scholarly journals Primary Mucinous Adenocarcinoma of the Upper Eyelid in an African American Female: A Rare Clinical Entity. A Case Report and Literature Review

Cureus ◽  
2019 ◽  
Author(s):  
Prashanth Ashok Kumar ◽  
Shweta Paulraj ◽  
Seung S Hahn ◽  
Abirami Sivapiragasam
Keyword(s):  
African American ◽  
Case Report ◽  
Literature Review ◽  
Mucinous Adenocarcinoma ◽  
Clinical Entity ◽  
African American Female ◽  
Rare Clinical Entity ◽  
Upper Eyelid

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.

Brachymetatarsia of the Third and Fourth Metatarsals

2001 ◽  
Vol 91 (7) ◽  
pp. 373-378 ◽  
Author(s):  
William P. Goforth ◽  
Troy D. Overbeek
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Bone Graft ◽  
Clinical Entity ◽  
Rare Clinical Entity ◽  
The Third ◽  
Diaphyseal Bone

A cylindrical autogenous diaphyseal bone graft from the neighboring second and fifth metatarsals to correct brachymetatarsia of the third and fourth metatarsals was last described by Biggs in 1979. The authors present a literature review and case report for the treatment of the rare clinical entity of brachymetatarsia. (J Am Podiatr Med Assoc 91(7): 373-378, 2001)

Skull Base Osseous Arteriovenous Fistula—A Rare Clinical Entity: Case Report and Literature Review

2017 ◽  
Vol 97 ◽  
pp. 760.e9-760.e12 ◽  
Author(s):  
Aneesh Mohimen ◽  
Santhosh Kumar Kannath ◽  
E.R. Jayadevan
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Skull Base ◽  
Arteriovenous Fistula ◽  
Clinical Entity ◽  
Rare Clinical Entity

scholarly journals Chronic Atypical Depression as an Early Feature of Pituitary Adenoma: A Case Report and Literature Review

2019 ◽  
Vol 2019 ◽  
pp. 1-10
Author(s):  
Filipa Cardoso ◽  
Heela Azizi ◽  
Alexander Kilpatrick ◽  
Olaniyi Olayinka ◽  
Tasmia Khan ◽  
...  
Keyword(s):  
African American ◽  
Case Report ◽  
Pituitary Adenoma ◽  
Early Diagnosis ◽  
Literature Review ◽  
Incidental Findings ◽  
Incidental Finding ◽  
African American Female ◽  
Atypical Depression ◽  
Mood Symptoms

Pituitary adenomas are often diagnosed as incidental findings on brain imaging. We present the case of a 52-year-old African American female patient with long standing depressed mood prior to the incidental finding of a pituitary adenoma. We explore the possibility of certain mood symptoms prompting an early diagnosis of pituitary adenoma.

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.

scholarly journals A Giant Cell Fibroma and Focal Fibrous Hyperplasia in a Young Child: A Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Rodney J. Vergotine
Keyword(s):  
African American ◽  
Case Report ◽  
Young Child ◽  
Giant Cell ◽  
Clinical Impact ◽  
The Other ◽  
African American Female ◽  
Distinct Entity ◽  
Anterior Maxilla ◽  
Attached Gingiva

A case of two fibrotic lesions of the oral mucosa in a 17-month-old African-American female is reported. Both lesions occurred on the anterior maxilla, one lesion pedunculated on the buccal attached gingiva and the other lesion sessile on the palate. Histological examination characterized the buccal lesion as focal fibrous hyperplasia (FFH) and the palatal lesion as a giant cell fibroma (GCF). A case is made for continuing the consideration of GCF as a histologically distinct entity from FFH but that no difference in clinical impact between the two lesions exists.

Metastasis of the right colon mucinous adenocarcinoma to aortocaval and retropancreatic space: case report and literature review

2021 ◽  
pp. 95
Author(s):  
A.L. Bedzhanyan ◽  
M.I. Bredikhin ◽  
T.N. Galyan ◽  
D.E. Arutyunyants ◽  
K.N. Petrenko ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Mucinous Adenocarcinoma ◽  
Right Colon ◽  
Space Case ◽  
The Right

scholarly journals Primary Mucinous Adenocarcinoma of the Thymus: A Case Report and Literature Review

2017 ◽  
Vol 32 (3) ◽  
pp. 201-203
Author(s):  
Yin-gai Yin ◽  
Yin-gai Yin ◽  
Hai-zhen Lu ◽  
Hai-zhen Lu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Mucinous Adenocarcinoma
Sign in / Sign up

Export Citation Format

Share Document