نتایج جستجو برای: histiocytic necrotizing lymphadenitis

تعداد نتایج: 15091  

Journal: :Revista medica de Chile 2013
Xiaojing Zhang Jianlan Xie Bing Yue Xiaoge Zhou

Histiocytic necrotizing lymphadenitis (also known as Kikuchi-Fujimoto's disease) is an uncommon, benign and self-limiting lymph disease. We report three patients aged 14, 22 and 50 years, who presented with fever and cervical lymphadenopathy, accompanied by skin lesions and joint pain in two of the three cases. One of the patient's sister suffered from histiocytic necrotizing lymphadenitis. Lab...

Journal: :Revista do Instituto de Medicina Tropical de São Paulo 2002

Journal: :JPMA. The Journal of the Pakistan Medical Association 1991
M Ahmad A H Khan J Iqbal

Seven cases of Histiocytic necrotizing Lymphadenitis (HNL) were studied. They constituted 0.56% of all lymph nodes biopsies. The condition primarily affects young women causing cervical lymph node enlargement and leukopenia. The basic lesion is characterized by proliferation of lymphocytes and histiocytes with nuclear debris in the para cortex and cortex. This study examined various bacterial, ...

2015
Şebnem İzmir Güner Didem Karacetin Ekrem Güner Mahmut Yüksel

Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a self-limiting, benign, and rare systemic lymphadenitis with unknown etiology. The cardinal symptoms are fever, lymphadenopathy and night sweat; consequently, it is first necessary to rule out infectious, lymphoproliferative, and connective tissue diseases such as systemic lupus erythematous. Histology can ...

Journal: :Acta otorrinolaringologica espanola 1996
P J Morillas Blasco M A González Martínez E Ferrandis Perepérez E Serrano Badía F Guallart Doménech R Ferrer Jiménez

Kikuchi-Fujimoto's disease (histiocytic necrotizing lymphadenitis) is a benign, self-limited disease of unknown cause that often presents with persistently enlarged cervical lymph nodes that are unresponsive to antibiotic therapy. The disease should be considered in the differential diagnosis of cervical lymphadenopaty: viral infection, tuberculosis, hyperplastic lymphadenopathy, and metastatic...

Journal: :Indian Journal of Case Reports 2023

Kikuchi–Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare and generally self-limiting of uncertain etiology that presents with fever cervical lymphadenopathy in both the pediatric adult populations. Here, we present case 5-year-old male who presented acute onset which was initially diagnosed managed staphylococcal lymphadenitis. He underwent an excisional bi...

Journal: :Revista do Instituto de Medicina Tropical de Sao Paulo 2002
José Vassallo João Carlos Coelho Filho Vânia Gondin Pires do Amaral

Histiocytic necrotizing lymphadenitis, or Kikuchi's lymphadenitis (KL), is an unusual form of lymphadenitis, generally with self-limited clinical course. KL has been reported in rare patients infected with the human immunodeficiency virus (HIV). Pathogenesis of the lesion is probably related to an impaired immune function. The purpose of the present article is to report on one case in which KL ...

Journal: : 2022

Kikuchi–Fujimoto disease, or necrotizing histiocytic lymphadenitis, is one of the rare causes benign lymphadeno-pathy. The diagnosis based on histological and immunohistochemical analysis lymph node biopsy. article presents four clinical cases disease. According to results primary tissue three patients were misdiagnosed with lymphoma. due unusual for lymphoid malignancy course material was revi...

Journal: :Rheumatology international 2001
Ghazala Mehdi Veena Maheshwari Priti Sood Hasan Haris

The etiology of cervical lymphadenopathy is multifactorial including infections and tumoral lesions. Histiocytic necrotising lymphadenitis or Kikuchi-Fujimoto's disease is a rare cause of cervical lymphadenopathy which does not have specific clinical signs. We report herewith a case of Kikuchi's disease (KD) diagnosed by histopathology.

Journal: :Journal of clinical pathology 2000
R W Blewitt S N Kumar J S Abraham

A 40 year old woman developed recurrent Kikuchi's disease 12 years after the original episode. The recurrence affected the same site (axilla) and occurred after the longest delay so far recorded in a European resident. Care must be taken to avoid misdiagnosis of Kikuchi's disease as lymphoma.

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