scholarly journals Teratoid Cyst with Nephrogenic Elements: A Rare Case

2020 ◽  
Vol 7 (11) ◽  
pp. C160-163
Author(s):  
Archana N Rijhsinghani
Keyword(s):  
Oral Cavity ◽  
Cyst Wall ◽  
Rare Case ◽  
Female Child ◽  
Duplication Cyst ◽  
Respiratory Epithelium ◽  
Intestinal Duplication ◽  
Common Location ◽  
Derivatives Of ◽  
Teratoid Cyst

Teratoid cyst is a type of dermoid cyst, the lining of which varies from stratified squamous to a ciliated respiratory epithelium containing derivatives of ectoderm, mesoderm and endoderm. The most common location of this cyst is oral cavity and presence of nephrogenic elements has been very rarely reported. We report a very uncommon rare case of teratoid cyst with nephrogenic elements in cyst wall and intestinal duplication cyst in a 6-month-old-female child.

Neonatal airway obstruction due to a massive lingual foregut duplication cyst

2020 ◽  
Vol 13 (10) ◽  
pp. e233907
Author(s):  
Sepehr Shabani ◽  
Bradley J Cheek ◽  
Katrin Post-Martens ◽  
Steven M Andreoli
Keyword(s):  
Oral Cavity ◽  
Airway Obstruction ◽  
Head And Neck ◽  
Alimentary Tract ◽  
Surgical Excision ◽  
Duplication Cyst ◽  
Respiratory Epithelium ◽  
Definitive Treatment ◽  
Foregut Duplication Cyst

Foregut duplication cysts (FDCs) are rare malformations arising along primitively derived alimentary tract. Head and neck cases comprise 0.3% of all FDCs with 60% occurring in the oral cavity. We present a case of neonatal airway obstruction secondary to a prenatally diagnosed massive lingual FDC. Definitive treatment requires surgical excision. Histologically, the cysts are lined gastric and respiratory epithelium. FDC should be a consideration in prenatally diagnosed masses affecting the oral cavity.

scholarly journals INTESTINAL DUPLICATION CYST PRESENTING AS VOLVULUS: A Rare Case Report

2014 ◽  
Vol 3 (2) ◽  
Author(s):  
Chanumolu Praveen ◽  
Prasan Kumar Hota ◽  
Ch.V. Pavan Kumar ◽  
And K. Maruthi Babu
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Duplication Cyst ◽  
Intestinal Duplication ◽  
Rare Case Report

scholarly journals A rare case of acute abdomen in the adult: The intestinal duplication cyst. case report and review of the literature

2019 ◽  
Vol 40 ◽  
pp. 18-21 ◽  
Author(s):  
Andrea Aurelio Ricciardolo ◽  
Tommaso Iaquinta ◽  
Alessandro Tarantini ◽  
Nicola Sforza ◽  
Donatella Mosca ◽  
...  
Keyword(s):  
Case Report ◽  
Acute Abdomen ◽  
Rare Case ◽  
Duplication Cyst ◽  
Review Of The Literature ◽  
Intestinal Duplication

scholarly journals Caecal duplication cyst: rare case report with review of literature

2019 ◽  
Vol 6 (11) ◽  
pp. 4190
Author(s):  
Muthukumaran J. ◽  
Udhayasankar V.
Keyword(s):  
Congenital Anomaly ◽  
Rare Case ◽  
Alimentary Tract ◽  
Female Child ◽  
Duplication Cyst ◽  
Paediatric Surgery ◽  
Review Of Literature ◽  
Rare Congenital Anomaly ◽  
Rare Case Report ◽  
Surgery Department

Duplication cysts of the alimentary tract are very rare congenital anomaly. Out of all these cases, two-thirds of them manifest before the age of 2 years. They are common in ileum, but very rare in cecum. We hereby report a case of 6 years female child presented in paediatric surgery department with abdominal pain, diagnosed as duplication cyst with intussusceptions.

scholarly journals Intestinal Duplication Cyst presenting as Volvulus: A rare case report with Review of Literatures

2015 ◽  
Vol 3 (3) ◽  
Author(s):  
Prasan Kumar Hota ◽  
Chanumolu Praveen ◽  
Chanumolu Praveen ◽  
Ch.V. Pavan Kumar ◽  
Chanumolu Praveen ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Duplication Cyst ◽  
Intestinal Duplication ◽  
Rare Case Report

Leiomyoma with Bizarre Nuclei (Symplastic Leiomyoma) in the Paratubal Cyst Wall: Report of a Rare Case

2021 ◽  
pp. 106689692199779
Author(s):  
Murat Celik
Keyword(s):  
Differential Diagnosis ◽  
Smooth Muscle ◽  
Cyst Wall ◽  
Rare Case ◽  
Clinical Behavior ◽  
Uterine Smooth Muscle ◽  
Smooth Muscle Neoplasm ◽  
Histological Variants ◽  
Eosinophilic Cytoplasm ◽  
Paratubal Cyst

Leiomyoma is a benign mesenchymal tumor that develops from smooth muscle cells. It can present in various histological variants. Leiomyoma with bizarre nuclei is an infrequent variant of uterine smooth muscle neoplasm. It is characterized by focally or diffusely distributed bizarre cells on the background of a typical leiomyoma. These bizarre cells are large, multinucleated, or multilobulated and have an eosinophilic cytoplasm. Even though leiomyomas with bizarre nuclei display benign clinical behavior, their differential diagnosis from leiomyosarcoma can sometimes be difficult. Leiomyoma has been described most commonly in the uterus. There is no case of leiomyoma originating from paratubal cysts described in the literature. In this article, we present a rare case of leiomyoma with bizarre nuclei originating from a paratubal cyst.

scholarly journals INTESTINAL DUPLICATION CYST OF ABDOMINAL ORIGIN PRESENTING IN THORAX

1959 ◽  
Vol 37 (6) ◽  
pp. 810-814
Author(s):  
Harold C. Spear ◽  
DeWitt C. Daughtry ◽  
John G. Chesney
Keyword(s):  
Duplication Cyst ◽  
Intestinal Duplication

scholarly journals Fourth mandibular molar in a pediatric patient – Case report

2015 ◽  
Vol 5 (20) ◽  
pp. 229-231
Author(s):  
Atanas Vlaykov ◽  
Dian Sharlanov ◽  
Dilyana Vicheva
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Treatment Modality ◽  
Treatment Plan ◽  
Female Child ◽  
Permanent Teeth ◽  
Radiographic Examination ◽  
Supernumerary Teeth ◽  
Patient Case ◽  
Mandibular Molar

Abstract Background. Supernumerary teeth are described as an excess of the normal teeth number of 20 deciduous and 32 permanent teeth and can occur in any dental region. Material and methods. The authors present the case of a 12-year-old female child with a paramolar in the maxilla, discovered accidentally during an orthopantomogram, emphasising the treatment modality and the complications that can appear. Conclusion. Supernumerary teeth can be present in any region of the oral cavity. Both practitioners and clinicians should be aware of the various types of paramolars and make a treatment plan after an accurate clinical and radiographic examination.

scholarly journals RARE CASE OF AN ISOLATED ENTERIC DUPLICATION CYST IN A TEENAGER

2020 ◽  
Vol 05 (02) ◽  
pp. 73-76
Author(s):  
Shubha H V ◽  
Archana Shetty ◽  
Vijaya C ◽  
Venkatachalapathy V
Keyword(s):  
Rare Case ◽  
Duplication Cyst ◽  
Enteric Duplication Cyst ◽  
Enteric Duplication
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