A rare case report of teen‐onset pica in a female patient with a clinical high risk for psychosis

2021 ◽  
Author(s):  
Feten Fekih‐Romdhane ◽  
Majda Cheour
Keyword(s):  
Case Report ◽  
High Risk ◽  
Female Patient ◽  
Rare Case ◽  
Clinical High Risk ◽  
Rare Case Report

scholarly journals Tuberculous Uveitis, Erythema Induratum, and Persistent Genital Warts in a Female Patient: A Rare Case Report

2019 ◽  
Vol 8 (1) ◽  
pp. 70
Author(s):  
Pedram Alirezaei ◽  
MohammadMahdi Majzoobi ◽  
Siamak Akbarzadeh ◽  
Golnoush Ebrahimi ◽  
HamidReza Ghasemibasir
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Genital Warts ◽  
Tuberculous Uveitis ◽  
Rare Case Report

scholarly journals Nasopharyngeal angiofibroma in an elderly female patient: A rare case report

2018 ◽  
Author(s):  
Massimo Ralli ◽  
Massimo Fusconi ◽  
Irene Visconti ◽  
Salvatore Martellucci ◽  
Marco de Vincentiis ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Nasopharyngeal Angiofibroma ◽  
Elderly Female ◽  
Rare Case Report

A Rare Case Report: Isolated Mediastinal Lymph Node Recurrence in High-Risk Endometrial Cancer at 5 Years after Primary Laparoscopic Surgery

2018 ◽  
Vol 25 (3) ◽  
pp. 537-540
Author(s):  
Luca Montanelli ◽  
Claudio Reato ◽  
Stefania Mauro ◽  
Sofia Meregalli ◽  
Marianna Spallino ◽  
...  
Keyword(s):  
Endometrial Cancer ◽  
Case Report ◽  
Lymph Node ◽  
Laparoscopic Surgery ◽  
High Risk ◽  
Rare Case ◽  
Mediastinal Lymph Node ◽  
Lymph Node Recurrence ◽  
Rare Case Report

scholarly journals Fibrous dysplasia of maxilla – A rare case report

2021 ◽  
pp. 485-488
Author(s):  
Vijaya R Kamble ◽  
Shalini N Waghmare ◽  
Aditi V Rangari ◽  
Mangala Meti ◽  
Pritam Pohankar ◽  
...  
Keyword(s):  
Case Report ◽  
Fibrous Dysplasia ◽  
Female Patient ◽  
Malignant Transformation ◽  
Histological Examination ◽  
Rare Case ◽  
Definitive Diagnosis ◽  
Developmental Anomaly ◽  
Rare Case Report ◽  
Examination Methods

Fibrous dysplasia (FD) is a skeletal developmental anomaly, which is non-hereditary in origin and idiopathic in nature. It is a benign fibro-osseous disease that affects one or more bones. It usually affects unilaterally and is seen in the posterior region. Approximately 0.5% of untreated cases show the malignant transformation. We report the case of a 35-year-old female patient with FD involving the maxilla. The clinical diagnostic approach, different imaging modalities, and histological examination methods for definitive diagnosis have been elaborated.

scholarly journals Van der woude syndrome with associated scaphocephaly: a rare case report

2021 ◽  
pp. 50749-50751
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Cleft Lip ◽  
Cleft Lip And Palate ◽  
Van Der Woude Syndrome ◽  
Sagittal Craniosynostosis ◽  
Three Generations ◽  
Bilateral Cleft Lip ◽  
Rare Case Report

The purpose of this case is to provide a descriptive report of a rare combination of Van der Woude syndrome, recurrent in three generations of the same family, in a female patient with bilateral cleft lip and palate associated with a sagittal craniosynostosis (scaphocephaly).

scholarly journals Odontome presenting as fibrotic mass in the upper lip: A rare case report

2015 ◽  
Vol 5 (1) ◽  
pp. 38-40
Author(s):  
B Shrestha ◽  
K J Cho ◽  
J H Lee ◽  
S Subedi
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Female Patient ◽  
Rare Case ◽  
Developmental Stages ◽  
Upper Lip ◽  
Predisposing Factor ◽  
Early Developmental Stages ◽  
Rare Case Report ◽  
Early Developmental

The extraosseous occurrence of Odontome is rare. Trauma to the tooth bud during its early developmental stages has been proposed as a possible predisposing factor for the origin of odontome. In many cases etiology cannot be identified. Here we report an unusual and rare case of odontome presenting as a fibrotic mass on the upper lip in 32 years old female patient. The authors believe this is the rare documented case of odontome occurring within the soft tissue of upper lip.DOI: http://dx.doi.org/10.3126/jcmc.v5i1.12573

scholarly journals Toxoplasmosis, a rare case report that led to a successful pregnancy

2021 ◽  
Vol 20 (3) ◽  
pp. 149-156
Author(s):  
Thomas Ntounis ◽  
Sofoklis Stavros ◽  
Antonios Koutras ◽  
Alexandros Katrachouras ◽  
Dimitrios Lentzaris ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Gold Standard ◽  
Rare Case ◽  
Successful Pregnancy ◽  
Serological Tests ◽  
Rare Case Report

A 19-year-old female patient was presented to our clinic for a pregnancy follow-up during which primary toxoplasmosis infection was diagnosed. The patient was successfully treated with spiramycin and finally delivered normally a healthy boy, on term. Serological tests (ELISA) for detection of anti-toxoplasma antibodies along with ultrasonography findings on the fetus are the gold standard for the diagnosis. Spiramycin was used for embryo protection to avoid T.gondii transmission to the fetus across the placenta.

scholarly journals Urinary Bladder Leiomyoma: A Rare Case Report

1970 ◽  
Vol 2 (2) ◽  
pp. 70-71
Author(s):  
HU Bhuiyan
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Key Words ◽  
Female Patient ◽  
Rare Case ◽  
Excision Biopsy ◽  
Key Words Urinary Bladder ◽  
Rare Case Report ◽  
Bladder Leiomyoma

A rare case of urinary bladder leiomyoma in a female patient is presented here. A quarter of these cases are asymptomatic only to be diagnosed by ultrasonography. Symptomatic cases are also misleading as in this case. Laparotomy, removal of mass and ultimately histopathology proved the case to be that of a urinary bladder leiomyoma. Ibrahim Med. Coll. J. 2008; 2(2): 70-71 Key Words: Urinary bladder leiomyoma, laparotomy, excision biopsy doi: 10.3329/imcj.v2i2.2943

scholarly journals Gastric Medullary Carcinoma: A Rare Case Report

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Ferit Aslan ◽  
Fisun Ardıç Yükrük ◽  
Fatma Buğdaycı Başal ◽  
Ayşe Durnalı
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Early Stage ◽  
Medullary Carcinoma ◽  
Review Of The Literature ◽  
Rare Case Report

A case of 64-year-old female patient with early stage gastric medullary carcinoma has been presented, along with a review of the literature.

scholarly journals Multiple sialolithiasis in submandibular gland duct: a rare case report

2020 ◽  
Vol 68 ◽  
Author(s):  
João Batista da SILVEIRA JUNIOR ◽  
Joaquim Barbosa MATIAS NETO ◽  
Ildeu ANDRADE JUNIOR ◽  
Herminia Marques CAPISTRANO
Keyword(s):  
Case Report ◽  
Salivary Glands ◽  
Submandibular Gland ◽  
Female Patient ◽  
Rare Case ◽  
Surgical Intervention ◽  
Pathological Process ◽  
Floor Of Mouth ◽  
Rare Case Report ◽  
Gland Duct

ABSTRACT Sialolithiasis is a pathological process that affects the major salivary glands. It consists of calcifications that obstruct the parenchyma of the gland and / or the lumen of the ducts. The 37 years old female patient, VBB, leucoderma, attended the stomatology service with a complaint of swelling in the floor of mouth, which she noticed 10 years ago. The clinical and radiographic exams indicated a diagnosis of multiple sialolithiasis in the left submandibular gland duct. Surgical intervention was indicated in this case. Amongst all sialolithiasis cases, 80% affect the submandibular glands. Of these, 70% are isolated sialoliths. Only 5% of cases present more than 3 calcifications. This study aims to report the diagnosis and treatment of a rare case of multiple sialoliths located in the duct of the submandibular gland, which were surgically removed via intraoral access.

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