Kawasaki Disease with an Initial Manifestation Mimicking Bacterial Inguinal Cellulitis

Joint Authors

Yamamoto, Hiroko
Tanaka, Tsukasa
Shimizu, Masaki
Tokuda, Oshi
Matsunoshita, Natsuki
Takenaka, Kanae
Kawasaki, Keiichiro

Source

Case Reports in Pediatrics

Issue

Vol. 2020, Issue 2020 (31 Dec. 2020), pp.1-6, 6 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2020-10-28

Country of Publication

Egypt

No. of Pages

6

Main Subjects

Medicine

Abstract EN

Background.

Kawasaki disease (KD) is typically characterized by fever, oral cavity erythematous changes, bilateral bulbar conjunctival injection, skin rash, erythema and edema of the hands and feet, and cervical lymphadenopathy.

Some atypical patients with KD initially develop cervical and pharyngeal cellulitis; however, an initial presentation with inguinal cellulitis is extremely rare.

In addition, to our knowledge, no report has documented the cytokine profile in a KD patient with cellulitis.

Case presentation.

A previously healthy 8-year-old Japanese girl was hospitalized following a 2-day history of fever and a 5-day history of pain and erythema in the left inguinal region.

She was diagnosed with bacterial inguinal cellulitis and was administered antibiotics.

The next day, a polymorphous rash emerged on her trunk.

After 3 days of antibiotics, however, her fever continued and the cellulitis had spread over the entire lower abdomen.

Simultaneously, the bilateral bulbar conjunctival injection without exudate became more prominent and her lips became erythematous.

In addition, erythematous changes on her palms appeared a few hours later, which led to the diagnosis of KD.

Since she had a high risk score that predicted no response to initial intravenous immunoglobulin (IVIG) at the initiation of treatment, she was treated with IVIG, intravenous prednisolone (PSL), and oral aspirin.

The KD symptoms improved the next day, but the cellulitis did not completely resolve until 2 months after discharge.

The patient’s serum cytokine profile at admission had an IL-6 dominant pattern which was consistent with that of patients with KD despite her initial lack of KD symptoms, and the pattern observed at admission was sustained until IVIG and PSL administration.

Conclusion.

KD should be included in the differential diagnosis for patients presenting with inguinal cellulitis who are unresponsive to initial empiric antibiotics.

American Psychological Association (APA)

Tanaka, Tsukasa& Shimizu, Masaki& Tokuda, Oshi& Yamamoto, Hiroko& Matsunoshita, Natsuki& Takenaka, Kanae…[et al.]. 2020. Kawasaki Disease with an Initial Manifestation Mimicking Bacterial Inguinal Cellulitis. Case Reports in Pediatrics،Vol. 2020, no. 2020, pp.1-6.
https://search.emarefa.net/detail/BIM-1150836

Modern Language Association (MLA)

Tanaka, Tsukasa…[et al.]. Kawasaki Disease with an Initial Manifestation Mimicking Bacterial Inguinal Cellulitis. Case Reports in Pediatrics No. 2020 (2020), pp.1-6.
https://search.emarefa.net/detail/BIM-1150836

American Medical Association (AMA)

Tanaka, Tsukasa& Shimizu, Masaki& Tokuda, Oshi& Yamamoto, Hiroko& Matsunoshita, Natsuki& Takenaka, Kanae…[et al.]. Kawasaki Disease with an Initial Manifestation Mimicking Bacterial Inguinal Cellulitis. Case Reports in Pediatrics. 2020. Vol. 2020, no. 2020, pp.1-6.
https://search.emarefa.net/detail/BIM-1150836

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1150836