scholarly journals Primary Palpebral Tuberculosis: A Case Report

2021 ◽  
Vol 3 (1) ◽  
pp. 44-45
Author(s):  
Ayoub Redouan ◽  
Hind Hamdani ◽  
Loubna El Maaloum ◽  
Bouchra Allali ◽  
Asmae El Kettani ◽  
...  

Tuberculosis is a frequent disease in Morocco, palpebral localization remains very rare, often poorly managed because of its polymorphism. We report the case of a 6-year-old patient, without any notable antecedents, who presented repeated chalazions. Following frequent recurrences, despite surgical management, the patient benefited from an exeresis biopsy which confirmed the tuberculosis infection. A general check-up was performed to look for secondary localizations of tuberculosis, specifically a pulmonary localization, which was negative. The patient presented a good response to antibacillary treatment. In the light of this clinical case, we recall the importance of an anatomopathological study, which must be systematic before any excision of tissue material in the treatment of a chalazion with atypical localization or notion of recurrence.

2014 ◽  
Vol 4 (1) ◽  
pp. 31-37 ◽  
Author(s):  
Erich C. Schmidt ◽  
Dimitrios E. V. Papadimitriou ◽  
Jack G. Caton

2014 ◽  
Vol 45 (S 01) ◽  
Author(s):  
L. Voges ◽  
G. Stettner ◽  
D. Weise ◽  
K. Brockmann ◽  
J. Gärtner ◽  
...  

2008 ◽  
Vol 4 (1) ◽  
Author(s):  
MR Hoque ◽  
MA Hossain ◽  
Z Rahman ◽  
SMG Saklayen

2018 ◽  
Author(s):  
Tatiana Tarasova ◽  
Alexander Lutsenko ◽  
Elena Przhiyalkovskaya ◽  
Ekaterina Pigarova ◽  
Larisa Dzeranova ◽  
...  
Keyword(s):  

2012 ◽  
Vol 2 (5) ◽  
pp. 415-417
Author(s):  
Dr. Bansi M Bhusari ◽  
◽  
Dr. Shruti Sura ◽  
Dr. Kalpan Desai ◽  
Dr. Ridhima Mahajan
Keyword(s):  

Author(s):  
И.А. Синельникова ◽  
И.В. Сопрунова ◽  
О.П. Николаева

В статье представлено описание семейного случая миотонической дистрофии Россолимо-Штейнерта-Куршмана-Баттена. Диагноз подтвержден в результате ДНК-диагностики: выявлено увеличенное число копий CTG-повтора гена DMPK, ответственного за развитие миотонической дистрофии. A family case report of Rossolimo-Steinert-Curschmann myotonic dystrophy is presented. An increased number of copies of CTG-repeats of the DMPK gene responsible for the development of MD, i.e., the diagnosis was confirmed by molecular genetic method.


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