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Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report.
Racette, Samuel D; Alexiev, Borislav A; Angarone, Michael P; Bhasin, Ajay; Lima, Kaitlin; Jennings, Lawrence J; Balasubramanian, Senthil; Matsuoka, Akihiro J.
  • Racette SD; Department of Otolaryngology-Head and Neck Surgery, Feinberg School of Medicine, Northwestern University, 676 N. St. Clair Street, Suite 1325, Chicago, IL, 60611, USA. samuel.racette@northwestern.edu.
  • Alexiev BA; Department of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Angarone MP; Department of Medicine, Division of Infectious Diseases, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Bhasin A; Department of Medicine, Division of Hospital Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Lima K; Department of Pediatrics, Division of Hospital Based Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Jennings LJ; Department of Medicine, Division of Rheumatology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Balasubramanian S; Department of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Matsuoka AJ; NorthShore University Health System, Evanston, IL, 60201, USA.
BMC Infect Dis ; 21(1): 740, 2021 Aug 03.
Article in English | MEDLINE | ID: covidwho-1455924
ABSTRACT

BACKGROUND:

We present a yet to be described association of SARS-CoV-2 infection with Kikuchi-Fujimoto disease. CASE PRESENTATION A 32-year-old physician with history of SARS-CoV-2 infection presented to the emergency department with 2 weeks of fever, chills, and right sided cervical lymphadenopathy. He was treated empirically for presumed folliculitis with worsening of symptoms leading to repeat presentation to the emergency department. Extensive workup was unrevealing of an infectious cause and needle biopsy of the lesion was unrevealing. An excisional lymph node biopsy revealed follicular hyperplasia with necrotic foci showing abundance of histiocytes at the edge of necrosis with CD8 predominance of T-cells. Final diagnosis was deemed to be Kikuchi-Fujimoto disease. Antibiotic therapy was discontinued, and the patient's symptoms resolved with steroid therapy and expectant management.

CONCLUSIONS:

This is the first report of a patient developing Kikuchi-Fujimoto disease following SARS-CoV-2 infection. Clinicians should be aware of Kikuchi-Fujimoto disease as a possibility when approaching patients with hyper-inflammatory states who present with cervical lymphadenopathy.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Histiocytic Necrotizing Lymphadenitis / Lymphadenopathy / COVID-19 Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid Limits: Adult / Humans / Male Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: S12879-021-06048-0

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Histiocytic Necrotizing Lymphadenitis / Lymphadenopathy / COVID-19 Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid Limits: Adult / Humans / Male Language: English Journal: BMC Infect Dis Journal subject: Communicable Diseases Year: 2021 Document Type: Article Affiliation country: S12879-021-06048-0