scholarly journals Acquired digital fibrokeratoma: a rare case study

The Foot ◽  
2020 ◽  
Vol 44 ◽  
pp. 101681
Author(s):  
Michael Judah McCann ◽  
John Bonvillian ◽  
Cody Douglas Blazek
Keyword(s):  
Thorax ◽  
2016 ◽  
Vol 72 (7) ◽  
pp. 673-674
Author(s):  
Yasuhito Suzuki ◽  
Junpei Saito ◽  
Ryuichi Togawa ◽  
Hiroyuki Minemura ◽  
Mitsuru Munakata

2018 ◽  
Vol 24 (1) ◽  
pp. 29-32
Author(s):  
Arthur Fourcade ◽  
Benjamin Salmon ◽  
François Le Pelletier ◽  
Anne-Laure Ejeil

Introduction: Osteoma is a benign slow-growing osteogenic neoplasm characterized by the proliferation of cancellous and/or cortical bone. Jaw bones are seldom affected. Observation: We observed a rare case of a patient with a peripheral mandibular osteoma, which was surgically removed. Comments: Frequently asymptomatic, a peripheral osteoma looks like a bony swelling that may be sessile or pedunculated. Imaging examinations show a well-circumscribed radio-opaque mass. Symptomatic osteomas must be surgically excised and submitted for histological evaluation. Conclusion: Excessive osseous healing following a tooth extraction may explain this rare form of osteoma.


2014 ◽  
Vol 16 (5) ◽  
pp. 523-530
Author(s):  
Nitesh Gahlot ◽  
Uttam Saini ◽  
Shivprakash SS ◽  
Sameer Aggarwal

2019 ◽  
pp. 244-318
Author(s):  
Fredrik Hagen

The chapter surveys the evidence for ancient Egyptian libraries during the period 1600–800 BCE. It looks at both private and institutional libraries, defined as collections of papyri with literary texts, with a notable focus on archaeological context, and the use and materiality of manuscripts. Given the paucity of archaeological remains of temple and palace libraries, many indirect sources play a key role in the analysis, including book labels, administrative titles, and patterns of transmission for literary texts. Private libraries are better attested, and here the main groups are described with a particular focus on their importance for reconstructing the circulation and reception of literature. Finally, the chapter includes a rare case study where an historical individual and his family can be identified as the owners of a private library.


Author(s):  
I. Atallah ◽  
J. Gervasoni ◽  
E. Gay ◽  
C.A. Righini
Keyword(s):  

2017 ◽  
Vol 7 (2) ◽  
pp. 183-184
Author(s):  
Subhajeet Dey ◽  
Malwinder Singh ◽  
Ankit Kaura ◽  
Gaurav Diwakar

ABSTRACT Agenesis of dorsal pancreas (ADP) is an extremely rare congenital anomaly that results from defective development of pancreas. Most ADP patients are asymptomatic; if symptomatic, they present with epigastric pain. About half of affected individuals develop diabetes mellitus (DM), resulting from reduced islet cell mass secondary to the absence of endocrine structures. Being very rare, it is generally not kept in mind while dealing these cases and are not suspected until imaging investigations are not done. In our case study, ADP was diagnosed during evaluation of the patient for recurrent pain abdomen and generalized weakness. How to cite this article Jain A, Singh M, Dey S, Kaura A, Diwakar G. A Rare Case of Complete Agenesis of Dorsal Pancreas. Euroasian J Hepato-Gastroenterol 2017;7(2):183-184.


2003 ◽  
Vol 42 (3) ◽  
pp. 486 ◽  
Author(s):  
Kenneth Sassen
Keyword(s):  

2016 ◽  
Vol 27 ◽  
pp. 147-151 ◽  
Author(s):  
Natalie Swergold ◽  
Steven Kozusko ◽  
Carlos Rivera ◽  
Cindy Sturt

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