scholarly journals Abdominal cocoon syndrome, a case report of a rare disease entity causing intestinal obstruction

2021 ◽  
Vol 87 ◽  
pp. 106401
Author(s):  
Farah Mohammed ◽  
Mohamed Abdulkarim ◽  
Ammar Ibn Yasir ◽  
Osman Taleballah ◽  
Dafalla Shani ◽  
...  
2019 ◽  
Vol 10 (6) ◽  
pp. 613-617
Author(s):  
Dipanjan Pradhan ◽  
◽  
Saurav Karmakar ◽  
Abida Sabreen ◽  
◽  
...  

2020 ◽  
pp. 195-200
Author(s):  
Nidhi Mahajan ◽  
Mitali Agarwal ◽  
Arti Khatri ◽  
Yousuf Mohsin Bari Siddiqui ◽  
Mamta Sengar

2017 ◽  
Vol 10 (1) ◽  
Author(s):  
Jianwen Liu ◽  
Rockson Wei ◽  
Xuefei Yang ◽  
Xinping Shen ◽  
Jing Guan ◽  
...  

JRSM Open ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 205427042110012
Author(s):  
Bence Csongor Baljer ◽  
Lauren Shelmerdine ◽  
Gerard Stansby

Femoral venous aneurysms are a rare disease entity, yet they carry the risk of significant mortality due to venous thromboembolism, as demonstrated by a case report of an otherwise fit and well 74-year-old gentleman.


2020 ◽  
Vol 71 (1) ◽  
pp. 59-62
Author(s):  
Mircea-Constantin Diaconu ◽  
Laura-Georgiana Moise ◽  
Agripina Rașcu

AbstractCaplan’s syndrome, known as rheumatoid pneumoconiosis, was first described by Anthony Caplan in 1953, who identified a rare lung disorder found in coal mine workers with rheumatoid arthritis. Although Caplan’s syndrome was found in patients with a variety of pneumoconioses, it mostly affects individuals with long exposure to crystalline silica. We present a case of Caplan’s syndrome in a patient with advanced stage of rheumatoid arthritis and silicosis.


2013 ◽  
Vol 2 (1) ◽  
pp. 12 ◽  
Author(s):  
Safwan Ahmad ◽  
Kanchan Kayastha ◽  
Sana Javed ◽  
Arsalan Wasti

Abdominal cocoon is a complete or partial encasement of intestines and rarely viscera by a fibrocollagenous sac which is usually formed by a nonspecific chronic inflammatory reaction. We report a case of abdominal cocoon in a 2-day-old neonate presenting with intestinal obstruction.


2020 ◽  
pp. 014556132093195
Author(s):  
Hyun Jin Min ◽  
Kyung Soo Kim

Primary nasopharyngeal tuberculosis, defined as an isolated tuberculosis infection of the nasopharynx without systemic or pulmonary disease, is rare, even in areas endemic for tuberculosis. It is challenging for ENT specialists to diagnose primary nasopharyngeal tuberculosis at an early stage. In this report, we describe a new case of primary nasopharyngeal tuberculosis, focusing on its nasopharyngoscopic features and radiological findings that can help the understanding and aid in accurate diagnosis of this unusual disease entity. Our experience suggests that although primary nasopharyngeal tuberculosis is a relatively rare disease, it must be included in the differential diagnosis of various nasopharyngeal lesions, particularly in patients with unusual nasopharyngoscopic and computed tomography findings.


2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Vimal Master Sankar Raj ◽  
Diana Warnecke ◽  
Julia Roberts ◽  
Sarah Elhadi

Goodpasture’s syndrome (GPS) remains a very rare disease entity in the pediatric population characterized by the presence of pulmonary hemorrhage and rapidly evolving glomerulonephritis. We hereby describe the case of a 2-year-old girl who presented with renal failure and was diagnosed with GPS. A brief review of the literature in regard to data on demographics, pathogenesis, clinical features, diagnosis, treatment, and prognosis for renal recovery is also provided.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Cheng Chang ◽  
Chen Jiang ◽  
Yaoyao Miao ◽  
Bin Fang ◽  
Lili Zhang

Abstract Background Cryptogenic multifocal ulcer stenosing enteritis (CMUSE) is a rare disease characterized by multiple superficial ulcers, stenosis, and obstruction of the small intestine of unknown origin, and the course can recur. Case presentation We encountered a 62-year-old male patient with intestinal obstruction. The patient was admitted to the hospital for surgical treatment due to intestinal obstruction, and was diagnosed with cryptogenic multifocal ulcer stenosis enteritis due to comprehensive surgery and postoperative pathological considerations. Conclusion In the future, we will continue to follow up the patient. The present study aims to remind clinicians of this disease, and reduce the incidence of misdiagnosis.


Sign in / Sign up

Export Citation Format

Share Document