Kikuchi-Fujimoto disease triggered by Salmonella enteritidis in a child with concurrent auto-immune thyroiditis and papilloedema.
Esma Altinel AçoğluEyup SariGürses ŞahinMelahat Melek OguzMeltem AkçaboyPelin ZorluSaliha SenelPublished in: Paediatrics and international child health (2018)
Kikuchi-Fujimoto disease (KFD) is a histiocytic necrotising lymphadenitis characterised by painful cervical lymphadenopathy, fever, malaise and weight loss. Infections, auto-immune pathogenesis and a genetic association have been implicated. A 12-year-old boy presented with a 1-month history of fever, abdominal pain, constipation and weight loss, and a painful lymph node was detected in the right axilla. Chest CT demonstrated multiple lymph nodes, especially in the left mediastinum. Salmonella enteritidis group D was detected in a blood culture and he was treated with ceftriaxone, followed by meropenem. An axillary lymph node biopsy demonstrated necrotising histiocytic lymphadenitis and KFD was diagnosed. He was discharged 35 days after admission. He was re-admitted 3 weeks later with recurrence of symptoms and headache and was found to have papilloedema of the left eye and auto-immune thyroiditis. Intravenous immunoglobulin (IVIG) 400 mg/kg/day was administered for 5 days. The fever and papilloedema slowly resolved and, subsequently, the thyroiditis, and he has remained well on follow-up. This is the first report of an association of S. enteritidis infection and papilloedema with KFD. IVIG may be required in prolonged or recurrent cases and in those with an auto-immune association.
Keyphrases
- lymph node
- weight loss
- sentinel lymph node
- neoadjuvant chemotherapy
- abdominal pain
- escherichia coli
- bariatric surgery
- emergency department
- roux en y gastric bypass
- early stage
- gastric bypass
- high dose
- computed tomography
- type diabetes
- squamous cell carcinoma
- low dose
- gene expression
- depressive symptoms
- rectal cancer
- body mass index
- listeria monocytogenes
- magnetic resonance
- skeletal muscle