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JCR 2016
جستجوی مقالات
سه شنبه 25 آذر 1404
Middle East Journal of Digestive Diseases
، جلد ۱۵، شماره ۲، صفحات ۱۴۱-۱۴۳
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
A Case Report of Hereditary Palmoplantar Keratoderma with Esophageal Melanosis
چکیده انگلیسی مقاله
A 70-year-old man, a known case of diabetes mellitus since 10 years ago, presented with lower limb swelling and dyspnea on exertion for one month and dysphagia to solids associated with early satiety for 2 weeks. The patient had palmoplantar keratosis (PPK), which was present since birth with a similar family history. The patient was admitted to rule out esophageal malignancy. Upper gastrointestinal (UGI) gastroscopy revealed esophagitis and esophageal melanosis with gastric mucosal erythema. Biopsies samples were taken. Histopathological examination revealed reflux esophagitis and chronic active helicobacter pylori (H. pylori) gastritis with no evidence of malignancy. His symptoms improved following H. pylori eradication and treatment for coronary artery disease and heart failure. The patient was advised of regular follow-up as he had risk factors for the development of esophageal melanoma or squamous cell carcinoma.
کلیدواژههای انگلیسی مقاله
Palmoplantar keratosis, Esophageal melanosis, Carcinoma
نویسندگان مقاله
| Delvina Vincent Comraj
Department of General Medicine, Sri Ramachandra Medical College and Research, Institue, Chennai, India
| Ayisha Zainab
Department of General Medicine, Sri Ramachandra Medical College and Research, Institue, Chennai, India
| Manisha Arthur
Department of General Medicine, Sri Ramachandra Medical College and Research, Institue, Chennai, India
| Jaba Chauhan
Department of General Medicine, Sri Ramachandra Medical College and Research, Institue, Chennai, India
| Viswanathan Pandurangan
Department of General Medicine, Sri Ramachandra Medical College and Research, Institue, Chennai, India
| Devasena Srinivasan
نشانی اینترنتی
http://mejdd.org/index.php/mejdd/article/view/2831
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زبان مقاله منتشر شده
en
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نوع مقاله منتشر شده
Case Report
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