Flat Non-pigmented Lesions on the Face

2020 ◽  
pp. 35-37
Author(s):  
Danica Tiodorovic ◽  
Enzo Errichetti ◽  
Aimilios Lallas
Keyword(s):  
2020 ◽  
pp. 43-52
Author(s):  
Ahmed Sadek ◽  
André Oliveira ◽  
Gabriel Salerni ◽  
María Belén Marín ◽  
Rodrigo Schwartz ◽  
...  
Keyword(s):  

2020 ◽  
pp. 31-34
Author(s):  
Raimonds Karls ◽  
Emilia N. Cohen Sabban ◽  
Horacio Cabo
Keyword(s):  

Author(s):  
M. Kostaki ◽  
A. Stathopoulou ◽  
M. Plaka ◽  
A. Zaras ◽  
E. Chatzidimitriou ◽  
...  

Author(s):  
Aimilios Lallas ◽  
Chryssoula Papageorgiou ◽  
Elvira Moscarella
Keyword(s):  

2002 ◽  
Vol 19 (3) ◽  
pp. 177-181
Author(s):  
Victor A. Neel ◽  
Natalie Nyugen ◽  
Julie Iwasaki ◽  
Ronald L. Moy

Introduction: Facial dyschromias, particularly in Asian skin, represent a challenge to cosmetic surgeons. Intense pulsed light (IPL) has been reported to clear a number of pigmentary alterations, but we have found the results variable and the efficacy of treatment difficult to predict. Objective: To use epiluminescent microscopy (ELM) to predict the clearing of clinically pigmented lesions in Asian patients undergoing “fotofacials” with IPL. Methods: Clinically similar pigmented lesions on the face were photographed with standard techniques and with ELM before, during, and after multiple IPL treatments in 5 patients. Patients and physicians were asked to grade cosmetic improvement after 5 sequential treatments. ELM photographs were then evaluated after treatment to correlate clinical success with the type of lesion. Results: ELM was able to discriminate among several clinically similar lesions. Lentigines responded to IPL treatments, whereas macular seborrheic keratoses, melasma, and junctional nevi responded poorly. Conclusion: Careful evaluation of pigmented lesions in Asian skin before IPL treatment can predict the efficacy of treatment.


Author(s):  
Horacio Cabo ◽  
Aimilios Lallas ◽  
Wilhem Stolz ◽  
Zoe Apalla ◽  
Michael Kunz ◽  
...  
Keyword(s):  

2019 ◽  
Vol 2019 (6) ◽  
Author(s):  
Mhmmad Nassif ◽  
Bardisan Gawrieh ◽  
Aras Abdo ◽  
Zuheir Alshehabi ◽  
Wajih Ali

AbstractPeutz–Jeghers syndrome (PJS) is an unusual hamartomatous polyposis of the gastrointestinal tract associated with melanocytic mucocutaneous hyperpigmentation. This research paper examines the case of an 18-month-old Syrian female who had been diagnosed with intussusception. The patient underwent laparotomy, and multiple small bowel polyps were found to act as the lead point. For this reason, small bowel resection (~15 cm), with end-to-end anastomosis, were performed. Although PJS diagnosis was histopathologically confirmed, the patient had no pigmented lesions on the face, the lower lip or the buccal mucosa and neither had any history of hospitalization or family history of the disease. This case was examined and is reported in the present study because PJS is rarely present at this early age when significant medical history is lacking.


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