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DOI 10.1136/bcr-2014-205470

Медицинская библиотека · BMJ case reports · 2014

Kikuchi-Fujimoto disease: a rare but important differential diagnosis for lymphadenopathy.

Srikantharajah Mukunthan, Mahendra Prem, Vydianath Bindu, Lowe Gillian C

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Аннотация

A 23-year-old man presented with a 6-week history of fevers, cervical lymphadenopathy and fatigue. A CT of the neck, chest, abdomen and pelvis showed left cervical lymphadenopathy, enlarged lymph nodes in the axilla and groin and hepatomegaly. A left cervical excisional lymph node biopsy was undertaken and the histopathological findings were consistent with Kikuchi-Fujimoto disease. He was treated with high-dose prednisolone for 1 week, which was then tapered. Generalised arthralgia and daily episodes of malaise were experienced for a subsequent 2 months following the cessation of corticosteroids. The condition lasted 4 months from the onset of symptoms. This case report highlights the importance of including Kikuchi-Fujimoto disease as a differential diagnosis for lymphadenopathy. Kikuchi-Fujimoto disease has commonly been mistaken for tuberculosis and lymphoma, and unnecessary exposure to agents used to treat these conditions can be avoided by prompt histological diagnosis.

Для цитирования: Srikantharajah Mukunthan, Mahendra Prem, Vydianath Bindu, Lowe Gillian C. Kikuchi-Fujimoto disease: a rare but important differential diagnosis for lymphadenopathy.. BMJ case reports. 2014. DOI: 10.1136/bcr-2014-205470.

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