Back to Search Start Over

Case of cutaneous botryomycosis in an 8‐year‐old immunocompetent boy with a review of the published work

Authors :
Daisuke Yuki
Hiroki Fujikawa
Haruna Shimagaki
Naoya Shimizu
Akihiko Yuki
Kiyoto Kimura
Riichiro Abe
Source :
The Journal of Dermatology. 47:542-545
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

Botryomycosis is a rare chronic suppurative granulomatous infection caused by several genera of non-filamentous bacteria. The clinical and histopathological findings are similar to those of mycetoma caused by true fungi or aerobic actinomycetes. Botryomycosis is divided into cutaneous and visceral disease, with the cutaneous form being more common. Histopathology shows granules of etiologic bacteria called "sulfur granules". Botryomycosis occurs more commonly among immunocompromised patients, although some cases have also been reported in immunocompetent patients. We report the case of an 8-year-old immunocompetent boy who visited our hospital with a 4-mm diameter subcutaneous tumor with mild tenderness on his right heel for several months. We surgically removed the tumor with an initial diagnosis of epidermal cyst. Histopathology showed sulfur granules surrounded by an eosinophilic matrix, indicating the Splendore-Hoeppli phenomenon. The granules consisted of Gram-positive cocci, leading to a diagnosis of botryomycosis. The patient was successfully treated by excision and oral trimethoprim/sulfamethoxazole (240 mg b.i.d.) for 2 weeks as adjuvant therapy. No recurrence was noted following treatment. The subcutaneous tumor in this case was smaller than the typical in botryomycosis infections. We reviewed the infection duration and tumor size in reported cases of botryomycosis in immunocompetent patients. Small tumor size may suggest that the case is in an early stage; therefore, it is important to remove and investigate these lesions proactively.

Details

ISSN :
13468138 and 03852407
Volume :
47
Database :
OpenAIRE
Journal :
The Journal of Dermatology
Accession number :
edsair.doi.dedup.....0d1206ac02164f5d1f3e0339ec3b85d9
Full Text :
https://doi.org/10.1111/1346-8138.15308