A Child with Kimura’s Disease Had Multiple Lymph Nodes Enlargement as the Initial Sign: A Case Report and Literature Review

2020 ◽  
Vol 10 (06) ◽  
pp. 1039-1044
Author(s):  
天文 全
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymph Nodes ◽  
Kimura’S Disease ◽  
Initial Sign

scholarly journals Eosinophilic vasculitis affecting multiple middle-sized arteries in a patient with Kimura's disease: A case report and literature review

2018 ◽  
Vol 67 ◽  
pp. S45-S47 ◽  
Author(s):  
Hiroki Furuya ◽  
Kei Ikeda ◽  
Junya Suzuki ◽  
Kazumasa Suzuki ◽  
Kaito Nakamura ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Kimura’S Disease

scholarly journals Cutaneous and Inguinal Lymph Nodes Metastases Disseminated from an Endometrial Serous Carcinoma - Case Report and Literature Review

Chirurgia ◽  
2021 ◽  
Vol 116 (1) ◽  
pp. 109
Author(s):  
Laura Rebegea ◽  
Ana-Maria Ilie ◽  
Anca Neagu ◽  
Dorel Firescu ◽  
Georgiana Bianca Constantin ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymph Nodes ◽  
Serous Carcinoma ◽  
Inguinal Lymph Nodes ◽  
Lymph Nodes Metastases

scholarly journals Kimura's Disease: A Case Report

2000 ◽  
Vol 79 (3) ◽  
pp. 195-199 ◽  
Author(s):  
Sebastian J. Karavattathayyil ◽  
John R. Krause
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Lymph Nodes ◽  
Head And Neck ◽  
Salivary Glands ◽  
Immunoglobulin E ◽  
Elevated Serum ◽  
Neck Region ◽  
Kimura’S Disease ◽  
Head And Neck Region

Kimura's disease is a rare, idiopathic condition that usually affects young men of Asian descent. The disease is characterized by swelling and lesions in the head and neck region, with involvement of the subcutaneous soft tissue, major salivary glands, and lymph nodes. Patients almost always have eosinophilia and elevated serum immunoglobulin E levels. The diagnosis is established by biopsy. Kimura's disease is usually self-limiting. Its etiology is unknown but is thought to be a manifestation of an aberrant allergic response. In this paper, we describe the case of a 30-year-old patient who was diagnosed with Kimura's disease at our institution.

scholarly journals Eosinophilic Lung Disease Complicated by Kimura's Disease: A Case Report and Literature Review

2012 ◽  
Vol 51 (22) ◽  
pp. 3163-3167 ◽  
Author(s):  
Hidefumi Koh ◽  
Nobufumi Kamiishi ◽  
Atsushi Chiyotani ◽  
Hidenori Takahashi ◽  
Akihiko Sudo ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lung Disease ◽  
Kimura’S Disease

scholarly journals Kimura’s disease affecting the axillary lymph nodes: a case report

BMC Surgery ◽  
2017 ◽  
Vol 17 (1) ◽  
Author(s):  
Kenji Kuroda ◽  
Shinichiro Kashiwagi ◽  
Hitoshi Teraoka ◽  
Haruhito Kinoshita ◽  
Mikio Nanbara ◽  
...  
Keyword(s):  
Case Report ◽  
Lymph Nodes ◽  
Axillary Lymph Nodes ◽  
Kimura’S Disease ◽  
Axillary Lymph

scholarly journals Kikuchi-Fujimoto disease in the regional lymph nodes with node metastasis in a patient with tongue cancer: A case report and literature review

2017 ◽  
Vol 14 (1) ◽  
pp. 257-263 ◽  
Author(s):  
Tessho Maruyama ◽  
Kazuhide Nishihara ◽  
Masanao Saio ◽  
Toshiyuki Nakasone ◽  
Fumikazu Nimura ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymph Nodes ◽  
Tongue Cancer ◽  
Regional Lymph Nodes ◽  
Node Metastasis

scholarly journals Multiple pilomatrixomas: Case report and literature review

2008 ◽  
Vol 87 (4) ◽  
pp. 230-233 ◽  
Author(s):  
Shashidhar Sadda Reddy ◽  
Swarupa A. Gadre ◽  
Patrick Adegboyega ◽  
Arun K. Gadre
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Lymph Nodes ◽  
Black Woman ◽  
Clinical Examination ◽  
Surgical Excision ◽  
Hair Matrix ◽  
The Masses ◽  
Epithelial Neoplasm

Pilomatrixoma is a rare, benign, circumscribed, calcifying epithelial neoplasm that is derived from hair matrix cells. Multiple pilomatrixomas are uncommon. We describe a case of multiple pilomatrixomas in a 23-year-old black woman who presented with lesions on her face and back. Based on the results of the clinical examination, she was provisionally diagnosed with either calcified sebaceous cysts or calcified lymph nodes. She underwent surgical excision of the masses. On histopathology, the lesions were identified as pilomatrixomas. We attribute our original failure to diagnose this condition to our lack of familiarity with it. We discuss the presentation, differential diagnosis, and other characteristics of pilomatrixomas.

scholarly journals Kikuchi-Fujimoto Disease: A Case Report and Literature Review

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Vikrant Veer ◽  
Albert Lim ◽  
Wolfgang Issing
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymph Nodes ◽  
Needle Aspiration ◽  
Excision Biopsy ◽  
Asian Countries ◽  
Histiocytic Necrotising Lymphadenitis ◽  
History Of ◽  
Reticular Cells ◽  
The Uk

Case. 38-year-old lady was referred to the ENT clinic with history of right-sided facial pain, otalgia, and odynophagia. Clinical examination revealed enlarged right-sided lymph nodes in the neck. Further radiological scans showed a mass near the carotid and enlarged level V lymph nodes. Lymphoma was initially suspected. Fine-needle aspiration and excision biopsy were undertaken. Histological analysis later suggested Kikuchi-Fujimoto disease, also known as histiocytic necrotising lymphadenitis.Literature Review. Kikuchi-Fujimoto disease (KFD) was described in 1972 as lymphadenitis with focal proliferation of reticular cells accompanied by numerous histiocytes and extensive nuclear debris. KFD, frequently found in East Asian countries, is rare in the UK. No definite aetiology of KFD is known despite autoimmune and infection factors being suggested. The diagnostic hallmark is histological findings from lymph nodes. Malignancy should be excluded. This condition is mainly self-limiting; hence, management is limited to supportive care. Steroid therapy could be used in severe cases. KFD is relatively unknown in the UK and this case report aims to highlight its occurrence in our population.

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