scholarly journals Congenital Midline Cervical Cleft: A very rare clinical entity

2021 ◽  
Vol 1 (1) ◽  
pp. 34-36
Author(s):  
Ahmed H. Al-Salem ◽  
Abdullah O. Bawazir ◽  
Nawaf F. Halabi ◽  
Razan Bawazir
Keyword(s):  
Surgical Treatment ◽  
Early Diagnosis ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Anterior Neck ◽  
Midline Cervical Cleft

Congenital midline cervical cleft is an extremely rare anterior neck defect. We describe a case of a male newborn with midline cervical cleft outlining aspects of diagnosis and stressing the importance of early diagnosis and surgical treatment.

Congenital Midline Cervical Cleft — A Rare Clinical Entity

1994 ◽  
Vol 111 (1) ◽  
pp. 148-149 ◽  
Author(s):  
Nelson C. Goldman ◽  
Kelvin K. W. Liu ◽  
Kim H. Lee
Keyword(s):  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Midline Cervical Cleft

scholarly journals Prikaz slucaja hirurskog zbrinjavanja trudnoce u rudimentarnom rogu uterusa stare pet meseci

2006 ◽  
Vol 53 (3) ◽  
pp. 91-94
Author(s):  
V. Boskovic ◽  
S. Vrzic-Petronijevic ◽  
M. Petronijevic ◽  
M. Berisavac ◽  
I. Likic-Ladjevic
Keyword(s):  
Surgical Treatment ◽  
Maternal Mortality ◽  
Ectopic Pregnancy ◽  
Gestational Age ◽  
Therapeutic Approach ◽  
Haemorrhagic Shock ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Important Complication ◽  
Taking Care

Cornual ectopic pregnancy is rare clinical entity with high maternal mortality. In all cases surgical treatment is indicated, and taking care of most important complication - haemorrhagic shock. Therapeutic approach is individual and depending of simptomatplogy, gestational age of pregnancy and condition of the patient in time of diagnosis. Authors are presenting the case of cornual ectopic pregnancy of five months. .

scholarly journals Dural Arteriovenous Fistulas - Regarding Two Clinical Cases

2021 ◽  
Vol 6 (08) ◽  
pp. 460-463
Author(s):  
Cristiana Fernandes ◽  
Sara Varanda ◽  
José Manuel Amorim ◽  
José Nuno Alves ◽  
Carla Ferreira
Keyword(s):  
Early Diagnosis ◽  
Intracranial Hypertension ◽  
Vascular Dementia ◽  
Clinical Presentation ◽  
Vascular Malformations ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Drainage Pattern ◽  
Arteriovenous Fistulas ◽  
Dural Arteriovenous Fistulas

Dural arteriovenous fistulas (AVF) are rare intracranial vascular malformations, consisting of communications between dural venous arteries and sinuses, meningeal veins, cortical veins, or combinations thereof. In most cases the etiology is unknown. The clinical presentation is determined by the location and mainly by the drainage pattern. The recognition of this rare clinical entity is essential for an early diagnosis and intervention, to avoid the potentially serious complications of the disease, such as, intracranial hypertension, vascular dementia, hemorrhage, among others.

scholarly journals The Glans Schwannoma: A Rare Clinical Entity

2021 ◽  
Vol 2 (S1) ◽  
pp. 1-3
Author(s):  
Diallo Kadidiatou Folly ◽  
Dyatta Mayombo Kévin ◽  
Atsame Ebang Gabrielle ◽  
Ipouka Doussiemou Sergina ◽  
Nguele Ndjota ◽  
...  
Keyword(s):  
Surgical Treatment ◽  
Rare Case ◽  
Complete Resection ◽  
Clinical Entity ◽  
Histologic Examination ◽  
University Hospital ◽  
Rare Clinical Entity ◽  
Complete Excision ◽  
Surgical History ◽  
The University

Introduction: Schwannoma of the glans is a rare clinical entity. The diagnosis is histological. Treatment is surgical, with complete excision. The authors report this rare case encountered at the University Hospital of Libreville in order to identify its clinical and therapeutic characteristics. Observation: Mr. I.B, 50 years old, with no medical-surgical history, consulted for swelling of the glans evolving for 06 years, preventing coitus. He reported a notion of poor healing from an acorn sore after the trouser fly was closed. The diagnostic suspicion was a glans keloid. A complete resection was performed. Histologic examination favored a glans schwannoma. Healing was effective on D7 postoperatively. Erectile functions have been preserved. Conclusion: The glans schwannoma is rare. Surgical treatment gives good results.

scholarly journals Bronchoesophageal fistula secondary to esophageal diverticulum in an adult: a case report and literature review

2021 ◽  
Vol 49 (2) ◽  
pp. 030006052199223
Author(s):  
Xiaolin Zhang ◽  
Hongmei Jiao ◽  
Xinmin Liu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Respiratory Infections ◽  
Relevant Literature ◽  
Rare Condition ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Esophageal Diverticulum ◽  
Bronchoesophageal Fistula ◽  
Fatal Complications

Esophageal diverticulum with secondary bronchoesophageal fistula is a rare clinical entity that manifests as respiratory infections, coughing during eating or drinking, hemoptysis, and sometimes fatal complications. In the present study, we describe a case of bronchoesophageal fistula emanating from esophageal diverticulum in a 45-year-old man who presented with bronchiectasis. We summarize the characteristics of this rare condition based on a review of the relevant literature.

scholarly journals Primary tubercular caecal perforation: a rare clinical entity

BMC Surgery ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Devendra K Jain ◽  
Gaurav Aggarwal ◽  
Parvinder S Lubana ◽  
Sonia Moses ◽  
Nitin Joshi
Keyword(s):  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Caecal Perforation

scholarly journals Cartilaginous Choristoma of the Gingiva: A Rare Clinical Entity

2014 ◽  
Vol 2014 ◽  
pp. 1-4
Author(s):  
Ramalingam Suganya ◽  
Narasimhan Malathi ◽  
Subramani Vijaya Nirmala ◽  
Chinnaswami Ravindran ◽  
Harikrishnan Thamizhchelvan
Keyword(s):  
Connective Tissue ◽  
Histopathological Examination ◽  
Clinical Entity ◽  
Fibrous Connective Tissue ◽  
Rare Clinical Entity ◽  
Normal Cells ◽  
Connective Tissue Stroma

Choristomas are rare entities which are aggregates of microscopically normal cells or tissues in aberrant locations. They are a “heterotopic” rest of cells, as they appear as a tumor-like mass. Herein we report a case of cartilaginous choristoma in a 54-year-old male who presented with a swelling on right lower gingiva. The histopathological examination revealed features of a well circumscribed mass of mature cartilage in a dense fibrous connective tissue stroma.

scholarly journals Role of Immunotherapy in Pulmonary Angiosarcoma: A Case Report

2021 ◽  
pp. 797-801
Author(s):  
Quang Tien Nguyen ◽  
Anh Tuan Pham ◽  
Thuy Thi Nguyen ◽  
Tam Thi Thanh Nguyen ◽  
Ky Van Le
Keyword(s):  
Case Report ◽  
Poor Prognosis ◽  
Checkpoint Inhibitor ◽  
Therapeutic Strategies ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
Excellent Response ◽  
First Case

Pulmonary angiosarcoma is a rare clinical entity with a poor prognosis and no established therapeutic strategies. We present the first case to our knowledge of metastatic pulmonary angiosarcoma, treated with checkpoint inhibitor immunotherapy, and have an excellent response. Until now, patient has been treated with immunotherapy for 1 year, and his disease is stable and well-tolerated.

Sign in / Sign up

Export Citation Format

Share Document