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.    

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

Giant Aneurysmal Bone Cyst of the Mandible

2016 ◽  
Vol 6 (2) ◽  
pp. 149-153
Author(s):  
Rajshri U Gurav
Keyword(s):  
Female Patient ◽  
Genetic Predisposition ◽  
Aneurysmal Bone Cyst ◽  
Rare Case ◽  
Bone Cyst ◽  
Long Bones ◽  
Rare Presentation ◽  
Bony Lesions ◽  
Bony Lesion ◽  
Secondary Phenomenon

ABSTRACT An aneurysmal bone cyst (ABC) is a benign osteolytic bony lesion that commonly affects the long bones with rare presentation in the jaws. The etiopathogenesis of ABC is unsure. Several theories have been suggested like trauma, intramedullary hematoma, alterations in local hemodynamics, reactive malformation, and genetic predisposition. Though ABCs are considered as secondary phenomenon in preexisting benign and malignant bony lesions, intermittent reports of ABCs with primary/denovo origin are generating perplexity in the scenario. Here, we describe a rare case of giant ABC involving mandible extending from right angle of mandible to left canine region which crosses midline, in a 10-year-old female patient, without any evidence of preexisting bony lesion. How to cite this article Gurav RU, Pathak J, Patel S, Swain N. Giant Aneurysmal Bone Cyst of the Mandible. J Contemp Dent 2016;6(2):149-153.

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 presentation of disseminated invasive aspergillosis

2017 ◽  
Vol 5 (10) ◽  
pp. 4645
Author(s):  
Rituparna Banerjee ◽  
Smita Patil ◽  
Manish Pendse ◽  
Anannya Mukherji ◽  
Prashant Kashyap
Keyword(s):  
Invasive Aspergillosis ◽  
Female Patient ◽  
Young Female ◽  
Prior History ◽  
Rare Presentation ◽  
Systemic Steroids ◽  
Course Of Illness ◽  
History Of ◽  
High Index Of Suspicion ◽  
Variable Presentation

Here’s presenting a case of disseminated invasive aspergillosis in a young female patient with pulmonary and CNS complications and the difficulty one faces while diagnosing such a case due to variable presentation of symptoms with no prior history of any underlying immunodeficiency. It also focuses on how diagnosing such a case can be further delayed due to clinical and radiological miss-match. Thus, it is important to have a high index of suspicion in such patients as prolonged antibiotics and systemic steroids worsens the course of illness. 

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.

CYSTICERCOSIS CHEEK IN A PAEDIATRIC PATIENT – A RARE CASE

2021 ◽  
pp. 1-2
Author(s):  
Avinash Kumar ◽  
Manjari Kishore ◽  
Garima Sinha ◽  
S.K. Varma
Keyword(s):  
Rare Case ◽  
Cystic Lesion ◽  
Taenia Solium ◽  
Parasitic Infection ◽  
Needle Aspiration ◽  
Common Disease ◽  
Rare Entity ◽  
Aspiration Cytology ◽  
Needle Aspiration Cytology ◽  
Cheek Swelling

Cysticercosis cellulosae is a systemic parasitic infection caused by the larval stage of pork tapeworm, taenia solium which involve humans as either a denitive or secondary host. It is a common disease in developing countries. The cases presenting as an isolated muscle mass is an extremely rare entity and demands documentation. Herein, we present a case of healthy pediatric patient who presented with unilateral cheek swelling which on ultrasound suggested a benign cystic lesion. The diagnosis was conrmed on ne needle aspiration cytology (FNAC).

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 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 Occult Neoplasm (Mucoepidermoid Carcinoma) in a Parotid Cyst

2012 ◽  
Vol 3 (1) ◽  
pp. 53-55 ◽  
Author(s):  
Prabodh Karnik ◽  
Anuja Santosh Kulkarni
Keyword(s):  
Parotid Gland ◽  
Head And Neck ◽  
Female Patient ◽  
Mucoepidermoid Carcinoma ◽  
Young Female ◽  
Clinical Entity ◽  
Unusual Presentation ◽  
Low Grade ◽  
Rare Presentation

ABSTRACT A parotid cyst is a well-documented clinical entity. Here we report a case of low-grade mucoepidermoid carcinoma as an occult neoplasm; a rare presentation of a parotid cyst in a 35-year-old female patient who presented with well-defined small cystic swelling of right parotid gland; cytologically consistent with a simple parotid gland cyst. The purpose of this article is to create awareness about existence of an occult neoplasm (low-grade mucoepidermoid carcinoma in this case) in a small simple parotid cyst in a young female an unusual presentation and management of parotid cyst. How to cite this article Kulkarni AS, Karnik P. Occult Neoplasm (mucoepidermoid carcinoma) in a Parotid Cyst. Int J Head and Neck Surg 2012;3(1):53-55.

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