Female Patient ◽  
Bladder Neck ◽  
Rare Case ◽  
Young Female ◽  
Case Presentation

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
Keyword(s):  
Intestinal Obstruction ◽  
Female Patient ◽  
Rare Case ◽  
Young Female ◽  
Histologic Examination ◽  
Rare Entity ◽  
Ileocolic Intussusception ◽  
Intestinal Intussusception ◽  
Clinical Presentations

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.

scholarly journals A rare case of masseter muscle cysticercosis in a young female patient managed conservatively

2020 ◽  
Vol 7 (3) ◽  
pp. 15-17
Author(s):  
Hardik Dodia ◽  
Karnadev Solanki ◽  
Bhaumik Shah
Keyword(s):  
Young Woman ◽  
Female Patient ◽  
Clinical Examination ◽  
Conservative Management ◽  
Masseter Muscle ◽  
Rare Case ◽  
Taenia Solium ◽  
Young Female ◽  
Rare Presentation ◽  
Cheek Swelling

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.    

A rare case of fibromuscular dysplasia involving multiple vascular beds

Vascular ◽  
2020 ◽  
pp. 170853812097909
Author(s):  
Christian Renz ◽  
Nader Tehrani ◽  
Lillian Malach ◽  
Michael Soult ◽  
Matthew Blecha ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Carotid Arteries ◽  
Fibromuscular Dysplasia ◽  
Young Female ◽  
Review Of The Literature ◽  
Pubmed Search ◽  
History Of ◽  
Vascular Beds

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.

scholarly journals A rare case of retained fourth molar teeth in maxilla and mandible. Case report

2014 ◽  
Vol 27 (2) ◽  
pp. 118-120 ◽  
Author(s):  
Mansur Rahnama ◽  
Anna Szyszkowska ◽  
Marta Pulawska ◽  
Joanna Szczerba-Gwozdz
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Local Anesthesia ◽  
Orthodontic Treatment ◽  
Rare Case ◽  
Young Female ◽  
Third Molars ◽  
Supernumerary Teeth ◽  
Molar Teeth ◽  
Maxilla And Mandible

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.

scholarly journals A Case Report of Caries Incident in a Patient Wearing an Essix Type Retainer.

2021 ◽  
Author(s):  
Albandri Alowid ◽  
Bashayer Helaby ◽  
Lujain Alqarni
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Oral Hygiene ◽  
Rare Case ◽  
Young Female ◽  
Full Time ◽  
Poor Oral Hygiene ◽  
Carious Lesions ◽  
Cleaning Protocol ◽  
Orthodontic Retention

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.

scholarly journals Elbow Cystic Lymphangioma in an 8-Month-Old Boy

2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Mohammad Jawad H. Rahal ◽  
Morad R. Abou Al Ezz ◽  
Rabab A. El Hajj ◽  
Jad Z. Chokor ◽  
Selim M. Nasser ◽  
...  
Keyword(s):  
Head And Neck ◽  
Surgical Resection ◽  
Rare Case ◽  
Pediatric Population ◽  
Cystic Lymphangioma ◽  
Benign Tumors ◽  
Cystic Lymphangiomas ◽  
Complete Surgical Resection ◽  
The Right

Cystic lymphangiomas are benign tumors originating mainly in the head and neck of the pediatric population. The authors report a rare case of cystic lymphangioma in the right elbow of an 8-month-old baby treated successfully by complete surgical resection.

scholarly journals Endosonographic Appearances of a Rare Duodenal Tumour, Brunner’s Gland Hamartoma

2019 ◽  
Vol 13 (2) ◽  
pp. 310-320
Author(s):  
Ikram Hussain ◽  
Malcolm Tan ◽  
Meyyur Aravamudan Veeraraghavan ◽  
Lai Mun Wang ◽  
Andrew Eu Boon Kwek
Keyword(s):  
Gastrointestinal Bleeding ◽  
Surgical Resection ◽  
Rare Case ◽  
Gastrointestinal Symptoms ◽  
Young Female ◽  
Major Surgery ◽  
Epithelial Tumour ◽  
Brunner’S Gland ◽  
Brunner's Gland ◽  
Brunner’S Gland Hamartoma

Brunner’s gland hamartoma (BGH) is a rare sub-epithelial tumour of the duodenum, which may cause haemorrhagic or obstructive gastrointestinal symptoms. Their accurate histological diagnosis often remains elusive before resection. Although endoscopic ultrasonography (EUS) is considered an excellent modality to study lesions within the gastrointestinal wall, only a few reports have described endosonographic characteristics of BGHs. A reliable pre-resection diagnosis with EUS may not only allay fear of malignancy but may as well avert a major surgery for the patients. In this report, we present a rare case of a large BGH in a young female who presented with acute gastrointestinal bleeding. Here, the endosonographic features assuaged the concern for malignancy while aiding in complete and uneventful surgical resection of the tumour via a submucosal plane.

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