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Kikuchi-Fujimoto Disease: A Rare Presentation with Localized Iliac Lymphadenitis | ||
| Iranian Journal of Medical Sciences | ||
| مقاله 13، دوره 42، شماره 1، فروردین 2017، صفحه 94-97 اصل مقاله (1.27 M) | ||
| نوع مقاله: Case Report(s) | ||
| نویسندگان | ||
| Shrihari Anil Anikhindi1؛ Anil Arora1؛ Shashi Dhawan2؛ Naresh Bansal1؛ Praveen Sharma1؛ Vikas Singla1؛ Ashish Kumar* 1 | ||
| 1Department of Gastroenterology, Sir Ganga Ram Hospital, New Delhi | ||
| 2Department of Pathology, Sir Ganga Ram Hospital, New Delhi | ||
| چکیده | ||
| Kikuchi-Fujimoto disease (KFD) is a benign, self-limiting disease characterized by histiocytic necrotising lymphadenitis. Though several viral agents or an autoimmune etiology has been proposed as causative, the exact cause remains unknown. It has a female predilection and most commonly seen among young Asian people. Patients usually present with a febrile illness and the presence of lymphadenopathy may provide a clue to diagnosis. The most common site of lymphadenopathy is cervical lymph nodes while intra-abdominal involvement is uncommon. Cases of KFD presenting with intra-abdominal lymphadenopathy have been reported to occur with equal frequency in both sexes. Abdominal tuberculosis, non-Hodgkin’s lymphoma, and systemic lupus erythematosus are close differential diagnoses for this type of presentation. Treatment is mostly supportive as the disease usually resolves spontaneously; steroids are only required in severe cases. We report a 32-year-old male patient of intra-abdominal lymphadenitis that presented as fever of unknown origin (FUO) and diagnosed by excisional biopsy as a case of KFD. | ||
| کلیدواژهها | ||
| Histiocytic necrotising lymphadenitis؛ Fever of unknown origin؛ Abdomen | ||
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آمار تعداد مشاهده مقاله: 3,038 تعداد دریافت فایل اصل مقاله: 1,381 |
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