scholarly journals Foregut Duplication Cyst of the Stomach: A Case Report and Review of the Literature

2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Y. Tjendra ◽  
K. Lyapichev ◽  
J. Henderson ◽  
C. P. Rojas
Keyword(s):  
Soft Tissue Tumor ◽  
Laparoscopic Resection ◽  
Gastroesophageal Junction ◽  
Duplication Cyst ◽  
First Year ◽  
Review Of The Literature ◽  
Epigastric Discomfort ◽  
Foregut Duplication Cyst ◽  
Abdominal Symptoms ◽  
First Year Of Life

Duplication cyst of the stomach is a rare congenital malformation, typically diagnosed in the first year of life. In most adult cases the cyst remains asymptomatic, but patients may present with abdominal symptoms including epigastric discomfort or pain. We present a case of a 65-year-old male with an asymptomatic gastric tumor diagnosed incidentally during initial workup of his esophageal adenocarcinoma. Computed tomography revealed a low density soft tissue tumor near the gastroesophageal junction. Endoscopic ultrasonography demonstrated a cystic lesion as a hypoechoic round mass with well-defined borders. Following complete laparoscopic resection, microscopic review revealed a cyst lined with respiratory pseudostratified ciliated columnar epithelium and layers of smooth muscle with an outermost thin fibrous capsule consistent with a foregut duplication cyst.

Capillary haemangioma of the parotid in an adult: an unusual case and a review of the literature

1997 ◽  
Vol 111 (6) ◽  
pp. 588-589 ◽  
Author(s):  
R. G. M. Hughes ◽  
J. Oates
Keyword(s):  
Parotid Gland ◽  
Unusual Case ◽  
First Year ◽  
Review Of The Literature ◽  
Capillary Haemangioma ◽  
Parotid Tumours ◽  
First Year Of Life

AbstractHaemangioma of the parotid gland is a well-described condition that accounts for 50 per cent of parotid tumours presenting during the first year of life. Parotid haemangiomas in adults are much rarer and until now only the cavernous variety have been reported. We report a case of a capillary haemangioma in an adult and discuss the literature.

scholarly journals 355 Incomplete Intestinal Rotation with Appendicular Abscess Causing Diagnostic Dilemma in An Adult Patient

2021 ◽  
Vol 108 (Supplement_2) ◽  
Author(s):  
I Almafreji ◽  
N Nur
Keyword(s):  
Computed Tomography ◽  
Abdominal Pain ◽  
Literature Review ◽  
First Year ◽  
Inflammatory Mass ◽  
Diagnostic Dilemma ◽  
Abdominal Symptoms ◽  
History Of ◽  
First Year Of Life ◽  
Intestinal Rotation

Abstract Intestinal malrotation presents as an emergency in the neonate and within the first year of life. Incomplete intestinal rotation may remain asymptomatic and undiagnosed. Adult patients are usually diagnosed incidentally while being investigated for nonspecific abdominal symptoms. We report a case of a 43-year-old female who presented with a 10-day history of paraumbilical abdominal pain. Computed tomography demonstrated features of incomplete intestinal rotation and a centrally located inflammatory mass related to the appendix. She underwent a laparotomy and appendectomy. Upon a brief literature review of similar cases, there seems to be a conflict of views regarding the management of incidentally diagnosed adult incomplete intestinal rotation.

scholarly journals Ileal Duplication Cyst Presenting With Acute Abdomen at Adult Age: Report of a Rare Case and a Review of the Literature

2018 ◽  
Vol 103 (5-6) ◽  
pp. 295-299
Author(s):  
Emre Gunay ◽  
Hasan Abuoglu ◽  
Cebrail Akyuz ◽  
Fugen Aker
Keyword(s):  
Acute Abdomen ◽  
Rare Case ◽  
Duplication Cyst ◽  
Review Of The Literature ◽  
Adult Age ◽  
Abdominal Symptoms ◽  
Ileal Duplication ◽  
Gastrointestinal Duplication

Gastrointestinal duplication cysts are rare lesions that typically present with acute abdomen in childhood. They are rare in adults, with only a few adult cases having been reported thus far. Adults with these lesions are usually asymptomatic or manifest with subtle abdominal symptoms. They may, however, also present with obstruction, bleeding, perforation, or malignancy. Herein, we aimed to report a case of ileal duplication cyst at adult age that presenting with symptoms of acute abdomen and reviewed the reported cases of adult age duplication cysts.

Atypical teratoid rhabdoid tumor in the first year of life: the Canadian ATRT registry experience and review of the literature

2017 ◽  
Vol 132 (1) ◽  
pp. 155-162 ◽  
Author(s):  
Mary Fossey ◽  
Haocheng Li ◽  
Samina Afzal ◽  
Anne-Sophie Carret ◽  
David D. Eisenstat ◽  
...  
Keyword(s):  
Rhabdoid Tumor ◽  
First Year ◽  
Atypical Teratoid Rhabdoid Tumor ◽  
Review Of The Literature ◽  
Atypical Teratoid ◽  
First Year Of Life

Gastric Duplication Cyst: A Rare Case Report

2021 ◽  
Author(s):  
Veli Avcı ◽  
Ramazan Çelik ◽  
Mesur Özgökçe
Keyword(s):  
Weight Loss ◽  
Rare Case ◽  
Duplication Cyst ◽  
First Year ◽  
Common Symptom ◽  
Gastric Duplication ◽  
Palpable Mass ◽  
Gastric Duplication Cyst ◽  
Rare Case Report ◽  
First Year Of Life

Duplication cysts are developmental anomalies of gastrointestinal tract that can occur at any level from the oral cavity to the rectum, and are extremely rare in the stomach. Most patients show symptom and findings in the first year of life. The most common symptom and findings are abdominal pain, nausea, vomiting, anemia, weight loss and palpable mass. In this study, a gastric duplication cyst was presented in an 11-month-old patient.

Congenital cystic supratentorial hemangioblastoma

1995 ◽  
Vol 82 (1) ◽  
pp. 113-115 ◽  
Author(s):  
Bryan K. Richmond ◽  
John H. Schmidt
Keyword(s):  
First Year ◽  
Extensive Review ◽  
Review Of The Literature ◽  
Content Type ◽  
Documented Case ◽  
First Year Of Life ◽  
Fine Print

✓ The first documented case of congenital supratentorial hemangioblastoma is presented, occurring in a 3-week-old infant. Extensive review of the literature revealed approximately 83 cases of supratentorial hemangioblastoma; however, only one of these occurred in the first year of life, and that case was not presented in detail.

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